U.S. patent application number 10/419008 was filed with the patent office on 2004-02-05 for methods for treating an autoimmune disease using a soluble ctla4 molecule and a dmard or nsaid.
Invention is credited to Becker, Jean-Claude, Carr, Suzette, Cohen, Robert, Hagerty, David, Peach, Robert J..
Application Number | 20040022787 10/419008 |
Document ID | / |
Family ID | 46299178 |
Filed Date | 2004-02-05 |
United States Patent
Application |
20040022787 |
Kind Code |
A1 |
Cohen, Robert ; et
al. |
February 5, 2004 |
Methods for treating an autoimmune disease using a soluble CTLA4
molecule and a DMARD or NSAID
Abstract
The present invention relates to compositions and methods for
treating immune system diseases such as rheumatic disease, by
administering to a subject soluble CTLA4 molecules that block
endogenous B7 molecules from binding their ligands, alone, or in
conjunction with other agents including Disease Modifying
Anti-Rheumatic Drugs (DMARDs).
Inventors: |
Cohen, Robert; (Newtown,
PA) ; Carr, Suzette; (Hopewell, NJ) ; Hagerty,
David; (Pennington, NJ) ; Peach, Robert J.;
(San Diego, CA) ; Becker, Jean-Claude; (Princeton,
NJ) |
Correspondence
Address: |
STEPHEN B. DAVIS
BRISTOL-MYERS SQUIBB COMPANY
PATENT DEPARTMENT
P O BOX 4000
PRINCETON
NJ
08543-4000
US
|
Family ID: |
46299178 |
Appl. No.: |
10/419008 |
Filed: |
April 18, 2003 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10419008 |
Apr 18, 2003 |
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09898195 |
Jul 2, 2001 |
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60215913 |
Jul 3, 2000 |
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Current U.S.
Class: |
424/144.1 ;
424/649; 424/85.1; 514/109; 514/12.2; 514/16.6; 514/165; 514/17.9;
514/171; 514/251; 514/263.31; 514/282; 514/313; 514/406;
514/570 |
Current CPC
Class: |
C07K 14/70521 20130101;
A61K 39/395 20130101; A61K 39/0008 20130101; A61K 47/6811 20170801;
C07K 2319/00 20130101; A61P 19/02 20180101; A61P 19/00 20180101;
A61P 3/10 20180101; A61K 38/00 20130101; A61K 38/1774 20130101 |
Class at
Publication: |
424/144.1 ;
514/2; 514/165; 514/171; 424/85.1; 514/109; 514/263.31; 514/313;
514/570; 514/282; 514/406; 424/649; 514/251 |
International
Class: |
A61K 039/395; A61K
038/39; A61K 038/19; A61K 031/66; A61K 031/60; A61K 031/56; A61K
031/525; A61K 033/24; A61K 031/415; A61K 031/522 |
Claims
What is claimed:
1. A method for blocking B7 interactions with CTLA4 and/or CD28
comprising administering to a subject an effective amount of a
first agent and a second agent, wherein a) the first agent is a
soluble CTLA4 molecule, and b) the second agent is selected from a
group consisting of immunosuppressive agents, corticosteroids,
nonsteroidal antiinflammatory drugs, prednisone, azathioprine,
methotrexate, TNF.alpha.: blockers or antagonists, infliximab, any
biological agent targeting an inflammatory cytokine,
hydroxychloroquine, sulphasalazopryine, gold salts, etanercept,
anakinra, cyclophosphamide, leflunomide, collagen, dnaJ, a molecule
that blocks TNF receptors, pegsunercept, a molecule that blocks
cytokine function, AMG719, a molecule that blocks LFA-1 function,
efalizumab, acetyl salicylic acid, choline magnesium salicylate,
diflunisal, magnesium salicylate, salsalate, sodium salicylate,
diclofenac, etodolac, fenoprofen, flurbiprofen, indomethacin,
ketoprofen, ketorolac, meclofenamate, naproxen, nabumetone,
phenylbutazone, piroxicam, sulindac, tolmetin, acetaminophen,
ibuprofen, Cox-2 inhibitors, meloxicam, codeine phosphate,
propoxyphene napsylate, oxycodone hydrochloride, oxycodone
bitartrate and tramadol.
2. A method for treating an immune system disease comprising
administering to a subject an effective amount of a first agent and
a second agent, wherein a) the first agent is a soluble CTLA4
molecule, and b) the second agent is selected from a group
consisting of immunosuppressive agents, corticosteroids,
nonsteroidal antiinflammatory drugs, prednisone, azathioprine,
methotrexate, TNF.alpha. blockers or antagonists, infliximab, any
biological agent targeting an inflammatory cytokine,
hydroxychloroquine, sulphasalazopryine, gold salts, etanercept,
anakinra, cyclophosphamide, leflunomide, collagen, dnaJ, a molecule
that blocks TNF receptors, pegsunercept, a molecule that blocks
cytokine function, AMG719, a molecule that blocks LFA-1 function,
efalizumab, acetyl salicylic acid, choline magnesium salicylate,
diflunisal, magnesium salicylate, salsalate, sodium salicylate,
diclofenac, etodolac, fenoprofen, flurbiprofen, indomethacin,
ketoprofen, ketorolac, meclofenamate, naproxen, nabumetone,
phenylbutazone, piroxicam, sulindac, tolmetin, acetaminophen,
ibuprofen, Cox-2 inhibitors, meloxicam, codeine phosphate,
propoxyphene napsylate, oxycodone hydrochloride, oxycodone
bitartrate and tramadol.
3. The method of claim 1 or 2, wherein cytokine production is
regulated.
4. The method of claim 1 or 2, wherein ACR 20, 50 and/or 70
response rates are improved.
5. A method for blocking B7 interactions with CTLA4 and/or CD28
comprising administering to a subject an effective amount of a
soluble CTLA4 molecule, wherein the effective amount of soluble
CTLA4 is about 0.1 to 100 mg/kg weight of the subject, about 0.5 to
5 mg/kg weight of a subject, about 5 to 10 mg/kg weight of a
subject, about 10 to 15 mg/kg weight of a subject, about 15 to 20
mg/kg weight of a subject, about 20 to 25 mg/kg weight of a
subject, about 25 to 30 mg/kg weight of a subject, about 30 to 35
mg/kg weight of a subject, about 35 to 40 mg/kg weight of a
subject, about 40 to 45 mg/kg of a subject, about 45 to 50 mg/kg
weight of a subject, about 50 to 55 mg/kg weight of a subject,
about 55 to 60 mg/kg weight of a subject, about 60 to 65 mg/kg
weight of a subject, about 65 to 70 mg/kg weight of a subject,
about 70 to 75 mg/kg weight of a subject, about 75 to 80 mg/kg
weight of a subject, about 80 to 85 mg/kg weight of a subject,
about 85 to 90 mg/kg weight of a subject, about 90 to 95 mg/kg
weight of a subject, about 95 to 100 mg/kg weight of a subject,
about 2 to 10 mg/kg weight of a subject, about 0.1 to 4 mg/kg
weight of a subject, about 0.1 to 0.5 mg/kg weight of a subject,
about 0.5 to 1.0 mg/kg weight of a subject, about 1.0 to 1.5 mg/kg
weight of a subject, about 1.5 to 2.0 mg/kg weight of a subject,
about 2.0 to 2.5 mg/kg weight of a subject, about 2.5 to 3.0 mg/kg
weight of a subject, about 3.0 to 3.5 mg/kg weight of a subject,
about 3.5 to 4.0 mg/kg weight of a subject, about 4.0 to 4.5 mg/kg
weight of a subject, about 4.5 to 5.0 mg/kg weight of a subject,
about 5.0 to 5.5 mg/kg weight of a subject, about 5.5 to 6.0 mg/kg
weight of a subject, about 6.0 to 6.5 mg/kg weight of a subject,
about 6.5 to 7.0 mg/kg weight of a subject, about 7.0 to 7.5 mg/kg
weight of a subject, about 7.5 to 8.0 mg/kg weight of a subject,
about 8.0 to 8.5 mg/kg weight of a subject, about 8.5 to 9.0 mg/kg
weight of a subject, about 9.0 to 9.5 mg/kg weight of a subject,
about 9.5 to 10.0 mg/kg weight of a subject, about 0.1 to 2 mg/kg
weight of a subject, about 2 to 4 mg/kg weight of a subject, about
4 to 6 mg/kg weight of a subject, about 6 to 8 mg/kg weight of a
subject, about 8 to 10 mg/kg weight of a subject, about 10 to 12
mg/kg weight of a subject, about 12 to 14 mg/kg weight of a
subject, about 14 to 16 mg/kg weight of a subject, about 16 to 18
mg/kg weight of a subject, about 18 to 20 mg/kg weight of a
subject, about 0.5 mg/kg weight of the subject, 2 mg/kg weight of
the subject, 10 mg/kg weight of the subject, about 0.5 mg/kg to 100
weight of the subject, about 0.5 to 10 mg/kg weight of a subject,
about 0.1 to 20 mg/kg weight of a subject, about 500 mg for a
subject weighing less than 60 kg, 750 mg for a subject weighing
between 60-100 kg or 1000 mg for a subject weighing more than 100
kg).
6. A method for treating an immune system disease comprising
administering to a subject an effective amount of a soluble CTLA4
molecule, wherein the effective amount of soluble CTLA4 is about
0.1 to 100 mg/kg weight of the subject, about 0.5 to 5 mg/kg weight
of a subject, about 5 to 10 mg/kg weight of a subject, about 10 to
15 mg/kg weight of a subject, about 15 to 20 mg/kg weight of a
subject, about. 20 to 25 mg/kg weight of a subject, about 25 to 30
mg/kg weight of a subject, about 30 to 35 mg/kg weight of a
subject, about 35 to 40 mg/kg weight of a subject, about 40 to 45
mg/kg weight of a subject, about 45 to 50 mg/kg weight of a
subject, about 50 to 55 mg/kg weight of a subject, about 55 to 60
mg/kg weight of a subject, about 60 to 65 mg/kg weight of a
subject, about 65 to 70 mg/kg weight of a subject, about 70 to 75
mg/kg weight of a subject, about 75 to 80 mg/kg weight of a
subject, about 80 to 85 mg/kg weight of a subject, about 85 to 90
mg/kg weight of a subject, about 90 to 95 mg/kg weight of a
subject, about 95 to 100 mg/kg weight of a subject, about 2 to 10
mg/kg weight of a subject, about 0.1 to 4 mg/kg weight of a
subject, about 0.1 to 0.5 mg/kg weight of a subject, about 0.5 to
1.0 mg/kg weight of a subject, about 1.0 to 1.5 mg/kg weight of a
subject, about 1.5 to 2.0 mg/kg weight of a subject, about 2.0 to
2.5 mg/kg weight of a subject, about 2.5 to 3.0 mg/kg weight of a
subject, about 3.0 to 3.5 mg/kg weight of a subject, about 3.5 to
4.0 mg/kg weight of a subject, about 4.0 to 4.5 mg/kg weight of a
subject, about 4.5 to 5.0 mg/kg weight of a subject, about 5.0 to
5.5 mg/kg weight of a subject, about 5.5 to 6.0 mg/kg weight of a
subject, about 6.0 to 6.5 mg/kg weight of a subject, about 6.5 to
7.0 mg/kg weight of a subject, about 7.0 to 7.5 mg/kg weight of a
subject, about 7.5 to 8.0 mg/kg weight of a subject, about 8.0 to
8.5 mg/kg weight of a subject, about 8.5 to 9.0 mg/kg weight of a
subject, about 9.0 to 9.5 mg/kg weight of a subject, about 9.5 to
10.0 mg/kg weight of a subject, about 0.1 to 2 mg/kg weight of a
subject, about 2 to 4 mg/kg weight of a subject, about 4 to 6 mg/kg
weight of a subject, about 6 to 8 mg/kg weight of a subject, about
8 to 10 mg/kg weight of a subject, about 10 to 12 mg/kg weight of a
subject, about 12 to 14 mg/kg weight of a subject, about 14 to 16
mg/kg weight of a subject, about 16 to 18 mg/kg weight of a
subject, about 18 to 20 mg/kg weight of a subject, about 0.5 mg/kg
weight of the subject, 2 mg/kg weight of the subject, 10 mg/kg
weight of the subject, about 0.5 mg/kg to 100 weight of the
subject, about 0.5 to 10 mg/kg weight of a subject, about 0.1 to 20
mg/kg weight of a subject, about 500 mg for a subject weighing less
than 60 kg, 750 mg for a subject weighing between 60-100 kg or 1000
mg for a subject weighing more than 100 kg.
7. The method of claim 5 or 6, wherein cytokine production is
regulated.
8. The method of claim 5 or 6, wherein ACR 20, 50 and/or 70
response rates are improved.
9. The method of claim 1, 2, 5, or 6, wherein the soluble CTLA4
molecule comprises an extracellular domain of a CTLA4 molecule, or
portion thereof, which binds a B7 antigen expressed on activated B
cells.
10. The method of claim 9, wherein the extracellular domain of the
CTLA4 molecule comprises the amino acids shown in FIG. 23 (SEQ ID
NO: 17) beginning with methionine at position 1 and or with alanine
at position -1 and ending with aspartic acid at position 124.
11. The method of claim 1, 2, 5, or 6, wherein the soluble CTLA4
molecule is a CTLA4 fusion molecule.
12. The method of claim 11, wherein the CTLA4 fusion molecule
comprises an extracellular domain of a CTLA4 molecule which binds a
B7 antigen expressed on activated B cells joined to a non-CTLA4
molecule.
13. The method of 12, wherein the non-CTLA4 molecule comprises an
amino acid sequence which alters the solubility or affinity of the
soluble CTLA4 molecule.
14. The method of claim 13, wherein the amino acid sequence which
alters the solubility or affinity comprises an immunoglobulin
moiety.
15. The method of claim 14, wherein the immunoglubulin moiety
comprises one or more mutations to reduce effector function.
16. The method of claim 14, wherein the immunoglubulin moiety is an
immunoglubulin constant region or portion thereof.
17. The method of claim 15, wherein the immunoglubulin constant
region or portion thereof is mutated to reduce effector
function.
18. The method of claim 15, wherein the immunoglubulin constant
region comprises a hinge, CH2 and CH3 regions of an immunoglobulin
molecule.
19. The method of claim 15, wherein the immunoglubulin constant
region or portion thereof is a human or monkey immunoglobulin
constant region.
20. The method of claim 1, 2, 5, or 6, wherein the soluble CTLA4
further comprises an amino acid sequence which permits secretion of
the soluble CTLA4 molecule.
21. The method of claim 20, wherein the amino acid sequence which
permits secretion comprises an oncostatin M signal peptide.
22. The method of claim 11, wherein the CTLA4 fusion molecule is
CTLA4Ig.
23. The method of claim 22, wherein the CTLA4Ig is shown in FIG. 24
(SEQ ID NO:19) beginning with methionine at position +1 or with
alanine at position -1 and ending with lysine at position +357.
24. The method of claim 1, 2, 5, or 6, wherein the soluble CTLA4
molecule is a soluble CTLA4 mutant molecule.
25. The method of claim 24, wherein the soluble CTLA4 mutant
molecule binds a B7 antigen expressed on activated B cells and
comprises a mutation in the extracellular domain of a CTLA4
molecule.
26. The method of claim 24, wherein the soluble CTLA4 mutant
molecule comprises an extracellular domain of CTLA4, a) wherein the
extracellular domain of CTLA4 begins with methionine at position +1
or with alanine at position -1 and ends with aspartic acid at
position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or 19), and
b) wherein at position +104 of the extracellular domain of CTLA4,
leucine is substituted with any other amino acid.
27. The method of claim 24, wherein the soluble CTLA4 mutant
molecule comprises an extracellular domain of CTLA4, a) wherein the
extracellular domain of CTLA4 begins with methionine at position +1
or with alanine at position -1 and ends with aspartic acid at
position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or 19), b)
wherein at position +104 of the extracellular domain of CTLA4,
leucine is substituted with glutamic acid, and c) wherein at
position +29 of the extracellular domain of CTLA4, alanine is
substituted with tyrosine.
28. The method of claim 24, wherein the soluble CTLA4 mutant
molecule is L104EA29YIg as shown in FIG. 19 (SEQ ID NO: 9)
beginning with methionine at position +1 or with alanine at
position -1 and ending with lysine at position +357 as shown in
FIG. 19 (SEQ ID NO: 9).
29. A method for treating an immune system disease comprising
administering to a subject a combination of an effective amount of
a soluble CTLA4 and a second agent, wherein a) the soluble CTLA4 is
a CTLA4Ig beginning with methionine at position +1 or with alanine
at position -1 and ending with lysine as position +357 as shown in
FIG. 24 (SEQ ID NO: 19), and b) the second agent is selected from a
group consisting of immunosuppressive agents, corticosteroids,
nonsteroidal antiinflammatory drugs, prednisone, azathioprine,
methotrexate, TNF.alpha. blockers or antagonists, infliximab, any
biological agent targeting an inflammatory cytokine,
hydroxychloroquine, sulphasalazopryine, gold salts, etanercept,
anakinra, cyclophosphamide, leflunomide, collagen, dnaJ, a molecule
that blocks TNF receptors, pegsunercept, a molecule that blocks
cytokine function, AMG719, a molecule that blocks LFA-1 function,
efalizumab, acetyl salicylic acid, choline magnesium salicylate,
diflunisal, magnesium salicylate, salsalate, sodium salicylate,
diclofenac, etodolac, fenoprofen, flurbiprofen, indomethacin,
ketoprofen, ketorolac, meclofenamate, naproxen, nabumetone,
phenylbutazone, piroxicam, sulindac, tolmetin, acetaminophen,
ibuprofen, Cox-2 inhibitors, meloxicam, codeine phosphate,
propoxyphene napsylate, oxycodone hydrochloride, oxycodone
bitartrate and tramadol.
30. A method for treating an immune system disease comprising
administering to a subject a combination of an effective amount of
a soluble CTLA4 and a second agent, wherein a) the soluble CTLA4
comprises the extracellular domain of a CTLA4 molecule as shown in
FIG. 23 (SEQ ID NO: 17) beginning with methionine at position +1 or
with alanine at position -1 and ending with aspartic acid at
position +124, and b) the second agent is selected from a group
consisting of immunosuppressive agents, corticosteroids,
nonsteroidal antiinflammatory drugs, prednisone, azathioprine,
methotrexate, TNF.alpha. blockers or antagonists, infliximab, any
biological agent targeting an inflammatory cytokine,
hydroxychloroquine, sulphasalazopryine, gold salts, etanercept,
anakinra, cyclophosphamide, leflunomide, collagen, dnaJ, a molecule
that blocks TNF receptors, pegsunercept, a molecule that blocks
cytokine function, AMG719, a molecule that blocks LFA-1 function,
efalizumab, acetyl salicylic acid, choline magnesium salicylate,
diflunisal, magnesium salicylate, salsalate, sodium salicylate,
diclofenac, etodolac, fenoprofen, flurbiprofen, indomethacin,
ketoprofen, ketorolac, meclofenamate, naproxen, nabumetone,
phenylbutazone, piroxicam, sulindac, tolmetin, acetaminophen,
ibuprofen, Cox-2 inhibitors, meloxicam, codeine phosphate,
propoxyphene napsylate, oxycodone hydrochloride, oxycodone
bitartrate and tramadol.
31. A method for treating an immune system disease comprising
administering to a subject a combination of an effective amount of
a soluble CTLA4 and a second agent, wherein a) the soluble CTLA4
mutant molecule comprises an extracellular domain of CTLA4, i)
wherein the extracellular domain of CTLA4 begins with methionine at
position +1 or with alanine at position -1 and ends with aspartic
acid at position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or
19), and ii) wherein at position +104 of the extracellular domain
of CTLA4, leucine is substituted with any other amino acid. b) the
second agent is selected from a group consisting of
immunosuppressive agents, corticosteroids, nonsteroidal
antiinflammatory drugs, prednisone, azathioprine, methotrexate,
TNF.alpha. blockers or antagonists, infliximab, any biological
agent targeting an inflammatory cytokine, hydroxychloroquine,
sulphasalazopryine, gold salts, etanercept, anakinra,
cyclophosphamide, leflunomide, collagen, dnaJ, a molecule that
blocks TNF receptors, pegsunercept, a molecule that blocks cytokine
function, AMG719, a molecule that blocks LFA-1 function,
efalizumab, acetyl salicylic acid, choline magnesium salicylate,
diflunisal, magnesium salicylate, salsalate, sodium salicylate,
diclofenac, etodolac, fenoprofen, flurbiprofen, indomethacin,
ketoprofen, ketorolac, meclofenamate, naproxen, nabumetone,
phenylbutazone, piroxicam, sulindac, tolmetin, acetaminophen,
ibuprofen, Cox-2 inhibitors, meloxicam, codeine phosphate,
propoxyphene napsylate, oxycodone hydrochloride, oxycodone
bitartrate and tramadol.
32. The method of claim 31, wherein the soluble CTLA4 mutant
molecule comprises an extracellular domain of CTLA4, a) wherein the
extracellular domain of CTLA4 begins with methionine at position +1
or with alanine at position -1 and ends with aspartic acid at
position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or 19), b)
wherein at position +104 of the extracellular domain of CTLA4,
leucine is substituted with glutamic acid, and c) wherein at
position +29 of the extracellular domain of CTLA4, alanine is
substituted with tyrosine.
33. The method of claim 31, wherein the soluble CTLA4 mutant
molecule is L104EA29YIg as shown in FIG. 19 (SEQ ID NO: 9)
beginning with methionine at position +1 or with alanine at
position -1 and ending with lysine at position +357 as shown in
FIG. 19 (SEQ ID NO: 9).
34. A method for treating an immune system disease comprising
administering to a subject a combination of an effective amount of
a soluble CTLA4 and a second agent, wherein a) the soluble CTLA4 is
L104EA29YIg beginning with methionine at position +1 or with
alanine at position -1 and ending with lysine as position +357 as
shown in FIG. 19 (SEQ ID NO: 9), and b) the second agent is
selected from a group consisting of immunosuppressive agents,
corticosteroids, nonsteroidal antiinflammatory drugs, prednisone,
azathioprine, methotrexate, TNF.alpha. blockers or antagonists,
infliximab, any biological agent targeting an inflammatory
cytokine, hydroxychloroquine, sulphasalazopryine, gold salts,
etanercept, anakinra, cyclophosphamide, leflunomide, collagen,
dnaJ, a molecule that blocks TNF receptors, pegsunercept, a
molecule that blocks cytokine function, AMG719, a molecule that
blocks LFA-1 function, efalizumab, acetyl salicylic acid, choline
magnesium salicylate, diflunisal, magnesium salicylate, salsalate,
sodium salicylate, diclofenac, etodolac, fenoprofen, flurbiprofen,
indomethacin, ketoprofen, ketorolac, meclofenamate, naproxen,
nabumetone, phenylbutazone, piroxicam, sulindac, tolmetin,
acetaminophen, ibuprofen, Cox-2 inhibitors, meloxicam, codeine
phosphate, propoxyphene napsylate, oxycodone hydrochloride,
oxycodone bitartrate and tramadol.
35. A method for blocking B7 interactions with CTLA4 and/or CD28
comprising administering to a subject an effective amount of a
first agent and a second agent, wherein a) the first agent is a
soluble CTLA4 molecule, and b) the second agent is Methotrexate,
wherein the effective amount of Methotrexate is about 0.1 to 40 mg
per week, about 5 to 30 mg per week, about 0.1 to 5 mg/week, about
5 to 10 mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week,
about 20 to 25 mg/week, about 25 to 30 mg/week, about 30 to 35
mg/week, about 35 to 40 mg/week or about 10 to 30 mg/week.
36. A method for treating an immune system disease comprising
administering to a subject an effective amount of a first agent and
a second agent, wherein a) the first agent is a soluble CTLA4
molecule, and b) the second agent is Methotrexate, wherein the
effective amount of Methotrexate is about 0.1 to 40 mg per week,
about 5 to 30 mg per week, about 0.1 to 5 mg/week, about 5 to 10
mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week, about 20
to 25 mg/week, about 25 to 30 mg/week, about 30 to 35 mg/week,
about 35 to 40 mg/week or about 10 to 30 mg/week.
37. A method for blocking B7 interactions with CTLA4 and/or CD28
comprising administering to a subject an effective amount of a
first agent and a second agent, wherein a) the first agent is a
soluble CTLA4 molecule, and b) the second agent is Etanercept,
wherein the effective amount of Etanercept is about 10 to 100 mg
per week, about 50 mg per week, about 0.1 to 50 mg/kg body weight
per week
38. A method for treating an immune system disease comprising
administering to a subject an effective amount of a first agent and
a second agent, wherein a) the first agent is a soluble CTLA4
molecule, and b) the second agent is Etanercept, wherein the
effective amount of Etanercept is about 10 to 100 mg per week,
about 50 mg per week, about 0.1 to 50 mg/kg body weight per
week
39. A method for blocking B7 interactions with CTLA4 and/or CD28
comprising administering to a subject an effective amount of a
first agent and a second agent, wherein a) the first agent is a
soluble CTLA4 molecule, and b) the second agent is a DMARD, wherein
the effective amount of the DMARD is about 1 to about 5000 mg/day,
about 1 to 10 mg/day, about 10 to 50 mg/day, about 50 to 100
mg/day, about 100 to 150 mg/day, about 150 to 200 mg/day, about 200
to 250 mg/day, about 250 to 300 mg/day, about 300 to 350 mg/day,
about 350 to 400 mg/day, about 400 to 450 mg/day, about 450 to 500
mg/day, about 500 to 550 mg/day, about 550 to 600 mg/day, about 600
to 650 mg/day, about 650 to 700 mg/day, about 700 to 750 mg/day,
about 750 to 800 mg/day, about 800 to 850 mg/day, about 850 to 900
mg/day, about 900 to 950 mg/day, about 950 to 1000 mg/day, about
1000 to 1100 mg/day, about 1100 to 1200 mg/day, about 1200 to 1300
mg/day, about 1300 to 1400 mg/day, about 1400 to 1500 mg/day, about
1500 to 1600 mg/day, about 1600 to 1700 mg/day, about 1700 to 1800
mg/day, about 1800 to 1900 mg/day, about 1900 to 2000 mg/day, about
2000 to 2500 mg/day, about 2500 to 3000 mg/day, about 3000 to 3500
mg/day, about 3500 to 4000 mg/day, about 4000 to 4500 mg/day or
about 4500 to 5000 mg/day.
40. A method for treating an immune system disease administering to
a subject an effective amount of a first agent and a second agent,
wherein a) the first agent is a soluble CTLA4 molecule, and b) the
second agent is a DMARD, wherein the effective amount of the DMARD
is about 1 to about 5000 mg/day, about 1 to 10 mg/day, about 10 to
50 mg/day, about 50 to 100 mg/day, about 100 to 150 mg/day, about
150 to 200 mg/day, about 200 to 250 mg/day, about 250 to 300
mg/day, about 300 to 350 mg/day, about 350 to 400 mg/day, about 400
to 450 mg/day, about 450 to 500 mg/day, about 500 to 550 mg/day,
about 550 to 600 mg/day, about 600 to 650 mg/day, about 650 to 700
mg/day, about 700 to 750 mg/day, about 750 to 800 mg/day, about 800
to 850 mg/day, about 850 to 900 mg/day, about 900 to 950 mg/day,
about 950 to 1000 mg/day, about 1000 to 1100 mg/day, about 1100 to
1200 mg/day, about 1200 to 1300 mg/day, about 1300 to 1400 mg/day,
about 1400 to 1500 mg/day, about 1500 to 1600 mg/day, about 1600 to
1700 mg/day, about 1700 to 1800 mg/day, about 1800 to 1900 mg/day,
about 1900 to 2000 mg/day, about 2000 to 2500 mg/day, about 2500 to
3000 mg/day, about 3000 to 3500 mg/day, about 3500 to 4000 mg/day,
about 4000 to 4500 mg/day or about 4500 to 5000 mg/day.
41. The method of claim 40, wherein the DMARD is selected from a
group consisting of a dihydrofolic acid reductase inhibitor,
cyclophosphamide, cyclosporine, cyclosporin A, chloroquine,
hydroxychloroquine, sulfasalazine (sulphasalazopyrine), gold salts,
D-penicillamine, leflunomide, azathioprine, anakinra, a TNF
blocker, a biological agent that targets an inflammatory cytokine,
methotrexate or etanercept.
42. The method of claim 1, 2, 29, 30, 31, 34, 35, 36, 37, 38, 39 or
40, wherein the effective amount of soluble CTLA4 is between about
0.5 through 100 mg/kg weight of the subject, about 0.1 to 100 mg/kg
weight of the subject, about 0.5 to 10 mg/kg weight of a subject,
about 0.5 to 5 mg/kg weight of a subject, about 5 to 10 mg/kg
weight of a subject, about 10 to 15 mg/kg weight of a subject,
about 15 to 20 mg/kg weight of a subject, about 20 to 25 mg/kg
weight of a subject, about 25 to 30 mg/kg weight of a subject,
about 30 to 35 mg/kg weight of a subject, about 35 to 40 mg/kg
weight of a subject, about 40 to 45 mg/kg weight of a subject,
about 45 to 50 mg/kg weight of a subject, about 50 to 55 mg/kg
weight of a subject, about 55 to 60 mg/kg weight of a subject,
about 60 to 65 mg/kg weight of a subject, about 65 to 70 mg/kg
weight of a subject, about 70 to 75 mg/kg weight of a subject,
about 75 to 80 mg/kg weight of a subject, about 80 to 85 mg/kg
weight of a subject, about 85 to 90 mg/kg weight of a subject,
about 90 to 95 mg/kg weight of a subject, about 95 to 100 mg/kg
weight of a subject, about 2 to 10 mg/kg weight of a subject, about
0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg weight
of a subject, about 0.5 to 1.0 mg/kg weight of a subject, about 1.0
to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg weight of
a subject, about 2.0 to 2.5 mg/kg weight of a subject, about 2.5 to
3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg weight of a
subject, about 3.5 to 4.0 mg/kg about 4.0 to 4.5 mg/kg weight of a
subject, about 4.5 to 5.0 mg/kg weight of a subject, about 5.0 to
5.5 mg/kg weight of a subject, about 5.5 to 6.0 mg/kg weight of a
subject, about 6.0 to 6.5 mg/kg weight of a subject, about 6.5 to
7.0 mg/kg weight of a subject, about 7.0 to 7.5 mg/kg weight of a
subject, about 7.5 to 8.0 mg/kg weight of a subject, about 8.0 to
8.5 mg/kg weight of a subject, about 8.5 to 9.0 mg/kg weight of a
subject, about 9.0 to 9.5 mg/kg weight of a subject, about 9.5 to
10.0 mg/kg weight of a subject, weight of a subject, about 0.1 to
20 mg/kg weight of a subject, about 0.1 to 2 mg/kg weight of a
subject, about 2 to 4 mg/kg weight of a subject, about 4 to 6 mg/kg
weight of a subject, about 6 to 8 mg/kg weight of a subject, about
8 to 10 mg/kg weight of a subject, about 10 to 12 mg/kg weight of a
subject, about 12 to 14 mg/kg weight of a subject, about 14 to 16
mg/kg weight of a subject, about 16 to 18 mg/kg weight of a
subject, about 18 to 20 mg/kg weight of a subject, 0.5 mg/kg weight
of the subject, 2 mg/kg weight of a subject, 10 mg/kg weight of a
subject, about 0.5 mg/kg weight of the subject, 2 mg/kg weight of
the subject, 10 mg/kg weight of the subject, about 0.5 mg/kg to 100
weight of the subject, about 0.5 to 10 mg/kg weight of a subject,
about 0.1 to 20 mg/kg weight of a subject, about 500 mg for a
subject weighing less than 60 kg, 750 mg for a subject weighing
between 60-100 kg or 1000 mg for a subject weighing more than 100
kg.
43. The method of claim 2, 6, 29, 30, 31, 34, 36, 38 or 40, wherein
the immune system disease is a rheumatic disease.
44. The method of claim 43, wherein the rheumatic disease is
rheumatoid arthritis.
45. The method of claim 2, 6, 29, 30, 31, 34, 36, 38 or 40,,
wherein the immune system disease is selected from autoimmune
diseases, psoriasis, immune disorders associated with graft
transplantation rejection, T cell lymphoma, T cell acute
lymphoblastic leukemia, testicular angiocentric T cell lymphoma,
benign lymphocytic angiitis, lupus erythematosus, Hashimoto's
thyroiditis, primary myxedema, Graves' disease, pernicious anemia,
autoimmune atrophic gastritis, Addison's disease, insulin dependent
diabetes mellitis, good pasture's syndrome, myasthenia gravis,
pemiphigus, Crohn's disease, sympathetic ophthalmia, autoimmune
uveitis, multiple sclerosis, autoimmune hemolytic anemia,
idiopathic thrombocytopenia, primary biliary cirrhosis, chronic
action hepatitis, ulceratis colitis, Sjogren's syndrome, rheumatic
disease, rheumatoid arthritis, polymyositis, scleroderma, mixed
connective tissue disease, inflammatory rheumatism, degenerative
rheumatism, extra-articular rheumatism, collagen diseases, chronic
polyarthritis, psoriasis arthropathica, ankylosing spondylitis,
juvenile rheumatoid arthritis, periarthritis humeroscapularis,
panarteriitis nodosa, systemic lupus erythematosus, progressive
systemic scleroderma, arthritis uratica, dermatomyositis, muscular
rheumatism, myositis, myogelosis and chondrocalcinosis.
46. The method of claim 2, 6, 29, 30, 31, 34, 36, 38 or 40,,
wherein the immune system disease is selected from graft related
disorders, chronic rejection, tissue or cell allo- or xenografts,
skin allo- or xenografts, islet allo- or xenografts, muscle allo-
or xenografts, hepatocyte allo- or xenografts and neuron allo- or
xenografts.
47. The method of claim 2, 6, 29, 30, 31, 34, 36, 38 or 40,,
wherein a symptom associated with the immune system disease is
alleviated and wherein the symptom is selected from the group
consisting of joint swelling, pain, tenderness, morning stiffness,
structural damage, an elevated level of serum C-reactive protein,
an elevated level of soluble IL-2r, an elevated level of soluble
ICAM-1, an elevated level of soluble E-selectin and an elevated
erythrocyte sedimentation rate.
48. The method of claim 2, 6, 29, 30, 31, 34, 36, 38 or 40, wherein
treating a subject suffering from an immune system disease induces
a pathophysiological change.
49. The method of claim 48, wherein the pathophysiological change
associated with the immune system disease is reduced structural
damage.
50. A method for treating a disease selected from autoimmune
diseases, psoriasis, immune disorders associated with graft
transplantation rejection, T cell lymphoma, T cell acute
lymphoblastic leukemia, testicular angiocentric T cell lymphoma,
benign lymphocytic angiitis, lupus erythematosus, Hashimoto's
thyroiditis, primary myxedema, Graves' disease, pernicious anemia,
autoimmune atrophic gastritis, Addison's disease, insulin dependent
diabetes mellitis, good pasture's syndrome, myasthenia gravis,
pemphigus, Crohn's disease, sympathetic ophthalmia, autoimmune
uveitis, multiple sclerosis, autoimmune hemolytic anemia,
idiopathic thrombocytopenia, primary biliary cirrhosis, chronic
action hepatitis, ulceratis colitis, Sjogren's syndrome, rheumatic
disease, rheumatoid arthritis, polymyositis, scleroderma, mixed
connective tissue disease, inflammatory rheumatism, degenerative
rheumatism, extra-articular rheumatism, collagen diseases, chronic
polyarthritis, psoriasis arthropathica, ankylosing spondylitis,
juvenile rheumatoid arthritis, periarthritis humeroscapularis,
panarteriitis nodosa, systemic lupus erythematosus, progressive
systemic scleroderma, arthritis uratica, dermatomyositis, muscular
rheumatism, myositis, myogelosis and chondrocalcinosis, by
administering to a subject an effective amount of a soluble CTLA4
molecule comprising the sequence shown in FIG. 19 (SEQ ID NO: 9)
beginning with methionine at position +1 or with alanine at
position -1 and ending with aspartic acid at position +124, and
wherein the effective amount is about 0.1 to 100 mg/kg weight of
the subject, about 0.5 to 5 mg/kg weight of a subject, about 5 to
10 mg/kg weight of a subject, about 10 to 15 mg/kg weight of a
subject, about 15 to 20 mg/kg weight of a subject, about 20 to 25
mg/kg weight of a subject, about 25 to 30 mg/kg weight of a
subject, about 30 to 35 mg/kg weight of a subject, about 35 to 40
mg/kg weight of a subject, about 40 to 45 mg/kg weight of a
subject, about 45 to 50 mg/kg weight of a subject, about 50 to 55
mg/kg weight of a subject, about 55 to 60 mg/kg weight of a
subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, about 95 to 100
mg/kg weight of a subject, about 2 to 10 mg/kg weight of a subject,
about 0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg
weight of a subject, about 0.5 to 1.0 mg/kg weight of a subject,
about 1.0 to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg
weight of a subject, about 2.0 to 2.5 mg/kg weight of a subject,
about 2.5 to 3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg
weight of a subject, about 3.5 to 4.0 mg/kg weight of a subject,
about 4.0 to 4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg
weight of a subject, about 5.0 to 5.5 mg/kg weight of a subject,
about 5.5 to 6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg
weight of a subject, about 6.5 to 7.0 mg/kg weight of a subject,
about 7.0 to 7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg
weight of a subject, about 8.0 to 8.5 mg/kg weight of a subject,
about 8.5 to 9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg
weight of a subject, about 9.5 to 10.0 mg/kg weight of a subject,
about 0.1 to 2 mg/kg weight of a subject, about 2 to 4 mg/kg weight
of a subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8
mg/kg weight of a subject, about 8 to 10 mg/kg weight of a subject,
about 10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg
weight of a subject, about 14 to 16 mg/kg weight of a subject,
about 16 to 18 mg/kg weight of a subject, about 18 to 20 mg/kg
weight of a subject about 0.5 mg/kg weight of the subject, 2 mg/kg
weight of the subject, 10 mg/kg weight of the subject, about 0.5
mg/kg to 100 weight of the subject, about 0.5 to 10 mg/kg weight of
a subject, about 0.1 to 20 mg/kg weight of a subject, about 500 mg
for a subject weighing less than 60 kg, 750 mg for a subject
weighing between 60-100 kg or 1000 mg for a subject weighing more
than 100 kg.
51. A method for treating a disease selected from autoimmune
diseases, psoriasis, immune disorders associated with graft
transplantation rejection, T cell lymphoma, T cell acute
lymphoblastic leukemia, testicular angiocentric T cell lymphoma,
benign lymphocytic angiitis, lupus erythematosus, Hashimoto's
thyroiditis, primary myxedema, Graves' disease, pernicious anemia,
autoimmune atrophic gastritis, Addison's disease, insulin dependent
diabetes mellitis, good pasture's syndrome, myasthenia gravis,
pemphigus, Crohn's disease, sympathetic ophthalmia, autoimmune
uveitis, multiple sclerosis, autoimmune hemolytic anemia,
idiopathic thrombocytopenia, primary biliary cirrhosis, chronic
action hepatitis, ulceratis colitis, Sjogren's syndrome, rheumatic
disease, rheumatoid arthritis, polymyositis, scleroderma, mixed
connective tissue disease, inflammatory rheumatism, degenerative
rheumatism, extra-articular rheumatism, collagen diseases, chronic
polyarthritis, psoriasis arthropathica, ankylosing spondylitis,
juvenile rheumatoid arthritis, periarthritis humeroscapularis,
panarteriitis nodosa, systemic lupus erythematosus, progressive
systemic scleroderma, arthritis uratica, dermatomyositis, muscular
rheumatism, myositis, myogelosis and chondrocalcinosis, by
administering to a subject an effective amount of a soluble CTLA4
molecule L104EA29YIg having the sequence shown in FIG. 19 (SEQ ID
NO: 9) beginning with methionine at position +1 or with alanine at
position -1 and ending with lysine as position +357, and wherein
the effective amount is about 0.1 to 100 mg/kg weight of the
subject, about 0.5 to 5 mg/kg weight of a subject, about 5 to 10
mg/kg weight of a subject, about 10 to 15 mg/kg weight of a
subject, about 15 to 20 mg/kg weight of a subject, about 20 to 25
mg/kg weight of a subject, about 25 to 30 mg/kg weight of a
subject, about 30 to 35 mg/kg weight of a subject, about 35 to 40
mg/kg weight of a subject, about 40 to 45 mg/kg weight of a
subject, about 45 to 50 mg/kg weight of a subject, about 50 to 55
mg/kg weight of a subject, about 55 to 60 mg/kg weight of a
subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, about 95 to 100
mg/kg weight of a subject, about 2 to 10 mg/kg weight of a subject,
about 0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg
weight of a subject, about 0.5 to 1.0 mg/kg weight of a subject,
about 1.0 to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg
weight of a subject, about 2.0 to 2.5 mg/kg weight of a subject,
about 2.5 to 3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg
weight of a subject, about 3.5 to 4.0 mg/kg weight of a subject,
about 4.0 to 4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg
weight of a subject, about 5.0 to 5.5 mg/kg weight of a subject,
about 5.5 to 6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg
weight of a subject, about 6.5 to 7.0 mg/kg weight of a subject,
about 7.0 to 7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg
weight of a subject, about 8.0 to 8.5 mg/kg weight of a subject,
about 8.5 to 9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg
weight of a subject, about 9.5 to 10.0 mg/kg weight of a subject,
about 0.1 to 2 mg/kg weight of a subject, about 2 to 4 mg/kg weight
of a subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8
mg/kg weight of a subject, about 8 to 10 mg/kg weight of a subject,
about 10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg
weight of a subject, about 14 to 16 mg/kg weight of a subject,
about 16 to 18 mg/kg weight of a subject, about 18 to 20 mg/kg
weight of a subject, about 0.5 mg/kg weight of the subject, 2 mg/kg
weight of the subject, 10 mg/kg weight of the subject, about 0.5
mg/kg to 100 weight of the subject, about 0.5 to 10 mg/kg weight of
a subject, about 0.1 to 20 mg/kg weight of a subject, about 500 mg
for a subject weighing less than 60 kg, 750 mg for a subject
weighing between 60-100 kg or 1000 mg for a subject weighing more
than 100 kg.
52. A method for treating a disease selected from graft related
disorders, chronic rejection, tissue or cell allo- or xenografts,
skin allo- or xenografts, islet allo- or xenografts, muscle allo-
or xenografts, hepatocyte allo- or xenografts and neuron allo- or
xenografts, by administering to a subject an effective amount of a
soluble CTLA4 molecule comprising the sequence shown in FIG. 19
(SEQ ID NO: 9) beginning with methionine at position +1 or with
alanine at position -1 and ending with aspartic acid at position
+124, and wherein the effective amount is about 0.1 to 100 mg/kg
weight of the subject, about 0.5 to 5 mg/kg weight of a subject,
about 5 to 10 mg/kg weight of a subject, about 10 to 15 mg/kg
weight of a subject, about 15 to 20 mg/kg weight of a subject,
about 20 to 25 mg/kg weight of a subject, about 25 to 30 mg/kg
weight of a subject, about 30 to 35 mg/kg weight of a subject,
about 35 to 40 mg/kg weight of a subject, about 40 to 45 mg/kg
weight of a subject, about 45 to 50 mg/kg weight of a subject,
about 50 to 55 mg/kg weight of a subject, about 55 to 60 mg/kg
weight of a subject, about 60 to 65 mg/kg weight of a subject,
about 65 to 70 mg/kg weight of a subject, about 70 to 75 mg/kg
weight of a subject, about 75 to 80 mg/kg weight of a subject,
about 80 to 85 mg/kg weight of a subject, about 85 to 90 mg/kg
weight of a subject, about 90 to 95 mg/kg weight of a subject,
about 95 to 100 mg/kg weight of a subject, about 2 to 10 mg/kg
weight of a subject, about 0.1 to 4 mg/kg weight of a subject,
about 0.1 to 0.5 mg/kg weight of a subject, about 0.5 to 1.0 mg/kg
weight of a subject, about 1.0 to 1.5 mg/kg weight of a subject,
about 1.5 to 2.0 mg/kg weight of a subject, about 2.0 to 2.5 mg/kg
weight of a subject, about 2.5 to 3.0 mg/kg weight of a subject,
about 3.0 to 3.5 mg/kg weight of a subject, about 3.5 to 4.0 mg/kg
about 4.0 to 4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg
weight of a subject, about 5.0 to 5.5 mg/kg weight of a subject,
about 5.5 to 6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg
weight of a subject, about 6.5 to 7.0 mg/kg weight of a subject,
about 7.0 to 7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg
weight of a subject, about 8.0 to 8.5 mg/kg weight of a subject,
about 8.5 to 9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg
weight of a subject, about 9.5 to 10.0 mg/kg weight of a subject,
weight of a subject, about 0.1 to 2 mg/kg weight of a subject,
about 2 to 4 mg/kg weight of a subject, about 4 to 6 mg/kg weight
of a subject, about 6 to 8 mg/kg weight of a subject, about 8 to 10
mg/kg weight of a subject, about 10 to 12 mg/kg weight of a
subject, about 12 to 14 mg/kg weight of a subject, about 14 to 16
mg/kg weight of a subject, about 16 to 18 mg/kg weight of a
subject, about 18 to 20 mg/kg weight of a subject, about 0.5 mg/kg
weight of the subject, 2 mg/kg weight of the subject, 10 mg/kg
weight of the subject, about 0.5 mg/kg to 100 weight of the
subject, about 0.5 to 10 mg/kg weight of a subject, about 0.1 to 20
mg/kg weight of a subject, about 500 mg for a subject weighing less
than 60 kg, 750 mg for a subject weighing between 60-100 kg or 1000
mg for a subject weighing more than 100 kg.
53. A method for treating a disease selected from graft related
disorders, chronic rejection, tissue or cell allo- or xenografts,
skin allo- or xenografts, islet allo- or xenografts, muscle allo-
or xenografts, hepatocyte allo- or xenografts and neuron allo- or
xenografts, by administering to a subject an effective amount of a
soluble CTLA4 molecule L104EA29YIg having the sequence shown in
FIG. 19 (SEQ ID NO: 9) beginning with methionine at position +1 or
with alanine at position -1 and ending with lysine as position
+357, and wherein the effective amount is about 0.1 to 100 mg/kg
weight of the subject, about 0.5 to 5 mg/kg weight of a subject,
about 5 to 10 mg/kg weight of a subject, about 10 to 15 mg/kg
weight of a subject, about 15 to 20 mg/kg weight of a subject,
about 20 to 25 mg/kg weight of a subject, about 25 to 30 mg/kg
weight of a subject, about 30 to 35 mg/kg weight of a subject,
about 35 to 40 mg/kg weight of a subject, about 40 to 45 mg/kg
weight of a subject, about 45 to 50 mg/kg weight of a subject,
about 50 to 55 mg/kg weight of a subject, about 55 to 60 mg/kg
weight of a subject, about 60 to 65 mg/kg weight of a subject,
about 65 to 70 mg/kg weight of a subject, about 70 to 75 mg/kg
weight of a subject, about 75 to 80 mg/kg weight of a subject,
about 80 to 85 mg/kg weight of a subject, about 85 to 90 mg/kg
weight of a subject, about 90 to 95 mg/kg weight of a subject,
about 95 to 100 mg/kg weight of a subject, about 2 to 10 mg/kg
weight of a subject, about 0.1 to 4 mg/kg weight of a subject,
about 0.1 to 0.5 mg/kg weight of a subject, about 0.5 to 1.0 mg/kg
weight of a subject, about 1.0 to 1.5 mg/kg weight of a subject,
about 1.5 to 2.0 mg/kg weight of a subject, about 2.0 to 2.5 mg/kg
weight of a subject, about 2.5 to 3.0 mg/kg weight of a subject,
about 3.0 to 3.5 mg/kg weight of a subject, about 3.5 to 4.0 mg/kg
weight of a subject, about 4.0 to 4.5 mg/kg weight of a subject,
about 4.5 to 5.0 mg/kg weight of a subject, about 5.0 to 5.5 mg/kg
weight of a subject, about 5.5 to 6.0 mg/kg weight of a subject,
about 6.0 to 6.5 mg/kg weight of a subject, about 6.5 to 7.0 mg/kg
weight of a subject, about 7.0 to 7.5 mg/kg weight of a subject,
about 7.5 to 8.0 mg/kg weight of a subject, about 8.0 to 8.5 mg/kg
weight of a subject, about 8.5 to 9.0 mg/kg weight of a subject,
about 9.0 to 9.5 mg/kg weight of a subject, about 9.5 to 10.0 mg/kg
weight of a subject, about 0.9 to 2 mg/kg weight of a subject,
about 2 to 4 mg/kg weight of a subject, about 4 to 6 mg/kg weight
of a subject, about 6 to 8 mg/kg weight of a subject, about 8 to 10
mg/kg weight of a subject, about 10 to 12 mg/kg weight of a
subject, about 12 to 14 mg/kg weight of a subject, about 14 to 16
mg/kg weight of a subject, about 16 to 18 mg/kg weight of a
subject, about 18 to 20 mg/kg weight of a subject, about 0.5 mg/kg
weight of the subject, 2 mg/kg weight of the subject, 10 mg/kg
weight of the subject, about 0.5 mg/kg to 100 weight of the
subject, about 0.5 to 10 mg/kg weight of a subject, about 0.1 to 20
mg/kg weight of a subject, about 500 mg for a subject weighing less
than 60 kg, 750 mg for a subject weighing between 60-100 kg or 1000
mg for a subject weighing more than 100 kg.
54. A method for treating rheumatic disease comprising
administering to a subject an effective amount of a soluble CTLA4
molecule L104EA29YIg having the sequence shown in FIG. 19 (SEQ ID
NO: 9) beginning with methionine at position +1 or with alanine at
position -1 and ending with lysine as position +357, and wherein
the effective amount is about 0.1 to 100 mg/kg weight of the
subject, about 0.5 to 5 mg/kg weight of a subject, about 5 to 10
mg/kg weight of a subject, about 10 to 15 mg/kg weight of a
subject, about 15 to 20 mg/kg weight of a subject, about 20 to 25
mg/kg weight of a subject, about 25 to 30 mg/kg weight of a
subject, about 30 to 35 mg/kg weight of a subject, about 35 to 40
mg/kg weight of a subject, about 40 to 45 mg/kg weight of a
subject, about 45 to 50 mg/kg weight of a subject, about 50 to 55
mg/kg weight of a subject, about 55 to 60 mg/kg weight of a
subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, about 95 to 100
mg/kg weight of a subject, about 2 to 10 mg/kg weight of a subject,
about 0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg
weight of a subject, about 0.5 to 1.0 mg/kg weight of a subject,
about 1.0 to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg
weight of a subject, about 2.0 to 2.5 mg/kg weight of a subject,
about 2.5 to 3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg
weight of a subject, about 3.5 to 4.0 mg/kg weight of a subject,
about 4.0 to 4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg
weight of a subject, about 5.0 to 5.5 mg/kg weight of a subject,
about 5.5 to 6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg
weight of a subject, about 6.5 to 7.0 mg/kg weight of a subject,
about 7.0 to 7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg
weight of a subject, about 8.0 to 8.5 mg/kg weight of a subject,
about 8.5 to 9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg
weight of a subject, about 9.5 to 10.0 mg/kg weight of a subject,
about 0.1 to 2 mg/kg weight of a subject, about 2 to 4 mg/kg weight
of a subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8
mg/kg weight of a subject, about 8 to 10 mg/kg weight of a subject,
about 10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg
weight of a subject, about 14 to 16 mg/kg weight of a subject,
about 16 to 18 mg/kg weight of a subject, about 18 to 20 mg/kg
weight of a subject, about 0.5 mg/kg weight of the subject, 2 mg/kg
weight of the subject, 10 mg/kg weight of the subject, about 0.5
mg/kg to 100 weight of the subject, about 0.5 to 10 mg/kg weight of
a subject, about 0.1 to 20 mg/kg weight of a subject, about 500 mg
for a subject weighing less than 60 kg, 750 mg for a subject
weighing between 60-100 kg or 1000 mg for a subject weighing more
than 100 kg.
55. The method of claim 35, 37, or 39, cytokine production is
regulated.
56. The method of claim 35, 37, or 39, wherein improves ACR 20, 50
and/or 70 response rates is improved.
57. The method of claim 29, 30, 31, 34, 35, 36, 37, 38, 39, 40, 50,
51, 52, 53 or 54, wherein the soluble CTLA4 molecule comprises an
amino acid sequence which permits secretion of the soluble CTLA4
molecule.
58. The method of claim 57, wherein the amino acid sequence which
permits secretion comprises an oncostatin M signal peptide.
59. The method of claim 1, 2, 5, 6, 29, 30, 31, 34, 35, 36, 37, 38,
39, 40, 50, 51, 52, 53 or 54, wherein administration of the agents
is effected locally or systemically.
60. The method of claim 59, wherein administration is selected from
the group consisting of, intravenous, intramuscular,
intraperitoneal, oral, inhalation, subcutaneous, implantable pump,
continuous infusion, gene therapy, liposomes, suppositories,
topical contact, vesicles, capsules, biodegradable polymers,
hydrogels, controlled release patch and injection methods.
61. The method of claim 1, 2, 5, 6, 29, 30, 31, 34, 35, 36, 37, 38,
39, 40, 50, 51, 52, 53 or 54, wherein the subject is selected from
the group consisting of human, monkey, ape, dog, cat, cow, horse,
rabbit, mouse, and rat.
62. The method of claim 22 or 29, wherein the CTLA4Ig is encoded by
a nucleic acid molecule designated ATCC No. 68629.
63. The method of claim 28, 32, 51, 53 or 54, wherein L104EA29YIg
is encoded by a DNA sequence designated ATCC PTA-2104.
64. A pharmaceutical composition comprising a pharmaceutically
acceptable carrier and an effective amount of a first agent and a
second agent, wherein a) the first agent is soluble CTLA4, and b)
the second agent is selected from a group consisting of
immunosuppressive agents, corticosteroids, nonsteroidal
antiinflammatory drugs, prednisone, azathioprine, methotrexate,
TNF.alpha. blockers or antagonists, infliximab, any biological
agent targeting an inflammatory cytokine, hydroxychloroquine,
sulphasalazopryine, gold salts, etanercept, anakinra,
cyclophosphamide, leflunomide, collagen, dnaJ, a molecule that
blocks TNF receptors, pegsunercept, a molecule that blocks cytokine
function, AMG719, a molecule that blocks LFA-1 function,
efalizumab, acetyl salicylic acid, choline magnesium salicylate,
diflunisal, magnesium salicylate, salsalate, sodium salicylate,
diclofenac, etodolac, fenoprofen, flurbiprofen, indomethacin,
ketoprofen, ketorolac, meclofenamate, naproxen, nabumetone,
phenylbutazone, piroxicam, sulindac, tolmetin, acetaminophen,
ibuprofen, Cox-2 inhibitors, meloxicam, codeine phosphate,
propoxyphene napsylate, oxycodone hydrochloride, oxycodone
bitartrate and tramadol.
65. The pharmaceutical composition of claim 64, wherein the soluble
CTLA4 comprises the extracellular domain of a CTLA4 molecule, or
portion thereof, which binds a B7 antigen expressed on activated B
cells.
66. The pharmaceutical composition of claim 64, wherein the soluble
CTLA4 is a CTLA4 fusion molecule.
67. The pharmaceutical composition of claim 66, wherein the CTLA4
fusion molecule comprises an extracellular domain of a CTLA4
molecule which binds a B7 antigen expressed on activated B cells
joined to a non-CTLA4 molecule.
68. The pharmaceutical composition of claim 64, wherein the soluble
CTLA4 is a soluble CTLA4 mutant molecule.
69. The pharmaceutical composition of claim 68, wherein the soluble
CTLA4 mutant molecule comprises an extracellular domain of CTLA4,
a) wherein the extracellular domain of CTLA4 begins with methionine
at position +1 or with alanine at position -1 and ends with
aspartic acid at position +124 as shown in FIG. 23 or 24 (SEQ ID
NO: 17 or 19), and b) wherein at position +104 of the extracellular
domain of CTLA4, leucine is substituted with any other amino
acid.
70. The pharmaceutical composition of claim 68, wherein the soluble
CTLA4 mutant molecule comprises an extracellular domain of CTLA4,
a) wherein the extracellular domain of CTLA4 begins with methionine
at position +1 or with alanine at position -1 and ends with
aspartic acid at position +124 as shown in FIG. 23 or 24 (SEQ ID
NO: 17 or 19), b) wherein at position +104 of the extracellular
domain of CTLA4, leucine is substituted with glutamic acid, and c)
wherein at position +29 of the extracellular domain of CTLA4,
alanine is substituted with tyrosine.
71. The pharmaceutical composition of claim 68, wherein the soluble
CTLA4 mutant molecule is L104EA29YIg as shown in FIG. 19 (SEQ ID
NO: 9), beginning with methionine at position +1 or with alanine at
position -1 and ending with lysine at position +357.
72. The pharmaceutical composition of claim 64, wherein the
pharmaceutically acceptable carrier is selected ion exchangers,
alumina, aluminum stearate, lecithin, serum proteins, such as human
serum albumin, buffer substances, glycine, sorbic acid, potassium
sorbate, partial glyceride mixtures of saturated vegetable fatty
acids, phosphate buffered saline solution, water, emulsions, salts
or electrolytes, colloidal silica, magnesium trisilicate, polyvinyl
pyrrolidone, cellulose-based substances, polyethylene glycol,
sterile solutions, tablets, excipients, sucrose, glucose, maltose,
flavor and color additives, lipid compositions and polymeric
compositions.
73. Combination of a pharmaceutical composition comprising a
soluble CTLA4 with a pharmaceutical composition comprising an agent
selected from a group consisting of immunosuppressive agents,
corticosteroids, nonsteroidal antiinflammatory drugs, prednisone,
azathioprine, methotrexate, TNF.alpha. blockers or antagonists,
infliximab, any biological agent targeting an inflammatory
cytokine, hydroxychloroquine, sulphasalazopryine, gold salts,
etanercept, anakinra, cyclophosphamide, leflunomide, collagen,
dnaJ, a molecule that blocks TNF receptors, pegsunercept, a
molecule that blocks cytokine function, AMG719, a molecule that
blocks LFA-1 function, efalizumab, acetyl salicylic acid, choline
magnesium salicylate, diflunisal, magnesium salicylate, salsalate,
sodium salicylate, diclofenac, etodolac, fenoprofen, flurbiprofen,
indomethacin, ketoprofen, ketorolac, meclofenamate, naproxen,
nabumetone, phenylbutazone, piroxicam, sulindac, tolmetin,
acetaminophen, ibuprofen, Cox-2 inhibitors, meloxicam, codeine
phosphate, propoxyphene napsylate, oxycodone hydrochloride,
oxycodone bitartrate and tramadol, for use in therapy.
74. A kit comprising an effective amount of a first agent and a
second agent, wherein a) the first agent is soluble CTLA4, and b)
the second agent is selected from a group consisting of
immunosuppressive agents, corticosteroids, nonsteroidal
antiinflammatory drugs, prednisone, azathioprine, methotrexate,
TNF.alpha. blockers or antagonists, infliximab, any biological
agent targeting an inflammatory cytokine, hydroxychloroquine,
sulphasalazopryine, gold salts, etanercept, anakinra,
cyclophosphamide, leflunomide, corticosteroids, nonsteroidal
antiinflammatory drugs, prednisone, azathioprine, methotrexate,
TNF.alpha. blockers or antagonists, infliximab, any biological
agent targeting an inflammatory cytokine, hydroxychloroquine,
sulphasalazopryine, gold salts, etanercept, anakinra,
cyclophosphamide, leflunomide, collagen, dnaJ, a molecule that
blocks TNF receptors, pegsunercept, a molecule that blocks cytokine
function, AMG719, a molecule that blocks LFA-1 function,
efalizumab, acetyl salicylic acid, choline magnesium salicylate,
diflunisal, magnesium salicylate, salsalate, sodium salicylate,
diclofenac, etodolac, fenoprofen, flurbiprofen, indomethacin,
ketoprofen, ketorolac, meclofenamate, naproxen, nabumetone,
phenylbutazone, piroxicam, sulindac, tolmetin, acetaminophen,
ibuprofen, Cox-2 inhibitors, meloxicam, codeine phosphate,
propoxyphene napsylate, oxycodone hydrochloride, oxycodone
bitartrate and tramadol.
75. The kit of claim 74, further comprising a label indicating that
the first and second agents are useful to treat an immune system
disease.
76. The kit of claim 75, wherein the label indicates an effective
amount for the first agent being about 0.1 to 100 mg/kg weight of
the subject, about 0.5 to 5 mg/kg weight of a subject, about 5 to
10 mg/kg weight of a subject, about 10 to 15 mg/kg weight of a
subject, about 15 to 20 mg/kg weight of a subject, about 20 to 25
mg/kg weight of a subject, about 25 to 30 mg/kg weight of a
subject, about 30 to 35 mg/kg weight of a subject, about 35 to 40
mg/kg weight of a subject, about 40 to 45 mg/kg weight of a
subject, about 45 to 50 mg/kg weight of a subject, about 50 to 55
mg/kg weight of a subject, about 55 to 60 mg/kg weight of a
subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, about 95 to 100
mg/kg weight of a subject, about 2 to 10 mg/kg weight of a subject,
about 0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg
weight of a subject, about 0.5 to 1.0 mg/kg weight of a subject,
about 1.0 to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg
weight of a subject, about 2.0 to 2.5 mg/kg weight of a subject,
about 2.5 to 3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg
weight of a subject, about 3.5 to 4.0 mg/kg weight of a subject,
about 4.0 to 4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg
weight of a subject, about 5.0 to 5.5 mg/kg weight of a subject,
about 5.5 to 6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg
weight of a subject, about 6.5 to 7.0 mg/kg weight of a subject,
about 7.0 to 7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg
weight of a subject, about 8.0 to 8.5 mg/kg weight of a subject,
about 8.5 to 9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg
weight of a subject, about 9.5 to 10.0 mg/kg weight of a subject,
about 0.1 to 2 mg/kg weight of a subject, about 2 to 4 mg/kg weight
of a subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8
mg/kg weight of a subject, about 8 to 10 mg/kg weight of a subject,
about 10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg
weight of a subject, about 14 to 16 mg/kg weight of a subject,
about 16 to 18 mg/kg weight of a subject, about 18 to 20 mg/kg
weight of a subject, about 500 mg for a subject weighing less than
60 kg, 750 mg for a subject weighing between 60-100 kg or 1000 mg
for a subject weighing more than 100 kg.
77. The kit of claim 75, wherein the label indicates an effective
amount for the second agent being about 0.1 to 40 mg per week,
about 5 to 30 mg per week, about 0.1 to 5 mg/week, about 5 to 10
mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week, about 20
to 25 mg/week, about 25 to 30 mg/week, about 30 to 35 mg/week,
about 35 to 40 mg/week, about 10 to 30 mg/week, about 10 to 100
mg/week, about 50 mg/week, about 0.1 to 50 mg/kg body weight per
week, about 1 to about 5000 mg/day, about 1 to 10 mg/day, about 10
to 50 mg/day, about 50 to 100 mg/day, about 100 to 150 mg/day,
about 150 to 200 mg/day, about 200 to 250 mg/day, about 250 to 300
mg/day, about 300 to 350 mg/day, about 350 to 400 mg/day, about 400
to 450 mg/day, about 450 to 500 mg/day, about 500 to 550 mg/day,
about 550 to 600 mg/day, about 600 to 650 mg/day, about 650 to 700
mg/day, about 700 to 750 mg/day, about 750 to 800 mg/day, about 800
to 850 mg/day, about 850 to 900 mg/day, about 900 to 950 mg/day,
about 950 to 1000 mg/day, about 1000 to 1100 mg/day, about 1100 to
1200 mg/day, about 1200 to 1300 mg/day, about 1300 to 1400 mg/day,
about 1400 to 1500 mg/day, about 1500 to 1600 mg/day, about 1600 to
1700 mg/day, about 1700 to 1800 mg/day, about 1800 to 1900 mg/day,
about 1900 to 2000 mg/day, about 2000 to 2500 mg/day, about 2500 to
3000 mg/day, about 3000 to 3500 mg/day, about 3500 to 4000 mg/day,
about 4000 to 4500 mg/day or about 4500 to 5000 mg/day.
78. The kit of claim 75, wherein the label indicates an effective
amount for the first and second agent a. the effective amount of
the first agent being about 0.1 to 100 mg/kg weight of the subject,
about 0.5 to 5 mg/kg weight of a subject, about 5 to 10 mg/kg
weight of a subject, about 10 to 15 mg/kg weight of a subject,
about 15 to 20 mg/kg weight of a subject, about 20 to 25 mg/kg
weight of a subject, about 25 to 30 mg/kg weight of a subject,
about 30 to 35 mg/kg weight of a subject, about 35 to 40 mg/kg
weight of a subject, about 40 to 45 mg/kg weight of a subject,
about 45 to 50 mg/kg weight of a subject, about 50 to 55 mg/kg
weight of a subject, about 55 to 60 mg/kg weight of a subject,
about 60 to 65 mg/kg weight of a subject, about 65 to 70 mg/kg
weight of a subject, about 70 to 75 mg/kg weight of a subject,
about 75 to 80 mg/kg weight of a subject, about 80 to 85 mg/kg
weight of a subject, about 85 to 90 mg/kg weight of a subject,
about 90 to 95 mg/kg weight of a subject, about 95 to 100 mg/kg
weight of a subject, about 2 to 10 mg/kg weight of a subject, about
0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg weight
of a subject, about 0.5 to 1.0 mg/kg weight of a subject, about 1.0
to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg weight of
a subject, about 2.0 to 2.5 mg/kg weight of a subject, about 2.5 to
3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg weight of a
subject, about 3.5 to 4.0 mg/kg weight of a subject, about 4.0 to
4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg weight of a
subject, about 5.0 to 5.5 mg/kg weight of a subject, about 5.5 to
6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg weight of a
subject, about 6.5 to 7.0 mg/kg weight of a subject, about 7.0 to
7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg weight of a
subject, about 8.0 to 8.5 mg/kg weight of a subject, about 8.5 to
9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg weight of a
subject, about 9.5 to 10.0 mg/kg weight of a subject, about 0.1 to
2 mg/kg weight of a subject, about 2 to 4 mg/kg weight of a
subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8 mg/kg
weight of a subject, about 8 to 10 mg/kg weight of a subject, about
10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg weight of
a subject, about 14 to 16 mg/kg weight of a subject, about 16 to 18
mg/kg weight of a subject, about 18 to 20 mg/kg weight of a
subject, about 500 mg for a subject weighing less than 60 kg, 750
mg for a subject weighing between 60-100 kg or 1000 mg for a
subject weighing more than 100 kg, and b. the effective amount of
the second agent is about 0.1 to 40 mg per week, about 5 to 30 mg
per week, about 0.1 to 5 mg/week, about 5 to 10 mg/week, about 10
to 15 mg/week, about 15 to 20 mg/week, about 20 to 25 mg/week,
about 25 to 30 mg/week, about 30 to 35 mg/week, about 35 to 40
mg/week, about 10 to 30 mg/week, about 10 to 100 mg/week, about 50
mg/week, about 0.1 to 50 mg/kg body weight per week, about 1 to
about 5000 mg/day, about 1 to 10 mg/day, about 10 to 50 mg/day,
about 50 to 100 mg/day, about 100 to 150 mg/day, about 150 to 200
mg/day, about 200 to 250 mg/day, about 250 to 300 mg/day, about 300
to 350 mg/day, about 350 to 400 mg/day, about 400 to 450 mg/day,
about 450 to 500 mg/day, about 500 to 550 mg/day, about 550 to 600
mg/day, about 600 to 650 mg/day, about 650 to 700 mg/day, about 700
to 750 mg/day, about 750 to 800 mg/day, about 800 to 850 mg/day,
about 850 to 900 mg/day, about 900 to 950 mg/day, about 950 to 1000
mg/day, about 1000 to 1100 mg/day, about 1100 to 1200 mg/day, about
1200 to 1300 mg/day, about 1300 to 1400 mg/day, about 1400 to 1500
mg/day, about 1500 to 1600 mg/day, about 1600 to 1700 mg/day, about
1700 to 1800 mg/day, about 1800 to 1900 mg/day, about 1900 to 2000
mg/day, about 2000 to 2500 mg/day, about 2500 to 3000 mg/day, about
3000 to 3500 mg/day, about 3500 to 4000 mg/day, about 4000 to 4500
mg/day or about 4500 to 5000 mg/day.
79. The kit of claim 75, wherein the immune system disease is
selected from autoimmune diseases, psoriasis, immune disorders
associated with graft transplantation rejection, T cell lymphoma, T
cell acute lymphoblastic leukemia, testicular angiocentric T cell
lymphoma, benign lymphocytic angiitis, lupus erythematosus,
Hashimoto's thyroiditis, primary myxedema, Graves' disease,
pernicious anemia, autoimmune atrophic gastritis, Addison's
disease, insulin dependent diabetes mellitis, good pasture's
syndrome, myasthenia gravis, pemphigus, Crohn's disease,
sympathetic ophthalmia, autoimmune uveitis, multiple sclerosis,
autoimmune hemolytic anemia, idiopathic thrombocytopenia, primary
biliary cirrhosis, chronic action hepatitis, ulceratis colitis,
Sjogren's syndrome, rheumatic disease, rheumatoid arthritis,
polymyositis, scleroderma, mixed connective tissue disease,
inflammatory rheumatism, degenerative rheumatism, extra-articular
rheumatism, collagen diseases, chronic polyarthritis, psoriasis
arthropathica, ankylosing spondylitis, juvenile rheumatoid
arthritis, periarthritis humeroscapularis, panarteriitis nodosa,
systemic lupus erythematosus, progressive systemic scleroderma,
arthritis uratica, dermatomyositis, muscular rheumatism, myositis,
myogelosis and chondrocalcinosis.
80. The kit of claim 74, further comprising a container.
81. The kit of claim 74, wherein the soluble CTLA4 comprises the
extracellular domain of a CTLA4 molecule, or portion thereof, which
binds a B7 antigen expressed on activated B cells.
82. The kit of claim 74, wherein the soluble CTLA4 comprises the
extracellular domain of a CTLA4 molecule as shown in FIG. 23 (SEQ
ID NO: 17) beginning with methionine at position +1 or with alanine
at position -1 and ending with aspartic acid at position +124.
83. The kit of claim 74, wherein the soluble CTLA4 is a CTLA4
fusion molecule.
84. The kit of claim 83, wherein the CTLA4 fusion molecule
comprises an extracellular domain of a CTLA4 molecule which binds a
B7 antigen expressed on activated B cells joined to a non-CTLA4
molecule.
85. The kit of claim 84, wherein the non-CTLA4 molecule comprises
an amino acid sequence which alters the solubility or affinity
which comprises an immunoglobulin moiety.
86. The kit of claim 85, wherein the immunoglubulin moiety is an
immunoglubulin constant region or portion thereof.
87. The kit of claim 86, wherein the immunoglubulin constant region
or portion thereof is mutated to reduce effector function.
88. The kit of claim 83, wherein the CTLA4 fusion molecule is
CTLA4Ig.
89. The kit of claim 88, wherein the CTLA4Ig is shown in FIG. 24
(SEQ ID NO:19) beginning with methionine at position +1 or with
alanine at position -1 and ending with lysine at position +357.
90. The kit of claim 74, wherein the soluble CTLA4 is a soluble
CTLA4 mutant molecule.
91. The kit of claim 90, wherein the soluble CTLA4 mutant molecule
comprises an extracellular domain of CTLA4, a) wherein the
extracellular domain of CTLA4 begins with methionine at position +1
or with alanine at position -1 and ends with aspartic acid at
position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or 19), and
b) wherein at position +104 of the extracellular domain of CTLA4,
leucine is substituted with any other amino acid.
92. The kit of claim 90, wherein the soluble CTLA4 mutant molecule
comprises an extracellular domain of CTLA4, a) wherein the
extracellular domain of CTLA4 begins with methionine at position +1
or with alanine at position -1 and ends with aspartic acid at
position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or 19), b)
wherein at position +104 of the extracellular domain of CTLA4,
leucine is substituted with glutamic acid, and c) wherein at
position +29 of the extracellular domain of CTLA4, alanine is
substituted with tyrosine.
93. The kit of claim 90, wherein the soluble CTLA4 mutant molecule
is L104EA29YIg as shown in FIG. 19 (SEQ. ID NO: 9) beginning with
methionine at position +1 or with alanine at position -1 and ending
with lysine at position +357 as shown in FIG. 19 (SEQ ID NO:
9).
94. Use of a kit comprising the pharmaceutical composition of claim
68, a container and a label.
95. A kit comprising an effective amount of a first agent and a
label, wherein a) the first agent is soluble CTLA4, and b) the
label indicates that the first agent can be used with a second
agent selected from a group consisting of immunosuppressive agents,
corticosteroids, nonsteroidal antiinflammatory drugs, prednisone,
azathioprine, methotrexate, TNF.alpha. blockers or antagonists,
infliximab, any biological agent targeting an inflammatory
cytokine, hydroxychloroquine, sulphasalazopryine, gold salts,
etanercept, anakinra, cyclophosphamide, leflunomide, collagen,
dnaJ, a molecule that blocks TNF receptors, pegsunercept, a
molecule that blocks cytokine function, AMG719, a molecule that
blocks LFA-1 function, efalizumab, acetyl salicylic acid, choline
magnesium salicylate, diflunisal, magnesium salicylate, salsalate,
sodium salicylate, diclofenac, etodolac, fenoprofen, flurbiprofen,
indomethacin, ketoprofen, ketorolac, meclofenamate, naproxen,
nabumetone, phenylbutazone, piroxicam, sulindac, tolmetin,
acetaminophen, ibuprofen, Cox-2 inhibitors, meloxicam, codeine
phosphate, propoxyphene napsylate, oxycodone hydrochloride,
oxycodone bitartrate and tramadol.
96. The kit of claim 95, wherein the label further indicates an
effective amount for the first agent being about 0.1 to 100 mg/kg
weight of the subject, about 0.5 to 5 mg/kg weight of a subject,
about 5 to 10 mg/kg weight of a subject, about 10 to 15 mg/kg
weight of a subject, about 15 to 20 mg/kg weight of a subject,
about 20 to 25 mg/kg weight of a subject, about 25 to 30 mg/kg
weight of a subject, about 30 to 35 mg/kg weight of a subject,
about 35 to 40 mg/kg weight of a subject, about 40 to 45 mg/kg
weight of a subject, about 45 to 50 mg/kg weight of a subject,
about 50 to 55 mg/kg weight of a subject, about 55 to 60 mg/kg
weight of a subject, about 60 to 65 mg/kg weight of a subject,
about 65 to 70 mg/kg weight of a subject, about 70 to 75 mg/kg
weight of a subject, about 75 to 80 mg/kg weight of a subject,
about 80 to 85 mg/kg weight of a subject, about 85 to 90 mg/kg
weight of a subject, about 90 to 95 mg/kg weight of a subject,
about 95 to 100 mg/kg weight of a subject, about 2 to 10 mg/kg
weight of a subject, about 0.1 to 4 mg/kg weight of a subject,
about 0.1 to 0.5 mg/kg weight of a subject, about 0.5 to 1.0 mg/kg
weight of a subject, about 1.0 to 1.5 mg/kg weight of a subject,
about 1.5 to 2.0 mg/kg weight of a subject, about 2.0 to 2.5 mg/kg
weight of a subject, about 2.5 to 3.0 mg/kg weight of a subject,
about 3.0 to 3.5 mg/kg weight of a subject, about 3.5 to 4.0 mg/kg
weight of a subject, about 4.0 to 4.5 mg/kg weight of a subject,
about 4.5 to 5.0 mg/kg weight of a subject, about 5.0 to 5.5 mg/kg
weight of a subject, about 5.5 to 6.0 mg/kg weight of a subject,
about 6.0 to 6.5 mg/kg weight of a subject, about 6.5 to 7.0 mg/kg
weight of a subject, about 7.0 to 7.5 mg/kg weight of a subject,
about 7.5 to 8.0 mg/kg weight of a subject, about 8.0 to 8.5 mg/kg
weight of a subject, about 8.5 to 9.0 mg/kg weight of a subject,
about 9.0 to 9.5 mg/kg weight of a subject, about 9.5 to 10.0 mg/kg
weight of a subject, about 0.1 to 2 mg/kg weight of a subject,
about 2 to 4 mg/kg weight of a subject, about 4 to 6 mg/kg weight
of a subject, about 6 to 8 mg/kg weight of a subject, about 8 to 10
mg/kg weight of a subject, about 10 to 12 mg/kg weight of a
subject, about 12 to 14 mg/kg weight of a subject, about 14 to 16
mg/kg weight of a subject, about 16 to 18 mg/kg weight of a
subject, about 18 to 20 mg/kg weight of a subject, about 500 mg for
a subject weighing less than 60 kg, 750 mg for a subject weighing
between 60-100 kg or 1000 mg for a subject weighing more than 100
kg.
97. The kit of claim 95, wherein the label indicates an effective
amount for the second agent being about 0.1 to 40 mg per week,
about 5 to 30 mg per week, about 0.1 to 5 mg/week, about 5 to 10
mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week, about 20
to 25 mg/week, about 25 to 30 mg/week, about 30 to 35 mg/week,
about 35 to 40 mg/week, about 10 to 30 mg/week, about 10 to 100
mg/week, about 50 mg/week, about 0.1 to 50 mg/kg body weight per
week, about 1 to about 5000 mg/day, about 1 to 10 mg/day, about 10
to 50 mg/day, about 50 to 100 mg/day, about 100 to 150 mg/day,
about 150 to 200 mg/day, about 200 to 250 mg/day, about 250 to 300
mg/day, about 300 to 350 mg/day, about 350 to 400 mg/day, about 400
to 450 mg/day, about 450 to 500 mg/day, about 500 to 550 mg/day,
about 550 to 600 mg/day, about 600 to 650 mg/day, about 650 to 700
mg/day, about 700 to 750 mg/day, about 750 to 800 mg/day, about 800
to 850 mg/day, about 850 to 900 mg/day, about 900 to 950 mg/day,
about 950 to 1000 mg/day, about 1000 to 1100 mg/day, about 1100 to
1200 mg/day, about 1200 to 1300 mg/day, about 1300 to 1400 mg/day,
about 1400 to 1500 mg/day, about 1500 to 1600 mg/day, about 1600 to
1700 mg/day, about 1700 to 1800 mg/day, about 1800 to 1900 mg/day,
about 1900 to 2000 mg/day, about 2000 to 2500 mg/day, about 2500 to
3000 mg/day, about 3000 to 3500 mg/day, about 3500 to 4000 mg/day,
about 4000 to 4500 mg/day or about 4500 to 5000 mg/day.
98. The kit of claim 95, wherein the label indicates an effective
amount for the first and second agent, a. wherein the effective
amount of the first agent being about 0.1 to 100 mg/kg weight of
the subject, about 0.5 to 5 mg/kg weight of a subject, about 5 to
10 mg/kg weight of a subject, about 10 to 15 mg/kg weight of a
subject, about 15 to 20 mg/kg weight of a subject, about 20 to 25
mg/kg weight of a subject, about 25 to 30 mg/kg weight of a
subject, about 30 to 35 mg/kg weight of a subject, about 35 to 40
mg/kg weight of a subject, about 40 to 45 mg/kg weight of a
subject, about 45 to 50 mg/kg weight of a subject, about 50 to 55
mg/kg weight of a subject, about 55 to 60 mg/kg weight of a
subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, about 95 to 100
mg/kg weight of a subject, about 2 to 10 mg/kg weight of a subject,
about 0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg
weight of a subject, about 0.5 to 1.0 mg/kg weight of a subject,
about 1.0 to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg
weight of a subject, about 2.0 to 2.5 mg/kg weight of a subject,
about 2.5 to 3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg
weight of a subject, about 3.5 to 4.0 mg/kg weight of a subject,
about 4.0 to 4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg
weight of a subject, about 5.0 to 5.5 mg/kg weight of a subject,
about 5.5 to 6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg
weight of a subject, about 6.5 to 7.0 mg/kg weight of a subject,
about 7.0 to 7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg
weight of a subject, about 8.0 to 8.5 mg/kg weight of a subject,
about 8.5 to 9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg
weight of a subject, about 9.5 to 10.0 mg/kg weight of a subject,
about 0.1 to 2 mg/kg weight of a subject, about 2 to 4 mg/kg weight
of a subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8
mg/kg weight of a subject, about 8 to 10 mg/kg weight of a subject,
about 10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg
weight of a subject, about 14 to 16 mg/kg weight of a subject,
about 16 to 18 mg/kg weight of a subject, about 18 to 20 mg/kg
weight of a subject, about 500 mg for a subject weighing less than
60 kg, 750 mg for a subject weighing between 60-100 kg or 1000 mg
for a subject weighing more than 100 kg, and b. wherein the
effective amount of the second agent is about 0.1 to 40 mg per
week, about 5 to 30 mg per week, about 0.1 to 5 mg/week, about 5 to
10 mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week, about
20 to 25 mg/week, about 25 to 30 mg/week, about 30 to 35 mg/week,
about 35 to 40 mg/week, about 10 to 30 mg/week, about 10 to 100
mg/week, about 50 mg/week, about 0.1 to 50 mg/kg body weight per
week, about 1 to about 5000 mg/day, about 1 to 10 mg/day, about 10
to 50 mg/day, about 50 to 100 mg/day, about 100 to 150 mg/day,
about 150 to 200 mg/day, about 200 to 250 mg/day, about 250 to 300
mg/day, about 300 to 350 mg/day, about 350 to 400 mg/day, about 400
to 450 mg/day, about 450 to 500 mg/day, about 500 to 550 mg/day,
about 550 to 600 mg/day, about 600 to 650 mg/day, about 650 to 700
mg/day, about 700 to 750 mg/day, about 750 to 800 mg/day, about 800
to 850 mg/day, about 850 to 900 mg/day, about 900 to 950 mg/day,
about 950 to 1000 mg/day, about 1000 to 1100 mg/day, about 1100 to
1200 mg/day, about 1200 to 1300 mg/day, about 1300 to 1400 mg/day,
about 1400 to 1500 mg/day, about 1500 to 1600 mg/day, about 1600 to
1700 mg/day, about 1700 to 1800 mg/day, about 1800 to 1900 mg/day,
about 1900 to 2000 mg/day, about 2000 to 2500 mg/day, about 2500 to
3000 mg/day, about 3000 to 3500 mg/day, about 3500 to 4000 mg/day,
about 4000 to 4500 mg/day or about 4500 to 5000 mg/day.
99. The kit of claim 95, further comprising a label indicating that
the first and second agents are useful to treat an immune system
disease.
100. The kit of claim 99, wherein the immune system disease is
selected from autoimmune diseases, psoriasis, immune disorders
associated with graft transplantation rejection, T cell lymphoma, T
cell acute lymphoblastic leukemia, testicular angiocentric T cell
lymphoma, benign lymphocytic angiitis, lupus erythematosus,
Hashimoto's thyroiditis, primary myxedema, Graves' disease,
pernicious anemia, autoimmune atrophic gastritis, Addison's
disease, insulin dependent diabetes mellitis, good pasture's
syndrome, myasthenia gravis, pemphigus, Crohn's disease,
sympathetic ophthalmia, autoimmune uveitis, multiple sclerosis,
autoimmune hemolytic anemia, idiopathic thrombocytopenia, primary
biliary cirrhosis, chronic action hepatitis, ulceratis colitis,
Sjogren's syndrome, rheumatic disease, rheumatoid arthritis,
polymyositis, scleroderma, mixed connective tissue disease,
inflammatory rheumatism, degenerative rheumatism, extra-articular
rheumatism, collagen diseases, chronic polyarthritis, psoriasis
arthropathica, ankylosing spondylitis, juvenile rheumatoid
arthritis, periarthritis humeroscapularis, panarteriitis nodosa,
systemic lupus erythematosus, progressive systemic sclerodermia,
arthritis uratica, dermatomyositis, muscular rheumatism, myositis,
myogelosis and chondrocalcinosis.
101. A kit comprising an effective amount of a first agent and a
label, wherein a) the first agent is soluble CTLA4, and b) the
label indicates that the first agent can be used with a second
agent selected from a group consisting of immunosuppressive agents,
corticosteroids, nonsteroidal antiinflammatory drugs, prednisone,
azathioprine, methotrexate, TNF.alpha. blockers or antagonists,
infliximab, any biological agent targeting an inflammatory
cytokine, hydroxychloroquine, sulphasalazopryine, gold salts,
etanercept, anakinra, cyclophosphamide, leflunomide, collagen,
dnaJ, a molecule that blocks TNF receptors, pegsunercept, a
molecule that blocks cytokine function, AMG719, a molecule that
blocks LFA-1 function, efalizumab, acetyl salicylic acid, choline
magnesium salicylate, diflunisal, magnesium salicylate, salsalate,
sodium salicylate, diclofenac, etodolac, fenoprofen, flurbiprofen,
indomethacin, ketoprofen, ketorolac, meclofenamate, naproxen,
nabumetone, phenylbutazone, piroxicam, sulindac, tolmetin,
acetaminophen, ibuprofen, Cox-2 inhibitors, meloxicam, codeine
phosphate, propoxyphene napsylate, oxycodone hydrochloride,
oxycodone bitartrate and tramadol, wherein the label further
indicates an effective amount for the first agent being about 0.1
to 100 mg/kg weight of the subject, about 0.5 to 5 mg/kg weight of
a subject, about 5 to 10 mg/kg weight of a subject, about 10 to 15
mg/kg weight of a subject, about 15 to 20 mg/kg weight of a
subject, about 20 to 25 mg/kg weight of a subject, about 25 to 30
mg/kg weight of a subject, about 30 to 35 mg/kg weight of a
subject, about 35 to 40 mg/kg weight of a subject, about 40 to 45
mg/kg weight of a subject, about 45 to 50 mg/kg weight of a
subject, about 50 to 55 mg/kg weight of a subject, about 55 to 60
mg/kg weight of a subject, about 60 to 65 mg/kg weight of a
subject, about 65 to 70 mg/kg weight of a subject, about 70 to 75
mg/kg weight of a subject, about 75 to 80 mg/kg weight of a
subject, about 80 to 85 mg/kg weight of a subject, about 85 to 90
mg/kg weight of a subject, about 90 to 95 mg/kg weight of a
subject, about 95 to 100 mg/kg weight of a subject, about 2 to 10
mg/kg weight of a subject, about 0.1 to 4 mg/kg weight of a
subject, about 0.1 to 0.5 mg/kg weight of a subject, about 0.5 to
1.0 mg/kg weight of a subject, about 1.0 to 1.5 mg/kg weight of a
subject, about 1.5 to 2.0 mg/kg weight of a subject, about 2.0 to
2.5 mg/kg weight of a subject, about 2.5 to 3.0 mg/kg weight of a
subject, about 3.0 to 3.5 mg/kg weight of a subject, about 3.5 to
4.0 mg/kg weight of a subject, about 4.0 to 4.5 mg/kg weight of a
subject, about 4.5 to 5.0 mg/kg weight of a subject, about 5.0 to
5.5 mg/kg weight of a subject, about 5.5 to 6.0 mg/kg weight of a
subject, about 6.0 to 6.5 mg/kg weight of a subject, about 6.5 to
7.0 mg/kg weight of a subject, about 7.0 to 7.5 mg/kg weight of a
subject, about 7.5 to 8.0 mg/kg weight of a subject, about 8.0 to
8.5 mg/kg weight of a subject, about 8.5 to 9.0 mg/kg weight of a
subject, about 9.0 to 9.5 mg/kg weight of a subject, about 9.5 to
10.0 mg/kg weight of a subject, about 0.1 to 2 mg/kg weight of a
subject, about 2 to 4 mg/kg weight of a subject, about 4 to 6 mg/kg
weight of a subject, about 6 to 8 mg/kg weight of a subject, about
8 to 10 mg/kg weight of a subject, about 10 to 12 mg/kg weight of a
subject, about 12 to 14 mg/kg weight of a subject, about 14 to 16
mg/kg weight of a subject, about 16 to 18 mg/kg weight of a
subject, about 18 to 20 mg/kg weight of a subject, about 500 mg for
a subject weighing less than 60 kg, 750 mg for a subject weighing
between 60-100 kg or 1000 mg for a subject weighing more than 100
kg, and wherein the label indicates an effective amount for the
second agent being about 0.1 to 40 mg per week, about 5 to 30 mg
per week, about 0.1 to 5 mg/week, about 5 to 10 mg/week, about 10
to 15 mg/week, about 15 to 20 mg/week, about 20 to 25 mg/week,
about 25 to 30 mg/week, about 30 to 35 mg/week, about 35 to 40
mg/week, about 10 to 30 mg/week, about 10 to 100 mg/week, about 50
mg/week, about 0.1 to 50 mg/kg body weight per week, about 1 to
about 5000 mg/day, about 1 to 10 mg/day, about 10 to 50 mg/day,
about 50 to 100 mg/day, about 100 to 150 mg/day, about 150 to 200
mg/day, about 200 to 250 mg/day, about 250 to 300 mg/day, about 300
to 350 mg/day, about 350 to 400 mg/day, about 400 to 450 mg/day,
about 450 to 500 mg/day, about 500 to 550 mg/day, about 550 to 600
mg/day, about 600 to 650 mg/day, about 650 to 700 mg/day, about 700
to 750 mg/day, about 750 to 800 mg/day, about 800 to 850 mg/day,
about 850 to 900 mg/day, about 900 to 950 mg/day, about 950 to 1000
mg/day, about 1000 to 1100 mg/day, about 1100 to 1200 mg/day, about
1200 to 1300 mg/day, about 1300 to 1400 mg/day, about 1400 to 1500
mg/day, about 1500 to 1600 mg/day, about 1600 to 1700 mg/day, about
1700 to 1800 mg/day, about 1800 to 1900 mg/day, about 1900 to 2000
mg/day, about 2000 to 2500 mg/day, about 2500 to 3000 mg/day, about
3000 to 3500 mg/day, about 3500 to 4000 mg/day, about 4000 to 4500
mg/day or about 4500 to 5000 mg/day.
102. The kit of claim 101, wherein the label further indicates that
the first and second agents are useful to treat an immune system
disease selected from autoimmune diseases, psoriasis, immune
disorders associated with graft transplantation rejection, T cell
lymphoma, T cell acute lymphoblastic leukemia, testicular
angiocentric T cell lymphoma, benign lymphocytic angiitis, lupus
erythematosus, Hashimoto's thyroiditis, primary myxedema, Graves'
disease, pernicious anemia, autoimmune atrophic gastritis,
Addison's disease, insulin dependent diabetes mellitis, good
pasture's syndrome, myasthenia gravis, pemphigus, Crohn's disease,
sympathetic ophthalmia, autoimmune uveitis, multiple sclerosis,
autoimmune hemolytic anemia, idiopathic thrombocytopenia, primary
biliary cirrhosis, chronic action hepatitis, ulceratis colitis,
Sjogren's syndrome, rheumatic disease, rheumatoid arthritis,
polymyositis, scleroderma, mixed connective tissue disease,
inflammatory rheumatism, degenerative rheumatism, extra-articular
rheumatism, collagen diseases, chronic polyarthritis, psoriasis
arthropathica, ankylosing spondylitis, juvenile rheumatoid
arthritis, periarthritis humeroscapularis, panarteriitis nodosa,
systemic lupus erythematosus, progressive systemic scleroderma,
arthritis uratica, dermatomyositis, muscular rheumatism, myositis,
myogelosis and chondrocalcinosis.
103. The kit of claim 101, further comprising a container.
104. The kit of claim 101, wherein the soluble CTLA4 comprises the
extracellular domain of a CTLA4 molecule, or portion thereof, which
binds a B7 antigen expressed on activated B cells.
105. The kit of claim 101, wherein the soluble CTLA4 is a CTLA4
fusion molecule.
106. The kit of claim 105, wherein the CTLA4 fusion molecule
comprises an extracellular domain of a CTLA4 molecule which binds a
B7 antigen expressed on activated B cells joined to a non-CTLA4
molecule.
107. The kit of claim 106, wherein the non-CTLA4 molecule comprises
an amino acid sequence which alters the solubility or affinity
comprises an immunoglobulin moiety.
108. The kit of claim 107, wherein the immunoglubulin moiety is an
immunoglubulin constant region or portion thereof.
109. The kit of claim 108, wherein the immunoglubulin constant
region or portion thereof is mutated to reduce effector
function.
110. The kit of claim 105, wherein the CTLA4 fusion molecule is
CTLA4Ig.
111. The kit of claim 110, wherein the CTLA4Ig is shown in FIG. 24
(SEQ ID NO:19) beginning with methionine at position +1 or with
alanine at position -1 and ending with lysine at position +357.
112. The kit of claim 101, wherein the soluble CTLA4 is a soluble
CTLA4 mutant molecule.
113. The kit of claim 112, wherein the soluble CTLA4 mutant
molecule comprises an extracellular domain of CTLA4, a) wherein the
extracellular domain of CTLA4 begins with methionine at position +1
or with alanine at position -1 and ends with aspartic acid at
position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or 19), and
b) wherein at position +104 of the extracellular domain of CTLA4,
leucine is substituted with any other amino acid.
114. The kit of claim 112, wherein the soluble CTLA4 mutant
molecule comprises an extracellular domain of CTLA4, a) wherein the
extracellular domain of CTLA4 begins with methionine at position +1
or with alanine at position -1 and ends with aspartic acid at
position +124 as shown in FIG. 23 or 24 (SEQ ID NO: 17 or 19), b)
wherein at position +104 of the extracellular domain of CTLA4,
leucine is substituted with glutamic acid, and c) wherein at
position +29 of the extracellular domain of CTLA4, alanine is
substituted with tyrosine.
115. The kit of claim 101, wherein the soluble CTLA4 mutant
molecule is L104EA29YIg as shown in FIG. 19 (SEQ ID NO: 9)
beginning with methionine at position +1 or with alanine at
position -1 and ending with lysine at position +357 as shown in
FIG. 19 (SEQ ID NO: 9).
Description
[0001] This application is a continuation-in-part (CIP) of U.S.
Ser. No. 09/898,195, filed Jul. 2, 2001, and claims the priorities
of provisional applications, U.S. Serial No. 60/215,913, filed Jul.
3, 2000, U.S. Serial No. 60/373,852, filed Apr. 19, 2002 and U.S.
Serial No. 60/407,246, filed Aug. 30, 2002, the contents of which
are hereby incorporated by reference in their entirety into this
application.
[0002] Throughout this application various publications are
referenced. The disclosures of these publications in their
entireties are hereby incorporated by reference into this
application in order to more fully describe the state of the art to
which this invention pertains.
FIELD OF THE INVENTION
[0003] The present invention relates generally to the field of
immune system diseases, e.g., rheumatic diseases. In particular,
the invention relates to methods and compositions for treating
immune system diseases, e.g., rheumatic diseases, such as
rheumatoid arthritis, by administering to a subject an effective
amount of soluble CTLA4 molecules alone, or in conjunction with a
Disease Modifying Anti-Rheumatic Drug (DMARD).
BACKGROUND OF THE INVENTION
[0004] No cure currently exists for rheumatic diseases. Rather,
therapeutic agents are used to treat the symptoms. Typically, the
therapeutic agents are administered over long periods of time and
the therapeutic value is often diminished by adverse side
effects.
[0005] Rheumatic diseases encompass a group of diseases that affect
the musculo-skeletal and connective tissues of the body. These
diseases are characterized by chronic inflammation that often leads
to permanent tissue damage, deformity, atrophy and disability.
Rheumatic diseases affect the joints, bone, soft tissue, or spinal
cord (Mathies, H. 1983 Rheuma) and are classified as inflammatory
rheumatism, degenerative rheumatism, extra-articular rheumatism, or
collagen diseases. Some rheumatic diseases are known to be
autoimmune diseases caused by a subject's altered immune
response.
[0006] Rheumatoid arthritis is a progressive rheumatic disease,
affecting approximately 2% of the adult population of developed
countries (Utsinger, P. D., et al., 1985 Rheumatoid Arthritis, p.
140). This disease is characterized by persistent inflammatory
synovitis that causes destruction of cartilage and bone erosion,
leading to structural deformities in the peripheral joints. The
symptoms associated with rheumatoid arthritis include joint
swelling, joint tenderness, inflammation, morning stiffness, and
pain, especially upon flexing. Subjects having advanced stages of
arthritis suffer from structural damage, including joint
destruction with bone erosion (in: "Principals of Internal
Medicine, Harrison, 13.sup.th edition, pages 1648-1655). In
addition, patients can present other clinical symptoms of various
organic lesions, including lesions of the skin, kidney, heart,
lung, central nervous system, and eyes due to vasculitis related to
the autoimmune process.
[0007] Other symptoms that correlate with rheumatoid arthritis
include elevated erythrocyte sedimentation rates, and elevated
levels of serum C-reactive protein (CRP) and/or soluble IL-2
receptor (IL-2r). The erythrocyte sedimentation rate is increased
in nearly all patients with active rheumatoid arthritis. The level
of serum C-reactive protein is also elevated and correlates with
disease activity and the likelihood of progressive joint damage.
Additionally, the level of soluble IL-2r, a product of activated
T-cells, is elevated in blood serum and synovial fluid of patients
with active rheumatoid arthritis (see: "Principals of Internal
Medicine, Harrison, 13.sup.th edition, page 1650).
[0008] Rheumatoid arthritis is believed to be a T-cell-mediated
autoimmune disease, involving antigen-nonspecific intercellular
interactions between T-lymphocytes and antigen-presenting cells. In
general, the magnitude of the T-cell response is determined by the
co-stimulatory response elicited by the interaction between T-cell
surface molecules and their ligands (Mueller, et al., 1989 Ann.
Rev. Immunol. 7:445-480). Key co-stimulatory signals are provided
by the interaction between T-cell surface receptors, CD28 and
CTLA4, and their ligands, such as B7-related molecules CD80 (i.e.,
B7-1) and CD86 (i.e., B7-2), on antigen presenting cells (Linsley,
P. and Ledbetter, J. 1993 Ann. Rev. Immunol. 11:191-212).
[0009] T-cell activation in the absence of co-stimulation results
in anergic T-cell response (Schwartz, R. H., 1992 Cell
71:1065-1068) wherein the immune system becomes nonresponsive to
stimulation.
[0010] Since rheumatoid arthritis is thought to be a
T-cell-mediated immune system disease, one strategy to develop new
agents to treat rheumatoid arthritis is to identify molecules that
block co-stimulatory signals between T-lymphocytes and antigen
presenting cells, by blocking the interaction between endogenous
CD28 or CTLA4 and B7. Potential molecules include soluble CTLA4
molecules that are modified (i.e. CTLA4 mutant molecules) to bind
to B7 with higher avidity than wildtype CTLA4 (the sequence of
which is shown in FIG. 23) or CD28, thereby blocking the
co-stimulatory signals.
[0011] Soluble forms of CD28 and CTLA4 have been constructed by
fusing variable (V)-like extracellular domains of CD28 and CTLA4 to
immunoglobulin (Ig) constant domains resulting in CD28Ig and
CTLA4Ig. A nucleotide and amino acid sequence of CTLA4Ig is shown
in FIG. 24 with the protein beginning with methionine at position
+1 or alanine at position -1 and ending with lysine at position
+357. CTLA4Ig binds both CD80-positive and CD86-positive cells more
strongly than CD28Ig (Linsley, P., et al., 1994 Immunity 1:793-80).
Many T-cell-dependent immune responses have been found to be
blocked by CTLA4Ig both in vitro and in vivo. (Linsley, P., et al.,
1991b, supra; Linsley, P., et al., 1992a Science 257:792-795;
Linsley, P., et al., 1992b J. Exp. Med. 176:1595-1604; Lenschow, D.
J., et al. 1992 Science 257:789-792; Tan, P., et al., 1992 J. Exp.
Med. 177:165-173; Turka, L. A., 1992 Proc. Natl. Acad. Sci. USA
89:11102-11105).
[0012] To alter binding affinity to natural ligands, such as B7,
soluble CTLA4Ig fusion molecules were modified by mutation of amino
acids in the CTLA4 portion of the molecules. Regions of CTLA4 that,
when mutated, alter the binding affinity or avidity for B7 ligands
include the complementarity determining region 1 (CDR-1 as
described in U.S. Pat. Nos. 6,090,914, 5,773,253, 5,844,095; in
copending U.S. Patent Application Serial No. 60/214,065; and by
Peach et al, 1994. J. Exp. Med., 180:2049-2058) and complementarity
determining region 3 (CDR-3)-like regions (CDR-3 is the conserved
region of the CTLA4 extracellular domain as described in U.S. Pat.
Nos. 6,090,914, 5,773,253 and 5,844,095; in copending U.S. Patent
Application Serial No. 60/214,065; and by Peach, R. J., et al J Exp
Med 1994 180:2049-2058; the CDR-3-like region encompasses the CDR-3
region and extends, by several amino acids, upstream and/or
downstream of the CDR-3 motif). The CDR-3-like region includes a
hexapeptide motif MYPPPY (SEQ ID NO.: 20) that is highly conserved
in all CD28 and CTLA4 family members. Alanine scanning mutagenesis
through the hexapeptide motif in CTLA4, and at selected residues in
CD28Ig, reduced or abolished binding to CD80 (Peach, R. J., et al J
Exp Med 1994 180:2049-2058; U.S. Pat. No. 5,434,131; U.S. Pat. No.
6,090,914; U.S. Pat. No. 5,773,253.
[0013] Further modifications were made to soluble CTLA4Ig molecules
by interchanging homologous regions of CTLA4 and CD28. These
chimeric CTLA4/CD28 homologue mutant molecules identified the
MYPPPY hexapeptide motif common to CTLA4 and CD28, as well as
certain non-conserved amino acid residues in the CDR-1- and
CDR-3-like regions of CTLA4, as regions responsible for increasing
the binding avidity of CTLA4 with CD80 (Peach, R. J., et al., 1994
J Exp Med 180:2049-2058).
[0014] Soluble CTLA4 molecules, such as CTLA4Ig, CTLA4 mutant
molecules or chimeric CTLA4/CD28 homologue mutants as described
supra, introduce a new group of therapeutic drugs to treat
rheumatic diseases.
[0015] Present treatments for rheumatic diseases, such as
rheumatoid arthritis, include administering nonspecific cytotoxic
immunosuppressive drugs known as Disease Modifying Anti-Rheumatic
Drugs (DMARDs), such as methotrexate, infliximab, cyclophosphamide,
azathioprine, cyclosporin A, sulfasalazine, hydroxychloroquine,
leflunomide, etanercept, and tumor necrosis factor-alpha
(TNF.alpha.) or other cytokine blockers or antagonists. These
immunosuppressive drugs suppress the entire immune system of the
subject, and long-term use increases the risk of infection and
oncogenesis. Moreover, these drugs merely slow down the progress of
the rheumatoid arthritis, which resumes at an accelerated pace
after the therapy is discontinued. Additionally, prolonged therapy
with these nonspecific drugs produces toxic side effects, including
a tendency towards development of certain malignancies, kidney
failure, bone marrow suppression, pulmonary fibrosis, malignancy,
diabetes, and liver function disorders. These drugs may also
gradually cease being effective after about 2-5 years (Kelley's
Textbook of Rheumatology, 6.sup.th Edition, pages 1001-1022).
Newer, biologically based, DMARDs such as cytokine blockers may be
more potent and may have longer lasting effects than older DMARDS
such as hydrochloroquine, however, the long term safety of these
newer drugs is still unknown. Reports of multiple sclerosis and
lupus exist with the use of TNF blockers.
[0016] Alternatively, therapeutic agents that are non-specific
immunosuppressive and anti-inflammatory drugs have been used to
obtain symptomatic relief. These drugs are dose-dependent and do
not protect from disease progression. These drugs include
Non-Steroidal Anti-Inflammatory Drugs (NSAIDS) as well as steroid
compounds (e.g., corticosteroids or glucocorticoids), such as
prednisone and methylprednisolone. Steroids also have significant
toxic side effects associated with their long-term use. (Kelley's
Textbook of Rheumatology, 6.sup.th Edition, pages 829-833).
[0017] Thus, current treatments for rheumatoid arthritis are of
limited efficacy, involve significant toxic side effects, and
cannot be used continuously for prolonged periods of time.
[0018] Accordingly, there exists a need for treatments that are
effective and more potent for treating rheumatic diseases, such as
rheumatoid arthritis, and avoids the disadvantages of old
conventional methods and agents, by targeting a pathophysiological
mechanism of auto-immunity.
SUMMARY OF THE INVENTION
[0019] The present invention provides compositions and methods for
treating immune system diseases, by administering to a subject
soluble CTLA4 molecules, which bind to B7 molecules on B7-positive
cells, thereby inhibiting endogenous B7 molecules from binding
CTLA4 and/or CD28 on T-cells. Soluble CTLA4 molecules used in the
methods of the invention include CTLA4Ig and soluble CTLA4 mutant
molecule L104EA29YIg.
[0020] Alternatively, the present invention provides compositions
and methods for treating immune system diseases, by administering
to a subject a combination of a DMARD and a molecule that blocks B7
interaction with CTLA4 and/or CD28.
[0021] The present invention also provides methods for inhibiting
T-cell function, but not causing T-cell depletion, in a human by
contacting B7-positive cells in the human with soluble CTLA4.
Examples of soluble CTLA4 include CTLA4Ig and soluble CTLA4 mutant
molecules, such as L104EA29YIg.
[0022] The present invention also provides methods for treating
(e.g. reducing symptoms of) rheumatic diseases, such as rheumatoid
arthritis, by administering to a subject suffering from symptoms of
arthritis, soluble CTLA4 molecules such as CTLA4Ig and/or soluble
CTLA4 mutant molecule L104EA29YIg and/or a mix of any soluble CTLA
molecule. The CTLA4 mutant molecule L104EA29YIg e.g. beginning with
methionine at position +1 or alanine at position -1 and ending with
lysine at position +357, as shown in FIG. 19, is preferred for use
in the methods of the invention.
[0023] The present invention also provides methods for treating
(e.g. reducing symptoms of) rheumatic diseases, such as rheumatoid
arthritis, by administering to the subject a combination of 1) a
DMARD, such as methotrexate or a molecule that blocks TNF
interactions, and 2) soluble CTLA4 molecules, such as CTLA4Ig.
[0024] The present invention also provides methods for reducing
pathophysiological changes associated with an immune system disease
(e.g., rheumatic disease), such as structural damage, by
administering to the subject diagnosed with the immune system
disease (e.g., rheumatoid arthritis), soluble CTLA4 molecules alone
or in conjunction with other therapeutic drugs, such as a
DMARD.
[0025] The present invention also provides a pharmaceutical
composition for treating immune system diseases, such as rheumatic
diseases, comprising a pharmaceutically acceptable carrier and a
biologically effective agent, such as soluble CTLA4 molecules,
alone or in conjunction with other therapeutic drugs, such as a
DMARD, a NSAID, a corticosteroid and/or a glucocorticoid.
[0026] Kits comprising pharmaceutical compositions therapeutic for
immune system disease are also encompassed by the invention. In one
embodiment, a kit comprising one or more of the pharmaceutical
compositions of the invention is used to treat an immune system
disease, e.g. rheumatoid arthritis. For example, the pharmaceutical
composition comprises an effective amount of soluble CTLA4
molecules that bind to B7 molecules on B7-positive cells, thereby
blocking the B7 molecules from binding CTLA4 and/or CD28 on
T-cells. Further, the kit may contain one or more immunosuppressive
agents used in conjunction with the pharmaceutical compositions of
the invention. Potential immunosuppressive agents include, but are
not limited to, corticosteroids, nonsteroidal antiinflammatory
drugs (e.g. Cox-2 inhibitors), prednisone, cyclosporine,
cyclosporin A, azathioprine, methotrexate, TNF.alpha. blockers or
antagonists, hydroxychloroquine, sulphasalazopyrine
(sulfasalazine), gold salts, infliximab, etanercept, anakinra and
any biological agent targeting an inflammatory cytokine.
[0027] The present invention also provides methods for reducing the
erythrocyte sedimentation rate that is associated with rheumatoid
arthritis.
[0028] Additionally, the present invention provides methods for
reducing the levels of certain components of blood serum which are
associated with rheumatoid arthritis, including C-reactive protein,
IL-6, TNF-.alpha., soluble ICAM-1, soluble E-selectin and/or
soluble IL-2r.
BRIEF DESCRIPTION OF THE FIGURES
[0029] FIG. 1A: Demographic data of patient cohorts. Demographic
data including gender, race, and disease duration as described in
Example 3, infra.
[0030] FIG. 1B: Demographic data of patient cohorts. Demographic
data including gender, age, weight, and disease activity, evaluated
by the patient and by the physician, as described in Example 3,
infra.
[0031] FIG. 1C: Demographic data of patient cohorts as described in
Example 3, infra. Demographic data including disease activity,
erythrocyte sedimentation rate (ESR), physical function (disability
evaluated by health questionnaire), and C-reactive protein
(CRP).
[0032] FIG. 1D: Demographic data of patient cohorts as described in
Example 3, infra. Demographic data including joint swelling, joint
tenderness, morning stiffness, and pain.
[0033] FIG. 1E: Demographic data of patient cohorts as described in
Example 3, infra. Demographic data including prior treatments.
[0034] FIG. 2: Summary of discontinuations at day 85 by reason as
described in Example 3, infra.
[0035] FIG. 3A: ACR responses at Day 85 as described in Example 3,
infra: ACR-20, -50, and -70 responses.
[0036] FIG. 3B: ACR-20 responses at Day 85, including placebo
response, as described in Example 3, infra: ACR-20 response with
95% confidence limits.
[0037] FIG. 3C: ACR-20 responses at Day 85 as described in Example
3, infra: Difference in ACR-20 response with respect to 95%
confidence intervals.
[0038] FIG. 4A: Basic (20% improvement) clinical responses in
swollen and tender joint count in percentage of patients at Day 85
as described in Example 3, infra: basic clinical response,
ACR-20.
[0039] FIG. 4B: Clinical responses (in percentage improvement) in
swollen and tender joint count in percentage of patients at Day 85
as described in Example 3, infra: change in clinical response in
percentage improvement.
[0040] FIG. 5A: Pain response (by Likert scale by mean unit change
from baseline) in percentage of patients at Day 85 as described in
Example 3, infra: pain score changes from baseline.
[0041] FIG. 5B: Patient global disease changes (by Likert scale by
mean unit change from baseline) in percentage of patients at Day 85
as described in Example 3, infra: patient global disease activity
changes.
[0042] FIG. 5C: Physician global disease changes (by Likert scale
by mean unit change from baseline) in percentage of patients at Day
85 as described in Example 3, infra: physician global disease
activity changes.
[0043] FIG. 5D: Pain (by Likert scale by mean unit change from
baseline) in percentage of patients at Day 85 as described in
Example 3, infra: pain changes from baseline.
[0044] FIG. 6A: Patient global assessment of disease activity
change from baseline by range of 2 units at Day 85 as described in
Example 3, infra; disease activity improvement.
[0045] FIG. 6B: Physician global assessment of disease activity
change from baseline by range of 2 units at Day 85 as described in
Example 3, infra; disease activity improvement.
[0046] FIG. 7A: Percent reduction in C-reactive protein (CRP)
levels at Day 85 as described in Example 3, infra: percentage
reduction in CRP levels from baseline.
[0047] FIG. 7B: Difference in reduction in C-reactive protein (CRP)
levels at Day 85 as described in Example 3, infra: percent
reduction difference in CRP levels with 95% confidence
intervals.
[0048] FIG. 7C: Mean reduction in C-reactive protein (CRP) levels
at Day 85 as described in Example 3, infra: mean change from
baseline.
[0049] FIG. 8: Reduction in soluble IL-2 receptor levels mean
change from baseline at Day 85 as described in Example 3,
infra.
[0050] FIG. 9A: The effect of CTLA4Ig on tender joints over time as
described in Example 3, infra: median difference from baseline.
[0051] FIG. 9B: The effect of CTLA4Ig on tender joints over time as
described in Example 3, infra: mean difference from baseline.
[0052] FIG. 10A: The effect of CTLA4Ig on swollen joints over time
as described in Example 3, infra: median difference from
baseline.
[0053] FIG. 10B: The effect of CTLA4Ig on swollen joints over time
as described in Example 3, infra: mean difference from
baseline.
[0054] FIG. 11: The effect of CTLA4Ig on pain assessment mean
difference from baseline over time as described in Example 3,
infra.
[0055] FIG. 12A: The effect of CTLA4Ig on patient assessment of
disease activity mean difference from baseline over time as
described in Example 3, infra.
[0056] FIG. 12B: The effect of CTLA4Ig on physician assessment of
disease activity mean difference from baseline over time as
described in Example 3, infra.
[0057] FIG. 13A: The effect of L104EA29YIg on tender joints over
time as described in Example 3, infra: median difference from
baseline.
[0058] FIG. 13B: The effect of L104EA29YIg on tender joints over
time as described in Example 3, infra: mean change from
baseline.
[0059] FIG. 14A: The effect of L104EA29YIg on swollen joints over
time as described in Example 3, infra: median difference from
baseline.
[0060] FIG. 14B: The effect of L104EA29YIg on swollen joints over
time as described in Example 3, infra: mean change from
baseline.
[0061] FIG. 15: The effect of L104EA29YIg on pain assessment over
time as described in Example 3, infra: mean change from baseline
over time.
[0062] FIG. 16A: The effect of L104EA29YIg on patient assessment of
disease activity mean difference from baseline over time as
described in Example 3, infra.
[0063] FIG. 16B: The effect of L104EA29YIg on physician assessment
of disease activity mean difference from baseline over time as
described in Example 3, infra.
[0064] FIG. 17: Percent improvement in patient disability assessed
by Health Assessment Questionnaire (HAQ) compared to the baseline
at Day 85 with CTLA4Ig and L104EA29YIg treatment as described in
Example 3, infra.
[0065] FIG. 18: Nucleotide and amino acid sequence of L104EIg (SEQ
ID NOs: 6-7) as described in Example 1, infra.
[0066] FIG. 19: Nucleotide and amino acid sequence of L104EA29YIg
(SEQ ID NOs: 8-9) as described in Example 1, infra.
[0067] FIG. 20: Nucleotide and amino acid sequence of L104EA29LIg
(SEQ ID NOs: 10-11) as described in Example 1, infra.
[0068] FIG. 21: Nucleotide and amino acid sequence of L104EA29TIg
(SEQ ID NOs: 12-13) as described in Example 1, infra.
[0069] FIG. 22: Nucleotide and amino acid sequence of L104EA29WIg
(SEQ ID NOs: 14-15) as described in Example 1, infra.
[0070] FIG. 23: Nucleotide and amino acid sequence of CTLA4
receptor (SEQ ID NOs: 16-17).
[0071] FIG. 24: Nucleotide and amino acid sequence of CTLA4Ig (SEQ
ID NOs: 18-19). FIG. 25: SDS gel (FIG. 25A) for CTLA4Ig (lane 1),
L104EIg (lane 2), and L104EA29YIg (lane 3A); and size exclusion
chromatographs of CTLA4Ig (FIG. 25B) and L104EA29YIg (FIG.
25C).
[0072] FIG. 26 (left and right depictions): A ribbon diagram of the
CTLA4 extracellular Ig V-like fold generated from the solution
structure determined by NMR spectroscopy. FIG. 26 (right depiction)
shows an expanded view of the CDR-1 (S25-R33) region and the MYPPPY
region indicating the location and side-chain orientation of the
avidity enhancing mutations, L104 and A29.
[0073] FIGS. 27A & 27B: FACS assays showing binding of
L104EA29YIg, L104EIg, and CTLA4Ig to human CD80- or
CD86-transfected CHO cells as described in Example 2, infra.
[0074] FIGS. 28A & 28B: Graphs showing inhibition of
proliferation of CD80-positive and CD86-positive CHO cells as
described in Example 2, infra.
[0075] FIGS. 29A & 29B: Graphs showing that L104EA29YIg is more
effective than CTLA4Ig at inhibiting proliferation of primary and
secondary allostimulated T cells as described in Example 2,
infra.
[0076] FIGS. 30A-C: Graphs illustrating that L104EA29YIg is more
effective than CTLA4Ig at inhibiting IL-2 (FIG. 30A), IL-4 (FIG.
30B), and gamma (.gamma.)-interferon (FIG. 30C) cytokine production
of allostimulated human T cells as described in Example 2,
infra.
[0077] FIG. 31: A graph demonstrating that L104EA29YIg is more
effective than CTLA4Ig at inhibiting proliferation of
phytohemaglutinin-(PHA) stimulated monkey T cells as described in
Example 2, infra.
[0078] FIG. 32: A graph showing the equilibrium binding analysis of
L104EA29YIg, L104EIg, and wild-type CTLA4Ig to CD86Ig.
[0079] FIGS. 33A & B: Reduction in soluble ICAM-1 and soluble
E-selectin levels mean change from baseline at Day 85 as described
in Example 3, infra.
[0080] FIG. 34: A graph showing the summary of ACR20 response by
visit day in response to methotrexate and CTLA4Ig (2 and 10 mg/kg)
therapy, as described in Example 5, infra.
[0081] FIG. 35: A graph showing the summary of ACR50 response by
visit day in response to methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg) therapy, as described in Example 5,
infra.
[0082] FIG. 36: A graph showing the summary of ACR70 response by
visit day in response to methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg) therapy, as described in Example 5,
infra.
[0083] FIG. 37: A graph showing the mean ACR-N over time in
response to methotrexate alone or methotrexate and CTLA4Ig (2 and
10 mg/kg) therapy, as described in Example 5, infra.
[0084] FIG. 38: A bar graph showing the ACR response in response to
methotrexate alone or methotrexate and CTLA4Ig (2 and 10 mg/kg)
therapy on day 180 with a 95% confidence interval, as described in
Example 5, infra.
[0085] FIG. 39: A bar graph showing the proportion of New Active
Joints in response to methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg) therapy on day 180, as described in
Example 5, infra.
[0086] FIG. 40: A bar graph showing ACR response after therapy with
methotrexate alone or methotrexate and CTLA4Ig (2 and 10 mg/kg) on
day 180, as described in Example 5, infra.
[0087] FIG. 41: A graph showing percent improvement in tender
joints after therapy with methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg)--mean percent improvement from baseline,
as described in Example 5, infra.
[0088] FIG. 42: A graph showing percent improvement in swollen
joints after therapy with methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg)--mean percent improvement from baseline,
as described in Example 5, infra.
[0089] FIG. 43: A graph showing percent improvement in pain after
therapy with methotrexate alone or methotrexate and CTLA4Ig (2 and
10 mg/kg)--mean percent improvement from baseline, as described in
Example 5, infra.
[0090] FIG. 44: A graph showing percent improvement in regard to
disease activity as reported by the subject after therapy with
methotrexate alone or methotrexate and CTLA4Ig (2 and 10
mg/kg)--mean percent improvement from baseline, as described in
Example 5, infra.
[0091] FIG. 45: A graph showing percent improvement in regard to
disease activity as reported by the physician after therapy with
methotrexate alone or methotrexate and CTLA4Ig (2 and 10
mg/kg)--mean percent improvement from baseline, as described in
Example 5, infra.
[0092] FIG. 46: A graph showing percent improvement regarding
physical function after therapy with methotrexate alone or
methotrexate and CTLA4Ig (2 and 10 mg/kg)--mean percent improvement
from baseline as measured by HAQ, as described in Example 5,
infra.
[0093] FIG. 47: A graph showing percent improvement in CRP levels
function after therapy with methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg)--mean percent improvement from baseline,
as described in Example 5, infra.
[0094] FIG. 48: A graph showing percent improvement in CRP levels
function after therapy with methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg)--median percent improvement from baseline,
as described in Example 5, infra.
[0095] FIG. 49: A graph showing the difference in ACR response rate
on day 180 in two groups after therapy with CTLA4Ig (2 and 10
mg/kg) in comparison to a group treated with methotrexate (MTX)
only (95% Confidence Limits), as described in Example 5, infra.
[0096] FIG. 50: A graph showing the change from baseline for SF-36
Physical Health Component on day 180, in two groups after therapy
with CTLA4Ig (2 and 10 mg/kg) compared to a group treated with
methotrexate only (95% Confidence Limits), as described in Example
5, infra.
[0097] FIG. 51: A graph showing the change from baseline for SF-36
Mental Health Component on Day 180, in two groups after therapy
with CTLA4Ig (2 and 10 mg/kg) compared to a group treated with
methotrexate only (95% Confidence Limits), as described in Example
5, infra.
[0098] FIG. 52: A bar graph showing CRP levels at day 180 after
therapy with methotrexate alone or methotrexate and CTLA4Ig (2 and
10 mg/kg), as described in Example 5, infra.
[0099] FIG. 53: A bar graph showing Rheumatoid Factor levels on day
180 after therapy with methotrexate alone or methotrexate and
CTLA4Ig (2 and 10 mg/kg), as described in Example 5, infra.
[0100] FIG. 54: A bar graph showing IL-2r levels on day 180 after
therapy with methotrexate alone or methotrexate and CTLA4Ig (2 and
10 mg/kg), as described in Example 5, infra.
[0101] FIG. 55: A bar graph showing IL-6 levels on day 180 after
therapy with methotrexate alone or methotrexate and CTLA4Ig (2 and
10 mg/kg), as described in Example 5, infra.
[0102] FIG. 56: A bar graph showing TNF.alpha. levels on day 180
after therapy with methotrexate alone or methotrexate and CTLA4Ig
(2 and 10 mg/kg), as described in Example 5, infra.
[0103] FIG. 57: A table of the univariate methotrexate dose at
screening/enrollment for treatment group BMS 10-treated with
CTLA4Ig at 10 mg/kg body weight as described in Example 5,
infra.
[0104] FIG. 58: A table of the univariate methotrexate dose at
screening/enrollment for treatment group BMS 2-treated with CTLA4Ig
at 2 mg/kg body weight as described in Example 5, infra.
[0105] FIG. 59: A table of the univariate methotrexate dose at
screening/enrollment for the placebo group, as described in Example
5, infra.
[0106] FIG. 60: A table of the univariate methotrexate dose up to
and including day 180 of the study for treatment group BMS
10-treated with CTLA4Ig at 10 mg/kg body weight as described in
Example 5, infra.
[0107] FIG. 61: A table of the univariate methotrexate dose up to
and including day 180 of the study for treatment group BMS
2-treated with CTLA4Ig at 2 mg/kg body weight as described in
Example 5, infra.
[0108] FIG. 62: A table of the univariate methotrexate dose up to
and including day 180 of the study for the placebo group, as
described in Example 5, infra.
[0109] FIG. 63: A bar graph showing the difference in modified ACR
response rates on day 180 in two groups after therapy with
etanercept alone (25 mg twice weekly) or in combination with
CTLA4Ig (2 mg/kg), as described in Example 6, infra.
[0110] FIGS. 64A-C: Graphs showing percentage improvement of
individual components of the modified ACR criteria as assessed on
each visit day after therapy with etanercept alone (25 mg twice
weekly) or in combination with CTLA4Ig (2 mg/kg) as described in
Example 6, infra. A. Tender Joint Count. B. Swollen Joint Count. C.
Pain Assessment.
[0111] FIG. 65: A. A graph showing the change from baseline for
SF-36 Physical Health Component on day 180, in two groups after
therapy with etanercept (25 mg biweekly) alone or in combination
with CTLA4Ig (2 mg/kg) (95% Confidence Limits), as described in
Example 6, infra. B. A graph showing the change from baseline for
SF-36 Mental Health Component on day 180, in two groups after
therapy with etanercept (25 mg biweekly) alone or in combination
with CTLA4Ig (2 mg/kg) (95% Confidence Limits), as described in
Example 6, infra.
[0112] FIG. 66: Nucleotide sequence of a CTLA4Ig encoding a signal
peptide; a wild type amino acid sequence of the extracellular
domain of CTLA4 starting at methionine at position +1 to aspartic
acid at position +124, or starting at alanine at position -1 to
aspartic acid at position +124; and an Ig region (SEQ ID NO.:
21).
[0113] FIG. 67: Amino acid sequence of a CTLA4Ig having a signal
peptide; a wild type amino acid sequence of the extracellular
domain of CTLA4 starting at methionine at position +1 to aspartic
acid at position +124, or starting at alanine at position -1 to
aspartic acid at position +124; and an Ig region (SEQ ID NO.:
22).
[0114] FIG. 68: A schematic diagram showing the disposition of
subjects into three cohorts as described in Example 7, infra.
[0115] FIG. 69: A Kaplan-Meier plot of the cumulative proportion of
subjects who discontinued for any reason during the first 12 months
of the study, as described in Example 7, infra.
[0116] FIG. 70: A Kaplan-Meier plot of the cumulative proportion of
subjects who discontinued due to lack of efficacy during the first
12 months of study, as described in Example 7, infra.
[0117] FIG. 71A: A graph showing the ACR Responses on Day 180 for
patients administered methotrexate alone or methotrexate and
CTLA4Ig (2 or 10 mg/kg body weight) as described in Example 7,
infra.
[0118] FIG. 71B: A graph showing the 95 Percent Confidence
Intervals for Differences in ACR Responses on Day 180 for patients
administered methotrexate alone or methotrexate and CTLA4Ig (2 or
10 mg/kg body weight) as described in Example 7, infra.
[0119] FIG. 72A: A graph showing the ACR Responses on Day 360 for
patients administered methotrexate alone or methotrexate and
CTLA4Ig (2 or 10 mg/kg body weight) as described in Example 7,
infra.
[0120] FIG. 72B: A graph showing the 95 Percent Confidence
Intervals for Differences in ACR Responses on Day 360 for patients
administered methotrexate alone or methotrexate and CTLA4Ig (2 or
10 mg/kg body weight) as described in Example 7, infra.
[0121] FIG. 73A: A graph summarizing the ACR 20 Response by Visit
during a one year interval for patients administered methotrexate
alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as
described in Example 7, infra.
[0122] FIG. 73B: A graph summarizing the ACR 50 Response by Visit
during a one year interval for patients administered methotrexate
alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as
described in Example 7, infra.
[0123] FIG. 73C: A graph summarizing the ACR 70 Response by Visit
during a one year interval for patients administered methotrexate
alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as
described in Example 7, infra.
[0124] FIG. 74: A graph showing the Mean ACR-N over a one year time
interval for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
[0125] FIG. 75: A graph showing the Proportion of New Active Joints
at Day 180 for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
[0126] FIG. 76A: A graph showing the Frequency of New Tender Joints
per Subject at Day 180 for patients administered methotrexate alone
or methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as
described in Example 7, infra.
[0127] FIG. 76B: A graph showing the Frequency of New Tender Joints
per Subject at Day 360 for patients administered methotrexate alone
or methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as
described in Example 7, infra.
[0128] FIG. 77A: A graph showing the Frequency of New Swollen
Joints per Subject at Day 180 for patients administered
methotrexate alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body
weight) as described in Example 7, infra.
[0129] FIG. 77B: A graph showing the Frequency of New Swollen
Joints per Subject at Day 360 for patients administered
methotrexate alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body
weight) as described in Example 7, infra.
[0130] FIG. 78: A graph showing the Proportion of New Active Joints
at Day 360 for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
[0131] FIG. 79: Graphs showing the: A) Change from Baseline in the
Physical Health Domains on Day 180, and B) Change from Baseline in
the Mental Health Domains on 180, for patients administered
methotrexate alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body
weight) as described in Example 7, infra.
[0132] FIG. 80: Graphs showing the: A) Change from Baseline in the
Physical Health Domains on Day 360, and B) Change from Baseline in
the Mental Health Domains on Day 360, for patients administered
methotrexate alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body
weight) as described in Example 7, infra.
[0133] FIG. 81: A graph showing the Soluble IL-2r Levels at
Baseline, Days 180 and 360 for patients administered methotrexate
alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as
described in Example 7, infra.
[0134] FIG. 82: A graph showing the Rheumatoid Factor Levels at
Baseline, Days 180 and 360 for patients administered methotrexate
alone or methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as
described in Example 7, infra.
[0135] FIG. 83: A graph showing the ICAM-1 Levels at Baseline, Days
180 and 360 for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
[0136] FIG. 84: A graph showing the e-Selectin Levels at Baseline,
Days 180 and 360 for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
[0137] FIG. 85: A graph showing the Serum IL-6 at Baseline, Days
180 and 360 for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
[0138] FIG. 86A: A graph showing the CRP Levels at Baseline, Days
180 and 360 for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
[0139] FIG. 86B: A graph showing the TNF.alpha. Levels at Baseline,
Days 180 and 360 for patients administered methotrexate alone or
methotrexate and CTLA4Ig (2 or 10 mg/kg body weight) as described
in Example 7, infra.
DETAILED DESCRIPTION OF THE INVENTION
[0140] Definitions
[0141] All scientific and technical terms used in this application
have meanings commonly used in the art unless otherwise specified.
As used in this application, the following words or phrases have
the meanings specified.
[0142] As used herein, DMARD refers to a Disease Modifying
Anti-Rheumatic Drug. A DMARD is any agent that modifies the
symptoms and/or progression associated with an immune system
disease, including autoimmune diseases (e.g. rheumatic diseases),
graft-related disorders and immunoproliferative diseases. DMARDs
modify one or more of the symptoms and/or disease progression
associated with rheumatic disease. Symptoms of rheumatic diseases,
include the following: joint swelling, pain, tenderness, morning
stiffness, structural damage, an elevated level of serum C-reactive
protein (CRP), an elevated level of soluble IL-2r, an elevated
level of soluble ICAM-1, an elevated level of soluble E-selectin,
an elevated level of rheumatoid factor, an elevated level of IL-6
or an elevated erythrocyte sedimentation rate (ESR). These symptoms
and the reduction of these symptoms can be evaluated by any well
known evaluation methods including: Health Questionnaire
Assessments; ACR 20, 50, 70; and/or Medical Outcomes Study Short
Form-36.
[0143] DMARDs include, but are not limited to, dihydrofolic acid
reductase inhibitors e.g., methotrexate; cyclophosphamide;
cyclosporine; cyclosporin A; chloroquine; hydroxychloroquine;
sulfasalazine (sulphasalazopyrine) gold salts D-penicillamine;
leflunomide; azathioprine; anakinra; TNF blockers e.g., infliximab
(REMICADER) or etanercept; and a biological agent that targets an
inflammatory cytokine.
[0144] As used herein, NSAID refers to a Non-Steroidal
Anti-Inflammatory Drug. NSAIDs reduce inflammatory reactions in a
subject. NSAIDs include, but are not limited to acetyl salicylic
acid, choline magnesium salicylate, diflunisal, magnesium
salicylate, salsalate, sodium salicylate, diclofenac, etodolac,
fenoprofen, flurbiprofen, indomethacin, ketoprofen, ketorolac,
meclofenamate, naproxen, nabumetone, phenylbutazone, piroxicam,
sulindac, tolmetin, acetaminophen, ibuprofen, Cox-2 inhibitors,
meloxicam and tramadol.
[0145] As used herein, "ligand" refers to a molecule that
specifically recognizes and binds another molecule, for example, a
ligand for CTLA4 is a B7 molecule. In a further example, a ligand
for the B7 molecule is a CTLA4 and/or CD28 molecule. The
interaction of a molecule and its ligand can be regulated by
compositions of the invention. For example, CTLA4 interaction with
its ligand B7 can be blocked by administration of CTLA4Ig
molecules. Alternatively, Tumor Necrosis Factor (TNF) interaction
with its ligand, TNF receptor (TNFR), can be blocked by
administration of etanercept or other TNF/TNFR blocking
molecules.
[0146] As used herein "wild type CTLA4" or "non-mutated CTLA4" has
the amino acid sequence of naturally occurring, full length CTLA4
as shown in FIG. 23 (also as described in U.S. Pat. Nos. 5,434,131,
5,844,095, and 5,851,795 herein incorporated by reference in their
entirety), or any portion or derivative thereof, that recognizes
and binds a B7 or interferes with a B7 so that it blocks binding to
CD28 and/or CTLA4 (e.g., endogenous CD28 and/or CTLA4). In
particular embodiments, the extracellular domain of wild type CTLA4
begins with methionine at position +1 and ends at aspartic acid at
position +124, or the extracellular domain of wild type CTLA4
begins with alanine at position -1 and ends at aspartic acid at
position +124 as shown in FIG. 23. Wild type CTLA4 is a cell
surface protein, having an N-terminal extracellular domain, a
transmembrane domain, and a C-terminal cytoplasmic domain. The
extracellular domain binds to target molecules, such as a B7
molecule. In a cell, the naturally occurring, wild type CTLA4
protein is translated as an immature polypeptide, which includes a
signal peptide at the N-terminal end. The immature polypeptide
undergoes post-translational processing, which includes cleavage
and removal of the signal peptide to generate a CTLA4 cleavage
product having a newly generated N-terminal end that differs from
the N-terminal end in the immature form. One skilled in the art
will appreciate that additional post-translational processing may
occur, which removes one or more of the amino acids from the newly
generated N-terminal end of the CTLA4 cleavage product.
Alternatively, the signal peptide may not be removed completely,
generating molecules that begin before the common starting amino
acid methionine. Thus, the mature CTLA4 protein may start at
methionine at position +1 or alanine at position -1. The mature
form of the CTLA4 molecule includes the extracellular domain or any
portion thereof, which binds to B7.
[0147] As used herein, a "CTLA4 mutant molecule" means wildtype
CTLA4 as shown in FIG. 23 or any portion or derivative thereof,
that has a mutation or multiple mutations (preferably in the
extracellular domain of wildtype CTLA4). A CTLA4 mutant molecule
has a sequence that it is similar but not identical to the sequence
of wild type CTLA4 molecule, but still binds a B7. The mutations
may include one or more amino acid residues substituted with an
amino acid having conservative (e.g., substitute a leucine with an
isoleucine) or non-conservative (e.g., substitute a glycine with a
tryptophan) structure or chemical properties, amino acid deletions,
additions, frameshifts, or truncations. CTLA4 mutant molecules may
include a non-CTLA4 molecule therein or attached thereto. The
mutant molecules may be soluble (i.e., circulating) or bound to a
cell surface. Additional CTLA4 mutant molecules include those
described in U.S. patent application Ser. Nos. 09/865,321,
60/214,065 and 60/287,576; in U.S. Pat. Nos. 6,090,914 5,844,095
and 5,773,253; and as described by Peach, R. J., et al., in J Exp
Med 180:2049-2058 (1994)). CTLA4 mutant molecules can be made
synthetically or recombinantly.
[0148] "CTLA4Ig" is a soluble fusion protein comprising an
extracellular domain of wildtype CTLA4 that binds B7, or a portion
thereof, joined to an immunoglobulin constant region (Ig), or a
portion thereof. A particular embodiment comprises the
extracellular domain of wild type CTLA4 (as shown in FIG. 23)
starting at methionine at position +1 and ending at aspartic acid
at position +124, or starting at alanine at position -1 to aspartic
acid at position +124; a junction amino acid residue glutamine at
position +125; and an immunoglobulin portion encompassing glutamic
acid at position +126 through lysine at position +357 (DNA encoding
CTLA4Ig was deposited on May 31, 1991 with the American Type
Culture Collection (ATCC), 10801 University Blvd., Manassas, Va.
20110-2209 under the provisions of the Budapest Treaty, and has
been accorded ATCC accession number ATCC 68629; Linsley, P., et
al., 1994 Immunity 1:793-80). CTLA4Ig-24, a Chinese Hamster Ovary
(CHO) cell line expressing CTLA4Ig was deposited on May 31, 1991
with ATCC identification number CRL-10762). The soluble CTLA4Ig
molecules used in the methods and/or kits of the invention may or
may not include a signal (leader) peptide sequence. Typically, in
the methods and/or kits of the invention, the molecules do not
include a signal peptide sequence.
[0149] "L104EA29YIg" is a fusion protein that is a soluble CTLA4
mutant molecule comprising an extracellular domain of wildtype
CTLA4 with amino acid changes A29Y (a tyrosine amino acid residue
substituting for an alanine at position 29) and L104E (a glutamic
acid amino acid residue substituting for a leucine at position
+104), or a portion thereof that binds a B7 molecule, joined to an
Ig tail (included in FIG. 19; DNA encoding L104EA29YIg was
deposited on Jun. 20, 2000 with ATCC number PTA-2104; copending in
U.S. patent application Ser. Nos. 09/579,927, 60/287,576 and
60/214,065, incorporated by reference herein). The soluble
L104EA29YIg molecules used in the methods and/or kits of the
invention may or may not include a signal (leader) peptide
sequence. Typically, in the methods and/or kits of the invention,
the molecules do not include a signal peptide sequence.
[0150] As used herein, "soluble" refers to any molecule, or
fragments and derivatives thereof, not bound or attached to a cell,
i.e., circulating. For example, CTLA4, B7 or CD28 can be made
soluble by attaching an immunoglobulin (Ig) moiety to the
extracellular domain of CTLA4, B7 or CD28, respectively.
Alternatively, a molecule such as CTLA4 can be rendered soluble by
removing its transmembrane domain. Typically, the soluble molecules
used in the methods, compositions and/or kits of the invention do
not include a signal (or leader) sequence.
[0151] As used herein, "soluble CTLA4 molecules" means
non-cell-surface-bound (i.e. circulating) CTLA4 molecules or any
functional portion of a CTLA4 molecule that binds B7 including, but
not limited to: CTLA4Ig fusion proteins (e.g. encoded by DNA
deposited with ATCC accession number 68629), wherein the
extracellular domain of CTLA4 is fused to an immunoglobulin (Ig)
moiety such as IgC.gamma.1 (IgCgamma1), IgC.gamma.2 (IgCgamma2),
IgC.gamma.3 (IgCgamma3), IgC.gamma.4 (IgCgamma4), IgC.mu. (IgCmu),
IgC.alpha.1 (IgCalpha1), IgC.alpha.2 (IgCalpha2), IgC.delta.
(IgCdelta) or IgC.epsilon. (IgCepsilon), rendering the fusion
molecule soluble, or fragments and derivatives thereof; proteins
with the extracellular domain of CTLA4 fused or joined with a
portion of a biologically active or chemically active protein such
as the papillomavirus E7 gene product (CTLA4-E7),
melanoma-associated antigen p97 (CTLA4-p97) or HIV env protein
(CTLA4-env gp 120) (as described in U.S. Pat. No. 5,844,095, herein
incorporated by reference in its entirety), or fragments and
derivatives thereof; hybrid (chimeric) fusion proteins such as
CD28/CTLA4Ig (as described in U.S. Pat. No. 5,434,131, herein
incorporated by reference in its entirety), or fragments and
derivatives thereof; CTLA4 molecules with the transmembrane domain
removed to render the protein soluble (Oaks, M. K., et al., 2000
Cellular Immunology 201:144-153, herein incorporated by reference
in its entirety), or fragments and derivatives thereof. "Soluble
CTLA4 molecules" also include fragments, portions or derivatives
thereof, and soluble CTLA4 mutant molecules, having CTLA4 binding
activity. The soluble CTLA4 molecules used in the methods of the
invention may or may not include a signal (leader) peptide
sequence. Typically, in the methods, compositions and/or kits of
the invention, the molecules do not include a signal peptide
sequence.
[0152] As used herein "the extracellular domain of CTLA4" is the
portion of CTLA4 that recognizes and binds CTLA4 ligands, such as
B7 molecules. For example, an extracellular domain of CTLA4
comprises methionine at position +1 to aspartic acid at position
+124 (FIG. 23). Alternatively, an extracellular domain of CTLA4
comprises alanine at position -1 to aspartic acid at position +124
(FIG. 23). The extracellular domain includes fragments or
derivatives of CTLA4 that bind a B7 molecule. The extracellular
domain of CTLA4 as shown in FIG. 23 may also include mutations that
change the binding avidity of the CTLA4 molecule for a B7
molecule.
[0153] As used herein, the term "mutation" means a change in the
nucleotide or amino acid sequence of a wildtype molecule, for
example, a change in the DNA and/or amino acid sequences of the
wild-type CTLA4 extracellular domain. A mutation in DNA may change
a codon leading to a change in the amino acid sequence. A DNA
change may include substitutions, deletions, insertions,
alternative splicing, or truncations. An amino acid change may
include substitutions, deletions, insertions, additions,
truncations, or processing or cleavage errors of the protein.
Alternatively, mutations in a nucleotide sequence may result in a
silent mutation in the amino acid sequence as is well understood in
the art. In that regard, certain nucleotide codons encode the same
amino acid. Examples include nucleotide codons CGU, CGG, CGC, and
CGA encoding the amino acid, arginine (R); or codons GAU, and GAC
encoding the amino acid, aspartic acid (D). Thus, a protein can be
encoded by one or more nucleic acid molecules that differ in their
specific nucleotide sequence, but still encode protein molecules
having identical sequences. The amino acid coding sequence is as
follows:
1 One Letter Amino Acid Symbol Symbol Codons Alanine Ala A GCU,
GCC, GCA, GCG Cysteine Cys C UGU, UGC Aspartic Acid Asp D GAU, GAC
Glutamic Acid Glu E GAA, GAG Phenylalanine Phe F UUU, UUC Glycine
Gly G GGU, GGC, GGA, GGG Histidine His H CAU, CAC Isoleucine Ile I
AUU, AUC, AUA Lysine Lys K AAA, AAG Leucine Leu L UUA, UUG, CUU,
CUC, CUA, CUG Methionine Met M AUG Asparagine Asn N AAU, AAC
Proline Pro P CCU, CCC, CCA, CCG Glutamine Gln Q CAA, CAG Arginine
Arg R CGU, CGC, CGA, CGG, AGA, AGG Serine Ser S UCU, UCC, UCA, UCG,
AGU, AGC Threonine Thr T ACU, ACC, ACA, ACG Valine Val V GUU, GUC,
GUA, GUG Tryptophan Trp W UGG Tyrosine Tyr Y UAU, UAC
[0154] The mutant molecule may have one or more mutations. As used
herein, a "non-CTLA4 protein sequence" or "non-CTLA4 molecule"
means any protein molecule that does not bind B7 and does not
interfere with the binding of CTLA4 to its target. The non-CTLA4
molecule, attached to the extracellular domain of a CTLA4 molecule
can alter the solubility or affinity of the CTLA4 molecule. An
example includes, but is not limited to, an immunoglobulin (Ig)
constant region or portion thereof. Preferably, the Ig constant
region is a human or monkey Ig constant region, e.g., human
C(gamma)1, including the hinge, CH2 and CH3 regions. The Ig
constant region can be mutated to reduce its effector functions
(U.S. Pat. Nos. 5,637,481, 5,844,095 and 5,434,131).
[0155] As used herein, a "fragment" or "portion" is any part or
segment of a molecule e.g. CTLA4 or CD28, preferably the
extracellular domain of CTLA4 or CD28 or a part or segment thereof,
that recognizes and binds its target, e.g., a B7 molecule.
[0156] As used herein, "B7" refers to the B7 family of molecules
including, but not limited to, B7-1 (CD80) (Freeman et al, 1989, J.
Immunol. 143:2714-2722, herein incorporated by reference in its
entirety), B7-2 (CD86) (Freeman et al, 1993, Science 262:909-911
herein incorporated by reference in its entirety; Azuma et al,
1993, Nature 366:76-79 herein incorporated by reference in its
entirety) that may recognize and bind CTLA4 and/or CD28. A B7
molecule can be expressed on an activated B cell.
[0157] As used herein, "CD28" refers to the molecule that
recognizes and binds B7 as described in U.S. Pat. Nos. 5,580,756
and 5,521,288 (herein incorporated by reference in their
entirety).
[0158] As used herein, "B7-positive cells" are any cells with one
or more types of B7 molecules expressed on the cell surface.
[0159] As used herein, a "derivative" is a molecule that shares
sequence similarity and activity of its parent molecule. For
example, a derivative of CTLA4 includes a soluble CTLA4 molecule
having an amino acid sequence at least 70% similar to the
extracellular domain of wildtype CTLA4, and which recognizes and
binds B7 e.g. CTLA4Ig or soluble CTLA4 mutant molecule L104EA29YIg.
A derivative means any change to the amino acid sequence and/or
chemical quality of the amino acid e.g., amino acid analogs.
[0160] As used herein, to "regulate" an immune response is to
activate, stimulate, up-regulate, inhibit, block, down-regulate or
modify the immune response. The auto-immune diseases described
herein, may be treated by regulating an immune response e.g., by
regulating functional CTLA4- and/or CD28-positive cell interactions
with B7-positive cells. For example, a method for regulating an
immune response comprises contacting the B7-positive cells with a
soluble CTLA4 molecule of the invention so as to form soluble
CTLA4/B7 complexes, the soluble CTLA4 molecule interfering with
reaction of an endogenous CTLA4 and/or CD28 molecule with said B7
molecule.
[0161] As used herein, to "block" or "inhibit" a receptor, signal
or molecule means to interfere with the activation of the receptor,
signal or molecule, as detected by an art-recognized test. For
example, blockage of a cell-mediated immune response can be
detected by determining reduction of Rheumatic Disease associated
symptoms. Blockage or inhibition may be partial or total.
[0162] As used herein, "blocking B7 interaction" means to interfere
with the binding of B7 to its ligands, such as CD28 and/or CTLA4,
thereby obstructing T-cell and B7-positive cell interactions.
Examples of agents that block B7 interactions include, but are not
limited to, molecules such as an antibody (or portion or derivative
thereof) that recognizes and binds to the any of CTLA4, CD28 or B7
molecules (e.g. B7-1, B7-2); a soluble form (or portion or
derivative thereof) of the molecules such as soluble CTLA4; a
peptide fragment or other small molecule designed to interfere with
the cell signal through the CTLA4/CD28/B7-mediated interaction. In
a preferred embodiment, the blocking agent is a soluble CTLA4
molecule, such as CTLA4Ig (ATCC 68629) or L104EA29YIg (ATCC
PTA-2104), a soluble CD28 molecule such as CD28Ig (ATCC 68628), a
soluble B7 molecule such as B7Ig (ATCC 68627), an anti-B7
monoclonal antibody (e.g. ATCC HB-253, ATCC CRL-2223, ATCC
CRL-2226, ATCC HB-301, ATCC HB-11341 and monoclonal antibodies as
described in by Anderson et al in U.S. Pat. No. 6,113,898 or
Yokochi et al., 1982. J. Immun., 128(2)823-827), an anti-CTLA4
monoclonal antibody (e.g. ATCC HB-304, and monoclonal antibodies as
described in references 82-83) and/or an anti-CD28 monoclonal
antibody (e.g. ATCC HB 11944 and mAb 9.3 as described by Hansen
(Hansen et al., 1980. Immunogenetics 10: 247-260) or Martin (Martin
et al., 1984. J. Clin. Immun., 4(1):18-22)). Blocking B7
interactions can be detected by art-recognized tests such as
determining reduction of immune disease (e.g., rheumatic disease)
associated symptoms, by determining reduction in T-cell/B7-cell
interactions or by determining reduction in B7 interaction with
CTLA4 and/or CD28. Blockage may be partial or total.
[0163] As used herein, an "effective amount" of a molecule is
defined as an amount that blocks the interaction of the molecule
with its ligand. For example, an effective amount of a molecule
that blocks B7 interaction with CTLA4 and/or CD28 may be defined as
the amount of the molecule that, when bound to B7 molecules on
B7-positive cells, inhibit B7 molecules from binding endogenous
ligands such as CTLA4 and CD28. Alternatively, an effective amount
of a molecule that blocks B7 interaction with CTLA4 and/or CD28 may
be defined as the amount of the molecule that, when bound to CTLA4
and/or CD28 molecules on T cells, inhibit B7 molecules from binding
endogenous ligands such as CTLA4 and CD28. The inhibition or
blockage may be partial or complete.
[0164] As used herein, "treating" a disease means to manage a
disease by medicinal or other therapies. Treatment of a disease may
ameliorate the symptoms of a disease, reduce the severity of a
disease, alter the course of disease progression and/or ameliorate
or cure the basic disease problem. For example, to treat an
auto-immune disease may be accomplished by regulating an immune
response e.g., by regulating functional CTLA4- and/or CD28-positive
cell interactions with B7-positive cells. Alternatively, treating
an auto-immune disease may be accomplished by preventing the
disease from occurring or progressing through the use of the
compositions described herein.
[0165] As used herein, "immune system disease" means any disease
mediated by T-cell interactions with B7-positive cells including,
but not limited to, autoimmune diseases, graft related disorders
and immunoproliferative diseases. Examples of immune system
diseases include graft versus host disease (GVHD) (e.g., such as
may result from bone marrow transplantation, or in the induction of
tolerance), immune disorders associated with graft transplantation
rejection, chronic rejection, and tissue or cell allo- or
xenografts, including solid organs (e.g., kidney transplants),
skin, islets, muscles, hepatocytes, neurons. Examples of
immunoproliferative diseases include, but are not limited to,
psoriasis, T-cell lymphoma, T-cell acute lymphoblastic leukemia,
testicular angiocentric T-cell lymphoma, benign lymphocytic
angiitis, lupus (e.g. lupus erythematosus, lupus nephritis),
Hashimoto's thyroiditis, primary myxedema, Graves' disease,
pernicious anemia, autoimmune atrophic gastritis, Addison's
disease, diabetes (e.g. insulin dependent diabetes mellitis, type I
diabetes mellitis, type II diabetes mellitis), good pasture's
syndrome, myasthenia gravis, pemphigus, Crohn's disease,
sympathetic ophthalmia, autoimmune uveitis, multiple sclerosis,
autoimmune hemolytic anemia, idiopathic thrombocytopenia, primary
biliary cirrhosis, chronic action hepatitis, ulceratis colitis,
Sjogren's syndrome, rheumatic diseases (e.g. rheumatoid arthritis),
polymyositis, scleroderma, and mixed connective tissue disease.
[0166] As used herein, "rheumatic diseases" means any disease that
affects the joints, bone, soft tissue, or spinal cord (Mathies, H.
1983 Rheuma) and comprises inflammatory rheumatism, degenerative
rheumatism, extra-articular rheumatism, and collagen diseases.
Additionally, rheumatic diseases include, but are not limited to,
chronic polyarthritis, psoriasis arthropathica, ankylosing
spondylitis, rheumatoid arthritis, panarteriitis nodosa, systemic
lupus erythematosus, progressive systemic scleroderma,
periarthritis humeroscapularis, arthritis uratica,
chondrocalcinosis, dermatomyositis, muscular rheumatism, myositis,
and myogelosis. Some rheumatic diseases are known to be autoimmune
diseases caused by a subject's altered immune response.
[0167] As used herein, "gene therapy" is a process to treat a
disease by genetic manipulation. Gene therapy involves introducing
a nucleic acid molecule into a cell and the cell expressing a gene
product encoded by the nucleic acid molecule. For example, as is
well known by those skilled in the art, introducing the nucleic
acid molecule into a cell may be performed by introducing an
expression vector containing the nucleic acid molecule of interest
into cells ex vivo or in vitro by a variety of methods including,
for example, calcium phosphate precipitation, diethyaminoethyl
dextran, polyethylene glycol (PEG), electroporation, direct
injection, lipofection or viral infection (Sambrook et al.,
Molecular Cloning: A Laboratory Manual (Cold Spring Harbor
Laboratory Press 1989); Kriegler M. Gene Transfer ad Expression: A
Laboratory Manual (W. H. Freeman and Co, New York, N.Y., 1993) and
Wu, Methods in Enzymology (Academic Press, New York, 1993), each of
which is incorporated herein by reference). Alternatively,
nucleotide sequences of interest may be introduced into a cell in
vivo using a variety of vectors and by a variety of methods
including, for example: direct administration of the nucleic acid
into a subject (Williams et al, 1991 PNAS 88:2726-2730); or
insertion of the nucleic acid molecule into a viral vector,
production of the recombinant virus or viral particle, and
infection of the subject with the recombinant virus (Battleman et
al, 1993 J Neurosci 13:94-951; Carroll et al, 1993 J Cell Biochem
17E:241; Lebkowski et al, U.S. Pat. No. 5,354,678; Davison and
Elliott, Molecular Virology: A Practical Approach (IRL Press, New
York, 1993)). Other methods used for in vivo transfer include
encapsulation of the nucleic acid into liposomes, and direct
introduction of the liposomes, or liposomes combined with a
hemagglutinating Sendai virus, into a subject (U.S. Pat. No.
5,824,655, incorporated by reference herein). The transfected or
infected cells express the protein products encoded by the nucleic
acid in order to ameliorate a disease or the symptoms of a
disease.
[0168] As used herein, "Health Questionnaire Assessments (HAQs)"
refers to a set of questions used to evaluate patients for symptoms
of disease activity. These symptoms included: joint swelling, joint
tenderness, inflammation, morning stiffness, disease activity and
disability evaluated by each patient in a self-administered
questionnaire regarding their physical well-being and function,
disease activity and disability as evaluated a physician, and pain
(Fries, J. F., et al., 1982 J. of Rheumatology 9:789-793).
[0169] As used herein, "ACR" refers to clinical response studies
based on criteria established by the American College of
Rheumatology. A subject satisfied the "ACR20" criterion if there
was about a 20 percent improvement in tender and swollen joint
counts and 20 percent improvement in three of five remaining
symptoms measured, such as patient and physician global disease
changes, pain, physical disability, and an acute phase reactant
such as CRP or ESR (Felson, D. T., et al., 1993 Arthritis and
Rheumatism 36:729-740; Felson, D. T., et al., 1995 Arthritis and
Rheumatism 38:1-9). Similarly, a subject satisfied the "ACR50" or
"ACR70" criterion if there was about a 50 or 70 percent
improvement, respectively, in tender and swollen joint counts and
about 50 or 70 percent improvement, respectively, in three of five
remaining symptoms measured, such as patient and physician global
disease changes, pain, physical disability, and an acute phase
reactant such as CRP or ESR.
[0170] As used herein, the "Medical Outcomes Study Short Form-36
(SF-36)" refers to forms used to evaluate the impact of a DMARD
(e.g., methotrexate or etanercept) and CTLA4Ig therapy on
health-related quality of life (HRQOL). The SF-36 consists of 36
items which covers four physical and four mental domains (physical
function, role-physical, bodily pain, general health, vitality,
social function, role emotional, and mental health). These
individual domains are used to derive the physical and mental
component summary scores which range from about 0 to 100, with
higher scores indicating better quality of life. Absolute
differences of 5 or more in the SF-36 scores were considered
clinically meaningful.
[0171] As used herein, "alleviate" refers to lessening or making
less severe, one or more of the symptoms of an immune disease
(e.g., rheumatic disease) including, but not limited to, joint
swelling, pain, tenderness, morning stiffness, structural damage,
an elevated level of serum C-reactive protein (CRP), an elevated
level of soluble IL-2r, an elevated level of soluble ICAM-1, an
elevated level of soluble E-selectin, an elevated level of
rheumatoid factor, an elevated level of IL-6 or an elevated
erythrocyte sedimentation rate.
[0172] In order that the invention herein described may be more
fully understood the following description is set forth.
[0173] Compositions and Methods of the Invention
[0174] The present invention provides compositions and methods for
treating immune system diseases, such as rheumatic diseases, by
administering to a subject an effective amount of a ligand that
blocks B7 interactions with CTLA4 and/or CD28. For example, such
ligands include: soluble CTLA4 molecules (such as CTLA4Ig,
CTLA4-E7, CTLA4-p97, CTLA4-env gp120, and mutant CTLA4 molecules
such as, CTLA4/CD28Ig, L104EA29YIg, L104EA29LIg, L104EA29TIg and/or
L104EA29WIg), soluble CD28 molecules, soluble B7-1 molecules,
soluble B7-2 molecules, and monoclonal antibodies that recognize
and bind B7, CD28 and/or CTLA4 (e.g., an anti-CTLA4 monoclonal
antibody, an anti-CD28 monoclonal antibody, an anti-B7-1 monoclonal
antibody or an anti-B7-2 monoclonal antibody.
[0175] Further, the present invention provides compositions and
methods for treating immune system diseases, such as rheumatic
diseases, by administering to a subject a combination of an
effective amount of 1) a DMARD (such as methotrexate or a molecule
that blocks TNF interactions, e.g., blocks TNF interactions with
its ligand) or other therapeutic agent, plus 2) an effective amount
of a molecule that blocks B7 interaction with CTLA4 and/or CD28
such as soluble CTLA4 molecules (e.g., CTLA4Ig, CTLA4Ig/CD28Ig,
CTLA4-E7, CTLA4-p97, CTLA4-env gp120, L104EA29YIg, L104EA29LIg,
L104EA29TIg and/or L104EA29WIg), soluble CD28 molecules, soluble
B7-1 molecules, soluble B7-2 molecules, and monoclonal antibodies
that recognize and bind B7, CD28 and/or CTLA4 (e.g., an anti-CTLA4
monoclonal antibody, an anti-CD28 monoclonal antibody, an anti-B7-1
monoclonal antibody or an anti-B7-2 monoclonal antibody).
[0176] An effective amount of a molecule that blocks B7 interaction
with CTLA4 and/or CD28 may be defined as the amount of anti-B7
monoclonal antibodies, soluble CTLA4 and/or soluble CD28 molecules
that, when bound to B7 molecules on B7-positive cells, inhibit B7
molecules from binding endogenous ligands such as CTLA4 and CD28.
The inhibition may be partial or complete.
[0177] Alternatively, an effective amount of a molecule that blocks
B7 interaction with CTLA4 and/or CD28 may be defined as the amount
of anti-CTLA4 monoclonal antibody, anti-CD28 monoclonal antibody or
soluble B7 (B7-1 or B7-2) molecules that, when bound to CTLA4
and/or CD28 molecules on T cells, inhibit B7 molecules from binding
endogenous ligands such as CTLA4 and CD28. The inhibition may be
partial or complete.
[0178] An effective amount of a molecule that blocks B7 interaction
with CTLA4 and/or CD28 is an amount about 0.1 to 100 mg/kg weight
of a subject. In another embodiment, the effective amount is an
amount about 0.5 to 5 mg/kg weight of a subject, 0.1 to 5 mg/kg
weight of a subject, about 5 to 10 mg/kg weight of a subject, about
10 to 15 mg/kg weight of a subject, about 15 to 20 mg/kg weight of
a subject, about 20 to 25 mg/kg weight of a subject, about 25 to 30
mg/kg weight of a subject, about 30 to 35 mg/kg weight of a
subject, about 35 to 40 mg/kg weight of a subject, about 40 to 45
mg/kg of a subject, about 45 to 50 mg/kg weight of a subject, about
50 to 55 mg/kg weight of a subject, about 55 to 60 mg/kg weight of
a subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, or about 95 to
100 mg/kg weight of a subject.
[0179] In an embodiment, the effective amount of a molecule that
blocks B7 interaction with CTLA4 and/or CD28 is an amount about 2
mg/kg to about 10 mg/kg weight of a subject. The preferred amount
is 10 mg/kg weight of a subject. In another embodiment, the
effective amount is an amount about 0.1 to 4 mg/kg weight of a
subject. In another embodiment the effective amount is an amount
about 0.1 to 0.5 mg/kg weight of a subject, about 0.5 to 1.0 mg/kg
weight of a subject, about 1.0 to 1.5 mg/kg weight of a subject,
about 1.5 to 2.0 mg/kg weight of a subject, about 2.0 to 2.5 mg/kg
weight of a subject, about 2.5 to 3.0 mg/kg weight of a subject,
about 3.0 to 3.5 mg/kg weight of a subject, about 3.5 to 4.0 mg/kg
weight of a subject, about 4.0 to 4.5 mg/kg weight of a subject,
about 4.5 to 5.0 mg/kg weight of a subject, about 5.0 to 5.5 mg/kg
weight of a subject, about 5.5 to 6.0 mg/kg weight of a subject,
about 6.0 to 6.5 mg/kg weight of a subject, about 6.5 to 7.0 mg/kg
weight of a subject, about 7.0 to 7.5 mg/kg weight of a subject,
about 7.5 to 8.0 mg/kg weight of a subject, about 8.0 to 8.5 mg/kg
weight of a subject, about 8.5 to 9.0 mg/kg weight of a subject,
about 9.0 to 9.5 mg/kg weight of a subject, about 9.5 to 10.0 mg/kg
weight of a subject.
[0180] In another embodiment, the effective amount is an amount
about 0.1 to 20 mg/kg weight of a subject. In another embodiment,
the effective amount is an amount about 0.1 to 2 mg/kg weight of a
subject, about 2 to 4 mg/kg weight of a subject, about 4 to 6 mg/kg
weight of a subject, about 6 to 8 mg/kg weight of a subject, about
8 to 10 mg/kg weight of a subject, about 10 to 12 mg/kg weight of a
subject, about 12 to 14 mg/kg weight of a subject, about 14 to 16
mg/kg weight of a subject, about 16 to 18 mg/kg weight of a subject
or about 18 to 20 mg/kg weight of a subject.
[0181] In another embodiment, the effective amount is about 2 mg/kg
weight of a subject. In yet another embodiment, the effective
amount is about 10 mg/kg weight of a subject.
[0182] In a specific embodiment, the molecule that blocks B7
interaction with CTLA4 and/or CD28 is soluble CTLA4 and the
effective amount of a soluble CTLA4 molecule is about 2 mg/kg
weight of a subject. In another specific embodiment, the effective
amount of a soluble CTLA4 molecule is about 10 mg/kg weight of a
subject. In another specific embodiment, an effective amount of a
soluble CTLA4 is 500 mg for a subject weighing less than 60 kg, 750
mg for a subject weighing between 60-100 kg and 1000 mg for a
subject weighing more than 100 kg.
[0183] An effective amount of the molecule that blocks B7
interaction with CTLA4 and/or CD28 is soluble CTLA4 may be
administered to a subject daily, weekly, monthly and/or yearly, in
single or multiple times per hour/day/week/month/year, depending on
need. For example, in one embodiment, the molecule may initially be
administered once every two weeks for a month, and then once every
month thereafter.
[0184] In a preferred embodiment, the immune disease is a rheumatic
disease. Rheumatic diseases are any diseases which are
characterized by (i) inflammation or degeneration of
musculo-skeletal or connective tissue structures of the body,
particularly the joints, and including muscles, tendons, cartilage,
synovial and fibrous tissues, (ii) accompanied by joint swelling,
joint tenderness, inflammation, morning stiffness, and/or pain, or
impairment of locomotion or function of those structures and, in
some cases, (iii) often accompanied by serological evidence of
rheumatoid factor and other inflammatory surrogate markers.
[0185] Rheumatic diseases include, but are not limited to,
rheumatoid arthritis. The symptoms of rheumatoid arthritis include
joint swelling, joint tenderness, inflammation, morning stiffness,
and pain leading to physical disability. Subjects afflicted with
the advanced stages of arthritis suffer from symptoms of structural
damage and debilitating pain. Other organs also can be impaired by
the autoimmune mechanism.
[0186] In an embodiment of the invention used to treat an immune
system disease, the DMARD is methotrexate or a molecule that blocks
TNF interactions such as etanercept, and the molecule that blocks
B7 interaction with CTLA4 and/or CD28 is a soluble CTLA4. In a
further embodiment, the methods of the invention comprise
administering to a subject an effective amount of methotrexate or a
molecule that blocks TNF interactions in combination with an
effective amount of soluble CTLA4 in order to treat rheumatic
diseases such as rheumatoid arthritis.
[0187] Effective amounts of methotrexate range about 0.1 to 40
mg/week. In one embodiment, the effective amount includes ranges of
about 0.1 to 5 mg/week, about 5 to 10 mg/week, about 10 to 15
mg/week, about 15 to 20 mg/week, about 20 to 25 mg/week, about 25
to 30 mg/week, about 30 to 35 mg/week, or about 35 to 40 mg/week.
In one embodiment, methotrexate is administered in an amount
ranging about 5 to 30 mg/week.
[0188] In one embodiment, the effective amount of a soluble CTLA4
molecule is about 2 mg/kg weight subject and the effective amount
of methotrexate is about 10 to 30 mg/week. In another embodiment,
the effective amount of a soluble CTLA4 molecule is about 10 mg/kg
weight subject and the effective amount of methotrexate is about 10
to 30 mg/week.
[0189] In an embodiment of the invention used to treat an immune
system disease, the DMARD is etanercept and the molecule that
blocks B7 interaction with CTLA4 and/or CD28 is a soluble CTLA4. In
a further embodiment, the methods of the invention comprise
administering to a subject an effective amount of etanercept in
combination with an effective amount of soluble CTLA4 in order to
treat rheumatic diseases such as rheumatoid arthritis.
[0190] Effective amounts of etanercept range about 0.1 to 100
mg/week. In one embodiment, the effective amount includes ranges of
about 10 to 100 mg/week, about 0.1 to 50 mg/week, about 0.1 to 5
mg/week, about 5 to 10 mg/week, about 10 to 15 mg/week, about 15 to
20 mg/week, about 20 to 25 mg/week, about 25 to 30 mg/week, about
30 to 35 mg/week, about 35 to 40 mg/week, about 40 to 45 mg/week,
about 45 to 50 mg/week, about 50 to 55 mg/week, about 55 to 60
mg/week, about 60 to 65 mg/week, about 65 to 70 mg/week, about 70
to 75 mg/week, about 75 to 80 mg/week, about 80 to 85 mg/week,
about 85 to 90 mg/week, about 90 to 95 mg/week or about 95 to 100
mg/week. In one embodiment, etanercept is administered in an amount
of about 50 mg/week, alternatively etanercept may be administered
in an amount of about 25 mg twice weekly.
[0191] In one embodiment, the effective amount of a soluble CTLA4
molecule is about 2 mg/kg weight subject and the effective amount
of etanercept is about 25 mg twice a week. In another embodiment,
the effective amount of a soluble CTLA4 molecule is about 10 mg/kg
weight subject and the effective amount of etanercept is about 25
mg twice a week.
[0192] The invention also provides compositions and methods for
treating immune system diseases, such as rheumatic diseases, by
administering to a subject a combination of an effective amount of
an NSAID and/or other therapeutic agent plus an effective amount of
a molecule that blocks B7 interaction with CTLA4 and/or CD28.
[0193] The invention also provides compositions and methods for
treating immune system diseases, such as rheumatic diseases, by
administering to a subject a an effective amount of a
glucocorticoid, corticosteroid and/or other therapeutic agent plus
an effective amount of a molecule that blocks B7 interaction with
CTLA4 and/or CD28.
[0194] Compositions
[0195] The present invention provides compositions for treating
immune diseases, such as rheumatic diseases, comprising soluble
CTLA4 molecules. Further, the present invention provides
compositions comprising a biological agent that inhibits T-cell
function but not T-cell depletion in a human by contacting
B7-positive cells in the human with a soluble CTLA4. Examples of
soluble CTLA4 include CTLA4Ig and soluble CTLA4 mutant molecules
such as L104EA29YIg (FIG. 19), L104EA29LIg (FIG. 20), L104EA29TIg
(FIG. 21), and L104EA29WIg (FIG. 22).
[0196] CTLA4 molecules, with mutant or wildtype sequences, may be
rendered soluble by deleting the CTLA4 transmembrane segment (Oaks,
M. K., et al., 2000 Cellular Immunology 201:144-153).
[0197] Alternatively, soluble CTLA4 molecules, with mutant or
wildtype sequences, may be fusion proteins, wherein the CTLA4
molecules are fused to non-CTLA4 moieties such as immunoglobulin
(Ig) molecules that render the CTLA4 molecules soluble. For
example, a CTLA4 fusion protein may include the extracellular
domain of CTLA4 fused to an immunoglobulin constant domain,
resulting in the CTLA4Ig molecule (FIG. 24) (Linsley, P. S., et
al., 1994 Immunity 1:793-80). Examples of immunoglobulin domains
that may be fused to CTLA4 include, but are not limited to
IgC.gamma.1 (IgCgamma1), IgC.gamma.2 (IgCgamma2), IgC.gamma.3
(IgCgamma3), IgC.gamma.4 (IgCgamma4), IgC.mu. (IgCmu), IgC.alpha.1
(IgCalpha1), IgC.alpha.2 (IgCalpha2), IgC.delta. (IgCdelta) or
IgC.epsilon. (IgCepsilon).
[0198] For clinical protocols, it is preferred that the
immunoglobulin moiety does not elicit a detrimental immune response
in a subject. The preferred moiety is the immunoglobulin constant
region, including the human or monkey immunoglobulin constant
regions. One example of a suitable immunoglobulin region is human
C.gamma.1, including the hinge, CH2 and CH3 regions which can
mediate effector functions such as binding to Fc receptors,
mediating complement-dependent cytotoxicity (CDC), or mediate
antibody-dependent cell-mediated cytotoxicity (ADCC). The
immunoglobulin moiety may have one or more mutations therein,
(e.g., in the CH2 domain, to reduce effector functions such as CDC
or ADCC) where the mutation modulates the binding capability of the
immunoglobulin to its ligand, by increasing or decreasing the
binding capability of the immunoglobulin to Fc receptors. For
example, mutations in the immunoglobulin moiety may include changes
in any or all its cysteine residues within the hinge domain, for
example, the cysteines at positions +130, +136, and +139 are
substituted with serine (FIG. 24). The immunoglobulin moiety may
also include the proline at position +148 substituted with a
serine, as shown in FIG. 24. Further, the mutations in the
immunoglobulin moiety may include having the leucine at position
+144 substituted with phenylalanine, leucine at position +145
substituted with glutamic acid, or glycine at position +147
substituted with alanine.
[0199] Additional non-CTLA4 moieties for use in the soluble CTLA4
molecules or soluble CTLA4 mutant molecules include, but are not
limited to, p97 molecule, env gp120 molecule, E7 molecule, and ova
molecule (Dash, B. et al. 1994 J. Gen. Virol. 75 (Pt 6):1389-97;
Ikeda, T., et al. 1994 Gene 138(1-2):193-6; Falk, K., et al. 1993
Cell. Immunol. 150(2):447-52; Fujisaka, K. et al. 1994 Virology
204(2):789-93). Other molecules are also possible (Gerard, C. et
al. 1994 Neuroscience 62(3):721; Byrn, R. et al. 1989 63(10):4370;
Smith, D. et al. 1987 Science 238:1704; Lasky, L. 1996 Science
233:209).
[0200] The soluble CTLA4 molecule of the invention can include a
signal peptide sequence linked to the N-terminal end of the
extracellular domain of the CTLA4 portion of the molecule. The
signal peptide can be any sequence that will permit secretion of
the molecule, including the signal peptide from oncostatin M
(Malik, et al., (1989) Molec. Cell. Biol. 9: 2847-2853), or CD5
(Jones, N. H. et al., (1986) Nature 323:346-349), or the signal
peptide from any extracellular protein. The soluble CTLA4 molecule
of the invention can include the oncostatin M signal peptide linked
at the N-terminal end of the extracellular domain of CTLA4, and the
human immunoglobulin molecule (e.g., hinge, CH2 and CH3) linked to
the C-terminal end of the extracellular domain (wildtype or
mutated) of CTLA4. This molecule includes the oncostatin M signal
peptide encompassing an amino acid sequence having methionine at
position -26 through alanine at position -1, the CTLA4 portion
encompassing an amino acid sequence having methionine at position
+1 through aspartic acid at position +124, a junction amino acid
residue glutamine at position +125, and the immunoglobulin portion
encompassing an amino acid sequence having glutamic acid at
position +126 through lysine at position +357.
[0201] Specifically, the soluble CTLA4 mutant molecules of the
invention, comprising the mutated CTLA4 sequences described infra,
can be fusion molecules comprising human Ig, e.g., IgC(gamma)1
(i.e. IgC.gamma.1) moieties fused to the mutated CTLA4
fragments.
[0202] In one embodiment, the soluble CTLA4 mutant molecules
comprise IgC.gamma.1 (IgCgamma1) fused to an extracellular domain
of CTLA4 comprising a single-site mutation in the extracellular
domain. The extracellular domain of CTLA4 comprises methionine at
position +1 through aspartic acid at position +124 (e.g., FIG. 23).
The extracellular domain of the CTLA4 can comprise alanine at
position -1 through aspartic acid at position +124 (e.g., FIG. 23).
Examples of single-site mutations-include the following wherein the
leucine at position +104 is changed to any other amino acid.
2 Single-site mutant: Codon change: L104EIg Glutamic acid GAG
L104SIg Serine AGT L104TIg Threonine ACG L104AIg Alanine GCG
L104WIg Tryptophan TGG L104QIg Glutamine CAG L104KIg Lysine AAG
L104RIg Arginine CGG L104GIg Glycine GGG
[0203] Further, the invention provides mutant molecules having the
extracellular domain of CTLA4 with two mutations, fused to an Ig
C.gamma.1 (IgCgamma1) moiety. Examples include the following
wherein the leucine at position +104 is changed to another amino
acid (e.g. glutamic acid) and the glycine at position +105, the
serine at position +25, the threonine at position +30 or the
alanine at position +29 is changed to any other amino acid:
3 Double-site mutants: Codon change: L104EG105FIg Phenylalanine TTC
L104EG105WIg Tryptophan TGG L104EG105LIg Leucine CTT L104ES25RIg
Arginine CGG L104ET30GIg Glycine GGG L104ET30NIg Asparagine AAT
L104EA29YIg Tyrosine TAT L104EA29LIg Leucine TTG L104EA29TIg
Threonine ACT L104EA29WIg Tryptophan TGG
[0204] Further still, the invention provides mutant molecules
having the extracellular domain of CTLA4 comprising three
mutations, fused to an IgC.gamma.1 (IgCgamma1) moiety. Examples
include the following wherein the leucine at position +104 is
changed to another amino acid (e.g. glutamic acid), the alanine at
position +29 is changed to another amino acid (e.g. tyrosine) and
the serine at position +25 is changed to another amino acid:
4 Triple-site Mutants: Codon changes: L104EA29YS25KIg Lysine AAA
L104EA29YS25KIg Lysine AAG L104EA29YS25NIg Asparagine AAC
L104EA29YS25RIg Arginine CGG
[0205] Soluble CTLA4 mutant molecules may have a junction amino
acid residue which is located between the CTLA4 portion and the Ig
portion of the molecule. The junction amino acid can be any amino
acid, including glutamine. The junction amino acid can be
introduced by molecular or chemical synthesis methods known in the
art.
[0206] The soluble CTLA4 proteins of the invention, and fragments
thereof, can be generated by chemical synthesis methods. The
principles of solid phase chemical synthesis of polypeptides are
well known in the art and may be found in general texts relating to
this area (Dugas, H. and Penney, C. 1981 Bioorganic Chemistry, pp
54-92, Springer-Verlag, New York). The soluble CTLA4 proteins may
be synthesized by solid-phase methodology utilizing an Applied
Biosystems 430A peptide synthesizer (Applied Biosystems, Foster
City, Calif.) and synthesis cycles supplied by Applied Biosystems.
Protected amino acids, such as t-butoxycarbonyl-protected amino
acids, and other reagents are commercially available from many
chemical supply houses.
[0207] The present invention provides CTLA4 mutant molecules
including a signal peptide sequence linked to the N-terminal end of
the extracellular domain of the CTLA4 portion of the mutant
molecule. The signal peptide can be any sequence that will permit
secretion of the mutant molecule, including the signal peptide from
oncostatin M (Malik, et al., 1989 Molec. Cell. Biol. 9: 2847-2853),
or CD5 (Jones, N. H. et al., 1986 Nature 323:346-349), or the
signal peptide from any extracellular protein.
[0208] The invention provides soluble CTLA4 mutant molecules
comprising a single-site mutation in the extracellular domain of
CTLA4 such as L104EIg (as included in FIG. 18) or L104SIg, wherein
L104EIg and L104SIg are mutated in their CTLA4 sequences so that
leucine at position +104 is substituted with glutamic acid or
serine, respectively. The single-site mutant molecules further
include CTLA4 portions encompassing methionine at position +1
through aspartic acid at position +124, a junction amino acid
residue glutamine at position +125, and an immunoglobulin portion
encompassing glutamic acid at position +126 through lysine at
position +357. The immunoglobulin portion of the mutant molecule
may also be mutated so that the cysteines at positions +130, +136,
and +139 are substituted with serine, and the proline at position
+148 is substituted with serine. Alternatively, the single-site
soluble CTLA4 mutant molecule may have a CTLA4 portion encompassing
alanine at position -1 through aspartic acid at position +124.
[0209] The invention provides soluble CTLA4 mutant molecules
comprising a double-site mutation in the extracellular domain of
CTLA4, such as L104EA29YIg, L104EA29LIg, L104EA29TIg or
L104EA29WIg, wherein leucine at position +104 is substituted with a
glutamic acid and alanine at position +29 is changed to tyrosine,
leucine, threonine and tryptophan, respectively. The sequences for
L104EA29YIg, L104EA29LIg, L104EA29TIg and L104EA29WIg, starting at
methionine at position +1 and ending with lysine at position +357,
plus a signal (leader) peptide sequence are shown in FIGS. 19-22
respectively. The double-site mutant molecules further comprise
CTLA4 portions encompassing methionine at position +1 through
aspartic acid at position +124, a junction amino acid residue
glutamine at position +125, and an immunoglobulin portion
encompassing glutamic acid at position +126 through lysine at
position +357. The immunoglobulin portion of the mutant molecule
may also be mutated, so that the cysteines at positions +130, +136,
and +139 are substituted with serine, and the proline at position
+148 is substituted with serine. Alternatively, these mutant
molecules can have a CTLA4 portion encompassing alanine at position
-1 through aspartic acid at position +124.
[0210] The invention provides soluble CTLA4 mutant molecules
comprising a double-site mutation in the extracellular domain of
CTLA4, such as L104EG105FIg, L104EG105WIg and L104EG105LIg, wherein
leucine at position +104 is substituted with a glutamic acid and
glycine at position +105 is substituted with phenylalanine,
tryptophan and leucine, respectively. The double-site mutant
molecules further comprise CTLA4 portions encompassing methionine
at position +1 through aspartic acid at position +124, a junction
amino acid residue glutamine at position +125, and an
immunoglobulin portion encompassing glutamic acid at position +126
through lysine at position +357. The immunoglobulin portion of the
may also be mutated, so that the cysteines at positions +130, +136,
and +139 are substituted with serine, and the proline at position
+148 is substituted with serine. Alternatively, these mutant
molecules can have a CTLA4 portion encompassing alanine at position
-1 through aspartic acid at position +124.
[0211] The invention provides L104ES25RIg which is a double-site
mutant molecule comprising a CTLA4 portion encompassing methionine
at position +1 through aspartic acid at position +124, a junction
amino acid residue glutamine at position +125, and the
immunoglobulin portion encompassing glutamic acid at position +126
through lysine at position +357. The portion having the
extracellular domain of CTLA4 is mutated so that serine at position
+25 is substituted with arginine, and leucine at position +104 is
substituted with glutamic acid. Alternatively, L104ES25RIg can have
a CTLA4 portion encompassing alanine at position -1 through
aspartic acid at position +124.
[0212] The invention provides soluble CTLA4 mutant molecules
comprising a double-site mutation in the extracellular domain of
CTLA4, such as L104ET30GIg and L104ET30NIg, wherein leucine at
position +104 is substituted with a glutamic acid and threonine at
position +30 is substituted with glycine and asparagine,
respectively. The double-site mutant molecules further comprise
CTLA4 portions encompassing methionine at position +1 through
aspartic acid at position +124, a junction amino acid residue
glutamine at position +125, and an immunoglobulin portion
encompassing glutamic <acid at position +126 through lysine at
position +357. The immunoglobulin portion of the mutant molecule
may also be mutated, so that the cysteines at positions +130, +136,
and +139 are substituted with serine, and the proline at position
+148 is substituted with serine. Alternatively, these mutant
molecules can have a CTLA4 portion encompassing alanine at position
-1 through aspartic acid at position +124.
[0213] The invention provides soluble CTLA4 mutant molecules
comprising a triple-site mutation in the extracellular domain of
CTLA4, such as L104EA29YS25KIg, L104EA29YS25NIg, L104EA29YS25RIg,
wherein leucine at position +104 is substituted with a glutamic
acid, alanine at position +29 is substituted with tyrosine, and
serine at position +25 is substituted with lysine, asparagine and
arginine, respectively. The triple-site mutant molecules further
comprise CTLA4 portions encompassing methionine at position +1
through aspartic acid at position +124, a junction amino acid
residue glutamine at position +125, and an immunoglobulin portion
encompassing glutamic acid at position +126 through lysine at
position +357. The immunoglobulin portion of the mutant molecule
may also be mutated, so that the cysteines at positions +130, +136,
and +139 are substituted with serine, and the proline at position
+148 is substituted with serine. Alternatively, these mutant
molecules can have a CTLA4 portion encompassing alanine at position
-1 through aspartic acid at position +124.
[0214] Additional embodiments of soluble CTLA4 mutant molecules
include chimeric CTLA4/CD28 homologue mutant molecules that bind a
B7 (Peach, R. J., et al., 1994 J Exp Med 180:2049-2058). Examples
of these chimeric CTLA4/CD28 mutant molecules include HS1, HS2,
HS3, HS4, HS5, HS6, HS4A, HS4B, HS7, HS8, HS9, HS10, HS11, HS12,
HS13 and HS14 (U.S. Pat. No. 5,773,253) Preferred embodiments of
the invention are soluble CTLA4 molecules such as CTLA4Ig (as shown
in FIG. 24, starting at methionine at position +1 and ending at
lysine at position +357) and soluble CTLA4 mutant L104EA29YIg (as
shown in FIG. 19, starting at methionine at position +1 and ending
at lysine at position +357).
[0215] The invention further provides nucleic acid molecules
comprising nucleotide sequences encoding the amino acid sequences
corresponding to the soluble CTLA4 molecules of the invention. In
one embodiment, the nucleic acid molecule is a DNA (e.g., cDNA) or
a hybrid thereof. For example, a CTLA4Ig molecule can comprise a
GCT or GCC codon, encoding alanine, at nucleotide position +49 to
+51 as shown in FIG. 24. In another example, a CTLA4Ig molecule can
comprise a GGT or GGG codon, encoding glycine, at nucleotide
position +436 to +438 as shown in FIG. 24. In yet another example,
a CTLA4Ig molecule can comprise a CGG or CGT codon, encoding
arginine, at nucleotide position +631 to +633 as shown in FIG. 24.
DNA encoding CTLA4Ig (FIG. 24) was deposited on May 31, 1991 with
the American Type Culture Collection (ATCC), 10801 University
Blvd., Manassas, Va. 20110-2209 and has been accorded ATCC
accession number ATCC 68629. DNA encoding L104EA29YIg (sequence
included in FIG. 19) was deposited on Jun. 19, 2000 with ATCC and
has been accorded ATCC accession number PTA-2104. Alternatively,
the nucleic acid molecules are RNA or a hybrid thereof.
[0216] The nucleic acid molecules of the invention also include
derivative nucleic acid molecules which differ from DNA or RNA
molecules, and anti-sense molecules. Derivative molecules include
peptide nucleic acids (PNAs), and non-nucleic acid molecules
including phosphorothioate, phosphotriester, phosphoramidate, and
methylphosphonate molecules, that bind to single-stranded DNA or
RNA in a base pair-dependent manner (Zamecnik, P. C., et al., 1978
Proc. Natl. Acad. Sci. 75:280284; Goodchild, P. C., et al., 1986
Proc. Natl. Acad. Sci. 83:4143-4146). Peptide nucleic acid
molecules comprise a nucleic acid oligomer to which an amino acid
residue, such as lysine, and an amino group have been added. These
small molecules, also designated anti-gene agents, stop transcript
elongation by binding to their complementary (template) strand of
nucleic acid (Nielsen, P. E., et al., 1993 Anticancer Drug Des
8:53-63). Reviews of methods for synthesis of DNA, RNA, and their
analogues can be found in: Oligonucleotides and Analogues, eds. F.
Eckstein, 1991, IRL Press, New York; Oligonucleotide Synthesis, ed.
M. J. Gait, 1984, IRL Press, Oxford, England. Additionally, methods
for antisense RNA technology are described in U.S. Pat. Nos.
5,194,428 and 5,110,802. A skilled artisan can readily obtain these
classes of nucleic acid molecules using the herein described
soluble CTLA4 polynucleotide sequences, see for example Innovative
and Perspectives in Solid Phase Synthesis (1992) Egholm, et al. pp
325-328 or U.S. Pat. No. 5,539,082.
[0217] Additionally, the invention provides a vector, which
comprises the nucleotide sequences of the invention. The term
vector includes, but is not limited to, plasmids, cosmids, and
phagemids. In one embodiment, the vector can be an autonomously
replicating vector comprising a replicon that directs the
replication of the rDNA within the appropriate host cell.
Alternatively, the vector can direct integration of the recombinant
vector into the host cell. Various viral vectors may also be used,
such as, for example, a number of well known retroviral and
adenoviral vectors (Berkner 1988 Biotechniques 6:616-629).
[0218] The vectors can permit expression of the soluble CTLA4
transcript or polypeptide sequences in prokaryotic or eukaryotic
host cells. The vectors include expression vectors, comprising an
expression control element, such as a promoter sequence, which
enables transcription of the inserted soluble CTLA4 nucleic acid
sequences and can be used for regulating the expression (e.g.,
transcription and/or translation) of an operably linked soluble
CTLA4 sequence in an appropriate host cell. Expression control
elements are known in the art and include, but are not limited to,
inducible promoters, constitutive promoters, secretion signals,
enhancers, transcription terminators, and other transcriptional
regulatory elements. Other expression control elements that are
involved in translation are known in the art, and include the
Shine-Dalgarno sequence (e.g., prokaryotic host cells), and
initiation and termination codons.
[0219] Specific initiation signals may also be required for
efficient translation of a soluble CTLA4 sequence. These signals
include the ATG-initiation codon and adjacent sequences. In cases
where the soluble CTLA4 initiation codon and upstream sequences are
inserted into the appropriate expression vector, no additional
translational control signals may be needed. However, in cases
where only the coding sequence, or a portion thereof, is inserted,
exogenous transcriptional control signals including the
ATG-initiation codon may be provided. Furthermore, the initiation
codon should be in the correct reading-frame to ensure translation
of the entire insert. Exogenous transcriptional elements and
initiation codons can be of various origins, both natural and
synthetic. The efficiency of expression may be enhanced by the
inclusion of enhancers appropriate to the cell system in use
(Scharf, D., et al, 1994 Results Probl. Cell. Differ. 20:125-62;
Bittner, et al., 1987 Methods in Enzymol. 153:516-544).
[0220] The preferred vectors for expression of the soluble CTLA4
sequences in eukaryote host cells include expression control
elements, such as the baculovirus polyhedrin promoter for
expression in insect cells. Other expression control elements
include promoters or enhancers derived from the genomes of plant
cells (e.g., heat shock, RUBISCO, storage protein genes), viral
promoters or leader sequences or from plant viruses, and promoters
or enhancers from the mammalian genes or from mammalian
viruses.
[0221] The preferred vector includes at least one selectable marker
gene that encodes a gene product that confers drug resistance such
as resistance to ampicillin or tetracyline. The vector also
comprises multiple endonuclease restriction sites that enable
convenient insertion of exogenous DNA sequences. Methods for
generating a recombinant expression vector encoding the soluble
CTLA4 proteins of the invention are well known in the art, and can
be found in Sambrook et al., (Molecular Cloning; A Laboratory
Manual, 2.sup.nd edition, Sambrook, Fritch, and Maniatis 1989, Cold
Spring Harbor Press) and Ausubel et al. (1989 Current Protocols in
Molecular Biology, John Wiley & Sons, New York N.Y.).
[0222] The preferred vectors for generating soluble CTLA4
transcripts and/or the encoded soluble CTLA4 polypeptides are
expression vectors which are compatible with prokaryotic host
cells. Prokaryotic cell expression vectors are well known in the
art and are available from several commercial sources. For example,
pET vectors (e.g., pET-21, Novagen Corp.), BLUESCRIPT phagemid
(Stratagene, LaJolla, Calif.), pSPORT (Gibco BRL, Rockville, Md.),
or ptrp-lac hybrids may be used to express soluble CTLA4
polypeptides in bacterial host cells.
[0223] Alternatively, the preferred expression vectors for
generating soluble CTLA4 transcripts and/or the encoded soluble
CTLA4 polypeptides are expression vectors which are compatible with
eukaryotic host cells. The more preferred vectors are those
compatible with vertebrate cells. Eukaryotic cell expression
vectors are well known in the art and are available from several
commercial sources. Typically, such vectors are provided containing
convenient restriction sites for insertion of the desired DNA
segment. Typical of such vectors are PSVL and pKSV-10 (Pharmacia),
pBPV-1/pML2d (International Biotechnologies, Inc.), pTDT1 (ATCC,
#31255), and similar eukaryotic expression vectors.
[0224] Examples of expression vectors for include, but are not
limited to, vectors for mammalian host cells (e.g., BPV-1, pHyg,
pRSV, pSV2, pTK2 (Maniatis); pIRES (Clontech); pRc/CMV2, pRc/RSV,
pSFV1 (Life Technologies); pVPakc Vectors, pCMV vectors, pSG5
vectors (Stratagene)), retroviral vectors (e.g., pFB vectors
(Stratagene)), pcDNA-3 (Invitrogen) or modified forms thereof,
adenoviral vectors; adeno-associated virus vectors, baculovirus
vectors, yeast vectors (e.g., pESC vectors (Stratagene)).
[0225] A host vector system is also provided. The host vector
system comprises the vector of the invention in a suitable host
cell. Examples of suitable host cells include, but are not limited
to, prokaryotic and eukaryotic cells. In accordance with the
practice of the invention, eukaryotic cells are also suitable host
cells. Examples of eukaryotic cells include any animal cell,
whether primary or immortalized, yeast (e.g., Saccharomyces
cerevisiae, Schizosaccharomyces pombe, and Pichia pastoris), and
plant cells. Exemplary animal cells include cells from bovine,
ovine, porcine, murine, equine, monkey and ape. Myeloma, COS and
CHO cells are examples of animal cells that may be used as hosts.
Particular CHO cells include, but are not limited to, DG44 (Chasin,
et la., 1986 Som. Cell. Molec. Genet. 12:555-556; Kolkekar 1997
Biochemistry 36:10901-10909), CHO-K1 (ATCC No. CCL-61), CHO-K1
Tet-On cell line (Clontech), CHO designated ECACC 85050302 (CAMR,
Salisbury, Wiltshire, UK), CHO clone 13 (GEIMG, Genova, IT), CHO
clone B (GEIMG, Genova, IT), CHO-K1/SF designated ECACC 93061607
(CAMR, Salisbury, Wiltshire, UK), and RR-CHOK1 designated ECACC
92052129 (CAMR, Salisbury, Wiltshire, UK). Exemplary plant cells
include whole plants, cell culture, or callus, from tobacco, corn,
soybean, and rice cells. Corn, soybean, and rice seeds are also
acceptable.
[0226] The CTLA4 mutant molecules of the invention may be isolated
as naturally-occurring polypeptides, or from any source whether
natural, synthetic, semi-synthetic or recombinant. Accordingly, the
CTLA4 mutant polypeptide molecules may be isolated as
naturally-occurring proteins from any species, particularly
mammalian, including bovine, ovine, porcine, murine, equine, and
preferably human. Alternatively, the CTLA4 mutant polypeptide
molecules may be isolated as recombinant polypeptides that are
expressed in prokaryote or eukaryote host cells, or isolated as a
chemically synthesized polypeptide.
[0227] A skilled artisan can readily employ standard isolation
methods to obtain isolated CTLA4 mutant molecules. The nature and
degree of isolation will depend on the source and the intended use
of the isolated molecules.
[0228] CTLA4 mutant molecules and fragments or derivatives thereof,
can be produced by recombinant methods. Accordingly, an isolated
nucleotide sequence encoding wild-type CTLA4 molecules may be
manipulated to introduce mutations, resulting in nucleotide
sequences that encode the CTLA4 mutant polypeptide molecules. For
example, the nucleotide sequences encoding the CTLA4 mutant
molecules may be generated by site-directed mutagenesis methods,
using primers and PCR amplification. The primers can include
specific sequences designed to introduce desired mutations.
Alternatively, the primers can be designed to include randomized or
semi-randomized sequences to introduce random mutations. Standard
recombinant methods (Molecular Cloning; A Laboratory Manual,
2.sup.nd edition, Sambrook, Fritch, and Maniatis 1989, Cold Spring
Harbor Press) and PCR technology (U.S. Pat. No. 4,603,102) can be
employed for generating and isolating CTLA4 mutant polynucleotides
encoding CTLA4 mutant polypeptides.
[0229] The invention includes pharmaceutical compositions
comprising pharmaceutically effective amounts of a molecule that
blocks B7 interaction with CTLA4 and/or CD28 such as soluble CTLA4
molecules, CD28 molecules, B7 (B7-1 or B7-2) molecules, anti-CTLA4
monoclonal antibodies, anti-CD28 monoclonal antibodies or anti-B7
(B7-1 or B7-2) monoclonal antibodies. The pharmaceutical
compositions of the invention are useful for treatment of immune
system diseases. In certain embodiments, immune system diseases are
mediated by CD28/CTLA4/B7 interactions. The soluble CTLA4 molecules
are preferably soluble CTLA4 molecules with wildtype sequence
and/or soluble CTLA4 molecules having one or more mutations in the
extracellular domain of CTLA4. The pharmaceutical composition can
include soluble CTLA4 protein molecules and/or nucleic acid
molecules, and/or vectors encoding the molecules. In preferred
embodiments, the soluble CTLA4 molecules have the amino acid
sequence of the extracellular domain of CTLA4 as shown in either
FIG. 24 or 19 (CTLA4Ig or L104EA29Y, respectively). Even more
preferably, the soluble CTLA4 mutant molecule is L104EA29YIg as
disclosed herein. The compositions may additionally include other
therapeutic agents, including, but not limited to, DMARDs, NSAIDs,
corticosteroids, glucocorticoids, drug toxins, alkylating agents,
anti-neoplastic drugs, enzymes, antibodies, or conjugates.
[0230] An embodiment of the pharmaceutical composition of the
invention comprises an effective amount of a molecule that blocks
B7 interaction with CTLA4 and/or CD28, such as the molecules and
the suitable amounts of the molecules described supra, and an
effective amount of a DMARD.
[0231] The amount of DMARDS administered to a subject varies
depending on several factors including the efficacy of the drug on
a specific subject and the toxicity (i.e. the tolerability) of a
drug to a specific subject (Guidelines for the Management of
Rheumatoid Arthritis, Arthritis and Rheumatism Vol. 39, No. 5, May
1996, pages 713-711; Physician's Desk Reference 2002, Medical
Economics Company, Inc. Montvale, N.J. 07645). The following
provides a range of drug dosages for each DMARD. An attending
physician will determine specific dosages for each subject.
[0232] Depending on the DMARD, an effective amount can be in a
range of about 1 to about 5000 mg/day. This range can be modified
to an amount of about 1 to 10 mg/day, about 10 to 50 mg/day, about
50 to 100 mg/day, about 100 to 150 mg/day, about 150 to 200 mg/day,
about 200 to 250 mg/day, about 250 to 300 mg/day, about 300 to 350
mg/day, about 350 to 400 mg/day, about 400 to 450 mg/day, about 450
to 500 mg/day, about 500 to 550 mg/day, about 550 to 600 mg/day,
about 600 to 650 mg/day, about 650 to 700 mg/day, about 700 to 750
mg/day, about 750 to 800 mg/day, about 800 to 850 mg/day, about 850
to 900 mg/day, about 900 to 950 mg/day, about 950 to 1000 mg/day,
about 1000 to 1100 mg/day, about 1100 to 1200 mg/day, about 1200 to
1300 mg/day, about 1300 to 1400 mg/day, about 1400 to 1500 mg/day,
about 1500 to 1600 mg/day, about 1600 to 1700 mg/day, about 1700 to
1800 mg/day, about 1800 to 1900 mg/day, about 1900 to 2000 mg/day,
about 2000 to 2500 mg/day, about 2500 to 3000 mg/day, about 3000 to
3500 mg/day, about 3500 to 4000 mg/day, about 4000 to 4500 mg/day
or about 4500 to 5000 mg/day. It would be clear to one skilled in
the art that dosage will vary depending on the particular DMARD
being used. Specific examples of appropriate dosages, depending on
the DMARD, are described below.
[0233] In another embodiment, an effective amount of a DMARD can be
in a range of about 0.1 mg/week to 40 mg/week; 0.1 mg/week to 5
mg/week; 5 mg/week to 10 mg/week; 10 mg/week to 30 mg/week; 30
mg/week to 35 mg/week; 0.1 mg/week to 100 mg/week; or 30 mg/week to
50 mg/week. In another embodiment, a DMARD can be administered in
an amount of about 50 mg/week or 25 mg twice weekly. It would be
clear to one skilled in the art that dosage range will vary
depending on the particular DMARD being used, for example see
below.
[0234] Methotrexate is an antimetabolite molecule that interferes
with DNA synthesis, repair and cellular replication. Methotrexate
functions as an inhibitor of dihydrofolic acid reductase i.e. it is
a folic acid antagonist. Methotrexate is commonly administered in
an amount about 0.1 to 40 mg per week with a common dosage ranging
about 5 to 30 mg per week. Methotrexate may be administered to a
subject in various increments: about 0.1 to 5 mg/week, about 5 to
10 mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week, about
20 to 25 mg/week, about 25 to 30 mg/week, about 30 to 35 mg/week,
or about 35 to 40 mg/week. In one embodiment, an effective amount
of a DMARD, including methotrexate, is an amount about 10 to 30
mg/week.
[0235] Cyclophosphamide, an alkylating agent, may be administered
in dosages ranging about 1 to 10 mg/kg body weight per day.
[0236] Cyclosporine (e.g. NEORAL.sup.R) also known as Cyclosporin
A, is commonly administered in dosages ranging from about 1 to 10
mg/kg body weight per day. Dosages ranging about 2.5 to 4 mg per
body weight per day are commonly used.
[0237] Chloroquine or hydroxychloroquine (e.g. PLAQUENIL.sup.R), is
commonly administered in dosages ranging about 100 to 1000 mg
daily. Preferred dosages range about 200-600 mg administered
daily.
[0238] Sulfasalazine (e.g., AZULFIDINE EN-tabs.sup.R) is commonly
administered in amounts ranging about 50 to 5000 mg per day, with a
common dosage of about 2000 to 3000 mg per day for adults. Dosages
for children are commonly about 5 to 100 mg/kg of body weight, up
to 2 grams per day.
[0239] Gold salts are formulated for two types of administration:
injection or oral. Injectable gold salts are commonly prescribed in
dosages about 5 to 100 mg doses every two to four weeks. Orally
administered gold salts are commonly prescribed in doses ranging
about 1 to 10 mg per day.
[0240] D-penicillamine or penicillamine (CUPRIMINE.sup.R) is
commonly administered in dosages about 50 to 2000 mg per day, with
preferred dosages about 125 mg per day up to 1500 mg per day.
[0241] Azathioprine is commonly administered in dosages of about 10
to 250 mg per day. Preferred dosages range about 25 to 200 mg per
day.
[0242] Anakinra (e.g. KINERET.sup.R) is an interleukin-1 receptor
antagonist. A common dosage range for anakinra is about 10 to 250
mg per day, with a recommended dosage of about 100 mg per day.
[0243] Infliximab (REMICADE.sup.R) is a chimeric monoclonal
antibody that binds to tumor necrosis factor alpha (TNF.alpha.) and
inhibits the activity of TNF.alpha.. Infliximab is commonly
administered in dosages about 1 to 20 mg/kg body weight every four
to eight weeks. Dosages of about 3 to 10 mg/kg body weight may be
administered every four to eight weeks depending on the
subject.
[0244] Etanercept (e.g. ENBREL.sup.R) is a dimeric fusion protein
that binds the tumor necrosis factor (TNF) and blocks its
interactions with TNF receptors. Commonly administered dosages of
etanercept are about 10 to 100 mg per week for adults with a
preferred dosage of about 50 mg per week. Dosages for juvenile
subjects range about 0.1 to 50 mg/kg body weight per week with a
maximum of about 50 mg per week. For adult patients, etanercept is
commonly administered e.g., injected, in 25 mg doses twice weekly
e.g., 72-96 hours apart in time.
[0245] Leflunomide (ARAVA.sup.R) is commonly administered at
dosages about 1 and 100 mg per day. A common daily dosage is about
10 to 20 mg per day.
[0246] A further embodiment of the invention is a pharmaceutical
composition comprising an effective amount of a soluble CTLA4, such
as CTLA4Ig, and an effective amount of a DMARD, such as
methotrexate or etanercept.
[0247] A pharmaceutical composition comprising soluble CTLA4 can be
used for methods for blocking B7 interaction with CTLA4 and/or
CD28; or for treating immune system diseases. Effective amounts of
soluble CTLA4 in the pharmaceutical composition range about 0.1 to
100 mg/kg weight of the subject. In another embodiment, the
effective amount is an amount about 0.5 to 5 mg/kg weight of a
subject, about 5 to 10 mg/kg weight of a subject, about 10 to 15
mg/kg weight of a subject, about 15 to 20 mg/kg weight of a
subject, about 20 to 25 mg/kg weight of a subject, about 25 to 30
mg/kg weight of a subject, about 30 to 35 mg/kg weight of a
subject, about 35 to 40 mg/kg weight of a subject, about 40 to 45
mg/kg of a subject, about 45 to 50 mg/kg weight of a subject, about
50 to 55 mg/kg weight of a subject, about 55 to 60 mg/kg weight of
a subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, or about 95 to
100 mg/kg weight of a subject.
[0248] In an embodiment, the effective amount of soluble CTLA4 is
an amount about 2 mg/kg to about 10 mg/kg weight of a subject. In
another embodiment, the effective amount is an amount about 0.1 to
4 mg/kg weight of a subject. In another embodiment the effective
amount is an amount about 0.1 to 0.5 mg/kg weight of a subject,
about 0.5 to 1.0 mg/kg weight of a subject, about 1.0 to 1.5 mg/kg
weight of a subject, about 1.5 to 2.0 mg/kg weight of a subject,
about 2.0 to 2.5 mg/kg weight of a subject, about 2.5 to 3.0 mg/kg
weight of a subject, about 3.0 to 3.5 mg/kg weight of a subject or
about 3.5 to 4.0 mg/kg weight of a subject. In another embodiment,
the effective amount is an amount about 0.1 to 20 mg/kg weight of a
subject. In another embodiment, the effective amount is an amount
about 0.1 to 2 mg/kg weight of a subject, about 2 to 4 mg/kg weight
of a subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8
mg/kg weight of a subject, about 8 to 10 mg/kg weight of a subject,
about 10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg
weight of a subject, about 14 to 16 mg/kg weight of a subject,
about 16 to 18 mg/kg weight of a subject or about 18 to 20 mg/kg
weight of a subject. In an embodiment, the effective amount is 2
mg/kg weight of a subject. In another embodiment, the effective
amount is about 10 mg/kg weight of a subject.
[0249] In a specific embodiment, an effective amount of soluble
CTLA4 is 500 mg for a subject weighing less than 60 kg, 750 mg for
a subject weighing between 60-100 kg and 1000 mg for a subject
weighing more than 100 kg.
[0250] Effective amounts of methotrexate in the pharmaceutical
composition range about 0.1 to 40 mg/week. In one embodiment, the
effective amount is an amount about 0.1 to 5 mg/week, about 5 to 10
mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week, about 20
to 25 mg/week, about 25 to 30 mg/week, about 30 to 35 mg/week, or
about 35 to 40 mg/week. In one embodiment, an effective amount of a
DMARD, including methotrexate, is an amount about 10 to 30
mg/week.
[0251] In one embodiment, the effective amount of a soluble CTLA4
molecule is about 2 mg/kg weight subject and the effective amount
of methotrexate is about 10 to 30 mg/week. In another embodiment,
the effective amount of a soluble CTLA4 molecule is about 10 mg/kg
weight subject and the effective amount of methotrexate is about 10
to 30 mg/week.
[0252] Effective amounts of etanercept in the pharmaceutical
composition range about 0.1 to 100 mg/week. In one embodiment, the
effective amount is ranges about 0.1 to 5 mg/week, about 5 to 10
mg/week, about 10 to 15 mg/week, about 15 to 20 mg/week, about 20
to 25 mg/week, about 25 to 30 mg/week, about 30 to 35 mg/week,
about 35 to 40 mg/week, about 40 to 45 mg/week, about 45 to 50
mg/week, about 50 to 55 mg/week, about 55 to 60 mg/week, about 60
to 65 mg/week, about 65 to 70 mg/week, about 70 to 75 mg/week,
about 75 to 80 mg/week, about 80 to 85 mg/week, about 85 to 90
mg/week, about 90 to 95 mg/week or about 95 to 100 mg/week. In one
embodiment, etanercept is administered in an amount ranging about
50 mg/week e.g., 25 mg administered twice weekly.
[0253] In one embodiment, the effective amount of a soluble CTLA4
molecule is about 2 mg/kg weight subject and the effective amount
of etanercept is about 25 mg twice a week. In another embodiment,
the effective amount of a soluble CTLA4 molecule is about 10 mg/kg
weight subject and the effective amount of etanercept is about 25
mg twice a week.
[0254] The compositions of the invention further encompass a
pharmaceutical composition comprising soluble CTLA4 in combination
with other treatments for rheumatic disease including, but not
limited to: collagen, dnaJ, molecules that block TNF function
(e.g., pegsunercept), molecules that block cytokine function (e.g.,
AMG719), molecules that block LFA-1 function (e.g., efalizumab) and
stem cell transplants. These other treatments are currently being
studied in clinical trials (www.clinicaltrials.gov) to determine
their effect on rheumatoid arthritis.
[0255] Collagen, for example in the form of bovine II collagen, may
be orally administered to a patient suffering from rheumatoid
arthritis in order to alleviate one or more symptoms of rheumatoid
arthritis.
[0256] DnaJ is a small peptide which mimics a protein contained in
a gene in many patients with rheumatoid arthritis. The peptide is
derived from E. coli bacteria heat shock protein. DnaJ may be
orally administered to a patient suffering from rheumatoid
arthritis in order to alleviate one or more symptoms of rheumatoid
arthritis.
[0257] TNF is a molecule involved in the inflammatory response of
patients with rheumatoid arthritis. Conceivably, any molecule that
blocks TNF function e.g., by blocking TNF binding to the TNF
receptor (TNFR), may help modify the progression of rheumatoid
arthritis and alleviate some of its symptoms. Several TNF blockers
such as infliximab and etanercept, have been shown to be
efficacious in treating rheumatoid arthritis. Other TNF blockers
such as pegsunercept are being developed and tested (Phase II
clinical trial) for their efficacy in treating rheumatoid
arthritis.
[0258] Cytokines e.g., Interleukin-1 (IL-1), are cell secreted
molecules involved in mediating immune responses. Conceivably, any
molecule that blocks cytokine function e.g., by blocking IL-1
interaction with its receptor, may help modify the progression of
rheumatoid arthritis and alleviate one or more of its symptoms.
Anakinra, a recombinant protein that blocks IL-1 interaction with
its receptor (IL-IR) has been shown to be efficacious in treating
rheumatoid arthritis. An IL-1 inhibitor, AMG719, is being developed
and tested (Phase II clinical trial) for its efficacy in treating
rheumatoid arthritis.
[0259] Lymphocyte function associated molecule 1 (LFA-1) is a
molecule composed of two subunits, CD11a and CD18, which functions
by mediating lymphocyte adhesion to various cell types such as
endothelium. Conceivably, interference of LFA-1 function may help
modify the progression of rheumatoid arthritis and alleviate one or
more of its symptoms. An anti-LFA-1 antibody, efalizumab, is being
developed and tested (Phase II clinical trial) for its efficacy in
treating rheumatoid arthritis.
[0260] Blockage of TNF, cytokine or LFA-1 interaction to their
ligands by a potentially therapeutic molecule can be determined by
any number of assays known to those skilled in the art. For
example, competition assays may be used to test blockage by the
molecule of interest e.g., a molecule can be exposed to a TNF/TNFR
binding pair in order to compete with TNF to bind to TNFR.
Alternatively, functional assays can be performed to test blockage
e.g., a molecule can be tested for its ability to inhibit an
inflammatory cascade, or any part of an inflammatory reaction such
as swelling, redness or pain, caused by a cytokine.
[0261] The present invention also provides pharmaceutical
compositions comprising the molecules of the invention e.g.,
CTLA4Ig and an acceptable carrier or adjuvant which is known to
those of skill of the art. The pharmaceutical compositions
preferably include suitable carriers and adjuvants which include
any material which when combined with the molecules of the
invention (e.g., a soluble CTLA4 molecule, such as, CTLA4Ig or
L104EA29Y) retain the molecule's activity, and is non-reactive with
the subject's immune system. These carriers and adjuvants include,
but are not limited to, ion exchangers, alumina, aluminum stearate,
lecithin, serum proteins, such as human serum albumin, buffer
substances such as phosphates, glycine, sorbic acid, potassium
sorbate, partial glyceride mixtures of saturated vegetable fatty
acids, phosphate buffered saline solution, water, emulsions (e.g.
oil-water emulsion), salts or electrolytes such as protamine
sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate,
sodium chloride, zinc salts, colloidal silica, magnesium
trisilicate, polyvinyl pyrrolidone, cellulose-based substances and
polyethylene glycol. Other carriers may also include sterile
solutions; tablets, including coated tablets and capsules.
Typically such carriers contain excipients such as starch, milk,
sugar (e.g. sucrose, glucose, maltose), certain types of clay,
gelatin, stearic acid or salts thereof, magnesium or calcium
stearate, talc, vegetable fats or oils, gums, glycols, or other
known excipients. Such carriers may also include flavor and color
additives or other ingredients. Compositions comprising such
carriers are formulated by well known conventional methods. Such
compositions may also be formulated within various lipid
compositions, such as, for example, liposomes as well as in various
polymeric compositions, such as polymer microspheres.
[0262] In a further embodiment of the invention, the present
invention provides kits (i.e., a packaged combination of reagents
with instructions) containing the molecules of the invention useful
for blocking B7 interactions with its ligands and/or for treating
an immune system disease.
[0263] The kit can contain a pharmaceutical composition that
includes one or more agents, for example, a soluble CTLA4 molecule
alone, or with a second agent, and an acceptable carrier or
adjuvant, e.g., pharmaceutically acceptable buffer, such as
phosphate-buffered saline, Ringer's solution and dextrose solution.
It may further include other materials desirable from a commercial
and user standpoint, including other buffers, diluents, filters,
needles, syringes, and package inserts with instructions for use.
The agents may be provided as dry powders, usually lyophilized,
including excipients that upon dissolving will provide a reagent
solution having the appropriate concentration.
[0264] Second agents can include the following: steroids,
glucocorticoids, drug toxins, alkylating agents, anti-neoplastic
drugs, enzymes, antibodies, conjugates, immunosuppressive agents,
corticosteroids, DMARDs, nonsteroidal antiinflammatory drugs
(NSAIDs), prednisone, azathioprine, methotrexate, TNF.alpha.
blockers or antagonists, infliximab, any biological agent targeting
an inflammatory cytokine, chloroquine, hydroxychloroquine,
sulfasalazine (sulphasalazopryine), gold salts, etanercept,
anakinra, cyclophosphamide, leflunomide, collagen, dnaJ, a molecule
that blocks TNF receptors (e.g., pegsunercept), a molecule that
blocks cytokine function (e.g., AMG719), a molecule that blocks
LFA-1 function (e.g., efalizumab), acetyl salicylic acid, choline
magnesium salicylate, diflunisal, magnesium salicylate, salsalate,
sodium salicylate, diclofenac, etodolac, fenoprofen, flurbiprofen,
indomethacin, ketoprofen, ketorolac, meclofenamate, naproxen,
nabumetone, phenylbutazone, piroxicam, sulindac, tolmetin,
acetaminophen, ibuprofen, Cox-2 inhibitors, meloxicam, codeine
phosphate, propoxyphene napsylate, oxycodone hydrochloride,
oxycodone bitartrate, tramadol, dihydrofolic acid reductase
inhibitor, cyclosporine, cyclosporin A or D-penicillamine.
[0265] The kit comprises a container with a label and/or
instructions. Suitable containers include, for example, bottles,
vials, and test tubes. The containers can be formed from a variety
of materials such as glass or plastic. The container can have a
sterile access port (for example the container can be an
intravenous solution bag or a vial having a stopper pierceable by a
needle such as a hypodermic injection needle). The container can
hold a pharmaceutical composition such as a pharmaceutical
composition having an agent that is effective for blocking B7
interactions with its ligand and/or treating an immune system
disease.
[0266] The kit can also comprise a second container comprising one
or more second agents as described herein (e.g., any of the DMARDS
or NSAIDS) and/or a pharmaceutically acceptable buffer, such as
phosphate-buffered saline, Ringer's solution and dextrose solution.
It may further include other materials desirable from a commercial
and user standpoint, including other buffers, diluents, filters,
needles, syringes, and package inserts with instructions for
use.
[0267] The kit may also suitably include a label and/or
instructions on, or associated with the container. The label can
provide directions for carrying out the preparation of the agents
for example, dissolving of the dry powders, and/or treatment for a
specific immune system disease.
[0268] The label and/or the instructions can indicate directions
for either in vivo or in vitro use of the pharmaceutical
composition. The label and/or the instructions can indicate that
the pharmaceutical composition is used alone, or in combination
with a second agent.
[0269] The label can indicate appropriate dosages for the molecules
of the invention. For example, the label can indicate that dosages
for a molecule that is effective for blocking B7 interactions with
its ligand and/or treating an immune system disease is about 0.1 to
100 mg/kg weight of the subject, about 0.5 to 5 mg/kg weight of a
subject, about 5 to 10 mg/kg weight of a subject, about 10 to 15
mg/kg weight of a subject, about 15 to 20 mg/kg weight of a
subject, about 20 to 25 mg/kg weight of a subject, about 25 to 30
mg/kg weight of a subject, about 30 to 35 mg/kg weight of a
subject, about 35 to 40 mg/kg weight of a subject, about 40 to 45
mg/kg of a subject, about 45 to 50 mg/kg weight of a subject, about
50 to 55 mg/kg weight of a subject, about 55 to 60 mg/kg weight of
a subject, about 60 to 65 mg/kg weight of a subject, about 65 to 70
mg/kg weight of a subject, about 70 to 75 mg/kg weight of a
subject, about 75 to 80 mg/kg weight of a subject, about 80 to 85
mg/kg weight of a subject, about 85 to 90 mg/kg weight of a
subject, about 90 to 95 mg/kg weight of a subject, about 95 to 100
mg/kg weight of a subject, about 2 to 10 mg/kg weight of a subject,
about 0.1 to 4 mg/kg weight of a subject, about 0.1 to 0.5 mg/kg
weight of a subject, about 0.5 to 1.0 mg/kg weight of a subject,
about 1.0 to 1.5 mg/kg weight of a subject, about 1.5 to 2.0 mg/kg
weight of a subject, about 2.0 to 2.5 mg/kg weight of a subject,
about 2.5 to 3.0 mg/kg weight of a subject, about 3.0 to 3.5 mg/kg
weight of a subject, about 3.5 to 4.0 mg/kg weight of a subject,
about 4.0 to 4.5 mg/kg weight of a subject, about 4.5 to 5.0 mg/kg
weight of a subject, about 5.0 to 5.5 mg/kg weight of a subject,
about 5.5 to 6.0 mg/kg weight of a subject, about 6.0 to 6.5 mg/kg
weight of a subject, about 6.5 to 7.0 mg/kg weight of a subject,
about 7.0 to 7.5 mg/kg weight of a subject, about 7.5 to 8.0 mg/kg
weight of a subject, about 8.0 to 8.5 mg/kg weight of a subject,
about 8.5 to 9.0 mg/kg weight of a subject, about 9.0 to 9.5 mg/kg
weight of a subject, about 9.5 to 10.0 mg/kg weight of a subject,
about 0.1 to 2 mg/kg weight of a subject, about 2 to 4 mg/kg weight
of a subject, about 4 to 6 mg/kg weight of a subject, about 6 to 8
mg/kg weight of a subject, about 8 to 10 mg/kg weight of a subject,
about 10 to 12 mg/kg weight of a subject, about 12 to 14 mg/kg
weight of a subject, about 14 to 16 mg/kg weight of a subject,
about 16 to 18 mg/kg weight of a subject, about 18 to 20 mg/kg
weight of a subject, about 0.5 mg/kg weight of the subject, 2 mg/kg
weight of the subject, 10 mg/kg weight of the subject, about 0.5
mg/kg to 100 weight of the subject, about 0.5 to 10 mg/kg weight of
a subject, about 0.1 to 20 mg/kg weight of a subject, about 500 mg
for a subject weighing less than 60 kg, 750 mg for a subject
weighing between 60-100 kg or 1000 mg for a subject weighing more
than 100 kg
[0270] The label and/or instructions can also indicate dosages for
a second agent, such as a DMARD, is about 1 to about 5000 mg/day,
about 1 to 10 mg/day, about 10 to 50 mg/day, about 50 to 100
mg/day, about 100 to 150 mg/day, about 150 to 200 mg/day, about 200
to 250 mg/day, about 250 to 300 mg/day, about 300 to 350 mg/day,
about 350 to 400 mg/day, about 400 to 450 mg/day, about 450 to 500
mg/day, about 500 to 550 mg/day, about 550 to 600 mg/day, about 600
to 650 mg/day, about 650 to 700 mg/day, about 700 to 750 mg/day,
about 750 to 800 mg/day, about 800 to 850 mg/day, about 850 to 900
mg/day, about 900 to 950 mg/day, about 950 to 1000 mg/day, about
1000 to 1100 mg/day, about 1100 to 1200 mg/day, about 1200 to 1300
mg/day, about 1300 to 1400 mg/day, about 1400 to 1500 mg/day, about
1500 to 1600 mg/day, about 1600 to 1700 mg/day, about 1700 to 1800
mg/day, about 1800 to 1900 mg/day, about 1900 to 2000 mg/day, about
2000 to 2500 mg/day, about 2500 to 3000 mg/day, about 3000 to 3500
mg/day, about 3500 to 4000 mg/day, about 4000 to 4500 mg/day or
about 4500 to 5000 mg/day.
[0271] The label and/or the instructions can also indicate that the
pharmaceutical composition can be used alone, or in combination,
with a second agent to treat a condition of choice e.g., immune
system diseases, autoimmune diseases, immunoproliferative diseases,
graft-related disorders, graft versus host disease (GVHD) (e.g.,
such as may result from bone marrow transplantation, or in the
induction of tolerance), immune disorders associated with graft
transplantation rejection, immune disorders associated with chronic
rejection, immune disorders associated with tissue or cell allo- or
xenografts (e.g., kidneys, skin, islets, muscles, hepatocytes,
neurons, solid organs and the like), psoriasis, T cell lymphoma, T
cell acute lymphoblastic leukemia, testicular angiocentric T cell
lymphoma, benign lymphocytic angiitis, as lupus (e.g., lupus
erythematosus, lupus nephritis), Hashimoto's thyroiditis, primary
myxedema, Graves' disease, pernicious anemia, autoimmune atrophic
gastritis, Addison's disease, diabetes (e.g. insulin dependent
diabetes mellitus, type I diabetes mellitus, type II diabetes
mellitus), good pasture's syndrome, myasthenia gravis, pemphigus,
Crohn's disease, sympathetic ophthalmia, autoimmune uveitis,
multiple sclerosis, autoimmune hemolytic anemia, idiopathic
thrombocytopenia, primary biliary cirrhosis, chronic action
hepatitis, ulcerative colitis, Sjogren's syndrome, rheumatic
diseases (e.g., rheumatoid arthritis), polymyositis, scleroderma,
mixed connective tissue disease, and the like.
[0272] In a specific embodiment of the invention, the kit comprises
a pharmaceutical composition comprising a pharmaceutically
acceptable carrier and an effective amount of a first agent,
wherein the first agent is a molecule that blocks B7 interaction
with CTLA4 and/or CD28 such as soluble CTLA4 molecules, CD28
molecules, B7 (B7-1 or B7-2) molecules, anti-CTLA4 monoclonal
antibodies, anti-CD28 monoclonal antibodies or anti-B7 (B7-1 or
B7-2) monoclonal antibodies. In preferred embodiments, the soluble
CTLA4 molecules have the amino acid sequence of the extracellular
domain of CTLA4 as shown in either FIG. 24 or 19 (CTLA4Ig or
L104EA29Y, respectively).
[0273] Methods
[0274] The invention provides methods for regulating functional
CTLA4- and CD28-positive cell interactions with B7-positive cells.
The methods comprise contacting the B7-positive cells with a
soluble CTLA4 molecule of the invention so as to regulate
functional CTLA4- and CD28-positive cell interactions with
B7-positive cells, e.g., by interfering with reaction of an
endogenous CTLA4 and/or CD28 molecule with a B7 molecule. Suitable
amounts of soluble CTLA4 for use in the methods of the invention
are described supra.
[0275] The present invention also provides methods for inhibiting
T-cell function but not T-cell depletion in a human by contacting
B7-positive cells in the human with a soluble CTLA4. Examples of
soluble CTLA4 include CTLA4Ig and soluble CTLA4 mutant molecule
e.g. L104EA29YIg. The present invention further provides methods
for treating immune system diseases and auto-immune diseases such
as rheumatic diseases. The methods comprise administering a
therapeutic composition, comprising soluble CTLA4 molecules of the
invention, to a subject in an amount effective to relieve at least
one of the symptoms associated with immune system diseases.
Additionally, the invention may provide long-term therapy for
immune system diseases by blocking the T-cell/B7-positive cell
interactions, thereby blocking T-cell activation/stimulation by
co-stimulatory signals such as B7 binding to CD28, leading to
induction of T-cell anergy or tolerance. Immune system diseases
include, but are not limited to, autoimmune diseases,
immunoproliferative diseases, and graft-related disorders. Examples
of graft-related diseases include graft versus host disease (GVHD)
(e.g., such as may result from bone marrow transplantation, or in
the induction of tolerance), immune disorders associated with graft
transplantation rejection, chronic rejection, and tissue or cell
allo- or xenografts, including allo- or xenografts solid organs
(e.g., kidneys), skin, islets, muscles, hepatocytes, neurons.
Examples of immunoproliferative diseases include, but are not
limited to, psoriasis; T cell lymphoma; T cell acute lymphoblastic
leukemia; testicular angiocentric T cell lymphoma; benign
lymphocytic angiitis; and autoimmune diseases such as lupus (e.g.,
lupus erythematosus, lupus nephritis), Hashimoto's thyroiditis,
primary myxedema, Graves' disease, pernicious anemia, autoimmune
atrophic gastritis, Addison's disease, diabetes (e.g. insulin
dependent diabetes mellitus, type I diabetes mellitus, type II
diabetes mellitus), good pasture's syndrome, myasthenia gravis,
pemphigus, Crohn's disease, sympathetic ophthalmia, autoimmune
uveitis, multiple sclerosis, autoimmune hemolytic anemia,
idiopathic thrombocytopenia, primary biliary cirrhosis, chronic
action hepatitis, ulcerative colitis, Sjogren's syndrome, rheumatic
diseases (e.g., rheumatoid arthritis), polymyositis, scleroderma,
and mixed connective tissue disease.
[0276] The soluble CTLA4 molecules of the invention exhibit
inhibitory properties in vivo. Under conditions where
T-cell/B7-positive cell interactions, for example T cell/B cell
interactions, are occurring as a result of contact between T cells
and B7-positive cells, binding of introduced CTLA4 molecules to
react to B7-positive cells, for example B cells, may interfere,
i.e., inhibit, the T cell/B7-positive cell interactions resulting
in regulation of immune responses.
[0277] The invention provides methods for regulating immune
responses. Immune responses downregulated (reduced) by the soluble
CTLA4 molecules of the invention may be by way of inhibiting or
blocking an immune response already in progress or may involve
preventing the induction of an immune response. The soluble CTLA4
molecules of the invention may inhibit the functions of activated T
cells, such as T lymphocyte proliferation, cytokine secretion
and/or cytokine production, by suppressing T cell responses or by
inducing specific tolerance in T cells, or both. Further, the
soluble CTLA4 molecules of this invention, interfering with the
CTLA4/CD28/B7 pathway may inhibit T-cell proliferation and/or
cytokine secretion, and thus result in reduced tissue destruction
and induction of T-cell unresponsiveness or anergy.
[0278] A preferred embodiment of the invention comprises use of the
soluble CTLA4 mutant molecule L104EA29YIg to regulate functional
CTLA4- and CD28-positive cell interactions with B7-positive cells,
to treat immune system diseases such as rheumatic diseases and/or
to downregulate immune responses. The L104EA29YIg of the invention
is a soluble CTLA4 mutant molecule comprising at least the two
amino acid changes, the leucine (L) to glutamic acid (E) at
position +104 and the alanine (A) to tyrosine (Y) change at
position +29 (FIG. 19). The L104EA29YIg molecule may encompass
further mutations beyond the two specified herein.
[0279] A preferred embodiment of the invention comprises use of a
molecule to block the interaction of B7 with CTLA4 and/or CD28 in
conjunction with a DMARD to regulate an immune response in order to
treat an immune system disease such as a rheumatic disease.
Suitable amounts of the molecule used to block the B7 interaction
with CTLA4 and/or CD28 are described supra. The molecule used to
block the B7/CTLA4 interaction may be a soluble CTLA4 such as
CTLA4Ig, CTLA4Ig/CD28Ig or L104EA29YIg, a soluble CD28 such as
CD28Ig, a soluble B7 (B7-1 or B7-2) such as B7Ig, anti-CTLA4
monoclonal antibodies, anti-CD28 monoclonal antibodies or anti-B7
monoclonal antibodies. The DMARD may be a dihydrofolic acid
reductase inhibitor such as methotrexate, cyclophosphamide,
cyclosporine, cyclosporin A, chloroquine, hydroxychloroquine,
sulfasalazine, sulphasalazopyrine, leflunomide, gold salts,
D-penicillamine, azathioprine, anakinra, infliximab, etanercept,
TNF.alpha. blockers or a biological agent that targets an
inflammatory cytokine.
[0280] A preferred embodiment includes methods for treating a
rheumatic disease, such as rheumatoid arthritis, by administering
an effective amount of soluble CTLA4 molecules alone, or in
conjunction with an effective amount of methotrexate or a molecule
that blocks TNF interactions, to a subject. Administration of an
effective amount of the therapeutic composition(s), thereby
relieving the subject of at least one of the symptoms associated
with the disease, including reducing: joint swelling, joint
tenderness, inflammation, morning stiffness, and pain, and
structural damage subsequently decreasing the physical disability.
The methods of the invention also may be used to reduce at least
one symptom associated with rheumatoid arthritis, including
reducing erythrocyte sedimentation rates, serum levels of
C-reactive protein, soluble ICAM-1, soluble E-selectin and/or
soluble IL-2r.
[0281] The amount of symptom relief provided by the present
invention can be measured using any of the accepted criteria
established to measure and document symptom relief in a clinical
setting. Acceptable criteria for measuring symptom relief may
include scores based on the criteria established by the American
College of Rheumatology (e.g., ACR 20), the four measures of
symptom relief (in: "CDER Guideline for the Clinical Evaluation of
Anti-Inflammatory and Antirheumatic Drugs--FDA 1988), and the
Health Assessment Questionnaire (HAQ) (Fries, J. F., et al., 1982 J
of Rheumatology 9:789-793). For a general description of these
criteria, see "Guidance for Industry: Clinical Development Programs
for Drugs, Devices, and Biological products for the Treatment of
Rheumatoid Arthritis (RA)", February 1999.
[0282] The present invention provides improving ACR response rates
using the methods of the invention. The embodiments of the
invention include improving ACR response rates of ACR 20, 50,
and/or 70, using the methods of the invention.
[0283] The subjects treated by the present invention include
mammalian subjects, including, human, monkey, ape, dog, cat, cow,
horse, goat, pig, rabbit, mouse and rat.
[0284] The present invention provides various methods, local or
systemic, for administering the therapeutic compositions of the
invention such as soluble CTLA4 molecule alone or in conjunction
with a DMARD, such as methotrexate, a molecule that blocks TNF
interactions and/or other therapeutic drug. The methods include
intravenous, intramuscular, intraperitoneal, oral, inhalation and
subcutaneous methods, as well as implantable pump, continuous
infusion, gene therapy, liposomes, suppositories, topical contact,
vesicles, capsules, biodegradable polymers, hydrogels, controlled
release patch and injection methods. The therapeutic agent,
compounded with a carrier, is commonly lyophilized for storage and
is reconstituted with water or a buffered solution with a neutral
pH (about pH 7-8, e.g., pH 7.5) prior to administration.
[0285] As is standard practice in the art, the compositions of the
invention may be administered to the subject in any
pharmaceutically acceptable form.
[0286] In accordance with the practice of the invention, the
methods comprise administering to a subject the soluble CTLA4
molecules of the invention to regulate CD28- and/or CTLA4-positive
cell interactions with B7-positive cells. The B7-positive cells are
contacted with an effective amount of the soluble CTLA4 molecules
of the invention, or fragments or derivatives thereof, so as to
form soluble CTLA4/B7 complexes. Suitable amounts of soluble CTLA4
are described supra. The complexes interfere with interaction
between endogenous CTLA4 and CD28 molecules with B7 family
molecules.
[0287] The soluble CTLA4 molecules may be administered to a subject
in an amount and for a time (e.g. length of time and/or multiple
times) sufficient to block endogenous B7 molecules from binding
their respective ligands, in the subject. Blockage of endogenous
B7/ligand binding thereby inhibiting interactions between
B7-positive cells with CD28-and/or CTLA4-positive cells. In an
embodiment, soluble CTLA4 may be administered to a subject daily,
weekly, monthly and/or yearly, in single or multiple times per
day/week/month/year, depending on need. For example, in one
embodiment, the molecule may initially be administered once every
two weeks for a month, and then once every month thereafter.
[0288] Dosage of a therapeutic agent is dependant upon many factors
including, but not limited to, the type of tissue affected, the
type of autoimmune disease being treated, the severity of the
disease, a subject's health and response to the treatment with the
agents. Accordingly, dosages of the agents can vary depending on
each subject and the mode of administration. The soluble CTLA4
molecules may be administered in an amount from about 0.1 to 100
mg/kg weight of the patient/day. Suitable amounts of soluble CTLA4
are described supra. Methotrexate may be administered to a subject
in an amount from about 0.1 to 100 mg/week. Suitable amounts of
soluble methotrexate are described supra. A molecule that blocks
TNF interactions e.g., etanercept, may be administered to a subject
in an amount from about 0.1 to 100 mg/week. Suitable amounts of TNF
blockers are described supra.
[0289] The invention also encompasses the use of the compositions
of the invention together with other pharmaceutical agents to treat
immune system diseases. For example, rheumatic diseases may be
treated with molecules of the invention in conjunction with, but
not limited to, immunosuppressants such as corticosteroids,
cyclosporin (Mathiesen 1989 Cancer Lett. 44(2):151-156),
prednisone, azathioprine, (R. Handschumacher, in: "Drugs Used for
Immunosuppression" pages 1264-1276), TNF.alpha. blockers or
antagonists (New England Journal of Medicine, vol. 340: 253-259,
1999; The Lancet vol. 354: 1932-39, 1999, Annals of Internal
Medicine, vol. 130: 478-486), or any other biological agent
targeting any inflammatory cytokine, nonsteroidal antiinflammatory
drugs/Cox-2 inhibitors, hydroxychloroquine, sulphasalazopryine,
gold salts, etanercept, infliximab, rapamycin, mycophenolate
mofetil, azathioprine, tacrolismus, basiliximab, cytoxan,
interferon beta-1a, interferon beta-1b, glatiramer acetate,
mitoxantrone hydrochloride, anakinra and/or other biologics.
[0290] The soluble CTLA4 molecules (preferably, L104EA29YIg) can
also be used in combination with one or more of the following
agents to regulate an immune response: soluble gp39 (also known as
CD40 ligand (CD40L), CD154, T-BAM, TRAP), soluble CD29, soluble
CD40, soluble CD80 (e.g. ATCC 68627), soluble CD86, soluble CD28
(e.g. ATCC accession number 68628), soluble CD56, soluble Thy-1,
soluble CD3, soluble TCR, soluble VLA-4, soluble VCAM-1, soluble
LECAM-1, soluble ELAM-1, soluble CD44, antibodies reactive with
gp39 (e.g. ATCC HB-10916, ATCC HB-12055 and ATCC HB-12056),
antibodies reactive with CD40 (e.g. ATCC HB-9110), antibodies
reactive with B7 (e.g. ATCC HB-253, ATCC CRL-2223, ATCC CRL-2226,
ATCC HB-301, ATCC HB-11341, etc), antibodies reactive with CD28
(e.g. ATCC HB-11944 or mAb 9.3 as described by Martin et al (J.
Clin. Immun. 4(1):18-22, 1980), antibodies reactive with LFA-1
(e.g. ATCC HB-9579 and ATCC TIB-213), antibodies reactive with
LFA-2, antibodies reactive with IL-2, antibodies reactive with
IL-12, antibodies reactive with IFN-gamma, antibodies reactive with
CD2, antibodies reactive with CD48, antibodies reactive with any
ICAM (e.g., ICAM-1 (ATCC CRL-2252), ICAM-2 and ICAM-3), antibodies
reactive with CTLA4 (e.g. ATCC HB-304), antibodies reactive with
Thy-1, antibodies reactive with CD56, antibodies reactive with CD3,
antibodies reactive with CD29, antibodies reactive with TCR,
antibodies reactive with VLA-4, antibodies reactive with VCAM-1,
antibodies reactive with LECAM-1, antibodies reactive with ELAM-1,
antibodies reactive with CD44. In certain embodiments, monoclonal
antibodies are preferred. In other embodiments, antibody fragments
are preferred. As persons skilled in the art will readily
understand, the combination can include: the soluble CTLA4
molecules of the invention and one other immunosuppressive agent;
the soluble CTLA4 molecules with two other immunosuppressive
agents; the soluble CTLA4 molecules with three other
immunosuppressive agents; and the like. The determination of the
optimal combination and dosages can be determined and optimized
using methods well known in the art.
[0291] Some specific combinations include the following:
L104EA29YIg and CD80 monoclonal antibodies (mAbs); L104EA29YIg and
CD86 mAbs; L104EA29YIg, CD80 mAbs, and CD86 mAbs; L104EA29YIg and
gp39 mAbs; L104EA29YIg and CD40 mAbs; L104EA29YIg and CD28 mAbs;
L104EA29YIg, CD80 and CD86 mAbs, and gp39 mAbs; L104EA29YIg, CD80
and CD86 mAbs and CD40 mAbs; and L104EA29YIg, anti-LFA1 mAb, and
anti-gp39 mAb. A specific example of a gp39 mAb is MR1. Other
combinations will be readily appreciated and understood by persons
skilled in the art.
[0292] The soluble CTLA4 molecules of the invention, for example
L104EA29YIg, may be administered as the sole active ingredient or
together with other drugs in immunomodulating regimens or other
anti-inflammatory agents such as DMARDs e.g. for the treatment or
prevention of allo- or xenograft acute or chronic rejection or
inflammatory or autoimmune disorders, or to induce tolerance. For
example, it may be used in combination with a calcineurin
inhibitor, e.g. cyclosporin A or FK506; an immunosuppressive
macrolide, e.g. rapamycine or a derivative thereof (e.g.
40-O-(2-hydroxy)ethyl-rapamycin); a lymphocyte homing agent, e.g.
FTY720 or an analog thereof; corticosteroids; cyclophosphamide;
azathioprene; a dihydrofolic acid reductase inhibitor such as
methotrexate; leflunomide or an analog thereof; mizoribine;
mycophenolic acid; mycophenolate mofetil; 15-deoxyspergualine or an
analog thereof, immunosuppressive monoclonal antibodies, e.g.,
monoclonal antibodies to leukocyte receptors, e.g., MHC, CD2, CD3,
CD4, CD11a/CD18, CD7, CD25, CD 27, B7, CD40, CD45, CD58, CD137,
ICOS, CD150 (SLAM), OX40, 4-1BB or their ligands; or other
immunomodulatory compounds, e.g. CTLA4/CD28-Ig, or other adhesion
molecule inhibitors, e.g. mAbs or low molecular weight inhibitors
including LFA-1 antagonists, Selectin antagonists and VLA-4
antagonists. The compound is particularly useful in combination
with a compound that interferes with CD40 and its ligand, e.g.
antibodies to CD40 and antibodies to CD40-L.
[0293] Where the soluble CTLA4 mutant molecules of the invention
are administered in conjunction with other
immunosuppressive/immunomodulatory or anti-inflammatory therapy,
e.g. as hereinabove specified, dosages of the co-administered
immunosuppressant, immunomodulatory or anti-inflammatory compound
will of course vary depending on the type of co-drug employed, e.g.
whether it is a steroid or a cyclosporin, on the specific drug
employed, on the condition being treated and so forth.
[0294] In accordance with the foregoing the present invention
provides in a yet further aspect methods as defined above
comprising co-administration, e.g. concomitantly or in sequence, of
a therapeutically effective amount of soluble CTLA4 molecules of
the invention, e.g. CTLA4Ig and/or L104EA29YIg, in free form or in
pharmaceutically acceptable salt form, and a second drug substance,
said second drug substance being an immunosuppressant,
immunomodulatory or anti-inflammatory drug, e.g. as indicated
above.
[0295] Further provided are therapeutic combinations, e.g. a kit,
comprising a soluble CTLA4 molecule, in free form or in
pharmaceutically acceptable salt form, to be used concomitantly or
in sequence with at least one pharmaceutical composition comprising
an immunosuppressant, immunomodulatory or anti-inflammatory drug
e.g., a DMARD, NSAID, glucocorticoid or corticosteroid. The kit may
comprise instructions for its administration. The kits of the
invention can be used in any method of the present invention.
[0296] The invention also provides methods for producing the
soluble CTLA4 mutant molecules of the invention. Expression of
soluble CTLA4 mutant molecules can be in prokaryotic cells or
eukaryotic cells.
[0297] Prokaryotes most frequently are represented by various
strains of bacteria. The bacteria may be a gram positive or a gram
negative. Typically, gram-negative bacteria such as E. coli are
preferred. Other microbial strains may also be used. Sequences
encoding soluble CTLA4 mutant molecules can be inserted into a
vector designed for expressing foreign sequences in prokaryotic
cells such as E. coli. These vectors can include commonly used
prokaryotic control sequences which are defined herein to include
promoters for transcription initiation, optionally with an
operator, along with ribosome binding site sequences, including
such commonly used promoters as the beta-lactamase (penicillinase)
and lactose (lac) promoter systems (Chang, et al., (1977) Nature
198:1056), the tryptophan (trp) promoter system (Goeddel, et al.,
(1980) Nucleic Acids Res. 8:4057) and the lambda derived P.sub.L
promoter and N-gene ribosome binding site (Shimatake, et al.,
(1981) Nature 292:128).
[0298] Such expression vectors will also include origins of
replication and selectable markers, such as a beta-lactamase or
neomycin phosphotransferase gene conferring resistance to
antibiotics, so that the vectors can replicate in bacteria and
cells carrying the plasmids can be selected for when grown in the
presence of antibiotics, such as ampicillin or kanamycin.
[0299] The expression plasmid can be introduced into prokaryotic
cells via a variety of standard methods, including but not limited
to CaCl.sub.2-shock (Cohen, (1972) Proc. Natl. Acad. Sci. USA
69:2110, and Sambrook et al. (eds.), "Molecular Cloning: A
Laboratory Manual", 2nd Edition, Cold Spring Harbor Press, (1989))
and electroporation.
[0300] In accordance with the practice of the invention, eukaryotic
cells are also suitable host cells. Examples of eukaryotic cells
include any animal cell, whether primary or immortalized, yeast
(e.g., Saccharomyces cerevisiae, Schizosaccharomyces pombe, and
Pichia pastoris), and plant cells. Myeloma, COS and CHO cells are
examples of animal cells that may be used as hosts. Particular CHO
cells include, but are not limited to, DG44 (Chasin, et la., 1986
Som. Cell. Molec. Genet. 12:555-556; Kolkekar 1997 Biochemistry
36:10901-10909), CHO-K1 (ATCC No. CCL-61), CHO-K1 Tet-On cell line
(Clontech), CHO designated ECACC 85050302 (CAMR, Salisbury,
Wiltshire, UK), CHO clone 13 (GEIMG, Genova, IT), CHO clone B
(GEIMG, Genova, IT), CHO-K1/SF designated ECACC 93061607 (CAMR,
Salisbury, Wiltshire, UK), and RR-CHOK1 designated ECACC 92052129
(CAMR, Salisbury, Wiltshire, UK). Exemplary plant cells include
tobacco (whole plants, cell culture, or callus), corn, soybean, and
rice cells. Corn, soybean, and rice seeds are also acceptable.
[0301] Nucleic acid sequences encoding the CTLA4 mutant molecules
can also be inserted into a vector designed for expressing foreign
sequences in an eukaryotic host. The regulatory elements of the
vector can vary according to the particular eukaryotic host.
[0302] Commonly used eukaryotic control sequences for use in
expression vectors include promoters and control sequences
compatible with mammalian cells such as, for example, CMV promoter
(CDM8 vector) and avian sarcoma virus (ASV) (.pi.rLN vector). Other
commonly used promoters include the early and late promoters from
Simian Virus 40 (SV40) (Fiers, et al., (1973) Nature 273:113), or
other viral promoters such as those derived from polyoma,
Adenovirus 2, and bovine papilloma virus. An inducible promoter,
such as hMTII (Karin, et al., (1982) Nature 299:797-802) may also
be used.
[0303] Vectors for expressing CTLA4 mutant molecules in eukaryotes
may also carry sequences called enhancer regions. These are
important in optimizing gene expression and are found either
upstream or downstream of the promoter region.
[0304] Examples of expression vectors for eukaryotic host cells
include, but are not limited to, vectors for mammalian host cells
(e.g., BPV-1, pHyg, pRSV, pSV2, pTK2 (Maniatis); pIRES (Clontech);
pRc/CMV2, pRc/RSV, pSFV1 (Life Technologies); pVPakc Vectors, pCMV
vectors, pSG5 vectors (Stratagene)), retroviral vectors (e.g., pFB
vectors (Stratagene)), pcDNA-3 (Invitrogen) or modified forms
thereof, adenoviral vectors; Adeno-associated virus vectors,
baculovirus vectors, yeast vectors (e.g., pESC vectors
(Stratagene)).
[0305] Nucleic acid sequences encoding CTLA4 mutant molecules can
integrate into the genome of the eukaryotic host cell and replicate
as the host genome replicates. Alternatively, the vector carrying
CTLA4 mutant molecules can contain origins of replication allowing
for extrachromosomal replication.
[0306] For expressing the nucleic acid sequences in Saccharomyces
cerevisiae, the origin of replication from the endogenous yeast
plasmid, the 2.mu. circle can be used. (Broach, (1983) Meth. Enz.
101:307). Alternatively, sequences from the yeast genome capable of
promoting autonomous replication can be used (see, for example,
Stinchcomb et al., (1979) Nature 282:39); Tschemper et al., (1980)
Gene 10:157; and Clarke et al., (1983) Meth. Enz. 101:300).
[0307] Transcriptional control sequences for yeast vectors include
promoters for the synthesis of glycolytic enzymes (Hess et al.,
(1968) J. Adv. Enzyme Reg. 7:149; Holland et al., (1978)
Biochemistry 17:4900). Additional promoters known in the art
include the CMV promoter provided in the CDM8 vector (Toyama and
Okayama, (1990) FEBS 268:217-221); the promoter for
3-phosphoglycerate kinase (Hitzeman et al., (1980) J. Biol. Chem.
255:2073), and those for other glycolytic enzymes.
[0308] Other promoters are inducible because they can be regulated
by environmental stimuli or by the growth medium of the cells.
These inducible promoters include those from the genes for heat
shock proteins, alcohol dehydrogenase 2, isocytochrome C, acid
phosphatase, enzymes associated with nitrogen catabolism, and
enzymes responsible for maltose and galactose utilization.
[0309] Regulatory sequences may also be placed at the 3' end of the
coding sequences. These sequences may act to stabilize messenger
RNA. Such terminators are found in the 3' untranslated region
following the coding sequences in several yeast-derived and
mammalian genes.
[0310] Exemplary vectors for plants and plant cells include, but
are not limited to, Agrobacterium T.sub.i plasmids, cauliflower
mosaic virus (CaMV), and tomato golden mosaic virus (TGMV).
[0311] General aspects of mammalian cell host system
transformations have been described by Axel (U.S. Pat. No.
4,399,216 issued Aug. 16, 1983). Mammalian cells can be transformed
by methods including but not limited to, transfection in the
presence of calcium phosphate, microinjection, electroporation, or
via transduction with viral vectors.
[0312] Methods for introducing foreign DNA sequences into eukaryote
genomes, including plant and yeast genomes include; (1) mechanical
methods, such as microinjection of DNA into single cells or
protoplasts, vortexing cells with glass beads in the presence of
DNA, or shooting DNA-coated tungsten or gold spheres into cells or
protoplasts; (2) introducing DNA by making cell membranes permeable
to macromolecules through polyethylene glycol treatment or
subjection to high voltage electrical pulses (electroporation); or
(3) the use of liposomes (containing cDNA) which fuse to cell
membranes.
[0313] Once the CTLA4 mutant molecules of the inventions are
expressed, they can be harvested by methods well known in the art
such as cell lysis (e.g. sonication, lysozyme and/or detergents)
and protein recovery performed using standard protein purification
means, e.g., affinity chromatography or ion-exchange
chromatography, to yield substantially pure product (R. Scopes in:
"Protein Purification, Principles and Practice", Third Edition,
Springer-Verlag (1994); Sambrook et al. (eds.), "Molecular Cloning:
A Laboratory Manual", 2nd Edition, Cold Spring Harbor Press,
(1989)). Expression of CTLA4 mutant molecules can be detected by
methods known in the art. For example, the mutant molecules can be
detected by Coomassie staining SDS-PAGE gels and immunoblotting
using antibodies that bind CTLA4.
[0314] The following examples are presented to illustrate the
present invention and to assist one of ordinary skill in making and
using the same. The examples are not intended in any way to
otherwise limit the scope of the invention.
EXAMPLE 1
[0315] The following provides a description of the methods used to
generate the nucleotide sequences encoding the CTLA4 molecules of
the invention.
[0316] A CTLA4Ig encoding plasmid was first constructed, and shown
to express CTLA4Ig molecules as described in U.S. Pat. Nos.
5,434,131, 5,885,579 and 5,851,795. Then single-site mutant
molecules (e.g., L104EIg) were generated from the CTLA4Ig encoding
sequence, expressed and tested for binding kinetics for various B7
molecules. The L104EIg nucleotide sequence (as included in the
sequence shown in FIG. 18) was used as a template to generate the
double-site CTLA4 mutant sequences (as included in the sequences
shown in FIGS. 19-22) which were expressed as proteins and tested
for binding kinetics. The double-site CTLA4 mutant sequences
include: L104EA29YIg, L104EA29LIg, L104EA29TIg, and L104EA29WIg.
Triple-site mutants were also generated.
[0317] CTLA4Ig Construction
[0318] A genetic construct encoding CTLA4Ig comprising the
extracellular domain of CTLA4 and an IgCgamma1 domain was
constructed as described in U.S. Pat. Nos. 5,434,131, 5,844,095 and
5,851,795, the contents of which are incorporated by reference
herein. The extracellular domain of the CTLA4 gene was cloned by
PCR using synthetic oligonucleotides corresponding to the published
sequence (Dariavach et al., Eur. Journ. Immunol. 18:1901-1905
(1988)).
[0319] Because a signal peptide for CTLA4 was not identified in the
CTLA4 gene, the N-terminus of the predicted sequence of CTLA4 was
fused to the signal peptide of oncostatin M (Malik et al., Mol. and
Cell. Biol. 9:2847 (1989)) in two steps using overlapping
oligonucleotides. For the first step, the oligonucleotide,
CTCAGTCTGGTCCTTGCACTCCTGTTTCCAAGCATGGCGAGCATGG- CAATGCA
CGTGGCCCAGCC (SEQ ID NO: 1) (which encoded the C terminal 15 amino
acids from the oncostatin M signal peptide fused to the N terminal
7 amino acids of CTLA4) was used as forward primer, and
TTTGGGCTCCTGATCAGAATCTGGGCACGGTTG (SEQ ID NO: 2) (encoding amino
acid residues 119-125 of the amino acid sequence encoding CTLA4
receptor and containing a Bcl I restriction enzyme site) as reverse
primer. The template for this step was cDNA synthesized from 1
micro g of total RNA from H38 cells (an HTLV II infected T-cell
leukemic cell line provided by Drs. Salahudin and Gallo, NCI,
Bethesda, Md.). A portion of the PCR product from the first step
was reamplified, using an overlapping forward primer, encoding the
N terminal portion of the oncostatin M signal peptide and
containing a Hind III restriction endonuclease site,
CTAGCCACTGAAGCTTCACCAATGGGTGTACTGCTCACACAGAGGACGCTGCTCAGTCTGGTCCTTGCACTC
(SEQ ID NO: 3) and the same reverse primer. The product of the PCR
reaction was digested with Hind III and Bcl I and ligated together
with a Bcl 1/Xba I cleaved cDNA fragment encoding the amino acid
sequences corresponding to the hinge, CH2 and CH3 regions of
IgC(gamma)1 into the Hind III/Xba I cleaved expression vector, CDM8
or Hind III/Xba I cleaved expression vector piLN (also known as
7.pi.LN).
[0320] DNA encoding the amino acid sequence corresponding to
CTLA4Ig has been deposited with the ATCC under the Budapest Treaty
on May 31, 1991, and has been accorded ATCC accession number
68629.
[0321] CTLA4Ig Codon Based Mutagenesis:
[0322] A mutagenesis and screening strategy was developed to
identify mutant CTLA4Ig molecules that had slower rates of
dissociation ("off" rates) from CD80 and/or CD86 molecules i.e.
improved binding ability. In this embodiment, mutations were
carried out in and/or about the residues in the CDR-1, CDR-2 (also
known as the C' strand) and/or CDR-3 regions of the extracellular
domain of CTLA4 (as described in U.S. Pat. Nos. 6,090,914,
5,773,253 and 5,844,095; in copending U.S. Patent Application
Serial No. 60/214,065; and by Peach, R. J., et al J Exp Med 1994
180:2049-2058. A CDR-like region encompasses the each CDR region
and extends, by several amino acids, upstream and/or downstream of
the CDR motif). These sites were chosen based on studies of
chimeric CD28/CTLA4 fusion proteins (Peach et al., J. Exp. Med.,
1994, 180:2049-2058), and on a model predicting which amino acid
residue side chains would be solvent exposed, and a lack of amino
acid residue identity or homology at certain positions between CD28
and CTLA4. Also, any residue which is spatially in close proximity
(5 to 20 Angstrom Units) to the identified residues is considered
part of the present invention.
[0323] To synthesize and screen soluble CTLA4 mutant molecules with
altered affinities for a B7 molecule (e.g. CD80, CD86), a two-step
strategy was adopted. The experiments entailed first generating a
library of mutations at a specific codon of an extracellular
portion of CTLA4 and then screening these by BIAcore analysis to
identify mutants with altered reactivity to B7. The Biacore assay
system (Pharmacia, Piscataway, N.J.) uses a surface plasmon
resonance detector system that essentially involves covalent
binding of either CD80Ig or CD86Ig to a dextran-coated sensor chip
which is located in a detector. The test molecule can then be
injected into the chamber containing the sensor chip and the amount
of complementary protein that binds can be assessed based on the
change in molecular mass which is physically associated with the
dextran-coated side of the sensor chip; the change in molecular
mass can be measured by the detector system.
[0324] Specifically, single-site mutant nucleotide sequences were
generated using non-mutated (e.g., wild-type) DNA encoding CTLA4Ig
(U.S. Pat. Nos. 5,434,131, 5,844,095; 5,851,795; and 5,885,796;
ATCC Accession No. 68629) as a template. Mutagenic oligonucleotide
PCR primers were designed for random mutagenesis of a specific
codon by allowing any base at positions 1 and 2 of the codon, but
only guanine or thymine at position 3 (XXG/T or also noted as
NNG/T). In this manner, a specific codon encoding an amino acid
could be randomly mutated to code for each of the 20 amino acids.
In that regard, XXG/T mutagenesis yields 32 potential codons
encoding each of the 20 amino acids. PCR products encoding
mutations in close proximity to the CDR3-like loop of CTLA4Ig
(MYPPPY), were digested with SacI/XbaI and subcloned into similarly
cut CTLA4Ig (as included in FIG. 24) .pi.LN expression vector. This
method was used to generate the single-site CTLA4 mutant molecule
L104EIg (as included in FIG. 18).
[0325] For mutagenesis in proximity to the CDR-1-like loop of
CTLA4Ig, a silent NheI restriction site was first introduced 5' to
this loop, by PCR primer-directed mutagenesis. PCR products were
digested with NheI/XbaI and subcloned into similarly cut CTLA4Ig or
L104EIg expression vectors. This method was used to generate the
double-site CTLA4 mutant molecule L104EA29YIg (as included in FIG.
19). In particular, the nucleic acid molecule encoding the
single-site CTLA4 mutant molecule, L104EIg, was used as a template
to generate the double-site CTLA4 mutant molecule, L104EA29YIg.
[0326] The double-site mutant nucleotide sequences encoding CTLA4
mutant molecules, such as L104EA29YIg (deposited on Jun. 19, 2000
with the American Type Culture Collection (ATCC), 10801 University
Blvd., Manassas, Va. 20110-2209 and accorded ATCC accession number
PTA-2104), were generated by repeating the mutagenesis procedure
described above using L104EIg as a template. This method was used
to generate numerous double-site mutants nucleotide sequences such
as those encoding CTLA4 molecules L104EA29YIg (as included in the
sequence shown in FIG. 19), L104EA29LIg (as included in the
sequence shown in FIG. 20), L104EA29TIg (as included in the
sequence shown in FIG. 21), and L104EA29WIg (as included in the
sequence shown in FIG. 22). Triple-site mutants, such as those
encoding L104EA29YS25KIg, L104EA29YS25NIg and L104EA29YS25RIg, were
also generated
[0327] The soluble CTLA4 molecules were expressed from the
nucleotide sequences and used in the phase II clinical studies
described in Example 3, infra.
[0328] As those skilled-in-the-art will appreciate, replication of
nucleic acid sequences, especially by PCR amplification, easily
introduces base changes into DNA strands. However, nucleotide
changes do not necessarily translate into amino acid changes as
some codons redundantly encode the same amino acid. Any changes of
nucleotide from the original or wildtype sequence, silent (i.e.
causing no change in the translated amino acid) or otherwise, while
not explicitly described herein, are encompassed within the scope
of the invention.
EXAMPLE 2
[0329] The following example provides a description of the
screening methods used to identify the single- and double-site
mutant CTLA polypeptides, expressed from the constructs described
in Example 1, that exhibited a higher binding avidity for B7
molecules, compared to non-mutated CTLA4Ig molecules.
[0330] Current in vitro and in vivo studies indicate that CTLA4Ig
by itself is unable to completely block the priming of antigen
specific activated T cells. In vitro studies with CTLA4Ig and
either monoclonal antibody specific for CD80 or CD86 measuring
inhibition of T cell proliferation indicate that anti-CD80
monoclonal antibody did not augment CTLA4Ig inhibition. However,
anti-CD86 monoclonal antibody did augment the inhibition,
indicating that CTLA4Ig was not as effective at blocking CD86
interactions. These data support earlier findings by Linsley et al.
(Immunity, (1994), 1:793-801) showing inhibition of CD80-mediated
cellular responses required approximately 100 fold lower CTLA4Ig
concentrations than for CD86-mediated responses. Based on these
findings, it was surmised that soluble CTLA4 mutant molecules
having a higher avidity for CD86 than wild type CTLA4 should be
better able to block the priming of antigen specific activated
cells than CTLA4Ig.
[0331] To this end, the soluble CTLA4 mutant molecules described in
Example 1 above were screened using a novel screening procedure to
identify several mutations in the extracellular domain of CTLA4
that improve binding avidity for CD80 and CD86. This screening
strategy provided an effective method to directly identify mutants
with apparently slower "off" rates without the need for protein
purification or quantitation since "off" rate determination is
concentration independent (O'Shannessy et al., (1993) Anal.
Biochem., 212:457-468).
[0332] COS cells were transfected with individual miniprep purified
plasmid DNA and propagated for several days. Three day conditioned
culture media was applied to BIAcore biosensor chips (Pharmacia
Biotech AB, Uppsala, Sweden) coated with soluble CD80Ig or CD86Ig.
The specific binding and dissociation of mutant proteins was
measured by surface plasmon resonance (O'Shannessy, D. J., et al.,
1997 Anal. Biochem. 212:457-468). All experiments were run on
BIAcore.TM. or BIAcore.TM. 2000 biosensors at 25.degree. C. Ligands
were immobilized on research grade NCM5 sensor chips (Pharmacia)
using standard N-ethyl-N'-(dimethylaminopro- pyl)
carbodiimidN-hydroxysuccinimide coupling (Johnsson, B., et al.
(1991) Anal. Biochem. 198: 268-277; Khilko, S. N., et al.(1993) J.
Biol. Chem 268:5425-15434).
[0333] Screening Method
[0334] COS cells grown in 24 well tissue culture plates were
transiently transfected with mutant CTLA4Ig. Culture media
containing secreted soluble mutant CTLA4Ig was collected 3 days
later.
[0335] Conditioned COS cell culture media was allowed to flow over
BIAcore biosensor chips derivitized with CD86Ig or CD80Ig (as
described in Greene et al., 1996 J. Biol. Chem. 271:26762-26771),
and mutant molecules were identified with off-rates slower than
that observed for wild type CTLA4Ig. The DNAs corresponding to
selected media samples were sequenced and more DNA prepared to
perform larger scale COS cell transient transfection, from which
CTLA4Ig mutant protein was prepared following protein A
purification of culture media.
[0336] BIAcore analysis conditions and equilibrium binding data
analysis were performed as described in J. Greene et al. 1996 J.
Biol. Chem. 271:26762-26771 and in U.S. patent application Ser.
Nos. 09/579,927, and 60/214,065 which are herein incorporated by
reference.
[0337] BIAcore Data Analysis
[0338] Senosorgram baselines were normalized to zero response units
(RU) prior to analysis. Samples were run over mock-derivatized flow
cells to determine background RU values due to bulk refractive
index differences between solutions. Equilibrium dissociation
constants (K.sub.d) were calculated from plots of R.sub.eq versus
C, where R.sub.eq is the steady-state response minus the response
on a mock-derivatized chip, and C is the molar concentration of
analyte. Binding curves were analyzed using commercial nonlinear
curve-fitting software (Prism, GraphPAD Software).
[0339] Experimental data were first fit to a model for a single
ligand binding to a single receptor (1-site model, i.e., a simple
langmuir system, A+BAB), and equilibrium association constants
(K.sub.d=[A].multidot.[B].backslash.[AB]) were calculated from the
equation R=R.sub.max.multidot.C/(K.sub.d+C). Subsequently, data
were fit to the simplest two-site model of ligand binding (i.e., to
a receptor having two non-interacting independent binding sites as
described by the equation
R=R.sub.max1.multidot.C.backslash.(K.sub.d1+C)+R.sub.max2.multid-
ot.C.backslash.(K.sub.d2+C).
[0340] The goodness-of-fits of these two models were analyzed
visually by comparison with experimental data and statistically by
an F test of the sums-of-squares. The simpler one-site model was
chosen as the best fit, unless the two-site model fit significantly
better (p<0.1).
[0341] Association and disassociation analyses were performed using
BIA evaluation 2.1 Software (Pharmacia). Association rate constants
k.sub.on were calculated in two ways, assuming both homogenous
single-site interactions and parallel two-site interactions. For
single-site interactions, k.sub.on values were calculated according
to the equation R.sub.t=R.sub.eq(1-exp.sup.-ks(t-t.sub.0), where
R.sub.t is a response at a given time, t; R.sub.eq is the
steady-state response; to is the time at the start of the
injection; and k.sub.s=dR/dt=k.sub.on.multidot.Ck.sub.of- f, where
C is a concentration of analyte, calculated in terms of monomeric
binding sites. For two-site interactions k.sub.on values were
calculated according to the equation
R.sub.t=R.sub.eq1(1-exp.sup.-ks1(t-t.sub.0)+R.s-
ub.eq2(1-exp.sup.ks2(t-t.sub.0). For each model, the values of
k.sub.on were determined from the calculated slope (to about 70%
maximal association) of plots of k.sub.s versus C.
[0342] Dissociation data were analyzed according to one site
(AB=A+B) or two site (AiBj=Ai+Bj) models, and rate constants
(k.sub.off) were calculated from best fit curves. The binding site
model was used except when the residuals were greater than machine
background (2-10RU, according to machine), in which case the
two-binding site model was employed. Half-times of receptor
occupancy were calculated using the relationship
t.sub.1/2=0.693/k.sub.off.
[0343] Flow Cytometry:
[0344] Murine mAb L307.4 (anti-CD80) was purchased from Becton
Dickinson (San Jose, Calif.) and IT2.2 (anti-B7-0 [also known as
CD86]), from Pharmingen (San Diego, Calif.). For immunostaining,
CD80-positive and/or CD86-positive CHO cells were removed from
their culture vessels by incubation in phosphate-buffered saline
(PBS) containing 10 mM EDTA. CHO cells (1-10.times..sub.10.sup.5)
were first incubated with mAbs or immunoglobulin fusion proteins in
DMEM containing 10% fetal bovine serum (FBS), then washed and
incubated with fluorescein isothiocyanate-conjugat- ed goat
anti-mouse or anti-human immunoglobulin second step reagents (Tago,
Burlingame, Calif.). Cells were given a final wash and analyzed on
a FACScan (Becton Dickinson).
[0345] SDS-PAGE and Size Exclusion Chromatography
[0346] SDS-PAGE was performed on Tris/glycine 4-20% acrylamide gels
(Novex, San Diego, Calif.). Analytical gels were stained with
Coomassie Blue, and images of wet gels were obtained by digital
scanning. CTLA4Ig (25 .mu.g) and L104EA29YIg (25 .mu.g) were
analyzed by size exclusion chromatography using a TSK-GEL G300
SW.sub.XL column (7.8.times.300 mm, Tosohaas, Montgomeryville, Pa.)
equilibrated in phosphate buffered saline containing 0.02%
NAN.sub.3 at a flow rate of 1.0 ml/min.
[0347] CTLA4X.sub.C120S and L104EA29YX.sub.X120S.
[0348] Single chain CTLA4X.sub.C120S was prepared as previously
described (Linsley et al., (1995) J. Biol. Chem., 270:15417-15424).
Briefly, an oncostatin M CTLA4 (OMCTLA4) expression plasmid was
used as a template, the forward primer,
GAGGTGATAAAGCTTCACCAATGGGTGTACTGCTCACACAG (SEQ ID NO: 4) was chosen
to match sequences in the vector; and the reverse primer,
GTGGTGTATTGGTCTAGATCAATCAGAATCTGGGCACGGTTC (SEQ ID NO: 5)
corresponded to the last seven amino acids (i.e. amino acids
118-124) in the extracellular domain of CTLA4, and contained a
restriction enzyme site, and a stop codon (TGA). The reverse primer
specified a C120S (cysteine to serine at position 120) mutation. In
particular, the nucleotide sequence GCA (nucleotides 34-36) of the
reverse primer shown above is replaced with one of the following
nucleotide sequences: AGA, GGA, TGA, CGA, ACT, or GCT. As persons
skilled in the art will understand, the nucleotide sequence GCA is
a reversed complementary sequence of the codon TGC for cysteine.
Similarly, the nucleotide sequences AGA, GGA, TGA, CGA, ACT, or GCT
are the reversed complementary sequences of the codons for serine.
Polymerase chain reaction products were digested with HindIII/XbaI
and directionally subcloned into the expression vector 7rLN
(Bristol-Myers Squibb Company, Princeton, N.J.).
L104EA29YX.sub.C120S was prepared in an identical manner. Each
construct was verified by DNA sequencing.
[0349] Identification and Biochemical Characterization of High
Avidity Mutants
[0350] Twenty four amino acids were chosen for mutagenesis and the
resulting .about.2300 mutant proteins assayed for CD86Ig binding by
surface plasmon resonance (SPR; as described, supra). The
predominant effects of mutagenesis at each site are summarized in
Table II, infra. Random mutagenesis of some amino acids in the
CDR-1 region (S25-R33) apparently did not alter ligand binding.
Mutagenesis of E31 and R33 and residues M97-Y102 apparently
resulted in reduced ligand binding. Mutagenesis of residues, S25,
A29, and T30, K93, L96, Y103, L104, and G105, resulted in proteins
with slow "on" and/or slow "off" rates. These results confirm
previous findings that residues in the CDR-1 (S25-R33) region, and
residues in or near M97-Y102 influence ligand binding (Peach et
al., (1994) J. Exp. Med., 180:2049-2058).
[0351] Mutagenesis of sites S25, T30, K93, L96, Y103, and G105
resulted in the identification of some mutant proteins that had
slower "off" rates from CD86Ig. However, in these instances, the
slow "off" rate was compromised by a slow "on" rate that resulted
in mutant proteins with an overall avidity for CD86Ig that was
apparently similar to that seen with wild type CTLA4Ig. In
addition, mutagenesis of K93 resulted in significant aggregation
that may have been responsible for the kinetic changes
observed.
[0352] Random mutagenesis of L104 followed by COS cell transfection
and screening by SPR of culture media samples over immobilized
CD86Ig yielded six media samples containing mutant proteins with
approximately 2-fold slower "off" rates than wild type CTLA4Ig.
When the corresponding cDNA of these mutants were sequenced, each
was found to encode a leucine to glutamic acid mutation (L104E).
Apparently, substitution of leucine 104 to aspartic acid (L104D)
did not affect CD86Ig binding.
[0353] Mutagenesis was then repeated at each site listed in Table
II, this time using L104E as the PCR template instead of wild type
CTLA4Ig, as described above. SPR analysis, again using immobilized
CD86Ig, identified six culture media samples from mutagenesis of
alanine 29 with proteins having approximately 4-fold slower "off"
rates than wild type CTLA4Ig. The two slowest were tyrosine
substitutions (L104EA29Y), two were leucine (L104EA29L), one was
tryptophan (L104EA29W), and one was threonine (L104EA29T).
Apparently, no slow "off" rate mutants were identified when alanine
29 was randomly mutated, alone, in wild type CTLA4Ig.
[0354] The relative molecular mass and state of aggregation of
purified L104E and L104EA29YIg was assessed by SDS-PAGE and size
exclusion chromatography. L104EA29YIg (.about.1 .mu.g; lane 3) and
L104EIg (.about.1 .mu.g; lane 2) apparently had the same
electrophoretic mobility as CTLA4Ig (.about.1 .mu.g; lane 1) under
reducing (.about.50 kDa; +BME; plus 2-mercaptoethanol) and
non-reducing (.about.100 kDa; -.beta.ME) conditions (FIG. 25A).
Size exclusion chromatography demonstrated that L104EA29YIg (FIG.
25C) apparently had the same mobility as dimeric CTLA4Ig (FIG.
25B). The major peaks represent protein dimer while the faster
eluting minor peak in FIG. 25B represents higher molecular weight
aggregates. Approximately 5.0% of CTLA4Ig was present as higher
molecular weight aggregates but there was no evidence of
aggregation of L104EA29YIg or L104EIg. Therefore, the stronger
binding to CD86Ig seen with L104EIg and LI04EA29YIg could not be
attributed to aggregation induced by mutagenesis.
[0355] Equilibrium and Kinetic Binding Analysis
[0356] Equilibrium and kinetic binding analysis was performed on
protein A purified CTLA4Ig, L104EIg, and L104EA29YIg using surface
plasmon resonance (SPR). The results are shown in Table I, infra.
Observed equilibrium dissociation constants (K.sub.d; Table I) were
calculated from binding curves generated over a range of
concentrations (5.0-200 nM). L104EA29YIg binds more strongly to
CD86Ig than does L104EIg or CTLA4Ig. The lower K.sub.d of
L104EA29YIg (3.21 nM) than L104EIg (6.06 nM) or CTLA4Ig (13.9 nM)
indicates higher binding avidity of L104EA29YIg to CD86Ig. The
lower K.sub.d of L104EA29YIg (3.66 nM) than L104EIg (4.47 nM) or
CTLA4Ig (6.51 nM) indicates higher binding avidity of L104EA29YIg
to CD80Ig.
[0357] Kinetic binding analysis revealed that the comparative "on"
rates for CTLA4Ig, L104EIg, and L104EA29YIg binding to CD80 were
similar, as were the "on" rates for CD86Ig (Table I). However,
"off" rates for these molecules were not equivalent (Table I).
Compared to CTLA4Ig, L104EA29YIg had approximately 2-fold slower
"off" rate from CD80Ig, and approximately 4-fold slower "off" rate
from CD86Ig. L104E had "off" rates intermediate between L104EA29YIg
and CTLA4Ig. Since the introduction of these mutations did not
significantly affect "on" rates, the increase in avidity for CD80Ig
and CD86Ig observed with L104EA29YIg was likely primarily due to a
decrease in "off" rates.
[0358] To determine whether the increase in avidity of L104EA29YIg
for CD86Ig and CD80Ig was due to the mutations affecting the way
each monomer associated as a dimer, or whether there were avidity
enhancing structural changes introduced into each monomer, single
chain constructs of CTLA4 and L104EA29Y extracellular domains were
prepared following mutagenesis of cysteine 120 to serine as
described supra, and by Linsley et al., (1995) J. Biol. Chem.,
270:15417-15424 (84). The purified proteins CTLA4X.sub.C120S and
L104EA29YX.sub.C120S were shown to be monomeric by gel permeation
chromatography (Linsley et al., (1995), supra), before their ligand
binding properties were analyzed by SPR. Results showed that
binding affinity of both monomeric proteins for CD86Ig was
approximately 35-80-fold less than that seen for their respective
dimers (Table I). This supports previously published data
establishing that dimerization of CTLA4 was required for high
avidity ligand binding (Greene et al., (1996) J. Biol. Chem.,
271:26762-26771).
[0359] L104EA29YX.sub.C120S bound with approximately 2-fold higher
affinity than CTLA4X.sub.C120S to both CD80Ig and CD86Ig. The
increased affinity was due to approximately 3-fold slower rate of
dissociation from both ligands. Therefore, stronger ligand binding
by L104EA29Y was most likely due to avidity enhancing structural
changes that had been introduced into each monomeric chain rather
than alterations in which the molecule dimerized.
[0360] Location and Structural Analysis of Avidity Enhancing
Mutations
[0361] The solution structure of the extracellular IgV-like domain
of CTLA4 has recently been determined by NMR spectroscopy (Metzler
et al., (1997) Nature Struct. Biol., 4:527-531). This allowed
accurate location of leucine 104 and alanine 29 in the three
dimensional fold (FIG. 26 left and right depictions). Leucine 104
is situated near the highly conserved MYPPPY amino acid sequence.
Alanine 29 is situated near the C-terminal end of the CDR-1
(S25-R33) region, which is spatially adjacent to the MYPPPY region.
While there is significant interaction between residues at the base
of these two regions, there is apparently no direct interaction
between L104 and A29 although they both comprise part of a
contiguous hydrophobic core in the protein. The structural
consequences of the two avidity enhancing mutants were assessed by
modeling. The A29Y mutation can be easily accommodated in the cleft
between the CDR-1 (S25-R33) region and the MYPPPY region, and may
serve to stabilize the conformation of the MYPPPY region. In wild
type CTLA4, L104 forms extensive hydrophobic interactions with L96
and V94 near the MYPPPY region. It is highly unlikely that the
glutamic acid mutation adopts a conformation similar to that of
L104 for two reasons. First, there is insufficient space to
accommodate the longer glutamic acid side chain in the structure
without significant perturbation to the CDR-1 (S25-R33 region).
Second, the energetic costs of burying the negative charge of the
glutamic acid side chain in the hydrophobic region would be large.
Instead, modeling studies predict that the glutamic acid side chain
flips out on to the surface where its charge can be stabilized by
solvation. Such a conformational change can easily be accommodated
by G105, with minimal distortion to other residues in the
regions.
[0362] Binding of High Avidity Mutants to CHO Cells Expressing CD80
or CD86
[0363] FACS analysis (FIG. 27) of CTLA4Ig and mutant molecules
binding to stably transfected CD80+ and CD86+CHO cells was
performed as described herein. CD80-positive and CD86-positive CHO
cells were incubated with increasing concentrations of CTLA4Ig,
L104EA29YIg, or L104EIg, and then washed. Bound immunoglobulin
fusion protein was detected using fluorescein
isothiocyanate-conjugated goat anti-human immunoglobulin.
[0364] As shown in FIG. 27, CD80-positive or CD86-positive CHO
cells (1.5.times.10.sup.5) were incubated with the indicated
concentrations of CTLA4Ig (closed squares), L104EA29YIg (circles),
or L104EIg (triangles) for 2 hr. at 23.degree. C., washed, and
incubated with fluorescein isothiocyanate-conjugated goat
anti-human immunoglobulin antibody. Binding on a total of 5,000
viable cells was analyzed (single determination) on a FACScan, and
mean fluorescence intensity (MFI) was determined from data
histograms using PC-LYSYS. Data were corrected for background
fluorescence measured on cells incubated with second step reagent
only (MFI=7). Control L6 mAb (80 .mu.g/ml) gave MFI<30. These
results are representative of four independent experiments.
[0365] Binding of L104EA29YIg, L104EIg, and CTLA4Ig to human
CD80-transfected CHO cells is approximately equivalent (FIG. 27A).
L104EA29YIg and L104EIg bind more strongly to CHO cells stably
transfected with human CD86 than does CTLA4Ig (FIG. 27B).
[0366] Functional Assays:
[0367] Human CD4-positive T cells were isolated by immunomagnetic
negative selection (Linsley et al., (1992) J. Exp. Med.
176:1595-1604). Isolated CD4-positive T cells were stimulated with
phorbal myristate acetate (PMA) plus CD80-positive or CD86-positive
CHO cells in the presence of titrating concentrations of inhibitor.
CD4-positive T cells (8-10.times.10.sup.4/well) were cultured in
the presence of 1 nM PMA with or without irradiated CHO cell
stimulators. Proliferative responses were measured by the addition
of 1 .mu.Ci/well of [3H]thymidine during the final 7 hours of a 72
hour culture. Inhibition of PMA plus CD80-positive CHO, or
CD86-positive CHO, stimulated T cells by L104EA29YIg and CTLA4Ig
was performed. The results are shown in FIG. 28. L104EA29YIg
inhibits proliferation of CD80-positive PMA treated CHO cells more
than CTLA4Ig (FIG. 28A). L104EA29YIg is also more effective than
CTLA4Ig at inhibiting proliferation of CD86-positive PMA treated
CHO cells (FIG. 28B). Therefore, L104EA29YIg is a more potent
inhibitor of both CD80- and CD86-mediated costimulation of T
cells.
[0368] FIG. 29 shows inhibition by L104EA29YIg and CTLA4Ig of
allostimulated human T cells prepared above, and further
allostimulated with a human B lymphoblastoid cell line (LCL) called
PM that expressed CD80 and CD86 (T cells at 3.0.times.10.sup.4/well
and PM at 8.0.times.10.sup.3/well). Primary allostimulation
occurred for 6 days, then the cells were pulsed with
.sup.3H-thymidine for 7 hours, before incorporation of radiolabel
was determined.
[0369] Secondary allostimulation was performed as follows. Seven
day primary allostimulated T cells were harvested over lymphocyte
separation medium (LSM) (ICN, Aurora, Ohio) and rested for 24
hours. T cells were then restimulated (secondary), in the presence
of titrating amounts of CTLA4Ig or L104EA29YIg, by adding PM in the
same ratio as above. Stimulation occurred for 3 days, then the
cells were pulsed with radiolabel and harvested as above. The
effect of L104EA29YIg on primary allostimulated T cells is shown in
FIG. 29A. The effect of L104EA29YIg on secondary allostimulated T
cells is shown in FIG. 29B. L104EA29YIg inhibits both primary and
secondary T cell proliferative responses better than CTLA4Ig.
[0370] To measure cytokine production (FIG. 30), duplicate
secondary allostimulation plates were set up. After 3 days, culture
media was assayed using ELISA kits (Biosource, Camarillo, Calif.)
using conditions recommended by the manufacturer. L104EA29YIg was
found to be more potent than CTLA4Ig at blocking T cell IL-2, IL-4,
and .gamma.-IFN (gamma-IFN) cytokine production following a
secondary allogeneic stimulus (FIGS. 30A-C).
[0371] The effects of L104EA29YIg and CTLA4Ig on monkey mixed
lymphocyte response (MLR) are shown in FIG. 31. Peripheral blood
mononuclear cells (PBMC'S; 3.5.times.10.sup.4 cells/well from each
monkey) from 2 monkeys were purified over lymphocyte separation
medium (LSM) and mixed with 2 .mu.g/ml phytohemaglutinin (PHA). The
cells were stimulated 3 days then pulsed with radiolabel 16 hours
before harvesting. L104EA29YIg inhibited monkey T cell
proliferation better than CTLA4Ig.
5TABLE I Equilibrium and apparent kinetic constants are given in
the following table (values are means .+-. standard deviation from
three different experiments): Immobilized k.sub.on (.times.
10.sup.5) k.sub.off (.times. 10.sup.-3) K.sub.d Protein Analyte
M.sup.-1 S.sup.-1 S.sup.-1 nM CD80Ig CTLA4Ig 3.44 .+-. 0.29 2.21
.+-. 0.18 6.51 .+-. 1.08 CD80Ig L104EIg 3.02 .+-. 0.05 1.35 .+-.
0.08 4.47 .+-. 0.36 CD80Ig L104EA29YIg 2.96 .+-. 0.20 1.08 .+-.
0.05 3.66 .+-. 0.41 CD80Ig CTLA4X.sub.C120S 12.0 .+-. 1.0 230 .+-.
10 195 .+-. 25 CD80Ig L104EA29- 8.3 .+-. 0.26 71 .+-. 5 85.0 .+-.
2.5 YX.sub.C120S CD86Ig CTLA4Ig 5.95 .+-. 0.57 8.16 .+-. 0.52 13.9
.+-. 2.27 CD86Ig L104EIg 7.03 .+-. 0.22 4.26 .+-. 0.11 6.06 .+-.
0.05 CD86Ig L104EA29YIg 6.42 .+-. 0.40 2.06 .+-. 0.03 3.21 .+-.
0.23 CD86Ig CTLA4X.sub.C120S 16.5 .+-. 0.5 840 .+-. 55 511 .+-. 17
CD86Ig L104EA29- 11.4 .+-. 1.6 300 .+-. 10 267 .+-. 29
YX.sub.C120S
[0372]
6TABLE II The effect on CD86Ig binding by mutagenesis of CTLA4Ig at
the sites listed was determined by SPR, described supra. The
predominant effect is indicated with a "+" sign. Effects of
Mutagenesis No Apparent Slow "on"rate/slow Reduced ligand
Mutagenesis Site Effect "off rate binding S25 + P26 + G27 + K28 +
A29 + T30 + E31 + R33 + K93 + L96 + M97 + Y98 + P99 + P100 + P101 +
Y102 + Y103 + L104 + G105 + I106 + G107 + Q111 + Y113 + I115 +
EXAMPLE 3
[0373] The following provides a description of phase II clinical
studies of human patients administered soluble CTLA4 mutant
molecule L104EA29YIg (also known as LEA29Y or LEA) or CTLA4Ig, to
relieve at least one symptom associated with rheumatoid arthritis,
including reducing: joint swelling, joint tenderness, inflammation,
morning stiffness, and pain. The CTLA4Ig molecule used herein
begins with methionine at position +1 (or alternatively with
alanine at position -1) and ends with lysine at position +357 as
shown in FIG. 24. DNA encoding an embodiment of the CTLA4Ig
molecule has been deposited as ATCC 68629. The L104EA29YIg molecule
used herein begins with methionine at position +1 (or alternatively
with alanine at position -1) and ends with lysine at position +357
as shown in FIG. 19. DNA encoding an embodiment of the L104EA29YIg
molecule has been deposited as ATCC PTA 2104.
[0374] Additionally, the following provides a description of human
patients administered L104EA29YIg or CTLA4Ig to relieve at least
one biological surrogate marker associated with rheumatoid
arthritis, including reducing erythrocyte sedimentation rates, and
serum levels of C-reactive protein and/or IL2 receptor.
[0375] Patient Cohorts
[0376] A total of 214 patients, including 54 males and 160 females,
participated in the study (FIGS. 1A, 1B). The patients at baseline
had a mean disease duration of 3.4 (.+-.2.0) years and had failed
at least one Disease Modifying Antirheumatic Drug (DMARD). Stable
Nonsteroidal Anti-inflammatory Drugs (NSAIDS) or steroids
(.ltoreq.10 mg/day) were permitted and concomitant DMARDS were
prohibited. The patients were randomized into groups of 25 to 32
patients per treatment group. Thirty-two patients received a
placebo, 92 received L104EA29YIg, and 90 received CTLA4Ig. The
patients who followed protocol guidelines and did not discontinue
before day 57 received a total of 4 intravenous infusions, one
infusion each on days 1, 15, 29, and 57. All patients were
evaluated on days 1, 15, 29, 43, 57, 71, and 85. The doses
administered included 0.5, 2.0, or 10.0 mg/kg of L104EA29YIg
(denoted as LEA5, LEA2 and LEA10, respectively in FIGS. 1A-1E) or
of CTLA4Ig (denoted as CTLA5, CTLA2 and CTLA10, respectively in
FIGS. 1A-1E).
[0377] All subjects were monitored for peri-infusional adverse
events and global safety by answering a questionnaire listing
potential adverse events. The patients were questioned about
potential adverse events that may have occurred within twenty-four
hours post-infusion. In addition, the patients were encouraged to
spontaneously report any adverse events that they experienced. The
physicians routinely monitored laboratory samples from the patients
for abnormalities in blood chemistry and hematology e.g. assessed
the levels of inflammatory response mediators such as cytokines
(TNF, IL-6), tryptase and complement. The primary endpoint was the
proportion of subjects meeting the ACR 20 criteria on day 85.
[0378] Storage of Test Material
[0379] The CTLA4Ig and L104EA29YIg were supplied in single-use
glass vials containing 200 mg/vial of CTLA4Ig or 100 mg/vial of
L104EA29YIg, respectively. Prior to infusion, the CTLA4Ig and
L104EA29YIg were diluted to a final concentration of 25 mg/ml with
sterile water for injection (SWFI).
[0380] Administration Protocol
[0381] All infusions were administered intravenously over 1 hour
(FIGS. 1 through 17). All subjects received at least one infusion
of study medication.
[0382] Group 1: 32 patients, CTLA4Ig or LI04EA29YIg matching
placebo.
[0383] Group 2: 26 patients; dosage 0.5 mg/kg of CTLA4Ig.
[0384] Group 3: 32 patients; dosage 2.0 mg/kg of CTLA4Ig.
[0385] Group 4: 32 patients; dosage 10.0 mg/kg of CTLA4Ig.
[0386] Group 5: 32 patients; dosage 0.5 mg/kg of L104EA29YIg.
[0387] Group 6: 29 patients; dosage 2.0 mg/kg of L104EA29YIg.
[0388] Group 7: 31 patients; dosage 10.0 mg/kg of L104EA29YIg.
[0389] Clinical Monitoring
[0390] Patients were evaluated for baseline symptoms of disease
activity prior to receiving any infusions. These baseline
evaluations included: joint swelling, joint tenderness,
inflammation, morning stiffness, disease activity evaluated by
patient and physician as well as disability evaluated by Health
Questionnaire Assessment (HAQ) (reported as a physical function
score in FIG. 1C), and pain (FIGS. 1A to 1D). Additionally, the
baseline evaluations included erythrocyte sedimentation rates
(ESR), and serum levels of C-reactive protein (CRP) and soluble
IL-2 receptor (IL-2r) (FIGS. 1C and 1D).
[0391] The clinical response studies were based on the criteria
established by the American College of Rheumatology (ACR). A
subject satisfied the ACR20 criterion if there was a 20 percent
improvement in tender and swollen joint counts and 20 percent
improvement in three of the five remaining symptoms measured, such
as patient and physician global disease changes, pain, disability,
and an acute phase reactant (Felson, D. T., et al., 1993 Arthritis
and Rheumatism 36:729-740; Felson, D. T., et al., 1995 Arthritis
and Rheumatism 38:1-9). Similarly, a subject satisfied the ACR50 or
ACR70 criterion if there was a 50 or 70 percent improvement,
respectively, in tender and swollen joint counts and 50 or 70
percent improvement, respectively, in three of the five remaining
symptoms measured, such as patient and physician global disease
changes, pain, physical disability, and an acute phase reactant
such as CRP or ESR.
[0392] Biomarkers
[0393] Potential biomarkers of disease activity (rheumatoid factor,
CRP, ESR, soluble IL-2R, soluble ICAM-1, soluble E-selectin, and
MMP-3) were also assessed. Validated enzyme immunoassay (EIA)
methods were used to determine the serum concentration of
IL-2sR.alpha., sICAM-1, sE-selectin and MMP-3. TNF.alpha. and IL-6
were assessed at infusion pre and 2 hours post, if necessary.
[0394] IL-2sR.alpha., sICAM-1, and sE-selectin were measured using
commercially available calorimetric EIA kits from R&D Systems,
Inc. (Minneapolis, Minn.). The lower and upper limits of
quantitation were 312-20,000 pg/mL, 40-907 ng/mL and 10-206 ng/mL,
respectively. The inter-assay coefficient of variation ranged from
4.48-8.4%, 3.8-5.0% and 5.5-9.0% respectively. According to the kit
manufacturer, normal serum values range from 676-2,132 pg/mL,
respectively.
[0395] MMP-3 was measured using a commercially available
calorimetric EIA kit from Amersham Pharmacia Biotech (Piscataway,
N.J.). The lower and upper limits of quantitation were 30-7,680
ng/mL. The inter-assay coefficient of variation ranged from
6.3-10.6%. According to the kit manufacturer, normal serum values
range from 28-99 ng/mL.
[0396] IL-6 and TNF.alpha. were measured using commercially
available chemiluminescent EIA kits from R&D Systems, Inc.
(Minneapolis, Minn.). The lower and upper limits of quantitation
were 0.3-3,000 pg/mL and 0.7-7,000 pg/mL, respectively. The
inter-assay coefficient of variation ranged from 3.1-5.7% and
6.4-20.7%, respectively. According to the kit manufacturer, normal
serum values range from <0.3-12 pg/mL and <0.7-7.5 pg/mL.
[0397] Antibody Testing
[0398] Serum samples were obtained for assessment of drug-specific
antibodies prior to dosing on day 1, and approximately on days 15,
29, 57, 85 and 169. Due to high, preexisting titers directed to the
immunoglobulin (Ig) portion of the molecule, specific antibody
formation against CTLA4Ig and LEA29Y without Ig constant regions
was also assessed.
[0399] Ninety-six well Immulon II ELISA plates (Dynex, Chantilly,
Va.) were coated with CTLA4Ig, CTLA4Ig without the Ig constant
regions, LEA29Y, or LEA29Y without the Ig constant regions at 2, 4,
2, or 1 .mu.g/ml in phosphate buffered saline (PBS), respectively,
and incubated overnight at 2-8.degree. C. The plates were washed
with PBS containing 0.05% Tween 20 and blocked for 1 hour at
37.degree. C. with PBS containing 1% bovine serum albumin (BSA).
The plates were then washed and serial dilutions of the test sera
or quality control (QC) sera were added to the appropriate wells
and incubated for 2 hours at 37.degree. C. Sera was diluted
threefold in PBS with 0.25% BSA and 0.05% Tween 20 starting at a
1:10 dilution. Plates were washed and an
alkaline-phosphatase-conjug- ated goat anti-human kappa and lambda
(Southern Biotechnology Associates, Inc., Birmingham, Ala.)
antibody cocktail was added. Following a 1-hour incubation at
37.degree. C., the plates were washed and 1 mg/ml para-nitrophenyl
phosphate in diethanolamine buffer was added to each well. After 30
minutes at 25.degree. C., the reactions were stopped with 3N NaOH
and the absorbance (dual wavelength: 405 nm and 550 nm) was
recorded. Results were expressed as endpoint titer (EPT), defined
as the reciprocal of the highest dilution that resulted in an
absorbance reading fivefold greater than or equal to the mean
plate-background absorbance. Plate background was determined as the
absorbance measurement recorded in the absence of serum. Values
were considered positive for seroconversion if they were at least
two serial dilutions (ninefold) or greater relative to predose EPT
values. Serum QC samples positive for either CTLA4Ig- or
LEA29Y-specific antibodies were generated from immunized monkeys.
An aliquot of the appropriate QC sample was assayed during each
analytical run. Analytical runs were accepted only when the QC
samples were within the assay acceptance criteria.
[0400] Results
[0401] CTLA4Ig and L104EA29YIg were generally well-tolerated at all
dose-levels. Peri-infusional adverse events were similar across all
dose groups, with the exception of headaches. Headache response of
patients on day 85 increased dose-dependently 23%, 44%, and 53% in
CTLA4Ig-treated patients, and 34%, 45%, and 61% in
L104EA29YIg-treated patients, at 0.5, 2.0, and 10.0 mg/kg
respectively. In contrast, 31% of the patients administered
placebos experienced headaches.
[0402] The percent of patients that discontinued from the clinical
study due to arthritis flares and other adverse events is
summarized in FIG. 2. A much higher percentage of patients on
placebo discontinued treatment due to arthritis flare. The CTLA4Ig
treated patients discontinued treatment less with increasing doses.
Very few patients treated with L104EA29YIg discontinued treatment.
These results indicate a good inverse dose-dependent response for
CTLA4Ig, and a stronger therapeutic response with L104EA29YIg
therapy.
[0403] The ACR-20, -50, and -70 responses of patients treated with
CTLA4Ig, L104EA29YIg, or placebo at day 85 are summarized in FIG.
3A. Similarly, FIGS. 3B and C describe the ACR-20 responses with
95% confidence limits. The responses appear to be dose-dependent
with a clear significant response at 10 mg/kg per body weight of
the patient.
[0404] The percent of patients having reduced swollen and tender
joint counts compared to the patients having no response to
treatment with CTLA4Ig, L104EA29YIg, or placebo, is shown in FIGS.
4A and B. The therapeutic responses appear to be dose-dependent. A
larger percentage of patients show improvement of 20, 50, 70, and
even 100% in the 2 and 10 mg/kg groups for both products.
[0405] The percent of patients having reduced pain, disease
activity evaluated by patient and physician mean score units with
CTLA4Ig, L104EA29YIg, or placebo, is shown in FIGS. 5A, B, C, and
D. The therapeutic responses, as monitored by the Likert scale,
appear to be dose-dependent in favor of the active treatment groups
as compared to placebo on day 85. The Likert scale is a validated
verbal rating scale using adjectives to rank the symptoms (The
American College of Rheumatology Preliminary Core Set of Disease
Activity Measures for Rheumatoid Arthritis Clinical Trials:
Arthritis and Rheumatism, June 1993, 36(6):729-740).
[0406] The patient and physician assessments of disease activity
change from the baseline by at least 2 units, resulting from
treatment with CTLA4Ig, L104EA29YIg, or placebo, are shown in FIGS.
6A and B. The responses appear to be dose-dependent with more
marked improvement for the higher doses of active drugs.
[0407] The percent reduction in C-reactive protein (CRP) levels in
patients treated with CTLA4Ig, L104EA29YIg, or placebo, is shown in
FIGS. 7A and B. The responses appear to be dose-dependent with a
clear decrease for the 2 and 10 mg/kg active treatment groups. In
addition, FIG. 7B showed that the difference is quite significant
compared to placebo with 95% confidence intervals. FIG. 7C shows
the changes in serum level changes from baseline at day 85.
[0408] The amount of serum soluble IL-2 receptor in patients
treated with CTLA4Ig, L104EA29YIg, or placebo, is shown in FIG. 8.
The reduction in soluble IL-2 receptor levels appears to be
dose-dependent.
[0409] The amount of serum soluble ICAM-1 and soluble E-selectin in
patients treated with CTLA4Ig, L104EA29YIg, or placebo, is shown in
FIG. 33. The reduction in soluble ICAM-1 and soluble E-selectin
levels appears to be dose-dependent.
[0410] The median and mean tender joint counts in patients treated
with CTLA4Ig or placebo over time are shown in FIGS. 9A and B. The
change from baseline (e.g., reduction in tender joints) appears to
be more important in the 2 and 10 mg/kg treated groups, than in the
placebo or 0.5 mg/kg groups.
[0411] The median and mean swollen joint counts in patients treated
with CTLA4Ig or placebo over time are shown in FIGS. 10A and B. The
change from baseline (e.g., reduction in swollen joints) appears to
be more important in the 2 and 10 mg/kg treated groups than placebo
or 0.5 mg/kg groups.
[0412] The mean pain assessment scores over time in patients
treated with CTLA4Ig or placebo are shown in FIG. 11. The change
from baseline (e.g., reduction in pain) appears to be more
important in the 2 and 10 mg/kg treated groups than placebo or 0.5
mg/kg groups.
[0413] The mean disease activity assessment scores assessed by
patient or physician in patients treated with CTLA4Ig or placebo
over time are shown in FIGS. 12A and B. The change from baseline
(e.g., reduction in disease activity) appears to be more important
in the 2 and 10 mg/kg treated groups than placebo or 0.5 mg/kg
groups.
[0414] The median and mean tender joint counts in patients treated
with L104EA29YIg (denoted as LEA in the figures) or placebo over
time are shown in FIGS. 13A and B. The change from baseline (e.g.,
reduction in tender joints) appears to be dose-dependent.
[0415] The median and mean swollen joint counts in patients treated
with L104EA29YIg (denoted as LEA in the figures) or placebo over
time are shown in FIGS. 14A and B. The change from baseline (e.g.,
reduction in swollen joints) appears to be more important in the 2
and 10 mg/kg treated groups than placebo or 0.5 mg/kg groups.
[0416] The mean pain assessment scores in patients treated with
L104EA29YIg (denoted as LEA in the figures) or placebo over time
are shown in FIG. 15. The change from baseline (e.g., reduction in
pain) appears to be dose-dependent.
[0417] The mean disease activity assessment scores evaluated by
patient or physician in patients treated with L104EA29YIg (denoted
as LEA in the figures) or placebo over time are shown in FIGS. 16A
and B. The change from baseline (e.g., reduction in disease
activity) appears to be dose-dependent.
[0418] The percent improvement of physical disability assessed by
HAQ at day 85 for patients treated with CTLA4Ig, L104EA29YIg, or
placebo are shown in FIG. 17 (Health Assessment Questionnaire
(HAQ); Fries, J. F., et al., 1982 J. of Rheumatology 9:789-793).
There is a clear dose dependent improvement with this
parameter.
[0419] The changes from baseline for soluble IL-2r and C-reactive
protein levels were dose-dependent in both treatment groups. After
treatment, soluble IL-2r levels were -2%, -10%, and -22% for
CTLA4Ig and -4%, -18%, and -32% for L104EA29YIg at 0.5, 2.0, and
10.0 mg/kg respectively, compared to +3% for the placebo.
C-reactive protein levels were +12%, -15%, and -32% for CTLA4Ig and
+47%, -33%, and -47% for L104EA29YIg at 0.5, 2.0, and 10.0 mg/kg
respectively, compared to +20% for the placebo (FIG. 7A).
[0420] No clinically remarkable findings with respect to routine
hematology testing, chemistry laboratory testing with the exception
of slight suppressions in IgA and IgG levels at the higher doses of
both drugs, physical findings, or vital signs assessments were
observed. Notably, neither medication induced drug-specific
antibodies.
EXAMPLE 4
[0421] The following examples describe phase II clinical studies of
human patients that will be administered L104EA29YIg, to reduce or
prevent structural damage, including bone or joint erosion using
validated radiographic scales. This improvement in reducing or
preventing structural damage is parallel to the clinical
improvement measured by the clinical parameters.
[0422] The status of the bone structure is monitored in some of the
human patients prior to treatment with CTLA4Ig or L104EA29YIg.
These patients are administered from 0.5 to 20 mg/kg of CTLA4Ig or
L104EA29YIg chronically every two to twelve weeks (alone or in
combination with other agents) to maintain their therapeutic
improvement over time. Radiographs of patients' hands and feet are
taken at predefined intervals: 6 months, and then yearly, as
recommended by the FDA guidelines. These patients are monitored in
long-term extension after 6 and 12 months to determine if treatment
with CTLA4Ig or L104EA29YIg reduces the progression of bone
deterioration, and then yearly. The patients are monitored by
radiographic methods, including X-ray and/or magnetic resonance
imaging (MRI), according to standard practice in the art (Larsen,
A. K. and M. Eek 1977 Acta. Radiol. Diag. 18:481-491; Sharp, J. T.,
et al., 1985 Arthritis and Rheumatism 28:1326-1335). The results of
the radiographic data are evaluated for prevention of structural
damage, including slowing the progression of bone erosion and
cartilage damage, with joint space narrowing and/or prevention of
new erosions.
EXAMPLE 5
[0423] A Study to Evaluate the Safety and Clinical Efficacy of Two
Different Doses of CTLA4Ig Administered Intravenously to Subjects
with Active Rheumatoid Arthritis
[0424] While Receiving Methotrexate Rheumatoid Arthritis (RA)
treatment is rapidly changing with an increased willingness to use
more aggressive therapies to achieve larger increases in efficacy
and higher success rates. The ultimate goal is to improve the
subject condition in a more intensive way, by raising the rate of
major and complete clinical response, to treatment and maintaining
this benefit with acceptable safety.
[0425] Methotrexate remains the cornerstone of the RA treatment. It
was the first agent that demonstrated early onset of action,
superior efficacy and tolerability compared to the classical DMARDs
(e.g. gold, hydroxychloroquine, sulfasalazine) used to treat RA.
Clinical benefit may be seen as early as 3 weeks after initiating
treatment, and the maximal improvement is generally achieved by 6
months. However, methotrexate has a number of limitations. For
example, despite its increased tolerability, the window between
efficacy and liver toxicity is quite narrow. Subjects treated with
methotrexate require careful monitoring and unacceptable toxicity
is often the reason for discontinuation of treatment.
[0426] Methotrexate also does not appear to efficiently control
disease progression or joint deterioration. For some subjects,
practitioners feel compelled to add a second DMARD with the hope of
increasing efficacy despite the risk of increased toxicity.
Alternatively, co-treatment with methotrexate and a costimulator
blocker (e.g. CD80 and CD86 blockers such as CTLA4Ig) that target
the auto-immune mechanism that lies upstream of the cytokine
inflammatory cascade, may also increase efficacy.
[0427] As noted in Example 3, above, significant clinical responses
and reductions in surrogate markers of disease activity were
observed for CTLA4Ig at doses of 2 and 10 mg/kg with a good
tolerability profile. It has also been confirmed that the
composition CTLA4Ig, used in Example 3 above, did not induce any
side effects. As a result, it was decided to continue the clinical
development of CTLA4Ig for rheumatoid arthritis in Phase IIB.
[0428] The following provides a description of a Phase IIB clinical
study of human patients administered soluble CTLA4 molecule with
methotrexate, and the results of the study after six months.
[0429] This example describes a twelve month study in which primary
efficacy was assessed after all subjects completed six months of
treatment or discontinue therapy. Efficacy, safety, and disease
progression were also assessed throughout the duration of the
study.
[0430] The study utilized a randomized, double blind, placebo
controlled, parallel dosing design. The study was designed to
evaluate the safety, clinical activity, immunogenicity and
pharmacokinetics of two doses of CTLA4Ig: 2 or 10 mg/kg. A total of
approximately 330 subjects with active RA and receiving
methotrexate were randomized to 1 of 3 dosing arms: CTLA4Ig at 2
mg/kg (N=110), 10 mg/kg (N=110) and placebo control group (N=110)
given monthly infusions for 12 months. All groups continued on
weekly methotrexate treatment (10-30 mg weekly) (FIGS. 57-62).
[0431] CTLA4Ig or a placebo were also administered on Day 15. Each
dose of study medication was infused intravenously over
approximately 30 minutes. The primary efficacy endpoint was the ACR
20 response rate after 6 months.
[0432] For the first 6 months, subjects were not allowed to alter
their doses of corticosteroids, glucocorticoids or NSAIDs.
Increases in methotrexate were also not permitted during the first
six months. Decreases in methotrexate were permitted only if it was
felt to be causing toxicity. Subjects were treated with
methotrexate for at least 6 months, and at a stable dose for 28
days prior to first treatment of CTLA4Ig or placebo. DMARDs other
than methotrexate were not permitted. Low-dose stable
corticosteroids use (at 10 mg daily or less) and/or use of stable
non-steroidal anti-inflammatory drugs (NSAIDs), including acetyl
salicylic acid (ASA), was allowed. Analgesics that did not contain
ASA or NSAIDs were permitted in subjects experiencing pain not
adequately controlled by the baseline and study medications, except
for 12 hours before a joint evaluation. Decreases in NSAIDs were
permitted but only if due to adverse events such as
gastrointestinal toxicity.
[0433] Test Product, Dose and Mode of Administration, Duration of
Treatment
[0434] CTLA4Ig at 2 mg/kg or 10 mg/kg was infused every two weeks
for the first month, and monthly thereafter for 12 months.
[0435] All subjects received weekly doses of methotrexate (10-30
mg) for at least six months prior to randomization and maintained
at the entry dose for the first 6 months of the trial. Doses could
only be decreased for toxicity during the first six months.
[0436] Criteria for Evaluation
[0437] The primary endpoint of the first stage of the study was the
proportion of subjects meeting the American College of Rheumatology
criteria for 20% improvement (ACR 20) on Day 180 (month six). The
ACR 20 definition of improvement is a 20% improvement from baseline
in the number of tender and swollen joint counts, and a 20%
improvement from baseline in 3 of the following 5 core set
measurements: subject global assessment of pain, subject global
assessment of disease activity, physician global assessment of
disease activity, subject assessment of physical function and acute
phase reactant value (C-reactive protein (CRP)). The evaluation for
50% improvement (ACR 50) and 70% improvement (ACR 70) follow
similarly. Subjects who discontinued the study due to lack of
efficacy (i.e. worsening RA) were considered as ACR non-responders
from that time on. For all subjects who dropped out for other
reasons, their ACR response at the time of discontinuation was
carried forward.
[0438] Statistical Methods
[0439] Two doses of CTLA4Ig (2 mg/kg and 10 mg/kg) were compared
with the placebo control group. All subjects were maintained at the
same stable entry doses of methotrexate. The primary analysis was
the comparison of CTLA4Ig 10 mg/kg with placebo. Sample sizes were
based on a 5% level (2-tailed) of significance. Based on published
studies, the placebo plus methotrexate control ACR 20 response rate
at 6 months is about 25%. A sample of 107 subjects (adjusted for a
possible 15% dropout) per treatment arm was determined to yield a
94% power to detect a difference of 25% at the 5% level
(two-tailed). Similarly, the sample was determined to yield a power
of 95% and 90% to detect differences of 20% and 14% in ACR 50 and
ACR 70, respectively. If the comparison between CTLA4Ig 10 mg/kg
and placebo was significant with regards to ACR 20, then the
comparison between CTLA4Ig 2 mg/kg and placebo was carried out.
This second testing should have a power of 88%. This sequentially
rejective procedure based on Chi-square tests was also used to test
for differences in ACR 50 and ACR 70 responses.
[0440] All efficacy analyses were based on a data set containing
all available assessments from all subjects who received at least
one dose of study medication.
[0441] Percent changes from baseline were also reported for the
individual components of the ACR. For subjects who discontinued,
their last observation was carried forward.
[0442] Results
[0443] Demography and Baseline Characteristics:
7TABLE III Subject Disposition and Demographics Methotrexate +
Methotrexate + CTLA4Ig CTLA4Ig Methotrexate + 10 mg/kg 2 mg/kg
Placebo Enrolled/ 115 105 119 Randomized Completed 99 (86.1%) 82
(78.1%) 78 (65.5%) Discontinued 16 (13.9%) 23 (21.9%) 41 (34.5%)
Adverse Events 2 (1.7%) 7 (6.7%) 7 (5.9%) Lack of Efficacy 12
(10.4%) 13 (12.4%) 29 (24.4%) Other 2 (1.7%) 3 (2.9%) 5 (4.2%) Age
(yrs)-Mean 55.8 (17-83) 54.4 (23-80) 54.7 (23-80) (Range) Weight
(kg)-Mean 77.8 (40.1- 78.7 (48.4- 79.9 (44-140) (Range) 144) 186.8)
Sex 75% females 63% females 66% females Race 87% white 87% white
87% white Duration of Disease (yrs) Mean .+-. SD 9.7 .+-. 9.8 9.7
.+-. 8.1 8.9 .+-. 8.3
[0444] Demographic and baseline clinical characteristics were
similar among the treatment groups. Sixty three to 75 percent of
subjects were female, 87% were Caucasian. The mean duration of the
disease at entry was 9.7.+-.9.8, 9.7.+-.8.1, and 8.9.+-.8.3 years
respectively in the 10, 2 mg/kg and the control group. The mean
weight in kg was very similar between 77.8 and 79.9 kg with a range
of 40.1 to 186.8 kg (Table III).
[0445] After 6 months, more subjects had discontinued from the
control group (35.5%) than from the active treatment groups; 13.9%
and 21.9% for the 10 and 2 mg/kg treated groups, respectively. The
main reason was lack of efficacy: with 24.3% discontinuing in the
control group, as opposed to 12.4% and 10.4% discontinuing in the 2
and 10 mg/kg groups, respectively. The discontinuation rate due to
adverse events was lower in the 10 mg/kg group with 1.7%, while it
was 6.7% and 5.9% in the 2 mg/kg and the control groups,
respectively.
[0446] During the first 3-4 months, the discontinuations appeared
at a faster rate in the control group compared to the
active-treatment groups. After Day 120, the discontinuations for
all treatment groups stabilized for the duration of the primary
treatment period (six months).
8TABLE IV Baseline Clinical Characteristics Methotrexate +
Methotrexate + CTLA4Ig CTLA4Ig Methotrexate + 10 mg/kg 2 mg/kg
Placebo (n = 115) (n = 105) (n = 119) Tender Joints 30.8 .+-. 12.2
28.2 .+-. 12.0 29.2 .+-. 13.0 (mean .+-. SD) Swollen Joints 21.3
.+-. 8.4 20.2 .+-. 8.9 21.8 .+-. 8.8 (mean .+-. SD) Pain (VAS 100
mm) 62.1 .+-. 21.4 64.5 .+-. 22.3 65.2 .+-. 22.1 (mean .+-. SD)
Physical Function 1.0 .+-. 0.5 1.0 .+-. 0.5 1.0 .+-. 0.6 (MHAQ
score of 0 to 3)(mean .+-. SD) Subject global 60.1 .+-. 20.7 59.4
.+-. 23.7 62.8 .+-. 21.6 assessment (VAS 100 mm) (mean .+-. SD)
Physician global 62.1 .+-. 14.8 61.0 .+-. 16.7 63.3 .+-. 15.5
assessment (VAS 100 mm) (mean .+-. SD) CRP (mg/dL) 2.9 .+-. 2.8 3.2
.+-. 2.6 3.2 .+-. 3.2 Morning Stiffness 97.9 .+-. 63.1 104.1 .+-.
63.9 106.0 .+-. 64.2 (in min.)
[0447] The mean number of tender and swollen joints at baseline was
comparable among the three treatment groups. The mean number of
tender joints and swollen joints in the 10 mg group was
30.8.+-.12.2 and 21.3.+-.8.4, respectively. The mean number of
tender joints and swollen joints in the 2 mg group was
28.2.+-.12.0, and 20.2.+-.8.9, respectively. The mean number of
tender joints and swollen joints in the control group was
29.2.+-.13.0, and 21.8.+-.8.8, respectively. These assessments and
all other clinical assessments were similar among all treatment
groups (Table IV).
[0448] ACR Responses and Core Components:
9TABLE V ACR Response at 6 months Methotrexate + Methotrexate +
CTLA4Ig CTLA4Ig Methotrexate + 10 mg/kg 2 mg/kg Placebo (n = 115)
(n = 105) (n = 119) ACR 20 60.0% 41.9% 35.3% Difference from 24.7
6.6 -- control group 95% CI 11.9, 37.5 -6.2, 19.4 -- p-value
<0.001 0.31 -- ACR 50 36.5% 22.9% 11.8% Difference from 24.8
11.1 -- control group 95% CI 13.8, 35.7 1.2, 20.9 -- p-value
<0.001 0.027 -- ACR 70 16.5% 10.5% 1.7% Difference from 14.8 8.8
-- control group 95% CI 7.5, 22.2 2.7, 14.9 -- p-value <0.001
0.005 --
[0449] The improvements in ACR 20, 50, and 70 response rates in the
10 mg/kg treatment group, at six months relative to the
methotrexate control group, were statistically significant (FIGS.
34-38, 40). The improvements in ACR 50, and ACR 70 for the 2 mg/kg
group were also statistically significant. The difference in ACR 20
response between the 2 mg/kg group and the control group was 6.6%.
This difference was not statistically significant, p=0.31 (Table V,
FIG. 49).
[0450] FIGS. 34-37 presents the ACR response rates from Day 1 to
Day 180. FIGS. 38 and 40 presents the ACR20, -50 and -70 response
rates on day 180 for the various treatment groups. The ACR 50 and
ACR 70 response rates suggest the possibility that maximal efficacy
may not have been achieved at 10 mg/kg.
[0451] FIG. 39 shows the proportion of new tender and swollen
joints at day 180 of the study after therapy with methotrexate
alone or in combination with CTLA4Ig (administered at 2 or 10 mg/kg
body weight of subject).
[0452] FIG. 46 shows the mean percent improvement in physical
function from baseline as measured by HAQ.
10TABLE VI Individual ACR Components at Day 180 (Mean Percent
Improvement) Methotrexate + Methotrexate + CTLA4Ig CTLA4Ig
Methotrexate + 10 mg/kg 2 mg/kg Placebo Core Components (n = 115)
(n = 105) (n = 119) Tender Joints 59.9% 43.3% 32.1% Swollen Joints
54.9% 45.1% 33.4% Pain 46.4% 22.7% 8.4% Physical Function 41.5%
17.3% 14.1% (mHAQ) Subject global 40.8% 9.6% 17.6% assessment
Physician global 52.0% 38.6% 25.6% assessment CRP 31.5% 16.2%
-23.6%
[0453] The 2 and 10 mg/kg dose groups demonstrated some degree of
efficacy among all clinical components of the ACR response criteria
(Table VI; FIGS. 41-45, 47-48); the subject's global assessment in
the 2 mg/kg dose group being the only exception. The reduction of
tender and swollen joints appears dose-dependent. The number of
tender joints was decreased by 59.9%, 43.3% and 32.1% in the 10
mg/kg, 2 mg/kg and control groups, respectively. A similar pattern
was observed for the swollen joint counts with a decrease of 54.9%,
45.1% and 33.4% in the 10 mg/kg, 2 mg/kg and control groups,
respectively. The greatest differences relative to the control
group were observed with the pain assessment which decreased 46.4%
and 22.7% relative to baseline for 10 mg and 2 mg/kg CTLA4Ig,
respectively, compared to 8.4% in the control group. The mean CRP
decreased 31.5% and 16.2% relative to baseline in the 10 and 2
mg/kg groups compared to an increase of 23.6% in the control
group.
[0454] Health-Related Quality of Life
[0455] The impact of CTLA4Ig on health-related quality of life
(HRQOL) was measured by the Medical Outcomes Study Short Form-36
(SF-36). The SF-36 was administered to all subjects at baseline, 90
and 180 days. The SF-36 consists of 36 items which covers eight
domains (physical function, role-physical, bodily pain, general
health, vitality, social function, role emotional, and mental
health). These individual domains are used to derive the physical
and mental component summary scores which range from 0 to 100, with
higher scores indicating better quality of life. Absolute
differences of 5 or more in the SF-36 scores were considered
clinically meaningful.
[0456] Compared to subjects treated with placebo, subjects in the
CTLA4Ig 10 mg/kg group also experienced statistically significantly
greater improvement in all 8 domains of the SF-36 (FIGS. 50-51).
For subjects treated with CTLA4Ig 2 mg/kg, the improvements were
also greater than those treated with placebo, but the differences
were not statistically significant (FIGS. 50-51).
[0457] Baseline SF-36 scores were comparable between the three
treatment groups. Improvements in quality of life show a clear
dose-response trend after 6 months of treatment. Subjects in the
CTLA4Ig 10 mg/kg treatment group demonstrated clinically and
statistically significant improvements from baseline in all 8
domains of the SF-36. The greatest effects were shown in the
role-physical, bodily pain, and role-emotional domains. This
positive finding was consistent with the efficacy results. For
subjects treated with CTLA4Ig 2 mg/kg, improvements from baseline
were also statistically significant for all domains except mental
health.
[0458] Pharmacokinetics:
11 PHARMACOKINETIC PARAMETER VALUES CMAX TMAX AUC(TAU) T-HALF CLT
VSS (.mu.G/ML) (H) (.mu.G .multidot. H/ML) (Days) (ML/H/KG) (L/KG)
2 mg/kg MEAN 57.96 0.50* 10176.14 13.50 0.23 0.07 SD 16.93 (0.00,
4.00) 3069.84 5.91 0.13 0.04 N 15 15 15 15 15 15 10 mg/kg MEAN
292.09 0.50* 50102.56 13.11 0.22 0.07 SD 67.78 (0.00, 4.00)
15345.95 5.32 0.09 0.03 N 14 14 14 14 14 14 *Median (minimum,
maximum)
[0459] The pharmacokinetics of CTLA4Ig were derived from serum
concentration versus time data between dosing days 60 and 90.
Samples were collected prior to dosing on day 60, at 0.5, and 4 h
after dosing, on days 67, 74, 81, and prior to dosing on Day 90.
The preliminary data indicate that both Cmax and AUC values
increase in a proportion comparable to the dose increment. For
nominal doses increasing in a 1:5 proportion, both the Cmax and AUC
values increased in the proportion of 1:5.04 and 1:4.92,
respectively. T-HALF, CLT, and Vss values appeared to be comparable
and dose independent.
[0460] Mean Vss values were 0.07 L/kg for both dose levels, which
was approximately 1.6-fold the plasma volume.
[0461] Pharmacodynamics:
12TABLE VII Mean Baseline Values for Pharmacodynamic Biomarkers
Methotrexate + Methotrexate + CTLA4Ig CTLA4Ig Methotrexate + 10
mg/kg 2 mg/kg Placebo Biomarker (n = 115) (n = 105) (n = 119) CRP
(mg/dL) 2.9 3.2 3.2 RF (IU/L) 207 274 179 IL-2r (pg/ml) 1388 1407
1398 IL-6 (pg/ml) 26.7 31.7 21.4 TNF.alpha. (pg/ml) 11.8 6.0
11.9
[0462] Serum levels of pharmacodynamic biomarkers were analyzed at
various times during the study. Baseline values are shown in Table
VII. The values on Day 180 relative to baseline are shown in the
FIGS. 52-56.
[0463] CRP levels decreased from baseline in both CTLA4Ig-treated
groups more than in the control group, with greater reduction
observed in the 10 mg/kg dosing group (see FIGS. 47, 48 and
52).
[0464] Rheumatoid factor levels decreased from baseline in both
CTLA4Ig-treated groups more than in the control group, with greater
reduction observed in the 10 mg/kg dosing group (see FIG. 53).
[0465] Soluble IL-2r levels decreased from baseline in both
CTLA4Ig-treated groups more than in the control group, with greater
reduction observed in the 10 mg/kg dosing group (see FIG. 54).
[0466] Serum IL-6 levels decreased from in both CTLA4Ig-treated
groups more than in the control group (see FIG. 55).
[0467] The effects of CTLA4Ig on serum TNF.alpha. levels were
inconclusive. The 2 mg/kg group increased and the 10 mg/kg group
decreased relative to the control group (see FIG. 56).
[0468] Safety:
[0469] CTLA4Ig was well tolerated at all doses. There were no
deaths, malignancies or opportunistic infections in any subjects
receiving CTLA4Ig. Serious adverse events (SAEs) and non-serious
adverse events (NSAEs) were similar or less frequent in the
active-treatment groups compared to the control group.
[0470] Fewer subjects in the 10 mg/kg group discontinued due to
adverse events relative to the control group (1.7% vs 5.9%,
respectively). The discontinuations due to adverse events in the 2
mg/kg were similar to the control group (6.7% vs 5.9%,
respectively). The SAEs followed a pattern similar to the
discontinuations due to adverse events.
[0471] No serious adverse events in the 10 mg/kg dose group were
considered related to the study drug.
[0472] Immunogenicity:
[0473] No anti-drug antibody responses were detected through Day
180 at both dose levels of CTLA4Ig.
[0474] CTLA4Ig significantly reduced the signs and symptoms of
rheumatoid arthritis in subjects receiving methotrexate as assessed
by ACR response criteria. The effects of CTLA4Ig appear to increase
in proportion to dose level. The improvement from baseline in all
ACR core components is higher in the 10 mg/kg group than the 2
mg/kg group. CTLA4Ig at 10 mg/kg doses demonstrated clinically and
statistically significant improvements in all 8 domains of the
SF-36. All pharmacodynamic biomarkers assayed appeared to decrease
in proportion to CTLA4Ig dose level except for TNF.alpha.. CTLA4Ig
was safe and well tolerated in subjects with rheumatoid arthritis
receiving methotrexate. The adverse event profile for both CTLA4Ig
doses was similar to the control group.
EXAMPLE 6
[0475] A Study of a Co-Stimulation Blocker, CTLA4Ig, Given Monthly
in Combination with Etanercept to Patients with Active Rheumatoid
Arthritis.
[0476] The following example provides a description of the
administration of CTLA4Ig, in combination with etanercept, to treat
patients with active Rheumatoid Arthritis.
[0477] Etanercept, along with infliximab, comprises a new
generation of Rheumatoid Arthritis drugs which targets Tumor
Necrosis Factor (TNF. Etanercept is a dimeric fusion protein having
an extracellular portion of the TNF receptor linked to the Fc
portion of human immunoglobulin (IgG1). This fusion protein binds
to TNF, blocks its interactions with cell surface TNF receptors and
render TNF molecules biologically inactive.
[0478] This example describes a twelve month study in which
efficacy was assessed after all subjects completed six months of
treatment or discontinued therapy. Efficacy, safety and disease
progression were also assessed throughout the duration of the
study.
[0479] The study utilized a randomized, double-blind, placebo
controlled, parallel dosing design. A total of approximately 141
subjects with active RA and receiving etanercept (25 mg twice
weekly) were randomized to 1 of 2 dosing groups: 1) a group
receiving CTLA4Ig at 2 mg/kg (n=94) plus etanercept or 2) a placebo
group receiving etanercept only (n=47).
[0480] Test Product, Dose and Mode of Administration, Duration of
Treatment
[0481] All subjects received etanercept (25 mg twice weekly) for at
least 3 months prior to treatment.
[0482] Infusions of CTLA4Ig were given on Days 1, 15, 30, and
monthly thereafter, for 6 months (primary treatment phase). Each
dose of study medication was infused intravenously for
approximately 30 minutes.
[0483] The primary treatment phase of the study took place during
the first six months of treatment. During this period, subjects
were required to remain on stable doses of etanercept (25 mg twice
weekly). DMARDs other than etanercept were not permitted. Low-dose
stable corticosteroid (at 10 mg daily or less) and/or stable
non-steroidal anti-inflammatory drug (NSAID), including acetyl
salicylic acid (ASA), use was allowed. Analgesics (that do not
contain ASA or NSAIDs) were permitted in subjects experiencing pain
that was not adequately controlled by the baseline and study
medications, except for 12 hours before a joint evaluation.
[0484] Criteria for Evaluation
[0485] The primary endpoint of this study was to collect data
regarding the proportion of subjects meeting modified American
College of Rheumatology (ACR) criteria for 20% improvement (ACR 20)
after six months. The modified ACR 20 criteria were used to
accommodate the low CRP levels in this study's subject population.
The modified ACR criteria were defined as 1) a greater than 20%
improvement in tender and swollen joint count and 2) a greater than
20% improvement in 2 of the remaining 4 core data set measures
(global pain, physician, subject, functional assessment). CRP,
which is normally a part of the standard ACR core data sets, was
not included in the modified ACR criteria due to the low levels of
CRP in subjects using TNF blockers, such as etanercept. The
standard ACR criteria, and two alternative criteria (SF-36 Physical
Health and SF-36 Mental Health) were also evaluated as secondary
endpoints.
[0486] Statistical Methods
[0487] Treatment of a group of patients with CTLA4Ig 2 mg/kg in
combination with etanercept was compared with a control group
treated with placebo plus etanercept. Based on previous studies
with etanercept in similar patient populations, it was assumed that
the modified ACR 20 response rate (modified criteria for
evaluation) at 6 months would be 35% in the control group. This is
the rate of response expected among subjects who did not respond
adequately to etanercept therapy. Using a 2:1 randomization, a
sample of 141 (adjusted for a possible 10% dropout) subjects (47
control/94 CTLA4Ig) yields a 90% power to detect a difference of
30% at the 5% level of significance (2-tailed, based on a
chi-square test with no adjustment for continuity correction).
[0488] Similarly, the sample was determined to yield a power of 91%
and 83% to detect differences of 30 and 25% in ACR 50 and 70,
respectively. However, due to slow enrollment, only 122 subjects
were randomized and 121 treated and analyzed (one subject was
randomized but never received treatment).
[0489] Demography and Baseline Characteristics
13TABLE 1 Subject Disposition at Day 180 CTLA4Ig + Placebo +
etanercept etanercept TOTAL Randomized* 85 36 121 Completed 68
(80%) 22 (61%) 90 (74%) Discontinued 17 (20%) 14 (39%) 31 (26%)
Adverse Events 6 (7.0%) 1 (2.7%) 7 (6%) Lack of Efficacy 6 (7.0%)
12 (33%) 18 (15%) Other 5 (5.8%) 1 (2.7%) 6 (5%) *Excludes one
subject that did not receive treatment
[0490] After six months, the proportion of total discontinuations
were higher (39%) in the placebo plus etanercept treatment group
compared to the CTLA4Ig plus etanercept group (20%). The difference
was driven by a higher rate of discontinuation due to lack of
efficacy in the placebo plus etanercept group (Table 1).
[0491] Demographic characteristics were similar between treatment
groups. The majority of subjects were female and Caucasian. The
mean duration of the disease was 13 years and the mean age was 52
years (Table 2).
14TABLE 2 Mean Baseline Demographic and Clinical Characteristics
CTLA4Ig + Placebo + etanercept etanercept TOTAL N = 85 N = 36 N =
121 Mean Age: yrs (Range) 50 (24-74) 55 (28-72) 52 (24-74) Mean
Weight: kg (Range) 81 (45-154) 79 (46-126) 81 (45-154) Gender:
female: n (%) 66 (78%) 26 (72%) 92 (76%) Race: Caucasian-n (%) 80
(94%) 36 (100%) 116 (96%) Mean Duration of Disease: 13.0 .+-. 10.1
12.8 .+-. 8.6 13.0 .+-. 9.7 yrs .+-. sd Tender Joints (out of 68)-
28.7 .+-. 14.0 29.5 .+-. 13.7 28.9 .+-. 13.8 mean .+-. sd Swollen
Joints-(out of 66)- 19.6 .+-. 9.4 20.3 .+-. 11.0 19.8 .+-. 9.9 mean
.+-. sd
[0492] Baseline clinical characteristics were similar between
treatment groups including a mean of 29 tender joints and 20
swollen joints. With the exception of CRP values, which were lower,
the baseline characteristics were typical of subjects with active
rheumatoid arthritis and enrolled in clinical studies (Table
2).
[0493] ACR Responses and Core Components
[0494] The improvements in the ACR 20 and ACR 70 responses in the
CTLA4Ig+etanercept group were statistically significant compared to
the CTLA4Ig+placebo group (Table 3 and FIG. 63).
15TABLE 3 Modified ACR Response at Day 180-number of subjects (%)*
ACR 20 ACR 50 ACR 70 CTLA4Ig + etanercept*** 48.2% 25.9% 10.6%
Diff. from Placebo + etanercept 20.5% 6.4% 10.6% 95% CI (1.2, 39.7)
(-10.2, 23.1) (0.4, 20.8) p-Value 0.037** 0.448 0.042** *See
Criteria for Evaluation **p < 0.05 (probability for ACR response
in CTLA4Ig + etanercept vs. placebo + etanercept) ***N = 85 and N =
36 for CTLA4Ig + etanercept: and Placebo + etanercept,
respectively
[0495] By two months of treatment, numerically higher responses on
all components of the ACR criteria were observed for the CTLA4Ig
plus etanercept group. Three of the seven ACR components are shown
in FIGS. 64A-C.
[0496] The mean improvements in the individual components of the
ACR criteria on Day 180 were consistently greater in the CTLA4Ig
plus etanercept treatment group compared to the placebo plus
etanercept group (Table 4).
16TABLE 4 Mean Percent (SE) Improvement in Individual ACR
Components at Day 180 CTLA4Ig + Placebo + etanercept etanercept ACR
Component N = 85 N = 36 Tender Joints 42% (5.5) 24% (8.3) Swollen
Joints 37% (5.0) 21% (8.1) Pain 34% (4.3) -1% (10.8) Physical
Function (MHAQ) 31% (5.2) -5% (13.8) Subject Global Assessment 27%
(5.4) 3% (9.5) Physician Global Assessment 43% (4.3) 27% (5.8)
[0497] Quality of Life
[0498] Compared to baseline, subjects in the CTLA4Ig plus
etanercept group demonstrated statistically significant
improvements at Day 180 in all 8 subscales of the SF-36-compared to
only one (physical function) in subjects in the placebo plus
etanercept group. The absolute changes in HRQOL subscales were
considered clinically meaningful.
[0499] Compared to the placebo plus etanercept group, subjects in
the CTLA4Ig plus etanercept group experienced statistically
significantly greater improvement in 4 subscales of the SF-36:
role-physical, bodily pain, vitality, and social function (FIG.
65). Improvements in the other 4 subscales were also greater than
the placebo plus etanercept group, although they were not
statistically significant.
[0500] Safety
[0501] No deaths or opportunistic infections occurred during the
first six months of this study. Among the most frequently reported
adverse events, headache, upper respiratory infection,
musculo/skeletal pain, nausea/vomiting, hypertension, and diarrhea
occurred at a higher rate in the CTLA4Ig plus etanercept group
compared to the placebo plus etanercept group. Sinus abnormalities
and rash were slightly higher in the CTLA4Ig plus etanercept group,
as well.
[0502] More subjects in the CTLA4Ig plus etanercept group
experienced serious adverse events (SAE) (7.1%) than the etanercept
plus placebo group (2.8%). However, no SAEs were considered related
to the study drug.
[0503] Two subjects receiving CTLA4Ig and etanercept had a
dermatological malignancy. One subject had a basal cell carcinoma
that was excised after the Day 150 visit. The other subject had a
squamous cell carcinoma which was a pre-existing lesion that the
subject decided to have removed after the Day 120 visit. Another
subject experienced angioedema that was considered by the
investigator to be a drug reaction to azithromycin.
[0504] All adverse events (AEs) leading to discontinuation were of
either of mild or of moderate intensity. One discontinuation in the
CTLA4Ig plus etanercept group, due to a tremor, was considered a
serious adverse event.
[0505] Immunogenicity
[0506] No subjects receiving CTLA4Ig seroconverted for CTLA4Ig or
CTLA4-T specific antibodies. No significant change in GMTs for
CTLA4Ig or CTLA4-T specific antibodies was observed.
[0507] Comparison between CTLA4Ig/Etanercept and
CTLA4Ig/Mlthotrexate ACR Responses
17TABLE 5 CTLA4Ig + etanercept vs. CTLA4Ig + methotrexate ACR
responses (% improvement): CTLA4Ig + Etanercept.sup.a CTLA4Ig +
Methotrexate.sup.b (IM101-101) (IM101-100) 2 mg/kg 0 mg/kg.sup.c 10
mg/kg 2 mg/kg 0 mg/kg.sup.c N = 85 N = 36 N = 115 N = 105 N = 119
ACR 20 48.2%.sup.d 27.8% 60.0%.sup.d 41.9% 35.3% ACR 50 29.3% 19.4%
36.5%.sup.d 22.9%.sup.d 11.8% ACR 70 10.6%.sup.d 0% 16.5%.sup.d
10.5%.sup.d 1.7% .sup.aModified ACR. See criteria for evaluation
.sup.bStandard ACR criteria .sup.cPlacebo + Background therapy
(etanercept or methotrexate) .sup.dp < 0.05 for the difference
in ACR response vs placebo + background therapy
[0508] The efficacy of CTLA4Ig plus etanercept at 2 mg/kg was
similar to that observed in subjects receiving the same dose of
CTLA4Ig plus methotrexate therapy (Example 5). However, the
criteria for evaluation in the methotrexate (Example 5) trial was
the standard ACR, that includes CRP among the core components,
while in the etanercept trial (Example 6) the criteria for
evaluation was the modified ACR, that excludes CRP.
CONCLUSION
[0509] Preliminary assessment of the study at six months found that
CTLA4Ig (2 mg/kg) in combination with etanercept reduced the signs
and symptoms of rheumatoid arthritis, as compared with etanercept
alone. The increases in the modified ACR20 and ACR 70 assays were
statistically significant. Efficacy of CTLA4Ig plus etanercept
therapy was observed within one month of the start of treatment.
CTLA4Ig was generally safe and well tolerated when administered in
combination with etanercept with the safety profile similar to
etanercept therapy alone. CTLA4Ig was not immunogenic during the
six month trial period. Additionally, the efficacy of CTLA4Ig
therapy in combination with etanercept (Example 6) was similar to
the same dose of CTLA4Ig with methotrexate (Example 5).
EXAMPLE 7
[0510] One-Year Results of a Phase IIB, Multicenter, Randomized,
Double-Blind, Placebo-Controlled Study to Evaluate the Safety and
Clinical Efficacy of Two Different Doses of BMS-188667 Administered
Intravenously to Subjects with Active Rheumatoid Arthritis While
Receiving Methotrexate.
[0511] The following example provides the one-year results from a
Phase IIB, multi-center, randomized, double-blind, placebo
controlled clinical study to evaluate the safety and clinical
efficacy of administering two different doses of CTLA4Ig in
combination with methotrexate to treat patients with active
Rheumatoid Arthritis (RA). The study presented in this example is a
continuance of the six-month study presented in Example 5.
[0512] Based on preliminary efficacy results from Example 3, supra,
and the standard practice of adding other therapies to MTX in the
treatment of RA, this study was designed to test the hypothesis
that CTLA4Ig (BMS-188667) combined with MTX may have greater
clinical efficacy when compared with MTX plus placebo in RA
subjects who still have active disease despite MTX treatment.
[0513] The results presented in this clinical study report are
based on data from an analysis performed after all subjects
completed 6 months of treatment and again after all subjects
completed 12 months of treatment.
[0514] Throughout this Example, the 10 mg/kg CTLA4Ig plus MTX group
may be referred to as the 10 mg/kg group, the 2 mg/kg plus MTX
group is referred to as the 2 mg/kg group, and the CTLA4Ig
(BMS-188667) placebo plus MTX group is referred to as the placebo
group.
[0515] Study Methodology
[0516] This study compared the clinical efficacy of two different
doses (10 and 2 mg/kg) of CTLA4Ig (BMS-188667) combined with
methotrexate (MTX) or with MTX plus placebo in subjects with active
RA as assessed by ACR at 6 month and 12 month intervals. This study
enrolled adult subjects with active RA who had had an inadequate
response to MTX.
[0517] Results after one-year of monitoring subjects with active
rheumatoid arthritis who were intravenously administere: 1) CTLA4Ig
at a dosage of 2 mg/kg body weight with methotrexate, 2) CTLA4Ig at
a dosage of 10 mg/kg body weight with methotrexate, or 3) a placebo
with methotrexate (hereinafter known as placebo), are presented
herein.
[0518] Subjects with active RA, despite treatment with MTX and who
met the inclusion/exclusion criteria for this study were randomized
1:1:1 to receive one of the following treatments on a background of
MTX therapy: CTLA4Ig (BMS-188667) 10 mg/kg, CTLA4Ig (BMS-188667) 2
mg/kg, or placebo. Subjects must have been treated with MTX (10 mg
to 30 mg weekly) for at least 6 months, at a stable dose for 28
days prior to Day 1.
[0519] Treatment Groups: Subjects were randomized 1:1:1 to one of
three treatment groups:
[0520] 1) Group 1: CTLA4Ig (BMS-188667) 10 mg/kg by intravenous
infusion
[0521] 2) Group 2: CTLA4Ig (BMS-188667) 2 mg/kg by intravenous
infusion
[0522] 3) Group 3: CTLA4Ig (BMS-188667) placebo by intravenous
infusion
[0523] Infusion doses were based upon the subject's body weight
from the pre-treatment visit immediately prior to the Day 1 visit
(for a subject on MTX monotherapy, the weight was obtained at the
screening visit; for a subject on MTX combination therapy [in
combination with other DMARDs], the weight was obtained from the
washout visit, Day -2). The infusion doses were not modified during
Day 1 to Day 360.
[0524] Infusions were to occur at approximately the same time of
day throughout the study. All doses of study medication were
administered in a fixed volume of 75 mL at a constant rate over
approximately 30 minutes. The intravenous bag and line were flushed
with 25 mL of dextrose 5% in water (D5W) solution at the end of
each infusion. All intravenous infusions were administered with the
subject in the seated position. Subjects were observed for Adverse
Events (Aes) and changes in vital signs (blood pressure,
heart-rate, body temperature) from the start of each infusion
(pre-dose, 15, 30, 45, 60, 75, 90, 120 minutes) and for a minimum
of 2 hours after the start of the infusion. The observation period
could be extended, if clinically indicated.
[0525] During the primary phase (Day 1 to Day 180) of the study,
concomitant administration of selected medications was allowed. The
permitted medications included:
[0526] MTX: Continued use of current dose (no increases, and
decreases only for toxicity)
[0527] Systemic (non-topical) corticosteroids: Provided that the
dose was stable and the total dose was less than or equal to the
equivalent of prednisone 10 mg/day. Intra-articular injections were
to be avoided; however, if necessary, up to two intra-articular
injections were permitted. NOTE: A joint that received an
intra-articular injection was counted as "active" in ALL subsequent
assessments/evaluations.
[0528] NSAIDs, including ASA: Provided the dose was stable
[0529] Acetaminophen, combination products including acetaminophen
and narcotic analgesics (i.e., acetaminophen with codeine
phosphate, acetaminophen with propoxyphene napsylate, acetaminophen
with oxycodone hydrochloride, acetaminophen with oxycodone
bitartrate, etc.), or tramadol: For subjects experiencing pain not
adequately controlled by baseline or study medication (except for
12 hours before a joint evaluation)
[0530] Table 1 is a schedule of study procedures and
evaluations.
18TABLE 1 Schedule of Study Procedures and Evaluations Treatment
Period Pretreatment (Day) Treatment Day.sup.e,f,j,h Screen Visit
Day (-28 to -2) (-2) 1 15 30 60 90 120 150 180 210 240 270 300 330
360 Screening assessments Informed consent X Complete History and
Physical X X.sup.i CXR X.sup.a ECG X.sup.a X Stabilize/Withdraw
prohibited X medications (if necessary).sup.b Enroll Subject X
X.sup.m Randomize Subject.sup.k X Dosing.sup.h X X X X X X X X X X
X X X Interim Assessments.sup.f Duration of morning stiffness X X X
X X X X X X X X X Interim History and Physical X X X X X X X X X X
Tender joint count X X X X X X X X X X X X X Swollen joint count X
X X X X X X X X X X X X Subject's assessment of pain X X X X X X X
X X X X X Subject's global assess of disease X X X X X X X X X X X
X activity Physician's global assess of X X X X X X X X X X X X
disease activity Subject's assess of physical X X X X X X X X X X X
X function Short form-36 health X X X X X questionnaire (SF-36)
Subjects response to therapy X X X Safety Assessments Adverse event
monitoring X X X X X X X X X X X X X X.sup.o Weight.sup.g X X X
Mammogram (females only).sup.l X X Vital signs X X X X X X X X X X
X X X X X Labs CBC X X X X X X X X X X X X X X X Chemistry panel X
X X X X X X X X X X X X X X Urinalysis X X Urine/serum pregnancy
test.sup.d X X X X X X X X X X X X X X X Hepatitis B surface
antigen X Hepatitis C antibody X Pharmacodynamics (PD) Rheumatoid
factor X X X X CRP X X X X X X X X X X X X X IL-2R X X X X X X X X
X X Exploratory cytokines (ICAM-1 X X X X e-Selectin, IL-6 and
TNF.alpha.) Pharmacokinetics X X X X Immunoglobulin determinations
Quantitative immunoglobulins X X X (IgG, IgA, IgM) Immunogenicity
Anti-BMS-188667Ab testing X X X X X X Radiographic
assessments.sup.n X-rays (hands/wrists and feet) X X X .sup.aChest
X-ray and ECG was performed if not performed within 6 months or not
on file. .sup.bIf subject was being treated with DMARDs on top of
methotrexate therapy and did not meet initial entry # criteria, the
DMARDs must have been washed out for at least 28 days prior to Day
1. .sup.cThis visit was required only if the subject was on MTX
therapy. .sup.dUrine or serum pregnancy test performed within 48
hours prior to dosing, for all women of child bearing # potential.
Serum pregnancy test was to be processed locally. .sup.eSubjects
who discontinued must have had an "early termination" visit.
Assessments at this visit were # identical to assessments performed
on Day 360. The assessments for this visit replaced what might have
# been scheduled on the day of discontinuation. Changes in current
DMARD, steroid, or NSAIDs therapy # were not permitted until after
these assessments were performed. Subjects were to be contacted 30
days # after discontinuation to capture safety data (adverse
events). .sup.fEvery effort must have been made to insure the same
evaluator completed the assessment for each subject. .sup.gMost
recent weight should have been used to calculate study drug dosage.
All doses administered during the # study were be based on this
weight. .sup.hFor Day 15, a +/-3 day visit window was permitted.
For subsequent visits, a +/- 7 day visit window was permitted.
.sup.iComplete physical examination only. .sup.jAll assessments
should have been performed or administered prior to study drug
administration unless otherwise indicated. .sup.kThe results of all
assessments must have been reviewed for eligibility requirements
before contacting the # Central Randomization System for
randomization. .sup.lSee Section 2.1.4.3 of the protocol for
mammography rationale. If not performed within 6 months #
(documentation must be on file) prior to signing consent. Subjects
who discontinued from the study after # Day 1 required a follow-up
mammogram on the one year anniversary of the mammogram that was #
performed during the screening period. .sup.mSubject's body weight
was provided to central randomization system. .sup.nNo radiographic
assessments were required at the termination visit for subjects who
discontinued within the # first nine months of treatment.
.sup.oSubjects who were terminated early had adverse events and
concomitant medications recorded 30 and 60 # days after the last
dose of study medication.
[0531] Efficacy Assessments
[0532] Clinical Measurements and Responses
[0533] Clinical response was assessed using the American College of
Rheumatology (ACR) Core Data Set and Response Definitions. For this
assessment, data were collected on seven components: 1) tender
joint count (standardized 68 joint count); 2) swollen joint count
(standardized 66 joint count); 3) subject global assessment of
pain; 4) subject global assessment of disease activity; 5)
physician global assessment of disease activity; 6) subject
assessment of physical function (MHAQ); and 7) an acute phase
reactant value CRP.
[0534] The ACR 20, ACR 50, and ACR 70 definition of response
corresponds to a 20%, 50%, or 70% improvement, respectively, over
baseline in tender and swollen joints (components 1 and 2) and a
20%, 50%, and 70% improvement, respectively, in three of the five
remaining core data set measures (components 3 to 7). A Major
Clinical Response is defined as maintenance of an ACR 70 response
over a continuous 6-month period. See Table 1 for the days that
data for each component was collected.
[0535] The primary efficacy analysis tested for differences in ACR
20 response between the two CTLA4Ig (BMS-188667) treatment groups
and the placebo group at 6 months (Day 180). A sequential testing
procedure was employed. First, a Chi-square test was used to
compare the data for the 10 mg/kg CTLA4Ig group with the data for
the placebo group at the 0.05 level of significance. If this was
significant, the data for the 2 mg/kg CTLA4Ig group was compared
with the placebo group at the 0.05 level. This testing procedure
preserved the overall alpha level at 5%. Similar analyses were
carried out for the ACR 50 and ACR 70 responses at 6 months.
Differences in ACR 20, ACR 50 and ACR 70 responses between each
CTLA4Ig (BMS-188667) treatment group and the placebo group were
summarized using point estimates and 95% confidence intervals.
Subjects who discontinued the study due to lack of efficacy (i.e.,
worsening RA) were considered ACR non-responders at all subsequent
time points. For all subjects who discontinued for other reasons,
their last ACR response was carried forward.
[0536] ACR 20, ACR 50, and ACR 70 response rates on Day 360 were
compared between each CTLA4Ig (BMS-188667) treatment group and
placebo at the Dunnett-adjusted 0.027 (two-tailed) level of
significance.
[0537] The proportion of responders achieving an ACR 20 response at
each time point was also plotted over time, and the Cochran
Mantel-Haenszel test (W. G. Cochran, 1954, Some Methods of
Strengthening the Common Chi-Square Test, Biometrics 10:417-451; N.
Mantel and W. Haenszel, 1959, Biostatistical Aspects of the
Analysis of Data from Retrospective Studies of Disease, J Nat
Cancer Inst, 22:719-748) was used to compare the frequency of
subjects achieving an ACR 20 response in each CTLA4Ig (BMS-188667)
group versus the placebo group.
[0538] ACR 20, ACR 50, and ACR 70 responses on Days 15, 30, 60, 90,
120, 150, 180, 240, 300, and 360 were also presented for the two
CTLA4Ig (BMS-188667) groups and the placebo group. The differences
in ACR responses between the CTLA4Ig (BMS-188667) groups and
placebo group were summarized using 95% confidence intervals. The
ACR data plotted over time were used to assess onset-of-action and
to determine time to maximal response.
[0539] A Major Clinical Response was defined as the maintenance of
an ACR 70 response over a continuous 6-month period. At the
12-month analysis, the proportion of subjects who achieved a Major
Clinical Response among the three groups was summarized.
[0540] In order to assess the integrity of the planned analyses,
all subjects who received study medication and discontinued the
study for any reason were considered ACR non-responders at all
scheduled study visits subsequent to discontinuation.
[0541] The cumulative index, ACR-N, was evaluated at each follow-up
assessment, and the AUC was assessed for up to 6 months and up to
12 months. The trapezoidal rule was used to compute the AUC. The
ACR-N AUC was compared between the two CTLA4Ig (BMS-188667)
treatment groups and the placebo group using an analysis of
variance (ANOVA) for 6- and 12-month data. This allowed for the
assessment of subject response throughout the study. These analyses
were carried out on the LOCF data sets.
[0542] The distributional assumptions regarding the normality of
the ACR-N AUC data were checked using the Shapiro-Wilks test on
standardized residuals from the ANOVA model at the 10% level of
significance.
[0543] Surrogate biomarkers were also used to assess the efficacy
of the CTLA4Ig+MTX or placebo+MTX treatment regimens. Potential
biomarkers for immunomodulation or inflammation in RA include CRP,
soluble IL-2r, RF, soluble ICAM-1, E-selectin, serum IL-6, and
TNF.alpha.. These parameters were summarized by treatment group,
using frequencies and mean change from baseline to Day 180 and Day
360.
[0544] An Adverse Event (AE) was defined as any new or worsening
illness, sign symptom or clinically significant laboratory test
abnormality noted by the Investigator during the course of the
study, regardless of causality. A serious adverse event (SAE) was
defined as an AE that met any of the following criteria: was fatal;
was life-threatening; resulted in or prolonged hospitalization;
resulted in persistent or significant disability or incapacity, was
cancer, was a congenital anomaly/birth defect, resulted in an
overdose, resulted in the development of drug dependency or drug
abuse, or was an important medical event.
[0545] Vital sign measurements were obtained at screening and at
each study visit during and following study drug administration.
Vital sign measurements (seated blood pressure, heart rate, and
body temperature) were summarized by treatment group using
means.
[0546] The two CTLA4Ig (BMS-188667) treatment groups (10 and 2
mg/kg) were compared with the placebo group. The primary analysis
was the comparison of 6-month ACR response rate for 10 mg/kg and
placebo groups, to be followed by the comparison of 2 mg/kg with
placebo only if the former was significant. Sample sizes were based
on a 5% level (two-tailed) of significance. The ACR 20 response
rate for a placebo group at 6 months was estimated to be about 25%
(Weinblatt M, Kremer J M, Bankhurst A D et. al. A trial of
etanercept, a recombinant TNF:Tc fusion protein in patients with RA
receiving methotrexate. NEJM 1999; 340: 253-259). A sample of 107
subjects per treatment group (adjusted for a possible 15%
discontinuation rate) was determined to yield a 94% power to detect
a difference of 25% at the 5% level (two-tailed). Table 2
summarizes the power needed to detect the specified treatment
differences in ACR 20, ACR 50, and ACR 70 responses at 6
months.
19TABLE 2 Response Rates and Power with 107.sup.a Subjects per
Group Response Control Rate (%) Treatment Difference Power (%) ACR
20 25 25 94 ACR 50 5 20 95 ACR 70 1 14 90 .sup.aSample size was
adjusted for a possible 15% discontinuation rate; actual sample
size was 91.
[0547] If the primary comparisons of the 10 mg/kg CTLA4Ig with
placebo were significant, then for the comparison of the 2 mg/kg
CTLA4Ig with placebo groups, the power of the test would be at
least 0.88, 0.90, and 0.81 for the comparison involving ACR 20, ACR
50, and ACR 70 responses at 6 months, respectively (Koch D D,
Gansky S A. Statistical considerations for multiplicity in
confirmatory protocols. Drug Info Journal 1996; 30: 523-534).
[0548] Statistical Analyses
[0549] Study Population
[0550] Disposition of Subjects
[0551] Of 524 subjects who were enrolled in this study, 339
subjects were randomized: 115 to the 10 mg/kg group; 105 to the 2
mg/kg group; and 119 to the placebo group (FIG. 68). The most
frequent reason for not being randomized was failure to meet
inclusion and/or exclusion criteria.
[0552] Primary Phase (Days 1-180)
[0553] A total of 256 subjects (75.5% of those randomized)
completed the primary phase of the study; 83 subjects discontinued
during this period (Table 3). Overall, discontinuation was more
than 2-fold higher with placebo compared with 10 mg/kg CTLA4Ig
group. Discontinuation due to lack of efficacy and discontinuation
due to an AE were also more than 2-fold higher with placebo than
with 10 mg/kg CTLA4Ig group.
20TABLE 3 Reasons for Discontinuation: Primary Phase (Days 1-180)
CTLA4Ig (BMS 188667) 10 mg/kg 2 mg/kg Placebo Total No. Treated, n
115 105 119 339 No. Discontinued, n (%) 17 (14.8) 25 (23.8) 41
(34.5) 83 (24.5) Adverse Event 3 (2.6) 7 (6.7) 9 (7.6) 19 (5.6)
Lack of Efficacy 12 (10.4) 16 (15.2) 28 (23.5) 56 (16.5) Withdrawal
of Consent 2 (1.7) 2 (1.9) 4 (3.4) 8 (2.4) Completed 180 Days of 98
(85.2) 80 (76.2) 78 (65.5) 256 (75.5) Therapy, n (%)
[0554] Cumulative Discontinuations (Days 1-360)
[0555] A total of 235 subjects (69.3% of those randomized)
completed both phases of the study; 104 subjects discontinued by
Day 360 (Table 4). The same general pattern in disontinuations
noted in the primary phase (2-fold higher incidence with placebo
compared with 10 mg/kg CTLA4Ig group) was also observed overall
(Days 1-360). This included the overall discontinuation rate,
discontinuations due to a lack of efficacy and discontinuations due
to an AE.
21TABLE 4 Reasons for Discontinuation: Both Phases (Days 1-360)
CTLA4Ig (BMS-188667) 10 mg/kg 2 mg/kg Placebo Total No. Treated, n
115 105 119 339 No. Discontinued, n (%) 25 (21.7) 31 (29.5) 48
(40.3) 104 (30.7) Adverse Event 5 (43).sup.b 9 (8.6) 11 (9.2) 25
(7.4) Death 0 1 (1.0) 0 1 (0.3) Lost to Follow-up 1 (0.9) 2 (1.9) 0
3 (0.9) Other.sup.a 1 (0.9) 0 1 (0.8) 2 (0.6) Lack of Efficacy 13
(11.3) 17 (16.2) 30 (25.2) 60 (17.7) Withdrawal of Consent 5 (4.3)
2 (1.9) 6 (5.0) 13 (3.8) Completed 360 Days of 90 (78.3) 74 (70.5)
71 (59.7) 235 (69.3) Therapy, n (%) .sup.aOther reasons for
discontinuation were related to compliance .sup.bSubject
IM101100-32-5 in the 10 mg/kg CTLA4Ig group reported an AE that was
recorded as having resulted in discontinuation from the study;
however, this subject was not included in this table.
[0556] A Kaplan-Meier plot of the cumulative proportion of subjects
who discontinued for any reason during the first 12 months is
presented in FIG. 69; the cumulative proportion of subjects who
discontinued due to lack of efficacy in presented in FIG. 70. Note
that in both graphs after approximately 30 days of therapy,
discontinuation rates with placebo were consistently higher
compared with both CTLA4Ig (BMS-188667) groups. Additionally, after
approximately 150 days of therapy, discontinuation rates for 2
mg/kg CTLA4Ig group were higher than those for 10 mg/kg.
[0557] Demography and Subject Characteristics
[0558] Overall, baseline demographic characteristics and baseline
clinical RA characteristics were generally comparable across the
three treatment groups and were typical of relatively advanced RA
encountered in clinical practice (Table 5 and Table 6). The
majority of subjects were white females approximately 55 years old
with a mean duration of RA of approximately 9 to 10 years, a
relatively large number of active joints (approximately 29 tender
and 21 swollen joints) and visual analogue scores (VAS)
approximately 59-65 mm (100 mm scale).
22TABLE 5 Baseline Demographic Characteristics CTLA4Ig (BMS-188667)
10 mg/kg 2 mg/kg Placebo No. Randomized 115 105 119 Age (yrs) Mean
.+-. SD (Range) 55.8 .+-. 12.5 (17, 83) 54.4 .+-. 11.3 (23, 80)
54.7 .+-. 12.0 (23, 80) Weight (kg) Mean .+-. SD (Range) 77.8 .+-.
18.6 (40.1, 144.0) 78.7 .+-. 21.4 (48.4, 186.8) 79.9 .+-. 17.6
(44.0, 140.0) Gender Males, n (%) 29 (25) 39 (37) 40 (34) Females,
n (%) 86 (75) 66 (63) 79 (66) Race White, n (%) 100 (87) 91 (87)
104 (87) Black, n (%) 6 (5) 0 3 (3) Other, n (%) 9 (8) 14 (13) 12
(10) Duration of RA (yrs) n = 114.sup.a n = 105 n = 117.sup.a Mean
.+-. SD (Range) 9.7 .+-. 9.8 (0, 38) 9.7 .+-. 8.1 (0, 36) 8.9 .+-.
8.3 (0, 41) Error! Bookmark not defined. Duration of RA was not
reported for 3 subjects.
[0559] Although not a component of the ACR criteria, duration of
morning stiffness was also assessed and was nearly 2-hours in each
of the three groups. Positive results for RF at baseline were also
assessed, and the CTLA4Ig (BMS-188667) treatment groups had higher
percentages of subjects who tested positive for RF (86% for both
the 10 mg/kg and 2 mg/kg CTLA4Ig groups compared to 76% for the
placebo group).
23TABLE 6 Baseline Clinical Rheumatoid Arthritis Characteristics
CTLA4Ig (BMS-188667) 10 mg/kg 2 mg/kg Placebo Characteristic (n =
115) (n = 105) (n = 119) Tender Joints, n 115 105 119 Mean .+-. SD
30.8 .+-. 12.2 28.2 .+-. 12.0 29.2 .+-. 13.0 Range 11.0, 66.0 3.0,
62.0 4.0, 68.0 Swollen Joints, n 115 105 119 Mean .+-. SD 21.3 .+-.
8.4 20.2 .+-. 8.9 21.8 .+-. 8.8 Range 9.0, 54.0 4.0, 48.0 8.0, 64.0
Pain (VAS 100 mm), n 113 104 119 Mean .+-. SD 62.1 .+-. 21.4 64.3
.+-. 22.3 65.2 .+-. 22.1 Range 0.0, 99.0 8.0, 100.0 3.0, 95.0
Physical Function (MHAQ 115 105 119 0-3), n Mean .+-. SD 1.0 .+-.
0.5 1.0 .+-. 0.5 1.0 .+-. 0.6 Range 0.0, 2.5 0.0, 2.5 0.0, 2.3
Subject Global Assess (VAS 113 105 119 100 mm), n Mean .+-. SD 60.1
.+-. 20.7 59.4 .+-. 23.7 62.8 .+-. 21.6 Range 10.0, 100.0 8.0, 99.0
4.0, 94.0 MD Global Assess (VAS 100 113 105 119 mm), n Mean .+-. SD
62.1 .+-. 14.8 61.0 .+-. 16.7 63.3 .+-. 15.5 Range 20.0, 98.0 8.0,
95.0 18.0, 93.0 CRP(mg/dL),n 112 99 115 Mean .+-. SD 2.9 .+-. 2.8
3.2 .+-. 2.5 3.2 .+-. 3.2 Range 0.2, 19.9 0.2, 10.8 0.2, 20.9
Morning Stiffness (in 115 103 119 minutes), n Mean .+-. SD 97.9
.+-. 63.1 104.1 .+-. 63.9 106.0 .+-. 64.2 Range 0.0, 180.0 0.0,
180.0 0.0, 180.0 Rheumatoid Factor (IU/mL), 99 90 90 n % Positive
86% 86% 76%
[0560] Baseline demographics and RA characteristics of the overall
population of subjects who had at least one dose of study drug and
discontinued due to lack of efficacy were generally comparable to
the entire study population, however, a greater proportion of
subjects in this subpopulation had been diagnosed with RA for
>10 years (45%) compared to the overall study population
(34%).
[0561] Medical History Findings and Prior Medications
[0562] Medical history findings for subjects in this study were
consistent with relatively advanced RA and were generally similar
among treatment groups. The most frequently occurring findings (in
>40% of the subjects) were musculoskeletal findings (not
including RA symptoms; 59.3%), gastrointestinal findings (45.1%),
and genitourinary findings (42.2%). Other important medical history
findings included cardiovascular disease in approximately 39% of
subjects in all treatment groups and endocrine/metabolic findings
in approximately 29% of all subjects.
[0563] Overall use of MTX, systemic (non-topical) corticosteroids,
DMARDs and biologic RA medications prior to entering the study was
generally comparable across the three treatment groups (Table 7).
All subjects were to have received prior treatment with rheumatic
medications, including MTX, to be eligible for the study. Prior
treatment with MTX was not recorded for 4 subjects. Systemic
(non-topical) corticosteroid use prior to randomization was
comparable among the three treatment groups, with slightly more
subjects in the 2 mg/kg CTLA4Ig and placebo groups taking systemic
(non-topical) corticosteroids (.about.67-68%) compared to subjects
in the 10 mg/kg CTLA4Ig group (60.0%). Use of other DMARDs and
biologic RA medications prior to entering the study varied from 0
to 12% across treatment groups with no overall predominance in any
treatment group. Mean dosing of MTX and of systemic (non-topical)
corticosteroids on Day 1 were comparable among all three treatment
groups (.about.15-16 mg/wk, .about.6-7 mgs/day, respectively.
24TABLE 7 Summary of Rheumatic Medications Prior to Enrollment
CTLA4Ig (BMS-188667) 10 mg/kg 2 mg/kg Placebo Prior Rheumatic
Medication, n (%).sup.a (n = 115) (n = 105) (n = 119) No. Subjects
on Prior Medications 114 (99.1) 103 (98.1) 118 (99.2)
Methotrexate.sup.b 114 (99.1) 103 (98.1) 118 (99.2) Systemic
(non-topical) corticosteroids 69 (60.0) 71 (67.6) 80 (67.2) Other
DMARDs 19 (16.5) 19 (18.1) 25 (21.0) Sulfasalazine 9 (7.8) 2 (1.9)
10 (8.4) Hydroxychloroquine 8 (7.0) 6 (5.7) 14 (11.8) Cyclosporine
2 (1.7) 4 (3.8) 4 (3.4) Infliximab 2 (1.7) 2 (1.9) 2 (1.7)
Etanercept 1 (0.9) 4 (3.8) 1 (0.8) Chloroquine 1 (0.9) 0 0
Leflunomide 0 2 (1.9) 2 (1.7) Error! Bookmark not defined.
Categories of prior rheumatic medications were not mutually
exclusive. Error! Bookmark not defined. Administration of MTX was
not recorded for 4 subjects
[0564] Study Therapy
[0565] Of the three treatment groups, the 10 mg/kg CTLA4Ig group
had the longest mean duration of exposure for both study phases and
the placebo group had the shortest mean duration of exposure for
both study phases (Day 180: 163 days, 156 days, 140 days; Day 360:
286 days, 268 days, and 234 days; 10 mg/kg, 2 mg/kg, and placebo,
respectively).
[0566] At Day 180 (end of the primary phase), the proportion of
subjects receiving infusions was higher in the 10 mg/kg CTLA4Ig
group (85%) compared with the 2 mg/kg CTLA4Ig group (79%) and the
placebo group (66%) (Table 8). At Day 330 (day of last scheduled
infusion in the secondary phase), the proportion of subjects
receiving infusions was also higher in the 10 mg/kg CTLA4Ig group
(78%) compared with the 2 mg/kg CTLA4Ig group (70%) and the placebo
group (59%).
25TABLE 8 Subjects Who Received Infusions on Given Study Days
Number (%) of Subjects CTLA4Ig (BMS-188667) 10 mg/kg 2 mg/kg
Placebo Day (n = 115) (n = 105) (n = 119) 1 115 (100) 105 (100) 119
(100) 15 114 (99) 104 (99) 117 (98) 30 113 (98) 101 (96) 111 (93)
60 108 (94) 97 (92) 103 (87) 90 106 (92) 94 (90) 94 (79) 120 100
(87) 86 (82) 83 (70) 150 98 (85) 83 (79) 81 (68) 180 98 (85) 83
(79) 78 (66) 210 94 (82) 80 (86) 78 (66) 240 95 (83) 78 (74) 76
(64) 270 93 (81) 77 (73) 73 (61) 300 90 (78) 74 (70) 72 (61) 330 90
(78) 73 (70) 70 (59)
[0567] Methotrexate
[0568] Subjects were to have been treated with a "stable" dose of
MTX (10-30 mg weekly) for at least 6 months, for 28 days prior to
Day 1. With the exception of 4 subjects, all subjects received
between 10 and 30 mg of MTX weekly in addition to CTLA4Ig
(BMS-188667) during the primary phase (Day 1-180). During the
secondary phase (Day 181-360), the dose of MTX could have been
adjusted provided it remained between 10 and 30 mg
[0569] Measurements of Treatment Compliance
[0570] During the primary phase, the number of missed infusions of
study drug was <2 at any time table (Table 9). During the
secondary phase, subjects in the placebo group appeared to have
missed slightly fewer infusions than subjects in the CTLA4Ig
(BMS-188667) groups. However, more placebo than CTLA4Ig
(BMS-188667) subjects discontinued by these later time points (see
supra).
26TABLE 9 Number of Missed Infusions of Study Drug CTLA4Ig
(BMS-188667) 10 mg/kg 2 mg/kg Placebo (n = 115) (n = 105) (n = 119)
Day 1 0 0 0 Day 15 1 1 0 Day 30 0 1 1 Day 60 0 0 0 Day 90 0 0 0 Day
120 0 1 2 Day 150 1 2 0 Day 180 1 0 1 Day 210 4 0 0 Day 240 1 2 1
Day 270 0 2 0 Day 300 1 1 0 Day 330 0 0 0
[0571] Concomitant Therapy
[0572] Systemic (non-topical) corticosteroid use was generally
comparable among the three groups during screening/enrollment
(58-67%) and during the primary phase of the study (67-71%), Tables
10 and 11, respectively. While corticosteroid use decreased in all
three treatment groups by Day 360, more subjects in the 10 mg/kg
CTLA4Ig group took systemic (non-topical) corticosteroids (63.5%)
compared to the other two treatment groups (53.3% and 45.4% for the
2 mg/kg CTLA4Ig and placebo groups, respectively). Several subjects
(CTLA4Ig: 0-3%, placebo: 0-10%) received DMARDs other than MTX
during screening/enrollment.
27TABLE 10 Summary of Rheumatic Concomitant Medications During
Screening/Enrollment CTLA4Ig (BMS-188667) 10 mg/kg 2 mg/kg Placebo
Rheumatic Medication, n (%).sup.a (n = 115) (n = 105) (n = 119) No.
Subjects on Prior Medications 114 (99.1) 103 (98.1) 118 (99.2)
Methotrexate 114 (99.1) 103 (98.1) 118 (99.2) Systemic
(non-topical) corticosteroids 67 (58.3) 70 (66.7) 75 (63.0) Other
DMARDs 5 (4.3) 6 (5.7) 14 (11.8) Sulfasalazine 3 (2.6) 1 (1.0) 4
(3.4) Hydroxychloroquine 2 (1.7) 3 (2.9) 12 (10.1) Cyclosporine 1
(0.9) 1 (1.0) 2 (1.7) Etanercept 0 1 (1.0) 0 Error! Bookmark not
defined. Drug categories were not mutually exclusive.
[0573]
28TABLE 11 Subjects Who Received Clinically Relevant Concomitant
Medications During Both Study Phases CTLA4Ig (BMS-188667) 10 mg/kg
2 mg/kg Placebo Medication.sup.a (n = 115) (n = 105) (n = 119)
Systemic (non-topical) corticosteroids 77 (67.0) 71 (67.6) 85
(71.4) (Primary Phase) Systemic (non-topical) corticosteroids 73
(63.5) 56 (53.3) 54 (45.4) (Secondary Phase) Error! Bookmark not
defined. Drug categories were not mutually exclusive. Note: Subject
IM101100-83-3 (10 mg/kg CTLA4Ig) took mefloquine and subject
IM101100-28-7 (placebo) took quinine between Days 1 and 180;
subject IM101100-18-11 (10 mg/kg CTLA4Ig) took quinine between Days
181 and 360 as an antimalarial, and was not considered a
significant protocol violation.
[0574] Efficacy Results
[0575] The CTLA4Ig (BMS-188667) 10 mg/kg group had superior
efficacy compared to the placebo group at Day 180 and Day 360. For
the 2 mg/kg CTLA4Ig group, results for some efficacy parameters
were significantly better compared to the placebo group, results
for most other efficacy parameters were numerically higher compared
to placebo.
[0576] ACR Responses at Day 180
[0577] Analysis of the primary efficacy variable for this study,
ACR20 response rate at Day 180, showed that the 10 mg/kg CTLA4Ig
group was significantly (p<0.001) more effective than placebo
(Table 12, FIG. 71A and FIG. 71B).
[0578] The ACR50 and ACR70 responses at Day 180 for the 10 mg/kg
CTLA4Ig group were also significantly higher compared to the
placebo group (Table 12, FIG. 71A and FIG. 71B). The ACR50 and the
ACR70 responses at Day 180 for the 2 mg/kg CTLA4Ig group were
significantly higher compared to the placebo group. The ACR20
response at Day 180 for the 2 mg/kg CTLA4Ig group was slightly
higher compared to the placebo group; however, no statistically
significant differences were observed.
29TABLE 12 ACR Responses at Day 180 CTLA4Ig (BMS-188667) 10 mg/kg 2
mg/kg Placebo (n = 115) (n = 105) (n = 119) ACR 20 n (%) 70 (60.9)
44 (41.9) 42 (35.3) CI 25.6 (12.8, 38.4) 6.6 (-6.2, 19.4) N/A
p-value <0.001.sup.a 0.31 N/A ACR 50 n (%) 42 (36.5) 24 (22.9)
14 (11.8) CI 24.8 (13.8, 35.7) 11.1 (1.2, 20.9) N/A p-value
<0.001.sup.a 0.027.sup.a N/A ACR 70 n (%) 19 (16.5) 11 (10.5) 2
(1.7) CI 14.8 (7.5, 22.2) 8.8 (2.7, 14.9) N/A p-value
<0.001.sup.a 0.005.sup.a N/A Error! Bookmark not defined.
Statistically significant difference for the comparison of
BMS-188667 vs placebo.
[0579] ACR Responses at Day 360
[0580] At Day 360, ACR20, ACR50 and ACR70 responses for the 10
mg/kg CTLA4Ig group were significantly (p<0.001) higher compared
to the placebo group (Table 13, FIG. 72A and FIG. 72B). Although
the same response rates for the 2 mg/kg CTLA4Ig group were
numerically higher compared to the placebo group, these differences
were not statistically significant.
30TABLE 13 ACR Responses at Day 360 CTLA4Ig (BMS-188667) 10 mg/kg 2
mg/kg Placebo (n = 115) (n = 105) (n = 119) ACR 20 n (%) 72 (62.6)
43 (41.0) 43 (36.1) CI 26.5 (13.7, 39.3) 4.8 (-7.9, 17.6) N/A
p-value <0.001.sup.a 0.459 N/A ACR 50 n (%) 48 (41.7) 23 (21.9)
24 (20.2) CI 21.6 (9.7, 33.4) 1.7 (-8.9, 12.4) N/A p-value
<0.001.sup.a 0.75 N/A ACR 70 n (%) 24 (20.9) 13 (12.4) 9 (7.6)
CI 13.3 (4.4, 22.2) 4.8 (-3.0, 12.6) N/A p-value 0.003.sup.a 0.227
N/A Error! Bookmark not defined. Statistically significant
difference for the comparison of 10/mg/kg CTLA4Ig group vs
placebo.
[0581] ACR Responses by Visit
[0582] For the comparison of the 10 mg/kg CTLA4Ig group to the
placebo group, statistically significant improvements were observed
for all three response rates (ACR 20, ACR 50, and ACR 70) by Day
90, and these values remained statistically significant at every
time point up to and including Day 360 (p<0.008 for all three
ACR response rates) (FIG. 73A, FIG. 73B, and FIG. 73C). In fact,
statistically significant improvements in ACR 50 and ACR 70
response for the 10 mg/kg CTLA4Ig group occurred as early as Day 30
(p=0.039 and p=0.04, respectively).
[0583] For the 2 mg/kg CTLA4Ig group, statistically significant
improvements compared to placebo were observed in ACR 50 and ACR 70
responses at Day 180 (p=0.027 and p=0.005, respectively). At Day
360, improvements in ACR response were slightly greater in the 2
mg/kg CTLA4Ig group compared to the placebo group; however, no
statistically significant differences were observed.
[0584] After adjusting for visit using the Cochran-Mantel Haenszel
test, a significant difference in ACR 20 response was observed for
the 10 mg/kg CTLA4Ig group compared to the placebo group at both
Day 180 and Day 360. No significant difference was observed between
the 2 mg/kg CTLA4Ig and placebo groups at both timepoints. Similar
results were obtained for ACR 50 response at both time points. For
ACR 70 response at both time points, a significant difference was
observed for both CTLA4Ig (BMS-188667) treatment groups compared to
the placebo group.
[0585] Summary of Major Clinical Response
[0586] Major Clinical Response was defined as maintenance of an ACR
70 response over a continuous 6-month period. The percentages of
subjects who achieved a Major Clinical Response at Day 360 were
significantly higher in both the 10 mg/kg and 2 mg/kg CTLA4Ig
groups (7.8% and 5.7%, respectively) when compared to the placebo
group (0.8%; p=0.008 and 0.036, respectively) (Table 14).
31TABLE 14 Summary of Major Clinical Response by Day 360 CTLA4Ig
(BMS-188667) 10 mg/kg 2 mg/kg Placebo (n = 115) (n = 105) (n = 119)
No. Subjects with a Major 9 (7.8) 6 (5.7) 1 (0.8) Response Diff
(CI) 7.0 (1.8, 12.2) 4.9 (0.3, 9.4) N/A p-value 0.008.sup.a
0.036.sup.a N/A Error! Bookmark not defined. Indicates a
statisticall significant difference for the comparison of
BMS-188667 vs placebo.
[0587] Mean Numeric ACR (ACR-N) and ACR-N Area Under the Curve
(ACR-N-AUC)
[0588] Overall, mean numeric ACR (ACR-N) for all treatment groups
increased over time during the first 6 months of the study (FIG.
74). During the second 6 months, mean ACR-N increased slightly with
10 mg/kg CTLA4Ig, but remained relatively unchanged with 2 mg/kg
CTLA4Ig and placebo. At each study visit, the ACR-N was
consistently higher for the 10 mg/kg CTLA4Ig group compared to the
2 mg/kg CTLA4Ig and placebo groups.
[0589] Compared to the placebo group, the differences in values for
ACR-N AUC (area under the curve) for the 10 mg/kg CTLA4Ig group was
significantly (p<0.001) higher by Day 360.
[0590] Percentage Improvement from Baseline at Day 180
[0591] For the 10 mg/kg CTLA4Ig group, improvements in each
individual ACR component (tender and swollen joint counts, CRP,
pain, subject global assessment, physician global assessment, and
physical function) at Day 180 were statistically significant
relative to improvements for the placebo group (Table 15).
[0592] For the 2 mg/kg CTLA4Ig group, statistically significant
improvements compared to the placebo group were observed in
physician global assessment and CRP at Day 180. Furthermore, CRP
levels in the placebo group actually worsened at Day 180. Change
from baseline in mean duration of morning stiffness was comparable
among the three treatment groups at Day 180.
32TABLE 15 Mean Percentage Improvement from Baseline at Day 180
(Individual Components of ACR Criteria) CTLA4Ig (BMS-188667) 10
mg/kg 2 mg/kg Placebo Component (n = 115) (n = 105) (n = 119)
Tender Joints n = 114 n = 104 n = 118 Mean % Change 59.78* 43.15
31.88 Swollen Joints n = 114 n = 104 n = 118 Mean % Change 55.28*
45.34* 33.49 CRP n = 108 n = 98 n = 114 Mean % Change 31.79* 16.41*
-23.43 Pain n = 109 n = 102 n = 118 Mean % Change 46.19* 22.09*
8.20 Subject Global Assessment n = 111 n = 103 n = 118 Mean %
Change 40.76* 9.07 17.48 MD Global Assessment n = 111 n = 103 n =
116 Mean % Change 51.91* 38.71* 25.14 Physical Function n = 107 n =
98 n = 110 Mean % Change 41.21* 21.63 13.71 Duration Morning
Stiffness n = 98 n = 82 n =80 Mean .+-. SD (minutes) 61.9 .+-. 55.4
60.8 .+-. 66.1 55.9 .+-. 66.2 *Indicates p < 0.05 in comparison
with placebo since 95% CIs did not include zero
[0593] Percentage Improvement from Baseline at Day 360
[0594] For the 10 mg/kg CTLA4Ig group, improvements in each
individual ACR component (tender and swollen joint counts, CRP,
pain, subject global assessment, physician global assessment, and
physical function) at Day 360 were statistically significant
relative to improvements for the placebo group. Mean percentage
improvements from baseline to Day 360 are presented in Table 16 for
all clinical parameters of the ACR criteria.
[0595] For the 2 mg/kg CTLA4Ig group, statistically significant
improvements compared to the placebo group were observed in
physician global assessment and CRP at Day 360. Furthermore, CRP
levels in the placebo group actually worsened at Day 360. At Day
360, the CTLA4Ig (BMS-188667) treatment groups had greater changes
from baseline in duration of morning stiffness compared to the
placebo group.
33TABLE 16 Mean Percentage Improvement from Baseline at Day 360
(Individual Components of ACR Criteria) CTLA4Tg (BMS-188667) 10
mg/kg 2 mg/kg Placebo Component (n = 115) (n = 105) (n = 119)
Tender Joints n = 115 n = 105 n=119 Mean % Change 66.39* 43.54*
29.97 Swollen Joints n = 115 n = 105 n = 119 Mean % Change 59.74*
46.40 36.17 CRP n = 112 n = 98 n = 115 Mean % Change 27.59* 10.31*
-31.26 Pain n = 112 n = 104 n = 119 Mean % Change 44.93* 26.26
12.55 Subject Global Assessment n = 113 n = 105 n = 119 Mean %
Change 41.01* 16.08 1.99 MD Global Assessment n = 113 n = 105 n =
119 Mean % Change 53.48* 37.87* 24.14 Physical Function n = 109 n =
100 n = 111 Mean % Change 42.32* 22.94 10.25 Duration Morning
Stiffness n = 88 n = 71 n = 72 Mean .+-. SD 66.2 .+-. 59.5* 66.6
.+-. 72.2 49.7 .+-. 73.9 *Indicates p <0.05 in comparison with
placebo since 95% CIs did not include zero
[0596] New Active Joints
[0597] The proportion of new active joints was determined using the
validated 28-joint count (out of 68 total tender joints and out of
66 total swollen joints) proposed by Smollen et al (Smollen J S,
Breedveld F C, Eberl G, Jones I et al. Validity and reliability of
the twenty-eight joint count for the assessment of RA activity.
Arthritis & Rheum 1993; 38: 38-43). The proportion of new
active joints (both tender and swollen) at Day 180 was lowest for
subjects receiving 10 mg/kg CTLA4Ig (FIG. 75).
[0598] At Day 180, the percentages of subjects reporting no new
tender joints and no new swollen joints was highest in the 10 mg/kg
CTLA4Ig group (FIG. 76A, FIG. 77A). The percentage of subjects who
reported no new tender joints and no new swollen joints was
approximately 59% and 52%, respectively, in the 10 mg/kg CTLA4Ig
group; 38% and 44%, respectively, in the 2 mg/kg CTLA4Ig group; and
41% and 37%, respectively, in the placebo group.
[0599] The proportion of new active joints (both tender and
swollen) at Day 360 was lowest for subjects receiving 10 mg/kg
CTLA4Ig (FIG. 78). This pattern for the proportion of new active
joints mirrored the pattern seen at Day 180.
[0600] Similarly, at Day 360, the proportion of subjects reporting
no new tender joints and no new swollen joints was highest in the
10 mg/kg CTLA4Ig group (FIG. 76B, and FIG. 77B). The percentage of
subjects who reported no new tender and no new swollen joints was
approximately 71% and 61%, respectively, in the 10 mg/kg CTLA4Ig
group; 41% and 44%, respectively, in the 2 mg/kg CTLA4Ig group; and
42% for both counts in the placebo group.
[0601] Improvement in Clinical Parameters Among Subjects with an
ACR Response
[0602] Among ACR 20, ACR 50, and ACR 70 responders, improvement in
the core components of the ACR criteria were slightly greater for
the two CTLA4Ig (BMS-188667) treatment groups compared to
placebo.
[0603] The onset of action for subjects who received the 10 mg/kg
CTLA4Ig dose occurred after approximately 15 days, with significant
increases in ACR 20 improvement occurring at .gtoreq.Day 60 for
ACR50 at .gtoreq.Day 90 for ACR70 at .gtoreq.Day 30 and in each
instance, continuing until Day 360 (see FIG. 73A, FIG. 73B and FIG.
73C).
[0604] Changes from Baseline for the Health Outcomes Short Form
Questionnaire (SF-36)
[0605] The impact of CTLA4Ig (BMS-188667) on health-related quality
of life was assessed using the Health Outcomes Short Form
Questionnaire SF-36 (summary scores range from 0 to 100 with higher
scores indicating a better quality of life). Analyses were
performed on the LOCF (last observation carried forward) data set
as well as the as the observed data set.
[0606] For the 10 mg/kg CTLA4Ig group, statistically significant
improvement from baseline compared to the placebo group was
observed in all four mental health and all four physical health
domains of the SF-36 at Day 180, using the LOCF analysis (i.e., 95%
CIs did not include 0) (FIGS. 79A, 79B). For the 2 mg/kg CTLA4Ig
group, there were numerical improvements in the mental health or
physical health domains compared to placebo at Day 180, however,
these improvements were not statistically significant.
[0607] Results of analyses performed on the as-observed data set
were similar to those observed for the LOCF data set except that
the "role emotional" domain at Day 180 was not significantly
improved (but was numerically improved) for the comparison between
the 10 mg/kg CTLA4Ig and placebo groups using the as-observed data
set.
[0608] The physical component and the mental health component
summary measures at Day 180 are shown in Table 17.
34TABLE 17 Mean Change from Baseline to Day 180 for the SF-36
(Physical and Mental Health Components) CTLA4Ig (BMS-188667) 10
mg/kg 2 mg/kg Placebo Summary Score (n = 115) (n = 105) (n = 119)
Mental Health Component n = 115 n = 103 n = 118 Baseline Mean 44.52
43.06 41.75 Postbaseline Mean 48.69 45.59 44.04 Mean Change from
Baseline 4.17 2.53 2.30 95% CI (2.46, 5.88) (0.39, 4.67) (0.42,
4.17) Physical Component n = 115 n = 103 n = 118 Baseline Mean
31.13 30.80 32.33 Postbaseline Mean 39.30 35.47 35.21 Mean Change
from Baseline 8.16 4.67 2.88 95% CI (6.33, 9.99) (3.25, 6.09)
(1.54, 4.22)
[0609] Results of the Health Outcomes at Day 360 were similar to
those seen at Day 180. For the 10 mg/kg CTLA4Ig group,
statistically significant improvements from baseline compared to
the placebo group were observed in all four mental and all four
physical domains of the SF-36 at Day 360, using the LOCF analysis
(i.e., 95% CIs did not include 0) (FIGS. 80A, and 80B). For the 2
mg/kg CTLA4Ig group, a statistically significant difference in
three of four physical domains at Day 360 and one of four mental
domains at Day 360 compared to the placebo group was observed.
[0610] Results of analyses performed on the as-observed data set
were similar to those observed for the LOCF data set.
[0611] The physical component and mental health component summary
measures at Day 360 is shown in Table 18.
35TABLE 18 Mean Change from Baseline to Day 360 for the SF-36
(Summaries of Physical Component and Mental Health Component)
CTLA4Ig (BMS-188667) 10 mg/kg 2 mg/kg Placebo Summary Score (n =
115) (n = 105) (n = 119) Mental Health Component n = 115 n = 103 n
= 118 Baseline Mean 44.52 43.06 44.75 Postbaseline Mean 48.83 45.65
43.22 Mean Change from Baseline 4.31 2.59 1.47 95% CI (2.64, 5.98)
(0.64, 4.55) (-0.14, 3.08) Physical Component n = 115 n = 103 n =
118 Baseline Mean 31.13 30.80 32.33 Postbaseline Mean 38.93 36.49
34.93 Mean Change from Baseline 7.79 5.69 2.60 95% CI (5.90, 9.68)
(4.10, 7.28) (1.09, 4.11)
[0612] Biomarker and Pharmacodynamic Data
[0613] There were significant improvements (decreases) in 5 of the
6 biomarker/pharmacodynamic (PD) parameters with 10 mg/kg CTLA4Ig
at Day 180 (soluble IL-2r, rheumatoid factor (RF), ICAM-1,
E-selectin and IL-6) and a numerical decrease in TNF-.alpha. (Table
19). There were significant improvements (decreases) in 3 of the 6
biomarker/PD parameters with 2 mg/kg CTLA4Ig at Day 180 (soluble
IL-2r, RF and IL-6) and a numerical improvement in ICAM-1. There
were no significant changes in any of the biomarker/PD parameters
with placebo at Day 180. There appears to be a dose response
relationship with the improvements (decreases) in biomarker/PD
parameters.
36TABLE 19 Pharmacodynamic Measures at Day 180 CTLA4Ig (BMS-188667)
10 mg/kg 2 mg/kg Placebo Parameter (n = 115) (n = 105) (n = 119)
Soluble IL-2r n = 95 n = 84 n = 76 (Normal range: 640-2543 pg/mL)
Baseline Mean (.+-. SD) 1426.19 .+-. 751.76 1396.82 .+-. 610.21
1429.13 .+-. 667.84 Postbaseline Mean (.+-. SD) 1112.62 .+-. 699.68
1261.31 .+-. 473.66 1470.03 .+-. 637.75 Mean Change -316.23 -135.51
43.59 95% CI (-417.73, -214.72) (-241.48, -29.53) (-71.24, 158.43)
Rheumatoid Factor n = 95 n = 84 n = 74 (Normal Range: 0-20 IU/mL)
Baseline Mean (.+-. SD) 289.71 .+-. 401.95 256.19 .+-. 307.92
196.11 .+-. 265.48 Postbaseline Mean (.+-. SD) 185.43 .+-. 269.52
227.82 .+-. 276.27 204.36 .+-. 320.09 Mean Change -104.27 -28.12
-0.62 95% CI (-151.53, -57.01) (-52.13, -4.11) (-31.67, 30.43)
ICAM-1 n = 95 n = 82 n = 75 Baseline Mean (.+-. SD) 404.89 .+-.
137.72 393.47 .+-. 150.85 387.33 .+-. 230.93 Postbaseline Mean
(.+-. SD) 364.74 .+-. 109.47 387.25 .+-. 142.73 386.17 .+-. 163.82
Mean Change -40.42 -6.22 1.09 95% CI (-58.06, -22.78) (-27.49,
15.05) (-31.88, 34.05) E-selectin n = 89 n = 80 n = 71 Baseline
Mean (.+-. SD) 68.07 .+-. 32.93 67.32 .+-. 37.13 68.23 .+-. 43.09
Postbaseline Mean (.+-. SD) 61.01 .+-. 31.53 67.86 .+-. 40.20 67.37
.+-. 35.66 Mean Change -8.41 0.54 -0.68 95% CI (-13.24, -3.58)
(-5.95, 7.03) (-6.87, 5.51) Serum IL-6 n = 86 n = 74 n = 69 (Normal
Range: 0.3-14.8 pg/mL) Baseline Mean (.+-. SD) 28.47 .+-. 38.28
31.75 .+-. 42.29 21.20 .+-. 26.51 Postbaseline Mean (.+-. SD) 9.25
.+-. 15.85 16.00 .+-. 22.13 23.98 .+-. 37.92 Mean Change -20.30
-16.10 1.98 95% CI (-27.55, -13.06) (-24.20, -8.00) (-7.21, 11.17)
TNF.alpha. n = 84 n = 74 n = 69 (1.2-8.0 pg/mL) Baseline Mean (.+-.
SD) 11.17 .+-. 23.72 7.51 .+-. 13.25 13.12 .+-. 23.20 Postbaseline
Mean (.+-. SD) 7.57 .+-. 7.90 6.20 .+-. 4.48 9.59 .+-. 11.21 Mean
Change -3.66 -1.21 -3.54 95% CI (-8.62, 1.30) (-4.32, 1.90) (-7.82,
0.75)
[0614] Overall, the pattern in the changes in biomarker/PD data at
Day 360 were similar to that seen at Day 180. There were
significant improvements (decreases) in 5 of the 6 biomarker/PD
parameters with 10 mg/kg CTLA4Ig at Day 360 (soluble IL-2r, RF,
ICAM-1, E-selectin and IL-6) and a numerical, but not statistically
significant improvement observed for TNF-.alpha. (Table 20). There
was a significant improvement (decrease) in IL-6 only with 2 mg/kg
CTLA4Ig at Day 360, however, numerical improvements were seen with
RF and ICAM-1. There were no significant changes in any of the
biomarker/PD parameters with placebo at Day 360. As seen with Day
180 data, it appeared that all of the improvements (decreases) in
biomarker/PD parameters occurred in a dose response manner.
[0615] A comparison of the postbaseline means for the biomarker/PD
parameters at Day 180 to those at Day 360 reveals important trends.
For the 10 mg/kg CTLA4Ig group, all biomarkers/PD measures
continued to decrease, with the exception of soluble IL-2r which
increased slightly. For the 2 mg/kg CTLA4Ig group, mean values for
3 of the biomarkers/PD parameters either decreased slightly
(ICAM-1, serum IL-6) or remained relatively constant (E-selectin)
and mean values for the other 3 biomarkers/PD measures increased
slightly (soluble IL-2r, RF, TNF .alpha.). For the placebo group,
mean values for all of the biomarkers/PD parameters increased
slightly at Day 360, with the exception of TNF .alpha. which
remained relatively unchanged.
37TABLE 20 Pharmacodynamic Measures at Day 360 CTLA4Ig (BMS-188667)
10 mg/kg 2 mg/kg Placebo Measure (n = 115) (n = 105) (n = 119)
Soluble IL-2r n = 68 n = 56 n = 55 (Normal range: 640-2543 pg/mL)
Baseline Mean (.+-. SD) 1372.10 .+-. 770.11 1373.86 .+-. 567.75
1459.93 .+-. 695.07 Postbaseline Mean (.+-. SD) 1185.51 .+-. 638.95
1413.84 .+-. 452.50 1666.59 .+-. 611.97 Mean Change -194.31 39.99
206.22 95% CI (-305.67, -82.96) (-69.87, 149.84) (35.88, 376.56)
Rheumatoid Factor n = 69 n = 55 n = 58 (Normal Range: 0-20 IU/mL)
Baseline Mean (.+-. SD) 261.43 .+-. 333.58 258.42 .+-. 318.65
179.12 .+-. 207.72 Postbaseline Mean (.+-. SD) 143.13 .+-. 180.80
236.61 .+-. 287.36 206.42 .+-. 256.27 Mean Change -118.30 -25.64
20.90 95% CI (-175.19, -61.42) (-58.50, 7.23) (-10.72, 52.51)
ICAM-1 n = 77 n = 68 n = 64 Baseline Mean (.+-. SD) 406.44 .+-.
145.22 393.41 .+-. 132.97 405.67 .+-. 245.16 Postbaseline Mean
(.+-. SD) 354.90 .+-. 111.40 380.42 .+-. 113.20 405.07 .+-. 194.15
Mean Change -55.15 -12.98 1.47 95% CI (-74.80, -35.49) (-35.36,
9.39) (-26.41, 29.35) E-selectin n = 75 n = 68 n = 62 Baseline Mean
(.+-. SD) 68.84 .+-. 34.38 66.75 .+-. 37.10 69.72 .+-. 44.38
Postbaseline Mean (.+-. SD) 58.77 .+-. 26.61 67.58 .+-. 31.50 71.90
.+-. 47.43 Mean Change -10.89 0.83 2.34 95% CI (-15.70, -6.08)
(-5.62, 7.28) (-4.53, 9.20) Serum IL-6 n = 56 n = 47 n = 48 (Normal
Range: 0.3-14.8 pg/mL) Baseline Mean (.+-. SD) 27.68 .+-. 38.56
27.19 .+-. 32.45 17.27 .+-. 22.47 Postbaseline Mean (.+-. SD) 7.64
.+-. 14.21 13.93 .+-. 19.00 17.72 .+-. 29.76 Mean Change -20.88
-12.72 -0.19 95% CI (-31.56, -10.19) (-22.49, -2.94) (-7.55, 7.18)
TNFa n = 61 n = 48 n = 50 (1.2-8.0 pg/mL) Baseline Mean (.+-. SD)
9.71 .+-. 22.80 6.27 .+-. 3.62 10.81 .+-. 21.24 Postbaseline Mean
(.+-. SD) 6.67 .+-. 4.80 7.18 .+-. 8.14 9.36 .+-. 26.43 Mean Change
-3.02 1.08 -1.41 95% CI (-8.70, 2.67) (-1.26, 3.42) (-5.14,
2.33)
[0616] The data are shown graphically for these biomarker/PD
measures, as well as for changes in CRP levels, in FIGS. 81 through
87.
[0617] In order to assess the integrity of the planned analyses,
all subjects who received study medication and discontinued the
study for any reason were considered ACR non-responders at all
scheduled study visits subsequent to discontinuation. Results of
these analyses (Table 21) were consistent with the efficacy results
already presented. The proportion of subjects who received 10 mg/kg
CTLA4Ig and achieved an ACR 20, ACR 50, or ACR 70 response at Day
180 was significantly (p<0.001) higher compared to the
proportion of subjects who received placebo. For the 2 mg/kg
CTLA4Ig group, a significantly (p.ltoreq.0.009) higher proportion
of subjects achieved either an ACR 50 or ACR 70 response.
38TABLE 21 ACR Response at Day 180 (Non-Completer Equals
Non-Responder) CTLA4Ig (BMS-188667) 10 mg/kg 2 mg/kg Placebo (n =
115) (n = 105) (n = 119) ACR 20, n (%) 67 (58.3) 41 (39.0) 38
(31.9) Diff (CI) 26.3 (13.6, 39.1) 7.1 (-5.4, 19.7) N/A p-value
<0.001.sup.a 0.266 N/A ACR 50, n (%) 41 (35.7) 24 (22.9) 12
(10.1) Diff (CI) 25.6 (14.8, 36.3) 12.8 (3.1, 22.4) N/A p-value
<0.001.sup.a 0.009.sup.a N/A ACR 70, n (%) 19 (16.5) 11 (10.5) 2
(1.7) Diff (CI) 14.8 (7.5, 22.2) 8.8 (2.7, 14.9) N/A p-value
<0.001.sup.a 0.005.sup.a N/A Error! Bookmark not defined.
Indicates a statistically significant difference for the comparison
of BMS-188667 vs placebo.
[0618] In addition, all primary efficacy analyses were performed on
the WOCF (worst observation carried forward) data set. ACR
responses based on the WOCF data set were slightly lower than those
reported in Table 13 and were comparable to those presented in
Table 21. These findings confirm the consistency of ACR response
rates in the CTLA4Ig (BMS-188667) treatment groups.
[0619] The dosages of anti-rheumatic concomitant medications were
to be collected to assess the need for these medications at 6 and
12 months; however, the available data were inadequate to perform
these analyses. Only baseline values for mean dose of methotrexate
and systemic (non-topical) corticosteroids are provided.
[0620] Efficacy Conclusions
[0621] CTLA4Ig (BMS-188667) administered at 10 mg/kg (+MTX) had
superior efficacy compared to placebo (+MTX) at Day 180 and Day
360. For the following efficacy parameters, administration of 10
mg/kg CTLA4Ig was significantly better than placebo:
[0622] Primary efficacy variable: ACR20 response at Day 180
(p<0.001)
[0623] ACR50 and ACR70 responses at Day 180 (p<0.001)
[0624] ACR20, ACR50 and ACR70 responses at Day 360
(p.ltoreq.0.003)
[0625] Statistically significant differences in ACR50 and ACR70
responses observed by Day 30 (p=0.039 and p=0.04), statistically
significant differences in all 3 response rates (ACR 20, ACR50 and
ACR70) observed by Day 90; these values remained statistically
significant at every timepoint up to and including Day 360
(p.ltoreq.0.008)
[0626] Proportions of subjects who achieved a Major Clinical
Response (maintenance of an ACR 70 response over a continuous
6-month period) at Day 360 (p=0.008)
[0627] Mean numeric ACR-AUC by Day 360 (p<0.001)
[0628] Mean percentage improvements in each individual ACR
component at Day 180 and Day 360 (p<0.05, 95% CIs did not
include 0)
[0629] Improvements in all four mental and all four physical
domains of the Health Outcomes evaluation (SF-36) at both Day 180
and Day 360 (p<0.05, 95% CIs did not include 0)
[0630] In addition to the above statistically significant
differences, the 10 mg/kg CTLA4Ig group had a lower number of new
active joints and a higher number of subjects reporting no new
active tender and swollen joints compared with the placebo group at
Day 180 and at Day 360.
[0631] Significant improvement with 10 mg/kg CTLA4Ig compared with
placebo was seen in nearly all measured pharmacodynamic paramenters
(soluble IL12r, RF, ICAM-1, E-selectin and IL-6) and numerical
improvement in TNF-.alpha. up to 1 year.
[0632] For the 2 mg/kg CTLA4Ig group, some efficacy parameters were
significantly better compared to the placebo group:
[0633] ACR50 response at Day 180 (p=0.027)
[0634] ACR70 response at Day 180 (p=0.005)
[0635] Statistically significant differences in ACR70 observed by
Day 60 (p=0.032) and statistically significant differences in ACR
50 and ACR 70 at Day 180 (p=0.027 and p=0.005)
[0636] Proportions of subjects who achieved a Major Clinical
Response (maintenance of an ACR 70 response over a continuous
6-month period) at Day 360 (p=0.036)
[0637] Mean percentage improvements in some of the individual ACR
component at Day 180 and Day 360 (p<0.05, 95% CIs did not
include 0)
[0638] For many other efficacy parameters, 2 mg/kg CTLA4Ig was
numerically better than placebo.
[0639] Safety Results
[0640] Overall, the safety profile of CTLA4Ig (BMS-188667) was
similar to placebo. There were no major safety problems.
[0641] Clinical Laboratory Evaluation
[0642] Overall, no new safety issues emerged from the evaluation of
mean changes in laboratory values. Mean values for hemoglobin,
WBCs, neutrophils, platelets, ALT, AST, GGT and total protein were
within the normal range at baseline and remained within the normal
range during the study. In general, results of the laboratory tests
did not reveal consistent out-of range values or abnormal trends
that could be attributed to study medication.
[0643] Vital Signs, Physical Findings, and Observations Related to
Safety
[0644] On each day of study drug administration, vital signs (body
temperature, heart rate, and seated blood pressure) were monitored
pre-dose and at 15, 30, 45, 60, 75, 90 and 120 minutes
post-infusion. Overall, mean values for all vital sign parameters
were within normal range and stable throughout the 360-day study
period for all treatment groups.
Sequence CWU 1
1
22 1 65 DNA Homo sapiens 1 ctcagtctgg tccttgcact cctgtttcca
agcatggcga gcatggcaat gcacgtggcc 60 cagcc 65 2 33 DNA Homo sapiens
2 tttgggctcc tgatcagaat ctgggcacgg ttg 33 3 72 DNA Homo sapiens 3
ctagccactg aagcttcacc aatgggtgta ctgctcacac agaggacgct gctcagtctg
60 gtccttgcac tc 72 4 41 DNA Artificial Oncostatin M CTLA4
(OMCTLA4) forward primer 4 gaggtgataa agcttcacca atgggtgtac
tgctcacaca g 41 5 42 DNA Artificial Oncostatin M CTLA4 (OMCTLA4)
reverse primer 5 gtggtgtatt ggtctagatc aatcagaatc tgggcacggt tc 42
6 1152 DNA Artificial L104EIg 6 atg ggt gta ctg ctc aca cag agg acg
ctg ctc agt ctg gtc ctt gca 48 Met Gly Val Leu Leu Thr Gln Arg Thr
Leu Leu Ser Leu Val Leu Ala -25 -20 -15 ctc ctg ttt cca agc atg gcg
agc atg gca atg cac gtg gcc cag cct 96 Leu Leu Phe Pro Ser Met Ala
Ser Met Ala Met His Val Ala Gln Pro -10 -5 -1 1 5 gct gtg gta ctg
gcc agc agc cga ggc atc gct agc ttt gtg tgt gag 144 Ala Val Val Leu
Ala Ser Ser Arg Gly Ile Ala Ser Phe Val Cys Glu 10 15 20 tat gca
tct cca ggc aaa gcc act gag gtc cgg gtg aca gtg ctt cgg 192 Tyr Ala
Ser Pro Gly Lys Ala Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35
cag gct gac agc cag gtg act gaa gtc tgt gcg gca acc tac atg atg 240
Gln Ala Asp Ser Gln Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40
45 50 ggg aat gag ttg acc ttc cta gat gat tcc atc tgc acg ggc acc
tcc 288 Gly Asn Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr
Ser 55 60 65 70 agt gga aat caa gtg aac ctc act atc caa gga ctg agg
gcc atg gac 336 Ser Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg
Ala Met Asp 75 80 85 acg gga ctc tac atc tgc aag gtg gag ctc atg
tac cca ccg cca tac 384 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met
Tyr Pro Pro Pro Tyr 90 95 100 tac gag ggc ata ggc aac gga acc cag
att tat gta att gat cca gaa 432 Tyr Glu Gly Ile Gly Asn Gly Thr Gln
Ile Tyr Val Ile Asp Pro Glu 105 110 115 ccg tgc cca gat tct gat cag
gag ccc aaa tct tct gac aaa act cac 480 Pro Cys Pro Asp Ser Asp Gln
Glu Pro Lys Ser Ser Asp Lys Thr His 120 125 130 aca tcc cca ccg tcc
cca gca cct gaa ctc ctg ggg gga tcg tca gtc 528 Thr Ser Pro Pro Ser
Pro Ala Pro Glu Leu Leu Gly Gly Ser Ser Val 135 140 145 150 ttc ctc
ttc ccc cca aaa ccc aag gac acc ctc atg atc tcc cgg acc 576 Phe Leu
Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165
cct gag gtc aca tgc gtg gtg gtg gac gtg agc cac gaa gac cct gag 624
Pro Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 170
175 180 gtc aag ttc aac tgg tac gtg gac ggc gtg gag gtg cat aat gcc
aag 672 Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala
Lys 185 190 195 aca aag ccg cgg gag gag cag tac aac agc acg tac cgt
gtg gtc agc 720 Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg
Val Val Ser 200 205 210 gtc ctc acc gtc ctg cac cag gac tgg ctg aat
ggc aag gag tac aag 768 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn
Gly Lys Glu Tyr Lys 215 220 225 230 tgc aag gtc tcc aac aaa gcc ctc
cca gcc ccc atc gag aaa acc atc 816 Cys Lys Val Ser Asn Lys Ala Leu
Pro Ala Pro Ile Glu Lys Thr Ile 235 240 245 tcc aaa gcc aaa ggg cag
ccc cga gaa cca cag gtg tac acc ctg ccc 864 Ser Lys Ala Lys Gly Gln
Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro 250 255 260 cca tcc cgg gat
gag ctg acc aag aac cag gtc agc ctg acc tgc ctg 912 Pro Ser Arg Asp
Glu Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu 265 270 275 gtc aaa
ggc ttc tat ccc agc gac atc gcc gtg gag tgg gag agc aat 960 Val Lys
Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290
ggg cag ccg gag aac aac tac aag acc acg cct ccc gtg ctg gac tcc
1008 Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp
Ser 295 300 305 310 gac ggc tcc ttc ttc ctc tac agc aag ctc acc gtg
gac aag agc agg 1056 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr
Val Asp Lys Ser Arg 315 320 325 tgg cag cag ggg aac gtc ttc tca tgc
tcc gtg atg cat gag gct ctg 1104 Trp Gln Gln Gly Asn Val Phe Ser
Cys Ser Val Met His Glu Ala Leu 330 335 340 cac aac cac tac acg cag
aag agc ctc tcc ctg tct ccg ggt aaa tga 1152 His Asn His Tyr Thr
Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys 345 350 355 7 383 PRT
Artificial L104EIg 7 Met Gly Val Leu Leu Thr Gln Arg Thr Leu Leu
Ser Leu Val Leu Ala -25 -20 -15 Leu Leu Phe Pro Ser Met Ala Ser Met
Ala Met His Val Ala Gln Pro -10 -5 -1 1 5 Ala Val Val Leu Ala Ser
Ser Arg Gly Ile Ala Ser Phe Val Cys Glu 10 15 20 Tyr Ala Ser Pro
Gly Lys Ala Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 Gln Ala
Asp Ser Gln Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45 50
Gly Asn Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser 55
60 65 70 Ser Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala
Met Asp 75 80 85 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr
Pro Pro Pro Tyr 90 95 100 Tyr Glu Gly Ile Gly Asn Gly Thr Gln Ile
Tyr Val Ile Asp Pro Glu 105 110 115 Pro Cys Pro Asp Ser Asp Gln Glu
Pro Lys Ser Ser Asp Lys Thr His 120 125 130 Thr Ser Pro Pro Ser Pro
Ala Pro Glu Leu Leu Gly Gly Ser Ser Val 135 140 145 150 Phe Leu Phe
Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165 Pro
Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 170 175
180 Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
185 190 195 Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val
Val Ser 200 205 210 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly
Lys Glu Tyr Lys 215 220 225 230 Cys Lys Val Ser Asn Lys Ala Leu Pro
Ala Pro Ile Glu Lys Thr Ile 235 240 245 Ser Lys Ala Lys Gly Gln Pro
Arg Glu Pro Gln Val Tyr Thr Leu Pro 250 255 260 Pro Ser Arg Asp Glu
Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu 265 270 275 Val Lys Gly
Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290 Gly
Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 295 300
305 310 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser
Arg 315 320 325 Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His
Glu Ala Leu 330 335 340 His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu
Ser Pro Gly Lys 345 350 355 8 1152 DNA Artificial L104EA29YIg 8 atg
ggt gta ctg ctc aca cag agg acg ctg ctc agt ctg gtc ctt gca 48 Met
Gly Val Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu Val Leu Ala -25 -20
-15 ctc ctg ttt cca agc atg gcg agc atg gca atg cac gtg gcc cag cct
96 Leu Leu Phe Pro Ser Met Ala Ser Met Ala Met His Val Ala Gln Pro
-10 -5 -1 1 5 gct gtg gta ctg gcc agc agc cga ggc atc gct agc ttt
gtg tgt gag 144 Ala Val Val Leu Ala Ser Ser Arg Gly Ile Ala Ser Phe
Val Cys Glu 10 15 20 tat gca tct cca ggc aaa tat act gag gtc cgg
gtg aca gtg ctt cgg 192 Tyr Ala Ser Pro Gly Lys Tyr Thr Glu Val Arg
Val Thr Val Leu Arg 25 30 35 cag gct gac agc cag gtg act gaa gtc
tgt gcg gca acc tac atg atg 240 Gln Ala Asp Ser Gln Val Thr Glu Val
Cys Ala Ala Thr Tyr Met Met 40 45 50 ggg aat gag ttg acc ttc cta
gat gat tcc atc tgc acg ggc acc tcc 288 Gly Asn Glu Leu Thr Phe Leu
Asp Asp Ser Ile Cys Thr Gly Thr Ser 55 60 65 70 agt gga aat caa gtg
aac ctc act atc caa gga ctg agg gcc atg gac 336 Ser Gly Asn Gln Val
Asn Leu Thr Ile Gln Gly Leu Arg Ala Met Asp 75 80 85 acg gga ctc
tac atc tgc aag gtg gag ctc atg tac cca ccg cca tac 384 Thr Gly Leu
Tyr Ile Cys Lys Val Glu Leu Met Tyr Pro Pro Pro Tyr 90 95 100 tac
gag ggc ata ggc aac gga acc cag att tat gta att gat cca gaa 432 Tyr
Glu Gly Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile Asp Pro Glu 105 110
115 ccg tgc cca gat tct gat cag gag ccc aaa tct tct gac aaa act cac
480 Pro Cys Pro Asp Ser Asp Gln Glu Pro Lys Ser Ser Asp Lys Thr His
120 125 130 aca tcc cca ccg tcc cca gca cct gaa ctc ctg ggg gga tcg
tca gtc 528 Thr Ser Pro Pro Ser Pro Ala Pro Glu Leu Leu Gly Gly Ser
Ser Val 135 140 145 150 ttc ctc ttc ccc cca aaa ccc aag gac acc ctc
atg atc tcc cgg acc 576 Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu
Met Ile Ser Arg Thr 155 160 165 cct gag gtc aca tgc gtg gtg gtg gac
gtg agc cac gaa gac cct gag 624 Pro Glu Val Thr Cys Val Val Val Asp
Val Ser His Glu Asp Pro Glu 170 175 180 gtc aag ttc aac tgg tac gtg
gac ggc gtg gag gtg cat aat gcc aag 672 Val Lys Phe Asn Trp Tyr Val
Asp Gly Val Glu Val His Asn Ala Lys 185 190 195 aca aag ccg cgg gag
gag cag tac aac agc acg tac cgt gtg gtc agc 720 Thr Lys Pro Arg Glu
Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser 200 205 210 gtc ctc acc
gtc ctg cac cag gac tgg ctg aat ggc aag gag tac aag 768 Val Leu Thr
Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys 215 220 225 230
tgc aag gtc tcc aac aaa gcc ctc cca gcc ccc atc gag aaa acc atc 816
Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile 235
240 245 tcc aaa gcc aaa ggg cag ccc cga gaa cca cag gtg tac acc ctg
ccc 864 Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu
Pro 250 255 260 cca tcc cgg gat gag ctg acc aag aac cag gtc agc ctg
acc tgc ctg 912 Pro Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu
Thr Cys Leu 265 270 275 gtc aaa ggc ttc tat ccc agc gac atc gcc gtg
gag tgg gag agc aat 960 Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val
Glu Trp Glu Ser Asn 280 285 290 ggg cag ccg gag aac aac tac aag acc
acg cct ccc gtg ctg gac tcc 1008 Gly Gln Pro Glu Asn Asn Tyr Lys
Thr Thr Pro Pro Val Leu Asp Ser 295 300 305 310 gac ggc tcc ttc ttc
ctc tac agc aag ctc acc gtg gac aag agc agg 1056 Asp Gly Ser Phe
Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg 315 320 325 tgg cag
cag ggg aac gtc ttc tca tgc tcc gtg atg cat gag gct ctg 1104 Trp
Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu 330 335
340 cac aac cac tac acg cag aag agc ctc tcc ctg tct ccg ggt aaa tga
1152 His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys
345 350 355 9 383 PRT Artificial L104EA29YIg 9 Met Gly Val Leu Leu
Thr Gln Arg Thr Leu Leu Ser Leu Val Leu Ala -25 -20 -15 Leu Leu Phe
Pro Ser Met Ala Ser Met Ala Met His Val Ala Gln Pro -10 -5 -1 1 5
Ala Val Val Leu Ala Ser Ser Arg Gly Ile Ala Ser Phe Val Cys Glu 10
15 20 Tyr Ala Ser Pro Gly Lys Tyr Thr Glu Val Arg Val Thr Val Leu
Arg 25 30 35 Gln Ala Asp Ser Gln Val Thr Glu Val Cys Ala Ala Thr
Tyr Met Met 40 45 50 Gly Asn Glu Leu Thr Phe Leu Asp Asp Ser Ile
Cys Thr Gly Thr Ser 55 60 65 70 Ser Gly Asn Gln Val Asn Leu Thr Ile
Gln Gly Leu Arg Ala Met Asp 75 80 85 Thr Gly Leu Tyr Ile Cys Lys
Val Glu Leu Met Tyr Pro Pro Pro Tyr 90 95 100 Tyr Glu Gly Ile Gly
Asn Gly Thr Gln Ile Tyr Val Ile Asp Pro Glu 105 110 115 Pro Cys Pro
Asp Ser Asp Gln Glu Pro Lys Ser Ser Asp Lys Thr His 120 125 130 Thr
Ser Pro Pro Ser Pro Ala Pro Glu Leu Leu Gly Gly Ser Ser Val 135 140
145 150 Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg
Thr 155 160 165 Pro Glu Val Thr Cys Val Val Val Asp Val Ser His Glu
Asp Pro Glu 170 175 180 Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu
Val His Asn Ala Lys 185 190 195 Thr Lys Pro Arg Glu Glu Gln Tyr Asn
Ser Thr Tyr Arg Val Val Ser 200 205 210 Val Leu Thr Val Leu His Gln
Asp Trp Leu Asn Gly Lys Glu Tyr Lys 215 220 225 230 Cys Lys Val Ser
Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile 235 240 245 Ser Lys
Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro 250 255 260
Pro Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu 265
270 275 Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser
Asn 280 285 290 Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val
Leu Asp Ser 295 300 305 310 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu
Thr Val Asp Lys Ser Arg 315 320 325 Trp Gln Gln Gly Asn Val Phe Ser
Cys Ser Val Met His Glu Ala Leu 330 335 340 His Asn His Tyr Thr Gln
Lys Ser Leu Ser Leu Ser Pro Gly Lys 345 350 355 10 1152 DNA
Artificial L104EA29LIg 10 atg ggt gta ctg ctc aca cag agg acg ctg
ctc agt ctg gtc ctt gca 48 Met Gly Val Leu Leu Thr Gln Arg Thr Leu
Leu Ser Leu Val Leu Ala -25 -20 -15 ctc ctg ttt cca agc atg gcg agc
atg gca atg cac gtg gcc cag cct 96 Leu Leu Phe Pro Ser Met Ala Ser
Met Ala Met His Val Ala Gln Pro -10 -5 -1 1 5 gct gtg gta ctg gcc
agc agc cga ggc atc gct agc ttt gtg tgt gag 144 Ala Val Val Leu Ala
Ser Ser Arg Gly Ile Ala Ser Phe Val Cys Glu 10 15 20 tat gca tct
cca ggc aaa ttg act gag gtc cgg gtg aca gtg ctt cgg 192 Tyr Ala Ser
Pro Gly Lys Leu Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 cag
gct gac agc cag gtg act gaa gtc tgt gcg gca acc tac atg atg 240 Gln
Ala Asp Ser Gln Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45
50 ggg aat gag ttg acc ttc cta gat gat tcc atc tgc acg ggc acc tcc
288 Gly Asn Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser
55 60 65 70 agt gga aat caa gtg aac ctc act atc caa gga ctg agg gcc
atg gac 336 Ser Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala
Met Asp 75 80 85 acg gga ctc tac atc tgc aag gtg gag ctc atg tac
cca ccg cca tac 384 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr
Pro Pro Pro Tyr 90 95 100 tac gag ggc ata ggc aac gga acc cag att
tat gta att gat cca gaa 432 Tyr Glu Gly Ile Gly Asn Gly Thr Gln Ile
Tyr Val Ile Asp Pro Glu 105 110 115 ccg tgc cca gat tct gat cag gag
ccc aaa tct tct gac aaa act cac 480 Pro Cys Pro Asp Ser Asp Gln Glu
Pro Lys Ser Ser Asp Lys Thr His 120 125 130 aca tcc cca ccg tcc cca
gca cct gaa ctc ctg ggg gga tcg tca gtc 528 Thr Ser Pro Pro Ser Pro
Ala Pro Glu Leu Leu Gly Gly Ser Ser Val 135 140 145 150 ttc ctc ttc
ccc cca aaa ccc aag gac acc ctc atg atc tcc cgg acc 576 Phe Leu Phe
Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165 cct
gag gtc aca tgc gtg gtg gtg gac gtg agc cac gaa gac cct gag 624 Pro
Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 170 175
180
gtc aag ttc aac tgg tac gtg gac ggc gtg gag gtg cat aat gcc aag 672
Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys 185
190 195 aca aag ccg cgg gag gag cag tac aac agc acg tac cgt gtg gtc
agc 720 Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val
Ser 200 205 210 gtc ctc acc gtc ctg cac cag gac tgg ctg aat ggc aag
gag tac aag 768 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys
Glu Tyr Lys 215 220 225 230 tgc aag gtc tcc aac aaa gcc ctc cca gcc
ccc atc gag aaa acc atc 816 Cys Lys Val Ser Asn Lys Ala Leu Pro Ala
Pro Ile Glu Lys Thr Ile 235 240 245 tcc aaa gcc aaa ggg cag ccc cga
gaa cca cag gtg tac acc ctg ccc 864 Ser Lys Ala Lys Gly Gln Pro Arg
Glu Pro Gln Val Tyr Thr Leu Pro 250 255 260 cca tcc cgg gat gag ctg
acc aag aac cag gtc agc ctg acc tgc ctg 912 Pro Ser Arg Asp Glu Leu
Thr Lys Asn Gln Val Ser Leu Thr Cys Leu 265 270 275 gtc aaa ggc ttc
tat ccc agc gac atc gcc gtg gag tgg gag agc aat 960 Val Lys Gly Phe
Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290 ggg cag
ccg gag aac aac tac aag acc acg cct ccc gtg ctg gac tcc 1008 Gly
Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 295 300
305 310 gac ggc tcc ttc ttc ctc tac agc aag ctc acc gtg gac aag agc
agg 1056 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys
Ser Arg 315 320 325 tgg cag cag ggg aac gtc ttc tca tgc tcc gtg atg
cat gag gct ctg 1104 Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val
Met His Glu Ala Leu 330 335 340 cac aac cac tac acg cag aag agc ctc
tcc ctg tct ccg ggt aaa tga 1152 His Asn His Tyr Thr Gln Lys Ser
Leu Ser Leu Ser Pro Gly Lys 345 350 355 11 383 PRT Artificial
L104EA29LIg 11 Met Gly Val Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu
Val Leu Ala -25 -20 -15 Leu Leu Phe Pro Ser Met Ala Ser Met Ala Met
His Val Ala Gln Pro -10 -5 -1 1 5 Ala Val Val Leu Ala Ser Ser Arg
Gly Ile Ala Ser Phe Val Cys Glu 10 15 20 Tyr Ala Ser Pro Gly Lys
Leu Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 Gln Ala Asp Ser
Gln Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45 50 Gly Asn
Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser 55 60 65 70
Ser Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala Met Asp 75
80 85 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr Pro Pro Pro
Tyr 90 95 100 Tyr Glu Gly Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile
Asp Pro Glu 105 110 115 Pro Cys Pro Asp Ser Asp Gln Glu Pro Lys Ser
Ser Asp Lys Thr His 120 125 130 Thr Ser Pro Pro Ser Pro Ala Pro Glu
Leu Leu Gly Gly Ser Ser Val 135 140 145 150 Phe Leu Phe Pro Pro Lys
Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165 Pro Glu Val Thr
Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 170 175 180 Val Lys
Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys 185 190 195
Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser 200
205 210 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr
Lys 215 220 225 230 Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile
Glu Lys Thr Ile 235 240 245 Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro
Gln Val Tyr Thr Leu Pro 250 255 260 Pro Ser Arg Asp Glu Leu Thr Lys
Asn Gln Val Ser Leu Thr Cys Leu 265 270 275 Val Lys Gly Phe Tyr Pro
Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290 Gly Gln Pro Glu
Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 295 300 305 310 Asp
Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg 315 320
325 Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
330 335 340 His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly
Lys 345 350 355 12 1152 DNA Artificial L104EA29TIg 12 atg ggt gta
ctg ctc aca cag agg acg ctg ctc agt ctg gtc ctt gca 48 Met Gly Val
Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu Val Leu Ala -25 -20 -15 ctc
ctg ttt cca agc atg gcg agc atg gca atg cac gtg gcc cag cct 96 Leu
Leu Phe Pro Ser Met Ala Ser Met Ala Met His Val Ala Gln Pro -10 -5
-1 1 5 gct gtg gta ctg gcc agc agc cga ggc atc gct agc ttt gtg tgt
gag 144 Ala Val Val Leu Ala Ser Ser Arg Gly Ile Ala Ser Phe Val Cys
Glu 10 15 20 tat gca tct cca ggc aaa act act gag gtc cgg gtg aca
gtg ctt cgg 192 Tyr Ala Ser Pro Gly Lys Thr Thr Glu Val Arg Val Thr
Val Leu Arg 25 30 35 cag gct gac agc cag gtg act gaa gtc tgt gcg
gca acc tac atg atg 240 Gln Ala Asp Ser Gln Val Thr Glu Val Cys Ala
Ala Thr Tyr Met Met 40 45 50 ggg aat gag ttg acc ttc cta gat gat
tcc atc tgc acg ggc acc tcc 288 Gly Asn Glu Leu Thr Phe Leu Asp Asp
Ser Ile Cys Thr Gly Thr Ser 55 60 65 70 agt gga aat caa gtg aac ctc
act atc caa gga ctg agg gcc atg gac 336 Ser Gly Asn Gln Val Asn Leu
Thr Ile Gln Gly Leu Arg Ala Met Asp 75 80 85 acg gga ctc tac atc
tgc aag gtg gag ctc atg tac cca ccg cca tac 384 Thr Gly Leu Tyr Ile
Cys Lys Val Glu Leu Met Tyr Pro Pro Pro Tyr 90 95 100 tac gag ggc
ata ggc aac gga acc cag att tat gta att gat cca gaa 432 Tyr Glu Gly
Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile Asp Pro Glu 105 110 115 ccg
tgc cca gat tct gat cag gag ccc aaa tct tct gac aaa act cac 480 Pro
Cys Pro Asp Ser Asp Gln Glu Pro Lys Ser Ser Asp Lys Thr His 120 125
130 aca tcc cca ccg tcc cca gca cct gaa ctc ctg ggg gga tcg tca gtc
528 Thr Ser Pro Pro Ser Pro Ala Pro Glu Leu Leu Gly Gly Ser Ser Val
135 140 145 150 ttc ctc ttc ccc cca aaa ccc aag gac acc ctc atg atc
tcc cgg acc 576 Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile
Ser Arg Thr 155 160 165 cct gag gtc aca tgc gtg gtg gtg gac gtg agc
cac gaa gac cct gag 624 Pro Glu Val Thr Cys Val Val Val Asp Val Ser
His Glu Asp Pro Glu 170 175 180 gtc aag ttc aac tgg tac gtg gac ggc
gtg gag gtg cat aat gcc aag 672 Val Lys Phe Asn Trp Tyr Val Asp Gly
Val Glu Val His Asn Ala Lys 185 190 195 aca aag ccg cgg gag gag cag
tac aac agc acg tac cgt gtg gtc agc 720 Thr Lys Pro Arg Glu Glu Gln
Tyr Asn Ser Thr Tyr Arg Val Val Ser 200 205 210 gtc ctc acc gtc ctg
cac cag gac tgg ctg aat ggc aag gag tac aag 768 Val Leu Thr Val Leu
His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys 215 220 225 230 tgc aag
gtc tcc aac aaa gcc ctc cca gcc ccc atc gag aaa acc atc 816 Cys Lys
Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile 235 240 245
tcc aaa gcc aaa ggg cag ccc cga gaa cca cag gtg tac acc ctg ccc 864
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro 250
255 260 cca tcc cgg gat gag ctg acc aag aac cag gtc agc ctg acc tgc
ctg 912 Pro Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu Thr Cys
Leu 265 270 275 gtc aaa ggc ttc tat ccc agc gac atc gcc gtg gag tgg
gag agc aat 960 Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp
Glu Ser Asn 280 285 290 ggg cag ccg gag aac aac tac aag acc acg cct
ccc gtg ctg gac tcc 1008 Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr
Pro Pro Val Leu Asp Ser 295 300 305 310 gac ggc tcc ttc ttc ctc tac
agc aag ctc acc gtg gac aag agc agg 1056 Asp Gly Ser Phe Phe Leu
Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg 315 320 325 tgg cag cag ggg
aac gtc ttc tca tgc tcc gtg atg cat gag gct ctg 1104 Trp Gln Gln
Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu 330 335 340 cac
aac cac tac acg cag aag agc ctc tcc ctg tct ccg ggt aaa tga 1152
His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys 345 350
355 13 383 PRT Artificial L104EA29TIg 13 Met Gly Val Leu Leu Thr
Gln Arg Thr Leu Leu Ser Leu Val Leu Ala -25 -20 -15 Leu Leu Phe Pro
Ser Met Ala Ser Met Ala Met His Val Ala Gln Pro -10 -5 -1 1 5 Ala
Val Val Leu Ala Ser Ser Arg Gly Ile Ala Ser Phe Val Cys Glu 10 15
20 Tyr Ala Ser Pro Gly Lys Thr Thr Glu Val Arg Val Thr Val Leu Arg
25 30 35 Gln Ala Asp Ser Gln Val Thr Glu Val Cys Ala Ala Thr Tyr
Met Met 40 45 50 Gly Asn Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys
Thr Gly Thr Ser 55 60 65 70 Ser Gly Asn Gln Val Asn Leu Thr Ile Gln
Gly Leu Arg Ala Met Asp 75 80 85 Thr Gly Leu Tyr Ile Cys Lys Val
Glu Leu Met Tyr Pro Pro Pro Tyr 90 95 100 Tyr Glu Gly Ile Gly Asn
Gly Thr Gln Ile Tyr Val Ile Asp Pro Glu 105 110 115 Pro Cys Pro Asp
Ser Asp Gln Glu Pro Lys Ser Ser Asp Lys Thr His 120 125 130 Thr Ser
Pro Pro Ser Pro Ala Pro Glu Leu Leu Gly Gly Ser Ser Val 135 140 145
150 Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr
155 160 165 Pro Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp
Pro Glu 170 175 180 Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val
His Asn Ala Lys 185 190 195 Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser
Thr Tyr Arg Val Val Ser 200 205 210 Val Leu Thr Val Leu His Gln Asp
Trp Leu Asn Gly Lys Glu Tyr Lys 215 220 225 230 Cys Lys Val Ser Asn
Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile 235 240 245 Ser Lys Ala
Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro 250 255 260 Pro
Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu 265 270
275 Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn
280 285 290 Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu
Asp Ser 295 300 305 310 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr
Val Asp Lys Ser Arg 315 320 325 Trp Gln Gln Gly Asn Val Phe Ser Cys
Ser Val Met His Glu Ala Leu 330 335 340 His Asn His Tyr Thr Gln Lys
Ser Leu Ser Leu Ser Pro Gly Lys 345 350 355 14 1152 DNA Artificial
L104EA29WIg 14 atg ggt gta ctg ctc aca cag agg acg ctg ctc agt ctg
gtc ctt gca 48 Met Gly Val Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu
Val Leu Ala -25 -20 -15 ctc ctg ttt cca agc atg gcg agc atg gca atg
cac gtg gcc cag cct 96 Leu Leu Phe Pro Ser Met Ala Ser Met Ala Met
His Val Ala Gln Pro -10 -5 -1 1 5 gct gtg gta ctg gcc agc agc cga
ggc atc gct agc ttt gtg tgt gag 144 Ala Val Val Leu Ala Ser Ser Arg
Gly Ile Ala Ser Phe Val Cys Glu 10 15 20 tat gca tct cca ggc aaa
tgg act gag gtc cgg gtg aca gtg ctt cgg 192 Tyr Ala Ser Pro Gly Lys
Trp Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 cag gct gac agc
cag gtg act gaa gtc tgt gcg gca acc tac atg atg 240 Gln Ala Asp Ser
Gln Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45 50 ggg aat
gag ttg acc ttc cta gat gat tcc atc tgc acg ggc acc tcc 288 Gly Asn
Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser 55 60 65 70
agt gga aat caa gtg aac ctc act atc caa gga ctg agg gcc atg gac 336
Ser Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala Met Asp 75
80 85 acg gga ctc tac atc tgc aag gtg gag ctc atg tac cca ccg cca
tac 384 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr Pro Pro Pro
Tyr 90 95 100 tac gag ggc ata ggc aac gga acc cag att tat gta att
gat cca gaa 432 Tyr Glu Gly Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile
Asp Pro Glu 105 110 115 ccg tgc cca gat tct gat cag gag ccc aaa tct
tct gac aaa act cac 480 Pro Cys Pro Asp Ser Asp Gln Glu Pro Lys Ser
Ser Asp Lys Thr His 120 125 130 aca tcc cca ccg tcc cca gca cct gaa
ctc ctg ggg gga tcg tca gtc 528 Thr Ser Pro Pro Ser Pro Ala Pro Glu
Leu Leu Gly Gly Ser Ser Val 135 140 145 150 ttc ctc ttc ccc cca aaa
ccc aag gac acc ctc atg atc tcc cgg acc 576 Phe Leu Phe Pro Pro Lys
Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165 cct gag gtc aca
tgc gtg gtg gtg gac gtg agc cac gaa gac cct gag 624 Pro Glu Val Thr
Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 170 175 180 gtc aag
ttc aac tgg tac gtg gac ggc gtg gag gtg cat aat gcc aag 672 Val Lys
Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys 185 190 195
aca aag ccg cgg gag gag cag tac aac agc acg tac cgt gtg gtc agc 720
Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser 200
205 210 gtc ctc acc gtc ctg cac cag gac tgg ctg aat ggc aag gag tac
aag 768 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr
Lys 215 220 225 230 tgc aag gtc tcc aac aaa gcc ctc cca gcc ccc atc
gag aaa acc atc 816 Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile
Glu Lys Thr Ile 235 240 245 tcc aaa gcc aaa ggg cag ccc cga gaa cca
cag gtg tac acc ctg ccc 864 Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro
Gln Val Tyr Thr Leu Pro 250 255 260 cca tcc cgg gat gag ctg acc aag
aac cag gtc agc ctg acc tgc ctg 912 Pro Ser Arg Asp Glu Leu Thr Lys
Asn Gln Val Ser Leu Thr Cys Leu 265 270 275 gtc aaa ggc ttc tat ccc
agc gac atc gcc gtg gag tgg gag agc aat 960 Val Lys Gly Phe Tyr Pro
Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290 ggg cag ccg gag
aac aac tac aag acc acg cct ccc gtg ctg gac tcc 1008 Gly Gln Pro
Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 295 300 305 310
gac ggc tcc ttc ttc ctc tac agc aag ctc acc gtg gac aag agc agg
1056 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser
Arg 315 320 325 tgg cag cag ggg aac gtc ttc tca tgc tcc gtg atg cat
gag gct ctg 1104 Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met
His Glu Ala Leu 330 335 340 cac aac cac tac acg cag aag agc ctc tcc
ctg tct ccg ggt aaa tga 1152 His Asn His Tyr Thr Gln Lys Ser Leu
Ser Leu Ser Pro Gly Lys 345 350 355 15 383 PRT Artificial
L104EA29WIg 15 Met Gly Val Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu
Val Leu Ala -25 -20 -15 Leu Leu Phe Pro Ser Met Ala Ser Met Ala Met
His Val Ala Gln Pro -10 -5 -1 1 5 Ala Val Val Leu Ala Ser Ser Arg
Gly Ile Ala Ser Phe Val Cys Glu 10 15 20 Tyr Ala Ser Pro Gly Lys
Trp Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 Gln Ala Asp Ser
Gln Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45 50 Gly Asn
Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser 55 60 65 70
Ser Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala Met Asp 75
80 85 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr Pro Pro Pro
Tyr 90 95 100 Tyr Glu Gly Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile
Asp Pro Glu 105 110 115 Pro Cys Pro Asp Ser Asp Gln Glu Pro Lys
Ser
Ser Asp Lys Thr His 120 125 130 Thr Ser Pro Pro Ser Pro Ala Pro Glu
Leu Leu Gly Gly Ser Ser Val 135 140 145 150 Phe Leu Phe Pro Pro Lys
Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165 Pro Glu Val Thr
Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 170 175 180 Val Lys
Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys 185 190 195
Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser 200
205 210 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr
Lys 215 220 225 230 Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile
Glu Lys Thr Ile 235 240 245 Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro
Gln Val Tyr Thr Leu Pro 250 255 260 Pro Ser Arg Asp Glu Leu Thr Lys
Asn Gln Val Ser Leu Thr Cys Leu 265 270 275 Val Lys Gly Phe Tyr Pro
Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290 Gly Gln Pro Glu
Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 295 300 305 310 Asp
Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg 315 320
325 Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu
330 335 340 His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly
Lys 345 350 355 16 636 DNA Homo sapiens CDS (1)..(636) mat_peptide
(79)..() 16 atg ggt gta ctg ctc aca cag agg acg ctg ctc agt ctg gtc
ctt gca 48 Met Gly Val Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu Val
Leu Ala -25 -20 -15 ctc ctg ttt cca agc atg gcg agc atg gca atg cac
gtg gcc cag cct 96 Leu Leu Phe Pro Ser Met Ala Ser Met Ala Met His
Val Ala Gln Pro -10 -5 -1 1 5 gct gtg gta ctg gcc agc agc cga ggc
atc gcc agc ttt gtg tgt gag 144 Ala Val Val Leu Ala Ser Ser Arg Gly
Ile Ala Ser Phe Val Cys Glu 10 15 20 tat gca tct cca ggc aaa gcc
act gag gtc cgg gtg aca gtg ctt cgg 192 Tyr Ala Ser Pro Gly Lys Ala
Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 cag gct gac agc cag
gtg act gaa gtc tgt gcg gca acc tac atg atg 240 Gln Ala Asp Ser Gln
Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45 50 ggg aat gag
ttg acc ttc cta gat gat tcc atc tgc acg ggc acc tcc 288 Gly Asn Glu
Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser 55 60 65 70 agt
gga aat caa gtg aac ctc act atc caa gga ctg agg gcc atg gac 336 Ser
Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala Met Asp 75 80
85 acg gga ctc tac atc tgc aag gtg gag ctc atg tac cca ccg cca tac
384 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr Pro Pro Pro Tyr
90 95 100 tac ctg ggc ata ggc aac gga acc cag att tat gta att gat
cca gaa 432 Tyr Leu Gly Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile Asp
Pro Glu 105 110 115 ccg tgc cca gat tct gac ttc ctc ctc tgg atc ctt
gca gca gtt agt 480 Pro Cys Pro Asp Ser Asp Phe Leu Leu Trp Ile Leu
Ala Ala Val Ser 120 125 130 tcg ggg ttg ttt ttt tat agc ttt ctc ctc
aca gct gtt tct ttg agc 528 Ser Gly Leu Phe Phe Tyr Ser Phe Leu Leu
Thr Ala Val Ser Leu Ser 135 140 145 150 aaa atg cta aag aaa aga agc
cct ctt aca aca ggg gtc tat gtg aaa 576 Lys Met Leu Lys Lys Arg Ser
Pro Leu Thr Thr Gly Val Tyr Val Lys 155 160 165 atg ccc cca aca gag
cca gaa tgt gaa aag caa ttt cag cct tat ttt 624 Met Pro Pro Thr Glu
Pro Glu Cys Glu Lys Gln Phe Gln Pro Tyr Phe 170 175 180 att ccc atc
aat 636 Ile Pro Ile Asn 185 17 212 PRT Homo sapiens 17 Met Gly Val
Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu Val Leu Ala -25 -20 -15 Leu
Leu Phe Pro Ser Met Ala Ser Met Ala Met His Val Ala Gln Pro -10 -5
-1 1 5 Ala Val Val Leu Ala Ser Ser Arg Gly Ile Ala Ser Phe Val Cys
Glu 10 15 20 Tyr Ala Ser Pro Gly Lys Ala Thr Glu Val Arg Val Thr
Val Leu Arg 25 30 35 Gln Ala Asp Ser Gln Val Thr Glu Val Cys Ala
Ala Thr Tyr Met Met 40 45 50 Gly Asn Glu Leu Thr Phe Leu Asp Asp
Ser Ile Cys Thr Gly Thr Ser 55 60 65 70 Ser Gly Asn Gln Val Asn Leu
Thr Ile Gln Gly Leu Arg Ala Met Asp 75 80 85 Thr Gly Leu Tyr Ile
Cys Lys Val Glu Leu Met Tyr Pro Pro Pro Tyr 90 95 100 Tyr Leu Gly
Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile Asp Pro Glu 105 110 115 Pro
Cys Pro Asp Ser Asp Phe Leu Leu Trp Ile Leu Ala Ala Val Ser 120 125
130 Ser Gly Leu Phe Phe Tyr Ser Phe Leu Leu Thr Ala Val Ser Leu Ser
135 140 145 150 Lys Met Leu Lys Lys Arg Ser Pro Leu Thr Thr Gly Val
Tyr Val Lys 155 160 165 Met Pro Pro Thr Glu Pro Glu Cys Glu Lys Gln
Phe Gln Pro Tyr Phe 170 175 180 Ile Pro Ile Asn 185 18 1152 DNA
Artificial CTLA4Ig 18 atg ggt gta ctg ctc aca cag agg acg ctg ctc
agt ctg gtc ctt gca 48 Met Gly Val Leu Leu Thr Gln Arg Thr Leu Leu
Ser Leu Val Leu Ala -25 -20 -15 ctc ctg ttt cca agc atg gcg agc atg
gca atg cac gtg gcc cag cct 96 Leu Leu Phe Pro Ser Met Ala Ser Met
Ala Met His Val Ala Gln Pro -10 -5 -1 1 5 gct gtg gta ctg gcc agc
agc cga ggc atc gct agc ttt gtg tgt gag 144 Ala Val Val Leu Ala Ser
Ser Arg Gly Ile Ala Ser Phe Val Cys Glu 10 15 20 tat gca tct cca
ggc aaa gcc act gag gtc cgg gtg aca gtg ctt cgg 192 Tyr Ala Ser Pro
Gly Lys Ala Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 cag gct
gac agc cag gtg act gaa gtc tgt gcg gca acc tac atg atg 240 Gln Ala
Asp Ser Gln Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45 50
ggg aat gag ttg acc ttc cta gat gat tcc atc tgc acg ggc acc tcc 288
Gly Asn Glu Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser 55
60 65 70 agt gga aat caa gtg aac ctc act atc caa gga ctg agg gcc
atg gac 336 Ser Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala
Met Asp 75 80 85 acg gga ctc tac atc tgc aag gtg gag ctc atg tac
cca ccg cca tac 384 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr
Pro Pro Pro Tyr 90 95 100 tac ctg ggc ata ggc aac gga acc cag att
tat gta att gat cca gaa 432 Tyr Leu Gly Ile Gly Asn Gly Thr Gln Ile
Tyr Val Ile Asp Pro Glu 105 110 115 ccg tgc cca gat tct gat cag gag
ccc aaa tct tct gac aaa act cac 480 Pro Cys Pro Asp Ser Asp Gln Glu
Pro Lys Ser Ser Asp Lys Thr His 120 125 130 aca tcc cca ccg tcc cca
gca cct gaa ctc ctg ggt gga tcg tca gtc 528 Thr Ser Pro Pro Ser Pro
Ala Pro Glu Leu Leu Gly Gly Ser Ser Val 135 140 145 150 ttc ctc ttc
ccc cca aaa ccc aag gac acc ctc atg atc tcc cgg acc 576 Phe Leu Phe
Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165 cct
gag gtc aca tgc gtg gtg gtg gac gtg agc cac gaa gac cct gag 624 Pro
Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu 170 175
180 gtc aag ttc aac tgg tac gtg gac ggc gtg gag gtg cat aat gcc aag
672 Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys
185 190 195 aca aag ccg cgg gag gag cag tac aac agc acg tac cgg gtg
gtc agc 720 Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val
Val Ser 200 205 210 gtc ctc acc gtc ctg cac cag gac tgg ctg aat ggc
aag gag tac aag 768 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly
Lys Glu Tyr Lys 215 220 225 230 tgc aag gtc tcc aac aaa gcc ctc cca
gcc ccc atc gag aaa acc atc 816 Cys Lys Val Ser Asn Lys Ala Leu Pro
Ala Pro Ile Glu Lys Thr Ile 235 240 245 tcc aaa gcc aaa ggg cag ccc
cga gaa cca cag gtg tac acc ctg ccc 864 Ser Lys Ala Lys Gly Gln Pro
Arg Glu Pro Gln Val Tyr Thr Leu Pro 250 255 260 cca tcc cgg gat gag
ctg acc aag aac cag gtc agc ctg acc tgc ctg 912 Pro Ser Arg Asp Glu
Leu Thr Lys Asn Gln Val Ser Leu Thr Cys Leu 265 270 275 gtc aaa ggc
ttc tat ccc agc gac atc gcc gtg gag tgg gag agc aat 960 Val Lys Gly
Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290 ggg
cag ccg gag aac aac tac aag acc acg cct ccc gtg ctg gac tcc 1008
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 295
300 305 310 gac ggc tcc ttc ttc ctc tac agc aag ctc acc gtg gac aag
agc agg 1056 Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp
Lys Ser Arg 315 320 325 tgg cag cag ggg aac gtc ttc tca tgc tcc gtg
atg cat gag gct ctg 1104 Trp Gln Gln Gly Asn Val Phe Ser Cys Ser
Val Met His Glu Ala Leu 330 335 340 cac aac cac tac acg cag aag agc
ctc tcc ctg tct ccg ggt aaa tga 1152 His Asn His Tyr Thr Gln Lys
Ser Leu Ser Leu Ser Pro Gly Lys 345 350 355 19 383 PRT Artificial
CTLA4Ig 19 Met Gly Val Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu Val
Leu Ala -25 -20 -15 Leu Leu Phe Pro Ser Met Ala Ser Met Ala Met His
Val Ala Gln Pro -10 -5 -1 1 5 Ala Val Val Leu Ala Ser Ser Arg Gly
Ile Ala Ser Phe Val Cys Glu 10 15 20 Tyr Ala Ser Pro Gly Lys Ala
Thr Glu Val Arg Val Thr Val Leu Arg 25 30 35 Gln Ala Asp Ser Gln
Val Thr Glu Val Cys Ala Ala Thr Tyr Met Met 40 45 50 Gly Asn Glu
Leu Thr Phe Leu Asp Asp Ser Ile Cys Thr Gly Thr Ser 55 60 65 70 Ser
Gly Asn Gln Val Asn Leu Thr Ile Gln Gly Leu Arg Ala Met Asp 75 80
85 Thr Gly Leu Tyr Ile Cys Lys Val Glu Leu Met Tyr Pro Pro Pro Tyr
90 95 100 Tyr Leu Gly Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile Asp
Pro Glu 105 110 115 Pro Cys Pro Asp Ser Asp Gln Glu Pro Lys Ser Ser
Asp Lys Thr His 120 125 130 Thr Ser Pro Pro Ser Pro Ala Pro Glu Leu
Leu Gly Gly Ser Ser Val 135 140 145 150 Phe Leu Phe Pro Pro Lys Pro
Lys Asp Thr Leu Met Ile Ser Arg Thr 155 160 165 Pro Glu Val Thr Cys
Val Val Val Asp Val Ser His Glu Asp Pro Glu 170 175 180 Val Lys Phe
Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys 185 190 195 Thr
Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser 200 205
210 Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys
215 220 225 230 Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu
Lys Thr Ile 235 240 245 Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln
Val Tyr Thr Leu Pro 250 255 260 Pro Ser Arg Asp Glu Leu Thr Lys Asn
Gln Val Ser Leu Thr Cys Leu 265 270 275 Val Lys Gly Phe Tyr Pro Ser
Asp Ile Ala Val Glu Trp Glu Ser Asn 280 285 290 Gly Gln Pro Glu Asn
Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser 295 300 305 310 Asp Gly
Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg 315 320 325
Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu 330
335 340 His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys
345 350 355 20 6 PRT Artificial MYPPPY amino acid sequence 20 Met
Tyr Pro Pro Pro Tyr 1 5 21 1152 DNA Artificial CTLA4Ig 21 atg ggt
gta ctg ctc aca cag agg acg ctg ctc agt ctg gtc ctt gca 48 Met Gly
Val Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu Val Leu Ala -25 -20 -15
ctc ctg ttt cca agc atg gcg agc atg gca atg cac gtg gcc cag cct 96
Leu Leu Phe Pro Ser Met Ala Ser Met Ala Met His Val Ala Gln Pro -10
-5 -1 1 5 gct gtg gta ctg gcc agc agc cga ggc atc gcc agc ttt gtg
tgt gag 144 Ala Val Val Leu Ala Ser Ser Arg Gly Ile Ala Ser Phe Val
Cys Glu 10 15 20 tat gca tct cca ggc aaa gcc act gag gtc cgg gtg
aca gtg ctt cgg 192 Tyr Ala Ser Pro Gly Lys Ala Thr Glu Val Arg Val
Thr Val Leu Arg 25 30 35 cag gct gac agc cag gtg act gaa gtc tgt
gcg gca acc tac atg atg 240 Gln Ala Asp Ser Gln Val Thr Glu Val Cys
Ala Ala Thr Tyr Met Met 40 45 50 ggg aat gag ttg acc ttc cta gat
gat tcc atc tgc acg ggc acc tcc 288 Gly Asn Glu Leu Thr Phe Leu Asp
Asp Ser Ile Cys Thr Gly Thr Ser 55 60 65 70 agt gga aat caa gtg aac
ctc act atc caa gga ctg agg gcc atg gac 336 Ser Gly Asn Gln Val Asn
Leu Thr Ile Gln Gly Leu Arg Ala Met Asp 75 80 85 acg gga ctc tac
atc tgc aag gtg gag ctc atg tac cca ccg cca tac 384 Thr Gly Leu Tyr
Ile Cys Lys Val Glu Leu Met Tyr Pro Pro Pro Tyr 90 95 100 tac ctg
ggc ata ggc aac gga acc cag att tat gta att gat cca gaa 432 Tyr Leu
Gly Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile Asp Pro Glu 105 110 115
ccg tgc cca gat tct gat cag gag ccc aaa tct tct gac aaa act cac 480
Pro Cys Pro Asp Ser Asp Gln Glu Pro Lys Ser Ser Asp Lys Thr His 120
125 130 aca tcc cca ccg tcc cca gca cct gaa ctc ctg ggg gga tcg tca
gtc 528 Thr Ser Pro Pro Ser Pro Ala Pro Glu Leu Leu Gly Gly Ser Ser
Val 135 140 145 150 ttc ctc ttc ccc cca aaa ccc aag gac acc ctc atg
atc tcc cgg acc 576 Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met
Ile Ser Arg Thr 155 160 165 cct gag gtc aca tgc gtg gtg gtg gac gtg
agc cac gaa gac cct gag 624 Pro Glu Val Thr Cys Val Val Val Asp Val
Ser His Glu Asp Pro Glu 170 175 180 gtc aag ttc aac tgg tac gtg gac
ggc gtg gag gtg cat aat gcc aag 672 Val Lys Phe Asn Trp Tyr Val Asp
Gly Val Glu Val His Asn Ala Lys 185 190 195 aca aag ccg cgg gag gag
cag tac aac agc acg tac cgt gtg gtc agc 720 Thr Lys Pro Arg Glu Glu
Gln Tyr Asn Ser Thr Tyr Arg Val Val Ser 200 205 210 gtc ctc acc gtc
ctg cac cag gac tgg ctg aat ggc aag gag tac aag 768 Val Leu Thr Val
Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys 215 220 225 230 tgc
aag gtc tcc aac aaa gcc ctc cca gcc ccc atc gag aaa acc atc 816 Cys
Lys Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile 235 240
245 tcc aaa gcc aaa ggg cag ccc cga gaa cca cag gtg tac acc ctg ccc
864 Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro
250 255 260 cca tcc cgg gat gag ctg acc aag aac cag gtc agc ctg acc
tgc ctg 912 Pro Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu Thr
Cys Leu 265 270 275 gtc aaa ggc ttc tat ccc agc gac atc gcc gtg gag
tgg gag agc aat 960 Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu
Trp Glu Ser Asn 280 285 290 ggg cag ccg gag aac aac tac aag acc acg
cct ccc gtg ctg gac tcc 1008 Gly Gln Pro Glu Asn Asn Tyr Lys Thr
Thr Pro Pro Val Leu Asp Ser 295 300 305 310 gac ggc tcc ttc ttc ctc
tac agc aag ctc acc gtg gac aag agc agg 1056 Asp Gly Ser Phe Phe
Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg 315 320 325 tgg cag cag
ggg aac gtc ttc tca tgc tcc gtg atg cat gag gct ctg 1104 Trp Gln
Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu 330 335 340
cac aac cac tac acg cag aag agc ctc tcc ctg tct ccg ggt aaa tga
1152 His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys
345 350 355 22 383 PRT Artificial CTLA4Ig 22 Met Gly Val
Leu Leu Thr Gln Arg Thr Leu Leu Ser Leu Val Leu Ala -25 -20 -15 Leu
Leu Phe Pro Ser Met Ala Ser Met Ala Met His Val Ala Gln Pro -10 -5
-1 1 5 Ala Val Val Leu Ala Ser Ser Arg Gly Ile Ala Ser Phe Val Cys
Glu 10 15 20 Tyr Ala Ser Pro Gly Lys Ala Thr Glu Val Arg Val Thr
Val Leu Arg 25 30 35 Gln Ala Asp Ser Gln Val Thr Glu Val Cys Ala
Ala Thr Tyr Met Met 40 45 50 Gly Asn Glu Leu Thr Phe Leu Asp Asp
Ser Ile Cys Thr Gly Thr Ser 55 60 65 70 Ser Gly Asn Gln Val Asn Leu
Thr Ile Gln Gly Leu Arg Ala Met Asp 75 80 85 Thr Gly Leu Tyr Ile
Cys Lys Val Glu Leu Met Tyr Pro Pro Pro Tyr 90 95 100 Tyr Leu Gly
Ile Gly Asn Gly Thr Gln Ile Tyr Val Ile Asp Pro Glu 105 110 115 Pro
Cys Pro Asp Ser Asp Gln Glu Pro Lys Ser Ser Asp Lys Thr His 120 125
130 Thr Ser Pro Pro Ser Pro Ala Pro Glu Leu Leu Gly Gly Ser Ser Val
135 140 145 150 Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile
Ser Arg Thr 155 160 165 Pro Glu Val Thr Cys Val Val Val Asp Val Ser
His Glu Asp Pro Glu 170 175 180 Val Lys Phe Asn Trp Tyr Val Asp Gly
Val Glu Val His Asn Ala Lys 185 190 195 Thr Lys Pro Arg Glu Glu Gln
Tyr Asn Ser Thr Tyr Arg Val Val Ser 200 205 210 Val Leu Thr Val Leu
His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys 215 220 225 230 Cys Lys
Val Ser Asn Lys Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile 235 240 245
Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro 250
255 260 Pro Ser Arg Asp Glu Leu Thr Lys Asn Gln Val Ser Leu Thr Cys
Leu 265 270 275 Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp
Glu Ser Asn 280 285 290 Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro
Pro Val Leu Asp Ser 295 300 305 310 Asp Gly Ser Phe Phe Leu Tyr Ser
Lys Leu Thr Val Asp Lys Ser Arg 315 320 325 Trp Gln Gln Gly Asn Val
Phe Ser Cys Ser Val Met His Glu Ala Leu 330 335 340 His Asn His Tyr
Thr Gln Lys Ser Leu Ser Leu Ser Pro Gly Lys 345 350 355
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