U.S. patent application number 15/926586 was filed with the patent office on 2018-07-26 for non-human animals having a humanized programmed cell death 1 gene.
This patent application is currently assigned to Regeneron Pharmaceuticals, Inc.. The applicant listed for this patent is Regeneron Pharmaceuticals, Inc.. Invention is credited to Elena Burova, Ka-Man Venus Lai, Alexander O. Mujica, Andrew J. Murphy.
Application Number | 20180206462 15/926586 |
Document ID | / |
Family ID | 53546709 |
Filed Date | 2018-07-26 |
United States Patent
Application |
20180206462 |
Kind Code |
A1 |
Burova; Elena ; et
al. |
July 26, 2018 |
NON-HUMAN ANIMALS HAVING A HUMANIZED PROGRAMMED CELL DEATH 1
GENE
Abstract
Non-human animals, and methods and compositions for making and
using the same, are provided, wherein the non-human animals
comprise a humanization of a Programmed cell death 1 (Pdcd1) gene.
The non-human animals may be described, in some embodiments, as
having a genetic modification to an endogenous Pdcd1 gene so that
the non-human animals express a PD-1 polypeptide that includes a
human portion and an endogenous portion (e.g., a non-human
portion).
Inventors: |
Burova; Elena; (Mount Kisco,
NY) ; Mujica; Alexander O.; (Elmsford, NY) ;
Lai; Ka-Man Venus; (Tarrytown, NY) ; Murphy; Andrew
J.; (Croton-on-Hudson, NY) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
US |
|
|
Assignee: |
Regeneron Pharmaceuticals,
Inc.
Tarrytown
NY
|
Family ID: |
53546709 |
Appl. No.: |
15/926586 |
Filed: |
March 20, 2018 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14744592 |
Jun 19, 2015 |
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15926586 |
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62138221 |
Mar 25, 2015 |
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62086518 |
Dec 2, 2014 |
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62014181 |
Jun 19, 2014 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C12Q 1/6886 20130101;
C12Q 2600/106 20130101; A01K 2207/15 20130101; A01K 2227/105
20130101; A01K 2217/05 20130101; C07K 14/435 20130101; C07K 2319/03
20130101; G01N 2500/10 20130101; G01N 2333/57 20130101; A01K
67/0278 20130101; G01N 2333/70503 20130101; C07K 2319/00 20130101;
A61P 35/00 20180101; A01K 2267/0331 20130101; A01K 2217/072
20130101; G01N 33/5038 20130101; A61K 49/0008 20130101; C07K
14/4747 20130101; C07K 16/2803 20130101; C12Q 2600/158 20130101;
C07K 2319/02 20130101 |
International
Class: |
A01K 67/027 20060101
A01K067/027; C12Q 1/6886 20180101 C12Q001/6886; C07K 14/47 20060101
C07K014/47; C07K 16/28 20060101 C07K016/28; G01N 33/50 20060101
G01N033/50; A61K 49/00 20060101 A61K049/00 |
Claims
1. A rodent that expresses a PD-1 polypeptide, which PD-1
polypeptide comprises a human portion and an endogenous
portion.
2. The rodent of claim 1, wherein the PD-1 polypeptide is
translated in a cell of the rodent with a rodent signal
peptide.
3. The rodent of claim 1 or 2, wherein the endogenous portion
comprises an intracellular portion of an endogenous PD-1
polypeptide.
4. The rodent of claim 3, wherein the endogenous portion further
comprises a transmembrane portion of an endogenous PD-1
polypeptide.
5. The rodent of claim 4, wherein the endogenous portion has an
amino acid sequence that is at least 50%, at least 60%, at least
70%, at least 80%, at least 90%, or at least 95% identical to a
corresponding amino acid sequence of a mouse PD-1 polypeptide that
appears in FIG. 8.
6. The rodent of claim 4, wherein the endogenous portion has an
amino acid sequence that is identical to a corresponding amino acid
sequence of a mouse PD-1 polypeptide that appears in FIG. 8.
7. The rodent of any one of claims 1-6, wherein the human portion
comprises amino acids 35-145 of a human PD-1 polypeptide.
8. The rodent of any one of claims 1-6, wherein the human portion
comprises amino acids 27-145 of a human PD-1 polypeptide.
9. The rodent of any one of claims 1-6, wherein the human portion
comprises amino acids 26-169 of a human PD-1 polypeptide.
10. The rodent of any one of claims 1-6, wherein the human portion
comprises an amino acid sequence that is at least 50%, at least
60%, at least 70%, at least 80%, at least 90%, or at least 95%
identical to a corresponding amino acid sequence of a human PD-1
polypeptide that appears in FIG. 8.
11. The rodent of any one of claims 1-6, wherein the human portion
comprises an amino acid sequence that is identical to a
corresponding amino acid sequence of a human PD-1 polypeptide that
appears in FIG. 8.
12. The rodent of any one of the preceding claims, wherein the PD-1
polypeptide, which comprises a human portion and an endogenous
portion, is encoded by an endogenous Pdcd1 gene.
13. The rodent of claim 12, wherein the endogenous Pdcd1 gene
comprises endogenous Pdcd1 exons 1, 4 and 5,
14. The rodent of claim 13, wherein the endogenous Pdcd1 gene
further comprises an endogenous Pdcd1 exon 3 in whole or in
part.
15. A rodent comprising a Pdcd1 gene that comprises an endogenous
portion and a human portion, wherein the endogenous and human
portions are operably linked to a rodent Pdcd1 promoter.
16. The rodent of claim 15, wherein the rodent Pdcd1 promoter is an
endogenous rodent Pdcd1 promoter.
17. The rodent of claim 15 or 16, wherein the endogenous portion
comprises endogenous Pdcd1 exons 1, 4 and 5.
18. The rodent of claim 17, wherein the endogenous portion further
comprises endogenous Pdcd1 exon 3 in whole or in part.
19. The rodent of claim 17 or 18, wherein exons 1, 3 in whole or in
part, 4 and 5 of the endogenous Pdcd1 gene are at least 50%, at
least 60%, at least 70%, at least 80%, at least 90%, or at least
95% identical to the corresponding exons 1, 3 in whole or in part,
4 and 5 of an endogenous Pdcd1 gene that appears in FIG. 8.
20. The rodent of any one of claims 15-19, wherein the human
portion encodes amino acids 26-169 of a human PD-1 polypeptide.
21. The rodent of any one of claims 15-19, wherein the human
portion comprises exon 2 of a human Pdcd1 gene.
22. The rodent of claim 21, wherein the human portion further
comprises a human Pdcd1 exon 3 in whole or in part.
23. The rodent of claim 22, wherein human Pdcd1 exons 2 and 3, in
whole or in part, are at least 50%, at least 60%, at least 70%, at
least 80%, at least 90%, or at least 95% identical to the
corresponding exons 2 and 3, in whole or in part, of a human Pdcd1
gene that appears in FIG. 8.
24. The rodent of claim 22, wherein the human portion comprises a
sequence that is codon-optimized for expression in the rodent.
25. The rodent of claim 22, wherein the human portion comprises SEQ
ID NO: 23,
26. The rodent of any one of claims 1-25, wherein the rodent is a
rat or mouse.
27. A PD-1 polypeptide produced by a rodent of any one of claims
1-26.
28. The PD-1 polypeptide of claim 27, wherein the PD-1 polypeptide
comprises an amino acid sequence that is at least 50%, at least
60%, at least 70%, at least 80%, at least 90%, or at least 95%
identical to a humanized. PD-1 polypeptide that appears in FIG.
8.
29. An isolated rodent cell or tissue whose genome comprises a
Pdcd1 gene that encodes a PD-1 polypeptide having a human portion
and an endogenous portion, which portions are operably linked to a
rodent Pdcd1 promoter.
30. The isolated rodent cell or tissue of claim 29, wherein the
rodent Pdcd1 promoter is an endogenous rodent Pdcd1 promoter.
31. The isolated cell or tissue of claim 29 or 30, wherein the
human portion comprises human Pdcd1 exon 2.
32. The isolated cell or tissue of claim 31, wherein the human
portion further comprises human Pdcd1 exon 3 in whole or in
part.
33. The isolated rodent cell or tissue of any one of claims 29-32,
wherein the rodent cell or tissue is a mouse cell or mouse tissue,
or a rat cell or rat tissue.
34. A rodent embryonic stem cell whose genome comprises a Pdcd1
gene that encodes a PD-1 polypeptide having a human portion and an
endogenous portion, which portions are operably linked to a rodent
Pdcd1 promoter.
35. The rodent embryonic stem cell of claim 34, wherein the rodent
Pdcd1 promoter is an endogenous rodent Pdcd1 promoter.
36. The rodent embryonic stem cell of claim 34 or 35, wherein the
human portion comprises human Pdcd 1 exon 2.
37. The rodent embryonic stem cell of claim 36, wherein the human
portion further comprises human Pdcd1 exon 3 in whole or in
part.
38. The rodent embryonic stem cell of any one of claims 34-37,
wherein the rodent embryonic stem cell is a mouse embryonic stem
cell and is from a 129 strain, C57BL strain, or a mixture
thereof.
39. The rodent embryonic stem cell of claim 38, wherein the rodent
embryonic stem cell is a mouse embryonic stern cell and is a
mixture of 129 and C57BL strains.
40. A rodent embryo generated from the embryonic stem cell of any
one of claims 34-39,
41. A method of making a rodent that expresses a PD-1 polypeptide
from an endogenous Pdcd1 gene, wherein the PD-1 polypeptide
comprises a human sequence, the method comprising (a) inserting a
genomic fragment into an endogenous Pdcd1 gene in a rodent
embryonic stem cell, said genomic fragment comprising a nucleotide
sequence that encodes a human PD-1 polypeptide in whole or in part;
(b) obtaining the rodent embryonic stem cell generated in (a); and,
(c) creating a rodent using the rodent embryonic stem cell of
(b).
42. The method of claim 41, wherein the human sequence comprises
amino acids 35-145 of a human PD-1 polypeptide.
43. The method of claim 41, wherein the human sequence comprises
amino acids 27-145 of a human PD-1 polypeptide.
44. The method of claim 41, wherein the human sequence comprises
amino acids 26-169 of a human PD-1 polypeptide.
45. The method of any one of claims 41-44, wherein the nucleotide
sequence comprises human Pdcd1 exon 2.
46. The method of claim 45, wherein the nucleotide sequence further
comprises human Pdcd1 exon 3 in whole or in part.
47. The method of any one of claims 41-46, wherein the nucleotide
sequence comprises one or more selection markers.
48. The method of any one of claims 41-47, wherein the nucleotide
sequence comprises one or more site-specific recombination
sites.
49. A method of making a rodent whose genome comprises a Pdcd1 gene
that encodes a P1)-1 polypeptide having a human portion and an
endogenous portion, which portions are operably linked to a rodent
Pdcd1 promoter, the method comprising modifying the genome of a
rodent so that it comprises a Pdcd1 gene that encodes a PD-1
polypeptide having a human portion and an endogenous portion, which
portions are operably linked to a rodent Pdcd1 promoter, thereby
making said rodent.
50. The method of claim 49, wherein the rodent Pdcd1 promoter is an
endogenous rodent Pdcd1 promoter.
51. The method of claim 49, wherein the human portion comprises
amino acids 35-145 of a human PD-1 polypeptide.
52. The method of claim 49, wherein the human portion comprises
amino acids 27-145 of a human PD-1 polypeptide.
53. The method of claim 49, wherein the human portion comprises
amino acids 26-169 of a human PD-1 polypeptide.
54. The method of any one of claims 49-53, wherein the Pdcd1 gene
is modified to include human Pdcd1 exon 2.
55. The method of claim 54, wherein the Pdcd1 gene is modified to
include human Pdcd1 exon 2 and human Pdcd1 exon 3 in whole or in
part.
56. The method of any one of claims 41-55, wherein the rodent is a
mouse or rat.
57. A rodent obtainable from the method of any one of claims
41-56.
58. The rodent of claim 57, wherein the rodent is a mouse or a
rat.
59. A method of reducing tumor growth in a rodent, the method
comprising the steps of administering a drug targeting human PD-1
to a rodent whose genome comprises a Pdcd1 gene that encodes a PD-1
polypeptide having a human portion and an endogenous portion, which
portions are operably linked to a rodent Pdcd1 promoter; the
administering being performed under conditions and for a time
sufficient that tumor growth is reduced in the rodent.
60. A method of killing tumor cells in a rodent, the method
comprising the steps of administering a drug targeting human PD-1
to a rodent whose genome comprises a Pdcd1 gene that encodes a PD-1
polypeptide having a human portion and an endogenous portion, which
portions are operably linked to a rodent Pdcd1 promoter; the
administering being performed under conditions and for a time
sufficient that the drug mediates killing of the tumor cells.
61. A method of assessing the pharmacokinetic properties of a drug
targeting human PD-1, the method comprising the steps of
administering the drug to a rodent whose genome comprises a Pdcd1
gene that encodes a PD-1 polypeptide having a human portion and an
endogenous portion, which portions are operably linked to a rodent
Pdcd1 promoter; and performing an assay to determine one or more
pharmacokinetic properties of the drug targeting human PD-1.
62. The method of any one of claims 59-61, wherein the human
portion comprises amino acids 35-145 of a human PD-1
polypeptide.
63. The method of any one of claims 59-61, wherein the human
portion comprises amino acids 27-145 of a human PD-1
polypeptide.
64. The method of any one of claims 59-61, wherein the human
portion comprises amino acids 26-169 of a human PD-1
polypeptide.
65. The method of any one of claims 59-64, wherein the drug
targeting human PD-1 is a PD-1 antagonist.
66. The method of any one of claims 59-64, wherein the drug
targeting human PD-1 is a PD-1 agonist.
67. The method of any one of claims 59-64, wherein the drug
targeting human PD-1 is an anti-PD-1 antibody.
68. The method of any one of claims 59-67, wherein the drug
targeting human PD-1 is administered to the rodent
intravenously.
69. The method of any one of claims 59-67, wherein the drug
targeting human PD-1 is administered to the rodent
intraperitoneally.
70. The method of any one of claims 59-67, wherein the drug
targeting human PD-1 is administered to the rodent
subcutaneously.
71. The method of any one of claims 59-70, wherein the rodent Pdcd1
promoter is an endogenous rodent Pdcd1 promoter.
72. The method of any one of claims 59-71, wherein the rodent is a
mouse or a rat.
73. A rodent tumor model, which rodent expresses a PD-1 polypeptide
comprising a human portion and an endogenous portion.
74. A rodent tumor model, which rodent has a genome comprising a
Pdcd1 gene that comprises an endogenous portion and a human
portion, wherein the endogenous and human portions are operably
linked to a rodent Pdcd1 promoter.
75. A rodent tumor model obtained by a) providing a rodent whose
genome comprises a Pdcd1 gene that includes an endogenous portion
and a human portion, which endogenous and human portions are
operatively linked to a rodent Pdcd1 promoter; and b) implanting
one or more tumor cells in the rodent of (a); thereby providing
said rodent tumor model.
76. The rodent tumor model of any one of claims 73-75, wherein the
rodent is a mouse or a rat.
77. The rodent tumor model of claim 76, wherein the rodent is a
mouse.
78. The rodent tumor model of claim 77, wherein the mouse is
selected from the group consisting of a 129 strain, a C57BL/6
strain, and a mixed 1129.times.C57BL/6 strain.
79. The rodent tumor model of claim 78, wherein the mouse is 25%
129 and 75% C57BL/6.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 14/744,592, filed Jun. 19, 2015, which claims
the benefit of priority of U.S. Provisional Application Nos.
62/138,221 filed Mar. 25, 2015, 62/086,518 filed Dec. 2, 2014 and
62/014,181 filed Jun. 19, 2014, the entire contents of which are
incorporated herein by reference.
INCORPORATION BY REFERENCE OF SEQUENCE LISTING
[0002] The Sequence Listing in an ASCII text file, named
31969_SEQ.txt of 23 KB, created on Jun. 4, 2015, and submitted to
the United States Patent and Trademark Office via EFS-Web, is
incorporated herein by reference.
BACKGROUND
[0003] Although an intense focus of medical research and
development has been devoted to cancer immunotherapy and
significant improvements have been made, cancer remains a major
challenge in the healthcare industry worldwide. This major
challenge is due, in part, to the ability of cancer cells to evade
the monitoring mechanisms of the immune system, which is partly the
result of inhibition and/or down-regulation of anti-tumor immunity.
Still, development of in vivo systems to optimally determine the
therapeutic potential of new cancer therapies that are designed to
activate and/or promote anti-tumor immunity and determine the
molecular aspects of how cancer cells provide inhibitory signals to
immune cells (e.g., T cells) is lacking. Such systems provide a
source for assays for assessing the therapeutic efficacy of
candidate agents that promote an anti-tumor environment in
vivo.
SUMMARY
[0004] The present invention encompasses the recognition that it is
desirable to engineer non-human animals to permit improved systems
for identifying and developing new therapeutics that can be used
for the treatment of cancer. The present invention also encompasess
the recognition that it is desirable to engineer non-human animals
to permit improved systems for identifying and developing new
therapeutics that can be used to treat autoimmune (or inflammatory)
disesases, disorders or conditions. Further, the present invention
also encompasses the recognition that non-human animals having a
humanized Pdcd1 gene and/or otherwise expressing, containing, or
producing a human or humanized PD-1 polypeptide are desirable, for
example for use in identifying and developing cancer therapeutics
that up-regulate anti-tumor immunity. In some embodiments,
non-human animals of the present invention provide improved in vivo
systems for the identification and development of combination
therapies that include targeting PD-1.
[0005] In some embodiments, the present invention provides a
non-human animal having a genome comprising a Pdcd1 gene that
includes genetic material from two different species (e.g., a human
and a non-human). In some embodiments, the Pdcd1 gene of a
non-human animal as described herein encodes a PD-1 polypeptide
that contains human and non-human portions, wherein the human and
non-human portions are linked together and form a functional PD-1
polypeptide. In some embodiments, the Pdcd1 gene of a non-human
animal as described herein encodes a PD-1 polypeptide that contains
an extracellular domain, in whole or in part, of a human PD-1
polypeptide.
[0006] In some embodiments, the present invention provides a
non-human animal that expresses a PD-1 polypeptide, which PD-1
polypeptide comprises a human portion and an endogenous portion. In
some embodiments, a PD-1 polypeptide of the present invention is
translated in a cell of the non-human animal with a non-human
signal peptide; in some certain embodiments, a rodent signal
peptide.
[0007] In some embodiments, an endogenous portion comprises an
intracellular portion of an endogenous PD-1 polypeptide. In some
embodiments, an endogenous portion further comprises a
transmembrane portion of an endogenous PD-1 polypeptide. In some
embodiments, an endogenous portion has an amino acid sequence that
is at least 50%, at least 60%, at least 70%, at least 80%, at least
90%, or at least 95% identical to a corresponding amino acid
sequence of a mouse PD-1 polypeptide that appears in FIG. 8. In
some embodiments, an endogenous portion has an amino acid sequence
that is substantially identical to a corresponding amino acid
sequence of a mouse PD-1 polypeptide that appears in FIG. 8. In
some embodiments, an endogenous portion has an amino acid sequence
that is identical to a corresponding amino acid sequence of a mouse
PD-1 polypeptide that appears in FIG. 8.
[0008] In some embodiments, a human portion comprises amino acids
35-145, 27-145, 27-169, 26-169 or 21-170 of a human PD-1
polypeptide. In some embodiments, a human portion comprises an
amino acid sequence that is at least 50%, at least 60%, at least
70%, at least 80%, at least 90%, or at least 95% identical to a
corresponding amino acid sequence of a human PD-1 polypeptide that
appears in FIG. 8. In some embodiments, a human portion comprises
an amino acid sequence that is substantially identical to a
corresponding amino acid sequence of a human PD-1 polypeptide that
appears in FIG. 8. In some embodiments, a human portion comprises
an amino acid sequence that is identical to a corresponding amino
acid sequence of a human PD-1 polypeptide that appears in FIG.
8.
[0009] In some embodiments, a PD-1 polypeptide, which comprises a
human portion and an endogenous portion, is encoded by an
endogenous Pdcd1 gene. In some certain embodiments, an endogenous
Pdcd1 gene comprises endogenous Pdcd1 exons 1, 4 and 5. In some
certain embodiments, an endogenous Pdcd1 gene further comprises an
endogenous Pdcd1 exon 3 in whole or in part. In some certain
embodiments, an endogenous Pdcd1 gene comprises SEQ ID NO: 21. In
some certain embodiments, an endogenous Pdcd1 gene comprises SEQ ID
NO: 22. In some certain embodiments, an endogenous Pdcd1 gene
comprises SEQ ID NO: 21 and SEQ ID NO: 22.
[0010] In some embodiments, a PD-1 polypeptide expressed by a
non-human animal as described herein has an amino acid sequence
that is at least 50%, at least 60%, at least 70%, at least 80%, at
least 90%, or at least 95% identical to SEQ ID NO: 6. In some
embodiments, a PD-1 polypeptide expressed by a non-human animal as
described herein has an amino acid sequence that is substantially
identical to SEQ ID NO: 6. in some embodiments, a PD-1 polypeptide
expressed by a non-human animal as described herein has an amino
acid sequence that is identical to SEQ ID NO: 6.
[0011] In some embodiments, the present invention provides a
humanized Pdcd1 locus comprising one or more exons of a non-human
Pdcd1 gene operably linked to one or more exons, in whole or in
part, of a human Pdcd1 gene. In some embodiments, a humanized Pdcd1
locus further comprises 5' and 3' non-human Pdcd1 untranslated
regions (UTRs) flanking the one or more exons of a human Pdcd1
gene. In some embodiments, a humanized Pdcd1 locus is under the
control of a rodent promoter; in some certain embodiments, an
endogenous rodent promoter.
[0012] In some embodiments, a humanized Pdcd1 locus comprises
non-human Pdcd1 exons 1, 3, 4 and 5 operably linked to a human
Pdcd1 exon 2. In some embodiments, a humanized Pdcd1 locus
comprises non-human Pdcd1 exons 1, 4 and 5, a human Pdcd1 exon 2
and further comprises a Pdcd1 exon 3, which Pdcd1 exon 3 comprises
a human portion and a non-human portion, and wherein said non-human
and human exons are operably linked. In some embodiments, a human
portion of a Pdcd1 exon 3 includes nucleotides that encode a PD-1
stalk sequence. In some embodiments, a human portion of a Pdcd1
exon 3 includes about 71 by of a human Pdcd1 exon 3. In some
embodiments, a non-human portion of a Pdcd1 exon 3 includes
nucleotides that encode a transmembrane sequence. In some
embodiments, a non-human portion of a Pdcd1 exon 3 includes about
91 bp of a rodent Pdcd1 exon 3.
[0013] In some embodiments, the present invention provides a
non-human animal comprising a Pdcd1 gene that comprises an
endogenous portion and a human portion, where the endogenous and
human portions are operably linked to a rodent Pdcd1 promoter. In
some embodiments, the rodent Pdcd1 promoter is an endogenous rodent
Pdcd1 promoter.
[0014] In some embodiments, an endogenous portion comprises
endogenous Pdcd1 exons 1, 4 and 5. In some embodiments, an
endogenous portion further comprises endogenous Pdcd1 exon 3 in
whole or in part. In some embodiments, exons 1, 3 in whole or in
part, 4 and 5 of an endogenous Pdcd1 gene are at least 50%, at
least 60%, at least 70%, at least 80%, at least 90%, or at least
95% identical to the corresponding exons 1, 3 in whole or in part,
4 and 5 of an endogenous Pdcd1 gene that appears in FIG. 8. In some
embodiments, exons 1, 3 in whole or in part, 4 and 5 of an
endogenous Pdcd1 gene are at substantially identical to the
corresponding exons 1, 3 in whole or in part, 4 and 5 of an
endogenous Pdcd1 gene that appears in FIG. 8. In some embodiments,
exons 1, 3 in whole or in part, 4 and 5 of an endogenous Pdcd1 gene
are at identical to the corresponding exons 1, 3 in whole or in
part, 4 and 5 of an endogenous Pdcd1 gene that appears in FIG.
8.
[0015] In some embodiments, a human portion encodes amino acids
21-170, 26-169, 27-169, 27-145 or 35-145 of a human PD-1
polypeptide.
[0016] In some embodiments, a human portion comprises exon 2 of a
human Pdcd1 gene. In some embodiments, a human portion further
comprises a human Pdcd1 exon 3 in whole or in part. In some
embodiments, human Pdcd1 exons 2 and 3, in whole or in part, are at
least 50%, at least 60%, at least 70%, at least 80%, at least 90%,
or at least 95% identical to the corresponding exons 2 and 3, in
whole or in part, of a human Pdcd1 gene that appears in FIG. 8. In
some embodiments, human Pdcd1 exons 2 and 3, in whole or in part,
are substantially identical to the corresponding exons 2 and 3, in
whole or in part, of a human Pdcd1 gene that appears in FIG. 8. In
some embodiments, human Pdcd1 exons 2 and 3, in whole or in part,
are identical to the corresponding exons 2 and 3, in whole or in
part, of a human Pdcd1 gene that appears in FIG. 8. In some
embodiments, a human portion comprises a sequence that is
codon-optimized for expression in a non-human animal; in some
embodiments, expression in a rodent; in some certain embodiments,
expression in a mouse; in some certain embodiments, expression in a
rat.
[0017] In some embodiments, a human portion comprises a sequence
that is at least 50%, at least 60%, at least 70%, at least 80%, at
least 90%, or at least 95% identical to S. EQ liD NO: 23. In some
embodiments, a human portion comprises a sequence that is
substantially identical to SEQ ID NO: 23. In some embodiments, a
human portion comprises a sequence that is identical to SEQ ID NO:
23. In some embodiments, a human portion comprises SEQ ID NO:
23.
[0018] In some embodiments, the present invention provides a PD-1
polypeptide produced (or generated) by a non-human animal as
described herein. In some certain embodiments, a PD-1 polypeptide
produced by a non-human animal as described herein comprises an
amino acid sequence that is at least 50%, at least 60%, at least
70%, at least 80%, at least 90%, or at least 95% identical to SEQ
ID NO: 6. In some certain embodiments, a PD-1 polypeptide produced
by a non-human animal as described herein comprises an amino acid
sequence that is substantially identical to SEQ ID NO: 6. In some
certain embodiments, a PD-1 polypeptide produced by a non-human
animal as described herein comprises an amino acid sequence that is
identical to SEQ ID NO: 6.
[0019] In some embodiments, the present invention provides an
isolated cell or tissue from a non-human animal as described
herein. In some embodiments, the present invention provides an
isolated cell or tissue that comprises a Pdcd1 gene as described
herein. In some embodiments, a cell is a lymphocyte. In some
embodiments, a cell is selected from a B cell, dendritic cell,
macrophage, monocyte (e.g., an activated monocyte), NK cell, and T
cell (e.g., an activated T cell). In some embodiments, a tissue is
selected from adipose, bladder, brain, breast, bone marrow, eye,
heart, intestine, kidney, liver, lung, lymph node, muscle,
pancreas, plasma, serum, skin, spleen, stomach, thymus, testis,
ovum, and a combination thereof.
[0020] In some embodiments, the present invention provides a
non-human embryonic stem cell whose genome comprises a Pdcd1 gene
as described herein. In some embodiments, a non-human embryonic
stem cell is a mouse embryonic stem cell and is from a 129 strain,
C57BL/6 strain or a BALB/c strain. In some embodiments, a non-human
embryonic stem cell is a mouse embryonic stem cell and is from a
129 strain, C57BL/6 strain or a mixture thereof. In some
embodiments, a non-human embryonic stern cell is a mouse embryonic
stem cell and is from a mixture of 129 and C57BL/6 strains.
[0021] In some embodiments, a non-human embryonic stem cell has a
genome comprising a Pdcd1 gene that comprises SEQ ID NO: 19, SEQ ID
NO: 20, SEQ ID NO: 21, SEQ ID NO: 22 or a combination thereof.
[0022] In some embodiments, the present invention provides the use
of a non-human embryonic stern cell as described herein to make a
non-human animal. In some certain embodiments, a non-human
embryonic stem cell is a mouse embryonic stem cell and is used to
make a mouse comprising a Pdcd1 gene as described herein. In some
certain embodiments, a non-human embryonic stem cell is a rat
embryonic stem cell and is used to make a rat comprising a Pdcd1
gene as described herein.
[0023] In some embodiments, the present invention provides a
non-human embryo comprising, made from, obtained from, or generated
from a non-human embryonic stem cell comprising a Pdcd1 gene as
described herein. In some certain embodiments, a non-human embryo
is a rodent embryo; in some embodiments, a mouse embryo; in some
embodiments, a rat embryo.
[0024] In some embodiments, the present invention provides the use
of a non-human embryo as described herein to make a non-human
animal. In some certain embodiments, a non-human embryo is a mouse
embryo and is used to make a mouse comprising a Pdcd1 gene as
described herein. In some certain embodiments, a non-human embryo
is a rat embryo and is used to make a rat comprising a Pdcd1 gene
as described herein.
[0025] In some embodiments, the present invention provides a
targeting vector (or nucleic acid construct) as described herein.
In some embodiments, the present invention provides a targeting
vector (or nucleic acid construct) that comprises a humanized Pdcd1
gene as described herein. In some embodiments, the present
invention provides a targeting vector (or nucleic acid construct)
that comprises a Pdcd1 gene that encodes a PD-1 polpeptide that
comprises a human extracellular domain in whole or in part; in some
certain embodiments a PD-1 polypeptide that comprises amino acids
21-170, 26-169, 27-169, 27-145 or 35-145 of a human PD-1
polypeptide.
[0026] In some embodiments, a targeting vector (or nucleic acid
construct) comprises one or more exons, in whole or in part, of a
non-human Pdcd1 gene operably linked to one or more exons, in whole
or in part, of a human Pdcd1 gene. In some embodiments, a targeting
vector (or nucleic acid construct) comprises 5' and 3' non-human
Pdcd1 untranslated regions (UTRs) flanking the one or more exons of
a human Pdcd1 gene. In some embodiments, a targeting vector (or
nucleic acid construct) comprises one or more selection markers. In
some embodiments, a targeting vector (or nucleic acid construct)
comprises one or more site-specific recombination sites. In some
embodiments, a targeting vector (or nucleic acid construct)
comprises a human Pdcd1 exon 2. In some embodiments, a targeting
vector (or nucleic acid construct) comprises a human Pdcd1 exon 2
and a human Pdcd1 exon 3 in whole or in part.
[0027] In some embodiments, the present invention provides use of a
targeting vector (or nucleic acid construct) as described herein to
make a modified non-human embryonic stem cell. In some embodiments,
the present invention provides use of a targeting vector (or
nucleic acid construct) as described herein to make a modified
non-human embryo. In some embodiments, the present invention
provides use of a targeting vector (or nucleic acid construct) as
described herein to make a non-human animal.
[0028] In some embodiments, the present invention provides a method
of making a non-human animal that expresses a PD-1 polypeptide from
an endogenous Pdcd1 gene, wherein the PD-1 polypeptide comprises a
human sequence, the method comprising (a) inserting a genomic
fragment into an endogenous Pdcd1 gene in a rodent embryonic stem
cell, said genomic fragment comprising a nucleotide sequence that
encodes a human PD-1 polypeptide in whole or in part; (b) obtaining
the rodent embryonic stem cell generated in (a); and, creating a
rodent using the rodent embryonic stem cell of (b).
[0029] In some embodiments, a human sequence comprises amino acids
35-145, 27-145, 27-169, 26-169 or 21-170 of a human PD-1
polypeptide.
[0030] In some embodiments, a nucleotide sequence comprises human
Pdcd1 exon 2. In some embodiments, a nucleotide sequence further
comprises human Pdcd1 exon 3 in whole or in part. In some
embodiments, a nucleotide sequence comprises one or more selection
markers. In some embodiments, a nucleotide sequence comprises one
or more site-specific recombination sites.
[0031] In some embodiments, the present invention provides a method
of making a non-human animal whose genome comprises a Pdcd1 gene
that encodes a PD-1 polypeptide having a human portion and an
endogenous portion, which portions are operably linked to a rodent
Pdcd1 promoter, the method comprising modifying the genome of a
non-human animal so that it comprises a Pdcd1 gene that encodes a
PD-1 polypeptide having a human portion and an endogenous portion,
which portions are operably linked to a rodent Pdcd1 promoter,
thereby making said non-human animal.
[0032] In some embodiments, a rodent Pdcd1 promoter is an
endogenous rodent Pdcd1 promoter.
[0033] In some embodiments, a human portion comprises amino acids
35-145, 27-145, 27-169, 26-169 or 21-170 of a human PD-1
polypeptide.
[0034] In some embodiments, a Pdcd1 gene is modified to include
human Pdcd1 exon 2. In some embodiments, a Pdcd1 gene is modified
to include human Pdcd1 exon 2 and human Pdcd1 exon 3 in whole or in
part.
[0035] In some embodiments, modifying the genome of a non-human
animal is performed in a non-human embryonic stem cell followed by
generating a non-human animal with said non-human embryonic stem
cell. In some certain embodiments, the non-human embryonic stem
cell is a rodent embryonic stem cell; in some embodiments, a mouse
embryonic stern cell; in some embodiments, a rat embryonic stern
cell.
[0036] In some embodiments, the present invention provides a
non-human animal obtainable by methods as described herein.
[0037] In some embodiments, the present invention provides a method
of reducing tumor growth in a non-human animal, the method
comprising the steps of administering a drug targeting human PD-1
to a non-human animal whose genome comprises a Pdcd1 gene that
encodes a PD-1 polypeptide having a human portion and an endogenous
portion, which portions are operably linked to a rodent Pdcd1
promoter; the administering being performed under conditions and
for a time sufficient that tumor growth is reduced in the non-human
animal.
[0038] In some embodiments, the present invention provides a method
of killing tumor cells in a non-human animal, the method comprising
the steps of administering a drug targeting human PD-1 to a
non-human animal whose genome comprises a Pdcd1 gene that encodes a
PD-1 polypeptide having a human portion and an endogenous portion,
which portions are operably linked to a rodent Pdcd1 promoter; the
administering being performed under conditions and for a time
sufficient that the drug mediates killing of the tumor cells in the
non-human animal.
[0039] In some embodiments, the present invention provides a method
of assessing the pharmacokinetic properties of a drug targeting
human PIM, the method comprising the steps of administering the
drug to a non-human animal whose genome comprises a Pdcd1 gene that
encodes a PD-1 polypeptide having a human portion and an endogenous
portion, which portions are operably linked a rodent Pdcd1
promoter; and performing an assay to determine one or more
pharmacokinetic properties of the drug targeting human PD-1.
[0040] In many embodiments, a non-human animal as described herein
is a rodent whose genome includes a Pdcd1 gene that encodes a PD-1
polypeptide having a human portion and an endogenous portion, which
portions are operably linked to a rodent Pdcd1 promoter. In many
embodiments, a rodent Pdcd1 promoter is an endogenous rodent Pdcd1
promoter. In many embodiments, a human portion comprises amino
acids 35-145, 27-145.sub.; 27-169, 26-169 or 21-170 of a human PD-1
polypeptide.
[0041] In some embodiments, a drug targeting human PD-1 is a PD-1
antagonist. In some embodiments, a drug targeting human PD-1 is a
PD-1 agonist. In some embodiments, a drug targeting human PD-1 is
an anti-PD-1 antibody. In some embodiments, a drug targeting human
PD-1 is administered intravenously, intraperitoneally, or
subcutaneously.
[0042] In some embodiments, the present invention provides a
non-human animal tumor model, which non-human animal expresses a
PD-1 polypeptide comprising a human portion and an endogenous
portion.
[0043] In some embodiments, the present invention provides a
non-human animal tumor model, which non-human animal has a genome
comprising a Pdcd1 gene that comprises an endogenous portion and a
human portion, wherein the endogenous and human portions are
operably linked to a non-human animal Pdcd1 promoter.
[0044] In some embodiments, the present invention provides a
non-human animal tumor model obtained by (a) providing a non-human
animal whose genome comprises a Pdcd1 gene that includes an
endogenous portion and a human portion, which endogenous and human
portions are operatively linked to a non-human animal Pdcd1
promoter; and (b) implanting one or more tumor cells in the rodent
of (a); thereby providing said non-human animal tumor model.
[0045] In some embodiments, a non-human animal tumor model of the
present invention is a rodent tumor model. In some embodiments, a
non-human animal Pdcd1 promoter is a rodent Pdcd1 promoter.
[0046] In some embodiments, the present invention provides a method
for identification or validation of a drug or vaccine, the method
comprising the steps of delivering a drug or vaccine to a non-human
animal whose genome includes a Pdcd1 gene that encodes a PD-1
polypeptide, which PD-1 polypeptide comprises a human portion and
an endogenous portion, and monitoring one or more of the immune
response to the drug or vaccine, the safety profile of the drug or
vaccine, or the effect on a disease, disorder or condition. In some
embodiments, monitoring the safety profile includes determining if
the non-human animal exhibits a side effect or adverse reaction as
a result of delivering the drug or vaccine. In some embodiments, a
side effect or adverse reaction is selected from morbidity,
mortality, alteration in body weight, alteration of the level of
one or more enzymes (e.g., liver), alteration in the weight of one
or more organs, loss of function (e.g., sensory, motor, organ,
etc.), increased susceptibility to one or more diseases,
alterations to the genome of the non-human animal, increase or
decrease in food consumption and complications of one or more
diseases. In some embodiments, the disease, disorder or condition
is induced in the non-human animal. In some embodiments, the
disease, disorder or condition induced in the non-human animal is
associated with a disease, disorder or condition suffered by one or
more human patients in need of treatment. In some certain
embodiments, the drug is an antibody.
[0047] In some embodiments, the present invention provides use of a
non-human animal as described herein in the development of a drug
or vaccine for use in medicine, such as use as a medicament.
[0048] In some embodiments, the present invention provides use of a
non-human animal as described herein in the manufacture of a
medicament for the treatment of cancer, neoplasm, an infectious
disease, an inflammatory disease, disorder or condition, or an
autoimmune disease, disorder or condition.
[0049] In various embodiments, a Pdcd1 gene of the present
invention includes a Pdcd1 gene as described herein. In various
embodiments, a Pdcd1 gene of the present invention encodes a PD-1
polypeptide having a human portion and an endogous portion, which
portions are operably linked to a rodent Pdcd1 promoter. In various
embodiments, a rodent promoter is an endogenous rodent promoter. In
various embodiments, a human portion comprises a human Pdcd1 exon
2. In various embodiments, a human portion comprises a human Pdcd1
exon 2 and further comprises a human Pdcd1 exon 3 in whole or in
part.
[0050] In various embodiments, a PD-1 polypeptide of the present
invention includes a PD-1 polypeptide as described herein. In
various embodiments, a non-human animal of the present invention
does not detectably express a full-length endogenous non-human PD-1
polypeptide. In various embodiments, a non-human animal of the
present invention does not detectably express an extracellular
portion of an endogenous PD-1 polypeptide. In various embodiments,
a non-human animal of the present invention does not detectably
express an N-terminal immunoglobulin V domain of an endogenous PD-1
polypeptide.
[0051] In various embodiments, a non-human animal of the present
invention is a rodent; in some embodiments, a mouse; in some
embodiments, a rat. In some embodiments, a mouse of the present
invention is selected from the group consisting of a 129 strain, a
BALB/C strain, a C57BL/6 strain, and a mixed 129.times.C57BL/6
strain; in some certain embodiments, 50% 129 and 50% C57BL/6; in
some certain embodiments, 25% 129 and 75% C57BL/6.
[0052] As used in this application, the terms "about" and
"approximately" are used as equivalents. Any numerals used in this
application with or without about/approximately are meant to cover
any normal fluctuations appreciated by one of ordinary skill in the
relevant art.
[0053] Other features, objects, and advantages of the present
invention are apparent in the detailed description of certain
embodiments that follows. It should be understood, however, that
the detailed description, while indicating certain embodiments of
the present invention, is given by way of illustration only, not
limitation. Various changes and modifications within the scope of
the invention will become apparent to those skilled in the art from
the detailed description.
BRIEF DESCRIPTION OF THE DRAWING
[0054] The Drawing included herein, which is composed of the
following Figures, is for illustration purposes only and not for
limitation.
[0055] FIG. 1 shows a diagram, not to scale, of the genomic
organization of a non-human (e.g., mouse) and human Programmed cell
death 1 (Pdcd1) genes. Exons and untranslated regions (UTRs) are
numbered beneath each exon and above each UTR.
[0056] FIG. 2 shows a diagram, not to scale, of an exemplary method
for humanization of a non-human Programmed cell death 1 (Pdcd1)
gene. Selected nucleotide junction locations are marked with a line
below each junction. Sequences of these selected nucleotide
junctions are indicated by SEQ ID NOs.
[0057] FIG. 3 shows a diagram, not to scale, of the genomic
organization of a mouse and human Programmed cell death 1 (Pdcd1)
genes indicating the approximate locations of probes used in an
assay described in Example 1.
[0058] FIG. 4 shows exemplary histograms of T cells gated on CD19
and. CD8 isolated from a wild-type mouse and a mouse heterozygous
for humanization of an endogenous Pdcd1 gene as described in
Example 1 that express mouse and/or humanized PD-1. Stimulated and
unstimulated cell populations are indicated, as are cells stained
with an isotype control.
[0059] FIG. 5 shows exemplary tumor growth curves over 21 days in
mice homozygous for humanization of an endogenous Pdcd1 gene as
described in Example 1. Control: antibody not specific for PD-1 ,
a-hPD-1 Ab: antibody specific for human PD-1. Arrows indicate the
days for antibody treatment. The number of tumor-free mice on day
21 is shown for each treatment group.
[0060] FIG. 6 shows exemplary real-time PCR analysis of CD8b, CD3,
DN-g and PD-1 mRNA expression in spleens in mice homozygous for
humanization of an endogenous Pdcd1 gene as described in Example 1
after treatment with anti-PD-1 antibody. A, mean of five mice per
group. B, expression levels for individual mice in each treatment
group. Control: antibody not specific for PD-1; a-PD-1: anti-PD-1
antibody.
[0061] FIG. 7 shows exemplary tumor growth curves over 60 days in
mice homozygous for humanization of an endogenous Pdcd1 gene as
described in Example 1 that were administered 0.3-25 mg/kg of
anti-hPD-1 antibody or 25 mg/kg of control antibody antibody not
specific for PD-1). Arrows indicate the days of antibody treatment.
The number of tumor-free mice on day 60 is shown for each treatment
group.
[0062] FIG. 8 sets forth exemplary murine, human and humanized
Pdcd1 and PD-1 sequences, and an exemplary human nucleic acid
sequence for humanization of a non-human Pdcd1 gene. For mRNA
sequences, bold font indicates coding sequence and consecutive
exons, where indicated, are separated by alternating underlined
text; for humanized mRNA sequences, human sequences are contained
within parentheses. For protein sequences, signal peptides are
underlined, extracellular sequences are bold font, immunoglobulin V
domain sequences are within parentheses, and intracellular
sequences are italicized; and for humanized protein sequences,
non-human sequences are indicated in regular font, and human
sequences are indicated in bold font.
DEFINITIONS
[0063] This invention is not limited to particular methods and
experimental conditions described herein, as such methods and
conditions may vary. It is also to be understood that the
terminology used herein is for the purpose of describing particular
embodiments only, and is not intended to be limiting, since the
scope of the present invention is defined by the claims.
[0064] Unless defined otherwise, all terms and phrases used herein
include the meanings that the terms and phrases have attained in
the art, unless the contrary is clearly indicated or clearly
apparent from the context in which the term or phrase is used.
Although any methods and materials similar or equivalent to those
described herein can be used in the practice or testing of the
present invention, particular methods and materials are now
described. All publications mentioned herein are hereby
incorporated by reference.
[0065] The term "approximately", as applied herein to one or more
values of interest, refers to a value that is similar to a stated
reference value. In certain embodiments, the term "approximately"
or "about" refers to a range of values that fall within 25%, 20%,
19%, 18%, 17%, 16%, 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%,
5%, 4%, 3%, 2%, 1%, or less in either direction (greater than or
less than) of the stated reference value unless otherwise stated or
otherwise evident from the context (except where such number would
exceed 100% of a possible value).
[0066] The term "biologically active" includes a characteristic of
any agent that has activity in a biological system, in vitro or in
vivo (e.g., in an organism). For instance, an agent that, when
present in an organism, has a biological effect within that
organism, is considered to be biologically active. In particular
embodiments, where a protein or polypeptide is biologically active,
a portion of that protein or polypeptide that shares at least one
biological activity of the protein or polypeptide is typically
referred to as a "biologically active" portion.
[0067] The term "comparable" includes to two or more agents,
entities, situations, sets of conditions, etc. that may not be
identical to one another but that are sufficiently similar to
permit comparison between them so that conclusions may reasonably
be drawn based on differences or similarities observed. Those of
ordinary skill in the art will understand, in context, what degree
of identity is required in any given circumstance for two or more
such agents, entities, situations, sets of conditions, etc. to be
considered comparable.
[0068] The term "conservative", e.g., as in a conservative amino
acid substitution, includes substitution of an amino acid residue
by another amino acid residue having a side chain R group with
similar chemical properties (e.g., charge or hydrophobicity). In
general, a conservative amino acid substitution will not
substantially change the functional properties of interest of a
protein, for example, the ability of a receptor to bind to a
ligand. Examples of groups of amino acids that have side chains
with similar chemical properties include: aliphatic side chains
such as glycine, alanine, valine, leucine, and isoleucine;
aliphatic-hydroxyl side chains such as serine and threonine;
amide-containing side chains such as asparagine and glutamine;
aromatic side chains such as phenylalanine, tyrosine, and
tryptophan; basic side chains such as lysine, arginine, and
histidine; acidic side chains such as aspartic acid and glutamic
acid; and, sulfur-containing side chains such as cysteine and
methionine. Conservative amino acids substitution groups include,
for example, valine/leucine/isoleucine, phenyl alanine/tyrosine,
lysine/arginine, alanine/valine, glutamate/aspartate, and
asparagine/glutamine. In some embodiments, a conservative amino
acid substitution can be a substitution of any native residue in a
protein with alanine, as used in, for example, alanine scanning
mutagenesis. In some embodiments, a conservative substitution is
made that has a positive value in the PAM250 log-likelihood matrix
disclosed in Gonnet et al. (1992) Exhaustive Matching of the Entire
Protein Sequence Database, Science 256:1443-45, hereby incorporated
by reference. In some embodiments, the substitution is a moderately
conservative substitution wherein the substitution has a
nonnegative value in the PAM250 log-likelihood matrix.
[0069] The term "control" includes the art-understood meaning of a
"control" being a standard against which results are compared.
Typically, controls are used to augment integrity in experiments by
isolating variables in order to make a conclusion about such
variables. In some embodiments, a control is a reaction or assay
that is performed simultaneously with a test reaction or assay to
provide a comparator. As used herein, a "control" may include a
"control animal". A "control animal" may have a modification as
described herein, a modification that is different as described
herein, or no modification (i.e., a wild-type animal). In one
experiment, the "test" (i.e., the variable being tested) is
applied. In the second experiment, the "control," the variable
being tested is not applied. In some embodiments, a control is a
historical control (i.e., of a test or assay performed previously,
or an amount or result that is previously known). In some
embodiments, a control is or comprises a printed or otherwise saved
record. A control may be a positive control or a negative
control.
[0070] The term "disruption" includes the result of a homologous
recombination event with a DNA molecule (e.g., with an endogenous
homologous sequence such as a gene or gene locus). In some
embodiments, a disruption may achieve or represent an insertion,
deletion, substitution, replacement, missense mutation, or a
frame-shift of a DNA sequence(s), or any combination thereof.
Insertions may include the insertion of entire genes or fragments
of genes, e.g., exons, which may be of an origin other than the
endogenous sequence (e.g., a heterologous sequence). In some
embodiments, a disruption may increase expression and/or activity
of a gene or gene product (e.g., of a protein encoded by a gene).
In some embodiments, a disruption may decrease expression and/or
activity of a gene or gene product. In some embodiments, a
disruption may alter sequence of a gene or an encoded gene product
(e.g., an encoded protein). In some embodiments, a disruption may
truncate or fragment a gene or an encoded gene product (e.g., an
encoded protein). In some embodiments, a disruption may extend a
gene or an encoded gene product; in some such embodiments, a
disruption may achieve assembly of a fusion protein. In some
embodiments, a disruption may affect level but not activity of a
gene or gene product. In some embodiments, a disruption may affect
activity but not level of a gene or gene product. In some
embodiments, a disruption may have no significant effect on level
of a gene or gene product. In some embodiments, a disruption may
have no significant effect on activity of a gene or gene product.
In some embodiments, a disruption may have no significant effect on
either level or activity of a gene or gene product.
[0071] The terms "determining", "measuring", "evaluating",
"assessing", "assaying" and "analyzing" are used interchangeably to
refer to any form of measurement, and include determining if an
element is present or not. These terms include both quantitative
and/or qualitative determinations. Assaying may be relative or
absolute. "Assaying for the presence of" can be determining the
amount of something present and/or determining whether or not it is
present or absent.
[0072] The term "dosing regimen" or "therapeutic regimen" includes
a set of unit doses, in some embodiments, more than one, that are
administered individually to a subject, typically separated by
periods of time. In some embodiments, a given therapeutic agent has
a recommended dosing regiment, which may involve one or more doses.
In some embodiments, a dosing regimen comprises a plurality of
doses each of which are separated from one another by a time period
of the same length; in some embodiments, a dosing regimen comprises
a plurality of doses and at least two different time periods
separating individual doses.
[0073] The phrase "endogenous locus" or "endogenous gene" includes
a genetic locus found in a parent or reference organism. In some
embodiments, the endogenous locus has a sequence found in nature.
In some embodiments, the endogenous locus is a wild type locus. In
some embodiments, the reference organism is a wild-type organism.
In some embodiments, the reference organism is an engineered
organism. In some embodiments, the reference organism is a
laboratory-bred organism (whether wild-type or engineered).
[0074] The phrase "endogenous promoter" includes a promoter that is
naturally associated, e.g., in a wild-type organism, with an
endogenous gene.
[0075] The term "heterologous" includes an agent or entity from a
different source. For example, when used in reference to a
polypeptide, gene, or gene product or present in a particular cell
or organism, the term clarifies that the relevant polypeptide,
gene, or gene product: 1) was engineered by the hand of man; 2) was
introduced into the cell or organism (or a precursor thereof)
through the hand of man (e.g., via genetic engineering); and/or 3)
is not naturally produced by or present in the relevant cell or
organism (e.g., the relevant cell type or organism type).
[0076] The term "host cell" includes a cell into which a
heterologous (e.g., exogenous) nucleic acid or protein has been
introduced. Persons of skill upon reading this disclosure will
understand that such terms refer not only to the particular subject
cell, but also is used to refer to the progeny of such a cell.
Because certain modifications may occur in succeeding generations
due to either mutation or environmental influences, such progeny
may not, in fact, be identical to the parent cell, but are still
included within the scope of the term "host cell". In some
embodiments, a host cell is or comprises a prokaryotic or
eukaryotic cell. In general, a host cell is any cell that is
suitable for receiving and/or producing a heterologous nucleic acid
or protein, regardless of the Kingdom of life to which the cell is
designated. Exemplary cells include those of prokaryotes and
eukaryotes (single-cell or multiple-cell), bacterial cells (e.g.,
strains of E. coli, Bacillus spp., Streptomyces spp., etc.),
mycobacteria cells, fungal cells, yeast cells (e.g., S. cerevisiae,
S. pombe, P. pastoris, P. methanolica, etc.), plant cells, insect
cells (e.g., SF-9, SF-21, baculovirus-infected insect cells,
Trichoplusia ni, etc.), non-human animal cells, human cells, or
cell fusions such as, for example, hybridomas or quadromas. In some
embodiments, the cell is a human, monkey, ape, hamster, rat, or
mouse cell. In some embodiments, the cell is eukaryotic and is
selected from the following cells: CHO (e.g., CHO K1, DXB-11 CHO,
Veggie-CHO), COS (e.g., COS-7), retinal cell, Vero, CV1, kidney
(e.g., HEK293, 293 EBNA, MSR 293, MDCK, HaK, BHK), HeLa, HepG2,
WI38, MRC 5, Colo205, HB 8065, HL-60, (e.g., BHK21), Jurkat, Daudi,
A431 (epidermal), CV-1, U937, 3T3, L cell, C127 cell, SP2/0, NS-0,
MMT 060562, Sertoli cell, BRL 3A cell, HT1080 cell, myeloma cell,
tumor cell, and a cell line derived from an aforementioned cell. In
some embodiments, the cell comprises one or more viral genes, e.g.,
a retinal cell that expresses a viral gene (e.g., a PER.C6.TM.
cell). In some embodiments, a host cell is or comprises an isolated
cell. In some embodiments, a host cell is part of a tissue. In some
embodiments, a host cell is part of an organism.
[0077] The term "humanized" includes nucleic acids or proteins
whose structures (i.e., nucleotide or amino acid sequences) include
portions that correspond substantially or identically with
structures of a particular gene or protein found in nature in a
non-human animal, and also include portions that differ from that
found in the relevant particular non-human gene or protein and
instead correspond more closely with comparable structures found in
a corresponding human gene or protein. In some embodiments, a
"humanized" gene is one that encodes a polypeptide having
substantially the amino acid sequence as that of a human
polypeptide (e.g., a human protein or portion thereof e.g.,
characteristic portion thereof). To give but one example, in the
case of a membrane receptor, a "humanized" gene may encode a
polypeptide having an extracellular portion, in whole or in part,
having an amino acid sequence as that of a human extracellular
portion and the remaining sequence as that of a non-human (e.g.,
mouse) polypeptide. In some embodiments, a humanized gene comprises
at least a portion of a DNA sequence of a human gene. In some
embodiment, a humanized gene comprises an entire DNA sequence of a
human gene. In some embodiments, a humanized protein comprises a
sequence having a portion that appears in a human protein. In some
embodiments, a humanized protein comprises an entire sequence of a
human protein and is expressed from an endogenous locus of a
non-human animal that corresponds to the homolog or ortholog of the
human gene.
[0078] The term "identity", e.g., as in connection with a
comparison of sequences, includes identity as determined by a
number of different algorithms known in the art that can be used to
measure nucleotide and/or amino acid sequence identity. In some
embodiments, identities as described herein are determined using a
ClustalW v. 1.83 (slow) alignment employing an open gap penalty of
10.0, an extend gap penalty of 0.1, and using a Gonnet similarity
matrix (MACVECTOR.TM. MacVector Inc., 2008).
[0079] The term "isolated" includes a substance and/or entity that
has been (1) separated from at least some of the components with
which it was associated when initially produced (whether in nature
and/or in an experimental setting), and/or (2) designed, produced,
prepared, and/or manufactured by the hand of man. Isolated
substances and/or entities may he separated from about 10%, about
20%, about 30%, about 40%, about 50%, about 60%, about 70%, about
80%, about 90%, about 91%, about 92%, about 93%, about 94%, about
95%, about 96%, about 97%, about 98%, about 99%, or more than about
99% of the other components with which they were initially
associated. In some embodiments, isolated agents are about 80%,
about 85%, about 90%, about 91%, about 92%, about 93%, about 94%,
about 95%, about 96%, about 97%, about 98%, about 99%, or more than
about 99% pure. A substance is "pure" if it is substantially free
of other components. In some embodiments, as will be understood by
those skilled in the art, a substance may still be considered
"isolated" or even "pure", after having been combined with certain
other components such as, for example, one or more carriers or
excipients (e.g., buffer, solvent, water, etc.); in such
embodiments, percent isolation or purity of the substance is
calculated without including such carriers or excipients. To give
but one example, in some embodiments, a biological polymer such as
a polypeptide or polynucleotide that occurs in nature is considered
to be "isolated" when: a) by virtue of its origin or source of
derivation is not associated with some or all of the components
that accompany it in its native state in nature; b) it is
substantially free of other polypeptides or nucleic acids of the
same species from the species that produces it in nature; or c) is
expressed by or is otherwise in association with components from a
cell or other expression system that is not of the species that
produces it in nature. Thus, for instance, in some embodiments, a
polypeptide that is chemically synthesized or is synthesized in a
cellular system different from that which produces it in nature is
considered to be an "isolated" polypeptide. Alternatively or
additionally, in some embodiments, a polypeptide that has been
subjected to one or more purification techniques may be considered
to be an "isolated" polypeptide to the extent that it has been
separated from other components: a) with which it is associated in
nature; and/or b) with which it was associated when initially
produced.
[0080] The phrase "non-human animal" includes any vertebrate
organism that is not a human. In some embodiments, a non-human
animal is a cyclostome, a bony fish, a cartilaginous fish (e.g., a
shark or a ray), an amphibian, a reptile, a mammal, and a bird. In
some embodiments, a non-human mammal is a primate, a goat, a sheep,
a pig, a dog, a cow, or a rodent. In some embodiments, a non-human
animal is a rodent such as a rat or a mouse.
[0081] The phrase "nucleic acid" includes any compound and/or
substance that is or can be incorporated into an oligonucleotide
chain. In some embodiments, a "nucleic acid" is a compound and/or
substance that is or can be incorporated into an oligonucleotide
chain via a phosphodiester linkage. As will be clear from context,
in some embodiments, "nucleic acid" includes individual nucleic
acid residues (e.g., nucleotides and/or nucleosides); in some
embodiments, "nucleic acid" includes an oligonucleotide chain
comprising individual nucleic acid residues. In some embodiments, a
"nucleic acid" is or comprises RNA; in some embodiments, a "nucleic
acid" is or comprises DNA. In some embodiments, a "nucleic acid"
is, comprises, or consists of one or more natural nucleic acid
residues. In some embodiments, a "nucleic acid" is, comprises, or
consists of one or more nucleic acid analogs. In some embodiments,
a nucleic acid analog differs from a "nucleic acid" in that it does
not utilize a phosphodiester backbone. For example, in some
embodiments, a "nucleic acid" is, comprises, or consists of one or
more "peptide nucleic acids", which are known in the art and have
peptide bonds instead of phosphodiester bonds in the backbone, are
considered within the scope of the present invention. Alternatively
or additionally, in some embodiments, a "nucleic acid" has one or
more phosphorothioate and/or 5'-N-phosphoramidite linkages rather
than phosphodiester bonds. In some embodiments, a "nucleic acid"
is, comprises, or consists of one or more natural nucleosides
(e.g., adenosine, thymidine, guanosine, cytidine, uridine,
deoxyadenosine, deoxythymidine, deoxyguanosine, and deoxycytidine).
In some embodiments, a "nucleic acid" is, comprises, or consists of
one or more nucleoside analogs (e.g., 2-aminoadenosine,
2-thiothymidine, inosine, pyrrolo-pyrimidine, 3-methyl
adenosine.sub.; 5-methylcytidine, C-5 propynyl-cytidine, C-5
propynyl-uridine, 2-aminoadenosine, C5-bromouridine,
C5-fluorouridine, C5-iodouridine, C5-propynyl-uridine,
C5-propynyl-cytidine, C5-methylcytidine, 2-aminoadenosine,
7-deazaadenosine, 7-deazaguanosine, 8-oxoadenosine, 8-oxoguanosine,
O(6)-methylguanine, 2-thiocytidine, methylated bases, intercalated
bases, and combinations thereof). In some embodiments, a "nucleic
acid" comprises one or more modified sugars (e.g., 2'-fluororibose,
ribose, 2'-deoxyribose, arabinose, and hexose) as compared with
those in natural nucleic acids. In some embodiments, a "nucleic
acid" has a nucleotide sequence that encodes a functional gene
product such as an RNA or protein. In some embodiments, a "nucleic
acid" includes one or more introns. In some embodiments, a "nucleic
acid" is prepared by one or more of isolation from a natural
source, enzymatic synthesis by polymerization based on a
complementary template (in vivo or in vitro), reproduction in a
recombinant cell or system, and chemical synthesis. In some
embodiments, a "nucleic acid" is at least 3, 4, 5, 6, 7, 8, 9, 10,
15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95,
100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 20, 225, 250,
275, 300, 325, 350, 375, 400, 425, 450, 475, 500, 600, 700, 800,
900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000 or more
residues long. In some embodiments, a "nucleic acid" is single
stranded; in some embodiments, a "nucleic acid" is double stranded.
In some embodiments, a "nucleic acid" has a nucleotide sequence
comprising at least one element that encodes, or is the complement
of a sequence that encodes, a polypeptide. In some embodiments, a
"nucleic acid" has enzymatic activity.
[0082] The phrase "operably linked" includes a juxtaposition
wherein the components described are in a relationship permitting
them to function in their intended manner. A control sequence
"operably linked" to a coding sequence is ligated in such a way
that expression of the coding sequence is achieved under conditions
compatible with the control sequences. "Operably linked" sequences
include both expression control sequences that are contiguous with
the gene of interest and expression control sequences that act in
trans or at a distance to control the gene of interest. The term
"expression control sequence" includes polynucleotide sequences,
which are necessary to effect the expression and processing of
coding sequences to which they are ligated. "Expression control
sequences" include: appropriate transcription initiation,
termination, promoter and enhancer sequences; efficient RNA
processing signals such as splicing and polyadenylation signals;
sequences that stabilize cytoplasmic mRNA, sequences that enhance
translation efficiency (i.e., Kozak consensus sequence); sequences
that enhance protein stability; and when desired, sequences that
enhance protein secretion. The nature of such control sequences
differs depending upon the host organism. For example, in
prokaryotes, such control sequences generally include promoter,
ribosomal binding site, and transcription termination sequence,
while in eukaryotes, typically, such control sequences include
promoters and transcription termination sequence. The term "control
sequences" is intended to include components whose presence is
essential for expression and processing, and can also include
additional components whose presence is advantageous, for example,
leader sequences and fusion partner sequences.
[0083] The term "patient" or "subject" includes any organism to
which a provided composition is or may be administered, e.g., for
experimental, diagnostic, prophylactic, cosmetic, and/or
therapeutic purposes. Typical patients include animals (e.g.,
mammals such as mice, rats, rabbits, non-human primates, and/or
humans). In some embodiments, a patient is a non-human animal. In
some embodiments, a patient (e.g., a non-human animal patient) may
have a modification as described herein, a modification that is
different as described herein or no modification (i.e., a wild-type
non-human animal patient). In some embodiments, a non-human animal
is suffering from or is susceptible to one or more disorders or
conditions. In some embodiments, a non-human animal displays one or
more symptoms of a disorder or condition. In some embodiments, a
non-human animal has been diagnosed with one or more disorders or
conditions.
[0084] The term "polypeptide" includes any polymeric chain of amino
acids. In some embodiments, a polypeptide has an amino acid
sequence that occurs in nature. In some embodiments, a polypeptide
has an amino acid sequence that does not occur in nature. In some
embodiments, a polypeptide has an amino acid sequence that contains
portions that occur in nature separately from one another (i.e.,
from two or more different organisms, for example, human and
non-human portions). In some embodiments, a polypeptide has an
amino acid sequence that is engineered in that it is designed
and/or produced through action of the hand of man.
[0085] The term "recombinant", is intended to include polypeptides
(e.g., PD-1 polypeptides as described herein) that are designed,
engineered, prepared, expressed, created or isolated by recombinant
means, such as polypeptides expressed using a recombinant
expression vector transfected into a host cell, polypeptides
isolated from a recombinant, combinatorial human polypeptide
library (Hoogenboom H. R., (1997) TIB Tech. 1:5:62-70; Azzazy H.,
and Highsmith W. E., (2002) Clin. Biochem. 35:425-445; Gavilondo J.
V., and Larrick J. W. (2002) BioTechniques 29:128-145; Hoogenboom
H., and Chames P. (2000) Immunology Today 21:371-378), antibodies
isolated from an animal (e.g., a mouse) that is transgenic for
human immunoglobulin genes (see e.g., Taylor, L. D., et al. (1992)
Nucl. Acids Res. 20:6287-6295; Kellermann S-A., and Green L. L.
(2002) Current Opinion in Biotechnology 13:593-597; Little M. et
al. (2000) Immunology Today 21:364-370; Murphy, A. J., et al.
(2014) Proc. Natl. Acad. Sci. U. S. A. 111(14):5153-5158) or
polypeptides prepared, expressed, created or isolated by any other
means that involves splicing selected sequence elements to one
another. In some embodiments, one or more of such selected sequence
elements is found in nature. In some embodiments, one or more of
such selected sequence elements is designed in silica. In some
embodiments, one or more such selected sequence elements result
from mutagenesis (e.g., in vivo or in vitro) of a known sequence
element, e.g., from a natural or synthetic source. For example, in
some embodiments, a recombinant polypeptide is comprised of
sequences found in the genome of a source organism of interest
(e.g., human, mouse, etc.). In some embodiments, a recombinant
polypeptide has an amino acid sequence that resulted from
mutagenesis (e.g., in vitro or in vivo, for example in a non-human
animal), so that the amino acid sequences of the recombinant
polypeptides are sequences that, while originating from and related
to polypeptides sequences, may not naturally exist within the
genome of a non-human animal in vivo.
[0086] The term "replacement" includes a process through which a
"replaced" nucleic acid sequence (e.g., a gene) found in a host
locus (e.g., in a genome) is removed from that locus, and a
different, "replacement" nucleic acid is located in its place. In
some embodiments, the replaced nucleic acid sequence and the
replacement nucleic acid sequences are comparable to one another in
that, for example, they are homologous to one another and/or
contain corresponding elements (e.g., protein-coding elements,
regulatory elements, etc.). In some embodiments, a replaced nucleic
acid sequence includes one or more of a promoter, an enhancer, a
splice donor site, a splice receiver site, an intron, an exon, an
untranslated region (UTR); in some embodiments, a replacement
nucleic acid sequence includes one or more coding sequences. In
some embodiments, a replacement nucleic acid sequence is a homolog
of the replaced nucleic acid sequence. In some embodiments, a
replacement nucleic acid sequence is an ortholog of the replaced
sequence. In some embodiments, a replacement nucleic acid sequence
is or comprises a human nucleic acid sequence. In some embodiments,
including where the replacement nucleic acid sequence is or
comprises a human nucleic acid sequence, the replaced nucleic acid
sequence is or comprises a rodent sequence (e.g., a mouse or rat
sequence). The nucleic acid sequence so placed may include one or
more regulatory sequences that are part of source nucleic acid
sequence used to obtain the sequence so placed (e.g., promoters,
enhancers, 5'- or 3'-untranslated regions, etc.). For example, in
various embodiments, the replacement is a substitution of an
endogenous sequence with a heterologous sequence that results in
the production of a gene product from the nucleic acid sequence so
placed (comprising the heterologous sequence), but not expression
of the endogenous sequence; the replacement is of an endogenous
genomic sequence with a nucleic acid sequence that encodes a
polypeptide that has a similar function as a polypeptide encoded by
the endogenous sequence (e.g., the endogenous genomic sequence
encodes a PD-1 polypeptide, and the DNA fragment encodes one or
more human PD-1 polypeptides). In various embodiments, an
endogenous gene or fragment thereof is replaced with a
corresponding human gene or fragment thereof. A corresponding human
gene or fragment thereof is a human gene or fragment that is an
ortholog of, or is substantially similar or the same in structure
and/or function, as the endogenous gene or fragment thereof that is
replaced.
[0087] The phrase "Programmed cell death 1 protein" or "P1)-1
protein" includes a type I transmembrane protein that belongs to
the CD28/CTLA-4 family of T cell regulators. The protein structure
of a PD-1 protein includes an extracellular amino-terminal
immunoglobulin V domain, a transmembrane domain and a
carboxyl-terminal intracellular tail, which intracellular tail
contains an immunoreceptor tyrosine-based inhibitory motif (ITIM)
and an immunoreceptor tyrosine-based switch motif. PD-1 is
expressed on the cell surface and interacts with PD-L1 and PD-L2,
members of the B7 family immune-regulatory ligands (Collins, M. et
at (2005) Genome Biol. 6:223). PD-1 is expressed in, inter alia,
activated T cells, B cells, macrophages, monocytes, mast cells, and
also in many tumors. PD-1 has been shown to be involved in negative
regulation of immune response and, in particular, negative
regulation of T cell responses. By way of illustration, nucleotide
and amino acid sequences of mouse and human Pdcd1 genes, which
encode PD-1 proteins, are provided in FIG. 8. Persons of skill upon
reading this disclosure will recognize that one or more endogenous
Pdcd1 genes in a genome (or all) can be replaced by one or more
heterologous Pdcd1 genes (e.g., polymorphic variants, subtypes or
mutants, genes from another species, humanized forms, etc.).
[0088] A "PD-1-expressing cell" includes a cell that expresses a
PD-1 type I membrane protein. In some embodiments, a
PD-1-expressing cell expresses a PD-1 type I membrane protein on
its surface. In some embodiments, a PD-1 protein is expressed on
the surface of the cell in an amount sufficient to mediate
cell-to-cell interactions. Exemplary PD-1-expressing cells include
B cells, macrophages and T cells. PD-1-expressing cells regulate
various cellular processes via the interaction of PD-1 expressed on
the surface of immune cells (e.g., T and B cells) and play a role
in determining the differentiation and fate of such cells. In some
embodiments, non-human animals of the present invention demonstrate
regulation of various cellular processes (as described herein) via
humanized PD-1 proteins expressed on the surface of one more cells
of the non-human animal. In some embodiments, non-human animals of
the present invention demonstrate negative regulation of signaling
through T cell receptors (TCRs) via humanized PD-1 proteins
expressed on the surface of one or more cells of the non-human
animal. In some embodiments, non-human animals demonstrate negative
regulation of immune responses via humanized PD-1 proteins
expressed on the surface of one or more cells of the non-human
animal.
[0089] The term "reference" includes a standard or control agent,
cohort, individual, population, sample, sequence or value against
which an agent, animal, cohort, individual, population, sample,
sequence or value of interest is compared. In some embodiments, a
reference agent, cohort, individual, population, sample, sequence
or value is tested and/or determined substantially simultaneously
with the testing or determination of the agent, cohort, individual,
population, sample, sequence or value of interest. In some
embodiments, a reference agent, cohort, individual, population,
sample, sequence or value is a historical reference, optionally
embodied in a tangible medium. In some embodiments, a reference may
refer to a control. As used herein, a "reference" may include a
"reference animal". A "reference animal" may have a modification as
described herein, a modification that is different as described
herein or no modification (i.e., a wild-type animal). Typically, as
would be understood by those skilled in the art, a reference agent,
animal, cohort, individual, population, sample, sequence or value
is determined or characterized under conditions comparable to those
utilized to determine or characterize the agent, animal (e.g., a
mammal), cohort, individual, population, sample, sequence or value
of interest.
[0090] The term "substantially" includes the qualitative condition
of exhibiting total or near-total extent or degree of a
characteristic or property of interest. One of ordinary skill in
the biological arts will understand that biological and chemical
phenomena rarely, if ever, go to completion and/or proceed to
completeness or achieve or avoid an absolute result. The term
"substantially" is therefore used herein to capture the potential
lack of completeness inherent in many biological and chemical
phenomena.
[0091] The phrase "substantial homology" includes a comparison
between amino acid or nucleic acid sequences. As will be
appreciated by those of ordinary skill in the art, two sequences
are generally considered to be "substantially homologous" if they
contain homologous residues in corresponding positions. Homologous
residues may be identical residues. Alternatively, homologous
residues may be non-identical residues will appropriately similar
structural and/or functional characteristics. For example, as is
well known by those of ordinary skill in the art, certain amino
acids are typically classified as "hydrophobic" or "hydrophilic"
amino acids, and/or as having "polar" or "non polar" side chains.
Substitution of one amino acid for another of the same type may
often be considered a "homologous" substitution. Typical amino acid
categorizations are summarized in Table 1 and 2.
TABLE-US-00001 TABLE 1 Alanine Ala A Nonpolar Neutral 1.8 Arginine
Arg R Polar Positive -4.5 Asparagine Asn N Polar Neutral -3.5
Aspartic acid Asp D Polar Negative -3.5 Cysteine Cys C Nonpolar
Neutral 2.5 Glutamic acid Glu E Polar Negative -3.5 Glutamine Gln Q
Polar Neutral -3.5 Glycine Gly G Nonpolar Neutral -0.4 Histidine
His H Polar Positive -3.2 Isoleucine Ile I Nonpolar Neutral 4.5
Leucine Leu L Nonpolar Neutral 3.8 Lysine Lys K Polar Positive -3.9
Methionine Met M Nonpolar Neutral 1.9 Phenylalanine Phe F Nonpolar
Neutral 2.8 Proline Pro P Nonpolar Neutral -1.6 Serine Ser S Polar
Neutral -0.8 Threonine Thr T Polar Neutral -0.7 Tryptophan Trp W
Nonpolar Neutral -0.9 Tyrosine Tyr Y Polar Neutral -1.3 Valine Val
V Nonpolar Neutral 4.2
TABLE-US-00002 TABLE 2 Ambiguous Amino Acids 3-Letter 1-Letter
Asparagine or aspartic acid Asx B Glutamine or glutamic acid Glx Z
Leucine or Isoleucine Xle J Unspecified or unknown amino Xaa X
acid
[0092] As is well known in this art, amino acid or nucleic acid
sequences may be compared using any of a variety of algorithms,
including those available in commercial computer programs such as
BLASTN for nucleotide sequences and BLASTP, gapped BLAST, and
PSI-BLAST for amino acid sequences. Exemplary such programs are
described in Altschul et al (1990) Basic local alignment search
tool, J. Mol. Biol., 215(3): 403-410; Altschul et al. (1997)
Methods in Enzymology; Altschul et al., "Gapped BLAST and
PSI-BLAST: a new generation of protein database search programs",
Nucleic Acids Res. 25:3389-3402; 13axevanis et al. (1998)
Bioinformatics: A Practical Guide to the Analysis of Genes and
Proteins, Wiley; and Misener et al. (eds.) (1999) Bioinformatics
Methods and Protocols (Methods in Molecular Biology, Vol, 132),
Humana Press. In addition to identifying homologous sequences, the
programs mentioned above typically provide an indication of the
degree of homology. In some embodiments, two sequences are
considered to be substantially homologous if at least 50%, 55%,
60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%,
97%, 98%, 99% or more of their corresponding residues are
homologous over a relevant stretch of residues. In some
embodiments, the relevant stretch is a complete sequence. In some
embodiments, the relevant stretch is at least 9, 10, 11, 12, 13,
14, 15, 16, 17 or more residues. In some embodiments. the relevant
stretch includes contiguous residues along a complete sequence. In
sonic embodiments, the relevant stretch includes discontinuous
residues along a complete sequence. In some embodiments, the
relevant stretch is at least 10, 15, 20, 25, 30, 35, 40, 45, 50, or
more residues.
[0093] The phrase "substantial identity" includes a comparison
between amino acid or nucleic acid sequences. As will be
appreciated by those of ordinary skill in the art, two sequences
are generally considered to be "substantially identical" if they
contain identical residues in corresponding positions. As is well
known in this art, amino acid or nucleic acid sequences may be
compared using any of a variety of algorithms, including those
available in commercial computer programs such as BLASTN for
nucleotide sequences and BLASTP, gapped BLAST, and PSI-BLAST for
amino acid sequences. Exemplary such programs are described in
Altschul et al. (1990) Basic local alignment search tool, J. Mol.
Biol., 215(3): 403-410; Altschul et al., Methods in Enzymology;
Altschul et al. (1997) Nucleic Acids Res. 25:3389-3402; Baxevanis
et al, (1998) Bioinformatics: A Practical Guide to the Analysis of
Genes and Proteins, Wiley; and Misener et al., (eds.) (1999)
Bioinformatics Methods and Protocols (Methods in Molecular Biology,
Vol. 132), Humana Press. In addition to identifying identical
sequences, the programs mentioned above typically provide an
indication of the degree of identity. In some embodiments.sub.; two
sequences are considered to be substantially identical if at least
50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94?,
95%, 96%, 97%, 98%, 99% or more of their corresponding residues are
identical over a relevant stretch of residues. In some embodiments,
the relevant stretch is a complete sequence. In some embodiments,
the relevant stretch is at least 10, 15, 20, 25, 30, 35, 40, 45,
50, or more residues.
[0094] The phrase "targeting vector" or "targeting construct"
includes a polynucleotide molecule that comprises a targeting
region. A targeting region comprises a sequence that is identical
or substantially identical to a sequence in a target cell, tissue
or animal and provides for integration of the targeting construct
into a position within the genome of the cell, tissue or animal via
homologous recombination. Targeting regions that target using
site-specific recombinase recognition sites loxP or Fri sites) are
also included. In some embodiments, a targeting construct of the
present invention further comprises a nucleic acid sequence or gene
of particular interest, a selectable marker, control and or
regulatory sequences, and other nucleic acid sequences that allow
for recombination mediated through exogenous addition of proteins
that aid in or facilitate recombination involving such sequences.
In some embodiments, a targeting construct of the present invention
further comprises a gene of interest in whole or in part, wherein
the gene of interest is a heterologous gene that encodes a protein,
in whole or in part, that has a similar function as a protein
encoded by an endogenous sequence. In some embodiments, a targeting
construct of the present invention further comprises a humanized
gene of interest, in whole or in part, wherein the humanized gene
of interest encodes a protein, in whole or in part, that has a
similar function as a protein encoded by the endogenous
sequence.
[0095] The phrase "therapeutically effective amount" includes an
amount that produces the desired effect for which it is
administered. In some embodiments, the term refers to an amount
that is sufficient, when administered to a subject (e.g., an
animal) suffering from or susceptible to a disease, disorder,
and/or condition in accordance with a therapeutic dosing regimen,
to treat the disease, disorder, and/or condition. In some
embodiments, a therapeutically effective amount is one that reduces
the incidence and/or severity of and/or delays onset of, one or
more symptoms of the disease, disorder, and/or condition. Those of
ordinary skill in the art will appreciate that the term
"therapeutically effective amount" does not in fact require
successful treatment be achieved in a particular individual.
Rather, a therapeutically effective amount may be that amount that
provides a particular desired pharmacological response in a
significant number of subjects when administered to subjects in
need of such treatment. In some embodiments, reference to a
therapeutically effective amount may be a reference to an amount as
measured in one or more specific tissues (e.g., a tissue affected
by the disease, disorder or condition) or fluids (e.g., blood,
saliva, serum, sweat, tears, urine, etc.). Those of ordinary skill
in the art will appreciate that, in some embodiments, a
therapeutically effective amount of a particular agent or therapy
may be formulated and/or administered in a single dose. In some
embodiments, a therapeutically effective agent may be formulated
and/or administered in a plurality of doses, for example, as part
of a dosing regimen.
[0096] The term "treatment" (also "treat" or "treating"), in its
broadest sense includes any administration of a substance (e.g.,
provided compositions) that partially or completely alleviates,
ameliorates, relives, inhibits, delays onset of, reduces severity
of, and/or reduces incidence of one or more symptoms, features,
and/or causes of a particular disease, disorder, and/or condition.
In some embodiments, such treatment may be administered to a
subject who does not exhibit signs of the relevant disease,
disorder and/or condition and/or of a subject who exhibits only
early signs of the disease, disorder, and/or condition.
Alternatively or additionally, in some embodiments, treatment may
be administered to a subject who exhibits one or more established
signs of the relevant disease, disorder and/or condition. In some
embodiments, treatment may be of a subject who has been diagnosed
as suffering from the relevant disease, disorder, and/or condition.
In some embodiments, treatment may be of a subject known to have
one or more susceptibility factors that are statistically
correlated with increased risk of development of the relevant
disease, disorder, and/or condition.
[0097] The term "variant" includes an entity that shows significant
structural identity with a reference entity, but differs
structurally from the reference entity in the presence or level of
one or more chemical moieties as compared with the reference
entity. In many embodiments, a "variant" also differs functionally
from its reference entity. In general, whether a particular entity
is properly considered to be a "variant" of a reference entity is
based on its degree of structural identity with the reference
entity. As will be appreciated by those skilled in the art, any
biological or chemical reference entity has certain characteristic
structural elements. A "variant", by definition, is a distinct
chemical entity that shares one or more such characteristic
structural elements. To give but a few examples, a small molecule
may have a characteristic core structural element (e.g., a
macrocycle core) and/or one or more characteristic pendent moieties
so that a variant of the small molecule is one that shares the core
structural element and the characteristic pendent moieties but
differs in other pendent moieties and/or in types of bonds present
(single vs. double, E vs. Z, etc.) within the core, a polypeptide
may have a characteristic sequence element comprised of a plurality
of amino acids having designated positions relative to one another
in linear or three-dimensional space and/or contributing to a
particular biological function, a nucleic acid may have a
characteristic sequence element comprised of a plurality of
nucleotide residues having designated positions relative to on
another in linear or three-dimensional space. For example, a
"variant polypeptide" may differ from a reference polypeptide as a
result of one or more differences in amino acid sequence and/or one
or more differences in chemical moieties e.g., carbohydrates,
lipids, etc.) covalently attached to the polypeptide backbone. In
some embodiments, a "variant polypeptide" shows an overall sequence
identity with a reference polypeptide that is at least 85%, 86%,
87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, or 99%.
Alternatively or additionally, in some embodiments, a "variant
polypeptide" does not share at least one characteristic sequence
element with a reference polypeptide. In some embodiments, the
reference polypeptide has one or more biological activities. In
some embodiments, a "variant polypeptide" shares one or more of the
biological activities of the reference polypeptide. In some
embodiments, a "variant polypeptide" lacks one or more of the
biological activities of the reference polypeptide. In some
embodiments, a "variant polypeptide" shows a reduced level of one
or more biological activities as compared with the reference
polypeptide. In many embodiments, a polypeptide of interest is
considered to be a "variant" of a parent or reference polypeptide
if the polypeptide of interest has an amino acid sequence that is
identical to that of the parent but for a small number of sequence
alterations at particular positions. Typically, fewer than 20%,
15%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2% of the residues in the
variant are substituted as compared with the parent. In some
embodiments, a "variant" has 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1
substituted residue as compared with a parent. Often, a "variant"
has a very small number (e.g., fewer than 5, 4, 3, 2, or 1) number
of substituted functional residues residues that participate in a
particular biological activity). Furthermore, a "variant" typically
has not more than 5, 3, 2, or 1 additions or deletions, and often
has no additions or deletions, as compared with the parent.
Moreover, any additions or deletions are typically fewer than about
25, about 20, about 19, about 18, about 17, about 16, about 15,
about 14, about 13, about 10, about 9, about 8, about 7, about 6,
and commonly are fewer than about 5, about 4, about 3, or about 2
residues. In some embodiments, the parent or reference polypeptide
is one found in nature. As will be understood by those of ordinary
skill in the art, a plurality of variants of a particular
polypeptide of interest may commonly be found in nature,
particularly when the polypeptide of interest is an infectious
agent polypeptide.
[0098] The term "vector" includes a nucleic acid molecule capable
of transporting another nucleic acid to which it is associated. In
some embodiment, vectors are capable of extra-chromosomal
replication and/or expression of nucleic acids to which they are
linked in a host cell such as a eukaryotic and/or prokaryotic cell.
Vectors capable of directing the expression of operatively linked
genes are referred to herein as "expression vectors."
[0099] The term "wild-type" includes an entity having a structure
and/or activity as found in nature in a "normal" (as contrasted
with mutant, diseased, altered, etc.) state or context. Those of
ordinary skill in the art will appreciate that wild- type genes and
polypeptides often exist in multiple different forms (e.g.,
alleles).
DETAILED DESCRIPTION OF CERTAIN EMBODIMENTS
[0100] The present invention provides, among other things, improved
and/or engineered non-human animals having humanized genetic
material encoding a Programmed cell death 1 (Pdcd1) gene for
determining the therapeutic efficacy of Pdcd1 modulators (e.g., an
anti-PD-1 antibody) for the treatment of cancer, and assays in T
cell responses and signal transduction. It is contemplated that
such non-human animals provide an improvement in determining the
therapeutic efficacy of PD-1 modulators and their potential for
PD-1 blockade. Therefore, the present invention is particularly
useful for the development of anti-PD-1 therapies for the treatment
of various cancers, as well as for augmenting immune responses to
treat and/or remove viral infection in non-human animals. In
particular, the present invention encompasses the humanization of a
murine Pdcd1 gene resulting in expression of a humanized PD-1
protein on the surface of cells of the non-human animal. Such
humanized PD-1 proteins have the capacity to provide a source of
human PD-1.sup.+ cells for determining the efficacy of anti-PD-1
therapeutics to promote anti-tumor immune responses. In some
embodiments, non-human animals of the present invention demonstrate
augmented immune responses via blockade of PD-1 signaling through
the humanized PD-1 protein expressed on the surface of cells of the
non-human animal. In some embodiments, humanized PD-1 proteins have
a sequence corresponding to the N-terminal immunoglobulin V domain,
in whole or in part, of a human PD-1 protein. In some embodiments,
humanized PD-1 proteins have a sequence corresponding to the
intracellular tail of a murine PD-1 protein; in some embodiments, a
sequence corresponding to the transmembrane domain and
intracellular tail of a murine PD-1 protein. In some embodiments,
humanized PD-1 proteins have a sequence corresponding to amino acid
residues 21-170 (or 26-169, 27-169, or 27-145, or 35-145) of a
human PD-1 protein. In some embodiments, non-human animals of the
present invention comprise an endogenous Pdcd1 gene that contains
genetic material from the non-human animal and a heterologous
species (e.g., a human). In some embodiments, non-human animals of
the present invention comprise a humanized Pdcd1 gene, wherein the
humanized Pdcd 1 gene comprises exon 2 and exon 3, in whole or in
part, of a human PDCD1 gene. In some certain embodiments, non-human
animals of the present invention comprise a humanized Pdcd1 gene,
wherein the humanized Pdcd1 gene compries 883 by of a human PDCD1
gene corresponding to exon 2 and the first 71 bp of exon 3 (i.e.,
encoding the stalk) of a human PDCD1 gene.
[0101] Various aspects of the invention are described in detail in
the following sections. The use of sections is not meant to limit
the invention. Each section can apply to any aspect of the
invention. In this application, the use of "or" means "and/or"
unless stated otherwise.
[0102] Programmed cell death 1 (Pdcd1) gene
[0103] Pdcd1 (also referred to as CD279) was originally discovered
as an upregulated gene in a T cell hybridoma that was undergoing
apoptosis (Ishida, Y. et al. (1992) EMBO J. 11(10:3887-3895). The
Pdcd1 gene consists of 5 exons that encode PD-1, which is a type
membrane protein (referred to as PD-1) that includes an N-terminal
immunoglobulin V (IgV) domain, a stalk (.about.20 amino acids in
length), a transmembrane domain, and an intracellular tail that
contains both an immunoreceptor tyrosine inhibitory motif (ITIM)
and an immunoreceptor tyrosine switch motif (ITSM). PD-1 is
expressed on many cell types such as, for example, B cells,
dendritic cells, activated monocytes, natural killer (NK) cells and
activated T cells (Keir, M. E., et al. (2008) Annu. Rev. Immunol.
26:677-704), Various splice variants of PD-1 have also been
reported and vary based on which exon is lacking (Nielsen, C. et
al. (2005) Cell. Immunol. 235:109-116). Indeed, certain splice
variants have been observed as a causitive factor in autoimmune
diseases (Wan, B. et al. (2006) J. Immunol. 177(12):8844-8850),
Further, Pdcd1-deficient mice have been reported to develop
autoimmune conditions (Nishimura, H. et al. (1998) Intern. Immunol.
10(10):1563-1572; Nishimura.sub.; H. et al. (1999) Immunity
11:141-151; Nishimura, H. et al. (2001) Science 291:319-322), which
have lead the way to solidifying PD-1 as a negative regulator of
activated lymphocytes and serves to protect against the development
of autoimmune disease. Interestingly, tumors have been discovered
to use PD-1 signaling to evade surveillance by the immune system.
Therefore, PD-1 and at least one of its ligands (i.e., PD-L1) are
currently being explored as targets for cancer therapy by promotion
of anti-tumor activity in tumor microenvironments via PIM blockade
(see e.g., Pedoeem, A. et al. (2014) Clin. Immunol. 153:145-152;
and Philips, G. K. and Atkins, M. (2014) Intern. Immunol. 8
pages)
[0104] A more thorough and detailed understanding of PD-1-mediated
functions and the PD-1 pathway is needed to develop practical
targeted therapies for future cancer treatment.
[0105] Pdcd1 and PD-1 Sequences
[0106] Exemplary murine, human and humanized Pdcd1 and PD-1
sequences are set forth in FIG. 8. An exemplary human nucleic acid
sequence for humanization of a non-human Pdcd1 gene is also set
forth in FIG. 8.
[0107] Humanized Pdcd1 Non-Human Animals
[0108] Non-human animals are provided that express humanized PD-1
proteins on the surface of cells of the non-human animals resulting
from a genetic modification of an endogenous locus (e.g., a Pdcd1
locus) of the non-human animal that encodes a PD-1 protein.
Suitable examples described herein include rodents, in particular,
mice.
[0109] A humanized Pdcd1 gene, in some embodiments, comprises
genetic material from a heterologous species (e.g., humans),
wherein the humanized Pdcd1 gene encodes a PD-1 protein that
comprises the encoded portion of the genetic material from the
heterologous species. In some embodiments, a humanized Pdcd1 gene
of the present invention comprises genomic DNA of a heterologous
species that encodes the extracellular portion of a PD-1 protein
that is expressed on the plasma membrane of a cell. Non-human
animals, embryos, cells and targeting constructs for making
non-human animals, non-human embryos, and cells containing said
humanized Pdcd1 gene are also provided.
[0110] In some embodiments, an endogenous Pdcd1 gene is deleted. In
some embodiments, an endogenous Pdcd1 gene is altered, wherein a
portion of the endogenous Pdcd1 gene is replaced with a
heterologous sequence (e.g., a human PDCD1 sequence, in whole or in
part). In some embodiments, all or substantially all of an
endogenous Pdcd1 gene is replaced with a heterologous gene (e.g., a
human PDCD1 gene). In some embodiments, a portion of a heterologous
Pdcd1 gene is inserted into an endogenous non-human Pdcd1 gene at
an endogenous Pdcd1 locus. In some embodiments, the heterologous
gene is a human gene. In some embodiments, the modification or
humanization is made to one of the two copies of the endogenous
Pdcd1 gene, giving rise to a non-human animal that is heterozygous
with respect to the humanized Pdcd1 gene. In other embodiments, a
non-human animal is provided that is homozygous for a humanized
Pdcd1 gene.
[0111] In various aspects, a non-human animal contains a human
PDCD1 gene, in whole or in part, at an endogenous non-human Pdcd1
locus. Thus, such non-human animals can be described as having a
heterologous Pdcd1 gene. The replaced, inserted, modified or
altered Pdcd1 gene at the endogenous Pdcd1 locus or a protein
expressed from such gene can be detected using a variety of methods
including, for example, PCR, Western blot, Southern blot,
restriction fragment length polymorphism (RFLP), or a gain or loss
of allele assay. In some embodiments, the non-human animal is
heterozygous with respect to the humanized Pdcd1 gene.
[0112] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a second exon
having a sequence at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to a second exon that appears in a human PDCD1 gene of
FIG. 8.
[0113] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a second exon
having a sequence that is subtantially identicial to a second exon
that appears in a human PDCD1 gene of FIG. 8.
[0114] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a second exon
having a sequence that is identicial to a second exon that appears
in a human PDCD1 gene of FIG. 8.
[0115] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a third exon
having a sequence at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to a third exon that appears in a humanized Pdcd1 mRNA
sequence of FIG. 8.
[0116] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a third exon
having a sequence that is subtantially identicial to a third exon
that appears in a humanized Pdcd1 mRNA sequence of FIG. 8.
[0117] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a third exon
having a sequence that is identicial to a third exon that appears
in a humanized Pdcd1 mRNA sequence of FIG. 8.
[0118] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that comprises a
sequence at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%, 80%,
85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to SEQ ID NO: 21 or SEQ ID NO: 23.
[0119] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that comprises a
sequence that is substantially identical to SEQ ID NO: 21 or SEQ ID
NO: 23.
[0120] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that comprises a
sequence that is identical to SEQ ID NO: 21 or SEQ ID NO: 23.
[0121] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a second exon
and a portion of a third exon each having a sequence at least 50%
(e.g., 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%,
94%, 95%, 96%, 97%, 98%, 99% or more) identical to a second exon
and a portion of a third exon that appear in a human PDCD1 gene of
FIG. 8.
[0122] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a first,
fourth and fifth exon each having a sequence at least 50% (e.g.,
50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%,
95%, 96%, 97%, 98%, 99% or more) identical to a first, fourth and
fifth exon that appear in a mouse Pdcd1 gene of FIG. 8.
[0123] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a first, a
portion of a third, a fourth and a fifth exon each having a
sequence at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%, 80%,
85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to a first, a portion of a third, a fourth and a fifth
exon that appear in a mouse Pdcd1 gene of FIG. 8.
[0124] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a 5'
untranslated region and a 3' untranslated region each having a
sequence at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%, 80%,
85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to a 5' untranslated region and a 3' untranslated region
that appear in a mouse Pdcd1 gene of FIG. 8.
[0125] In various embodiments, a humanized Pdcd1 gene according to
the present invention includes a Pdcd1 gene that has a nucleotide
coding sequence (e.g., a cDNA sequence) at least 50% (e.g., 50%,
55%, 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%,
97%, 98%, 99% or more) identical to a nucleotide coding sequence
that appears in a humanized Pdcd1 nucleotide coding sequence of
FIG. 8.
[0126] In various embodiments, a humanized Pdcd1 mRNA sequence
according to the present invention comprises a sequence that is at
least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%,
92%, 93%, 94%, 96%, 97%, 98%, 99% or more) identical to a humanized
mRNA sequence that appears in FIG. 8.
[0127] In various embodiments, a humanized Pdcd1 gene according to
the present invention encodes a PD-1 polypeptide having an amino
acid sequence at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 7%, 80%,
85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to an amino acid sequence that appears in a PD-1
polypeptide sequence of FIG. 8.
[0128] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion having an amino acid sequence that is at least 50% (e.g.,
50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%,
95%, 96%, 97%, 98%, 99% or more) identical to an extracellular
portion of a human PD-1 protein that appears in FIG. 8.
[0129] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to amino acid residues 21-170 that appear in a human or
humanized PD-1 protein of FIG. 8.
[0130] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is substantially identical to amino acid residues
21-170 that appear in a human or humanized PD-1 protein of FIG.
8.
[0131] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is identical to amino acid residues 21-170 that
appear in a human or humanized PD-1 protein of FIG. 8.
[0132] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion. comprises an amino acid
sequence that is at least 50%, (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to amino acid residues 26-169 that appear in a human or
humanized PD-1 protein of FIG. 8.
[0133] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is substantially identical to amino acid residues
26-169 that appear in a human or humanized PD-1 protein of FIG.
8.
[0134] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is identical to amino acid residues 26-169 that
appear in a human or humanized PD-1 protein of FIG. 8.
[0135] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to amino acid residues 27-169 that appear in a human or
humanized PD-1 protein of FIG. 8.
[0136] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is substantially identical to amino acid residues
27-169 that appear in a human or humanized PD-1 protein of FIG.
8.
[0137] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is identical to amino acid residues 27-169 that
appear in a human or humanized PD-1 protein of FIG. 8.
[0138] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to amino acid residues 27-145 that appear in a human or
humanized PD-1 protein of FIG. 8.
[0139] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is substantially identical to amino acid residues
27-145 that appear in a human or humanized PD-1 protein of FIG.
8.
[0140] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is identical to amino acid residues 27-145 that
appear in a human or humanized PD-1 protein of FIG. 8.
[0141] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to amino acid residues 35-145 that appear in a human or
humanized PD-1 protein of FIG. 8.
[0142] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is substantially identical to amino acid residues
35-145 that appear in a human or humanized PD-1 protein of FIG.
8,
[0143] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an extracellular
portion, which extracellular portion comprises an amino acid
sequence that is identical to amino acid residues 35-145 that
appear in a human or humanized PD-1 protein of FIG. 8.
[0144] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an N-terminal
immunoglobulin V domain having an amino acid sequence that is at
least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%,
92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more) identical to an
N-terminal immunoglobulin V domain of a human or humanized PD-1
protein that appears in FIG. 8.
[0145] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an N-terminal
immunoglobulin V domain having an amino acid sequence that is
substantially identical to an N-terminal immunoglobulin V domain
that appears in a human or humanized PD-1 protein of FIG. 8.
[0146] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an N-terminal
immunoglobulin V domain having an amino acid sequence that is
identical to an N-terminal immunoglobulin V domain that appears in
a human or humanized PD-1 protein of FIG. 8.
[0147] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has a transmembrane
domain having a sequence that is at least 50% (e.g., 50%, 55%, 60%,
65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%,
98%, 99% or more) identical to a transmembrane domain of a mouse
RD-1 protein that appears in FIG. 8.
[0148] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an intracellular
tail having a sequence that is at least 50% (e.g., 50%, 55%, 60%,
65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%,
98%, 99% or more) identical to an intracellular tail of a mouse
PD-1 protein that appears in FIG. 8.
[0149] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an amino acid
sequence that is at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to amino acid residues 27-169 (or 26-169) that appear in
a human PD-1 protein of FIG. 8.
[0150] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an amino acid
sequence that is substantially identical to amino acid residues
27-169 (or 26-169) that appear in a human PD-1 protein of FIG.
8.
[0151] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an amino acid
sequence that is identical to amino acid residues 27-169 (or
26-169) that appear in a human PD-1 protein of FIG. 8.
[0152] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invention has an amino acid
sequence that is at least 50% (e.g., 50%, 55%, 60%, 65%, 70%, 75%,
80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more)
identical to an amino acid sequence of a humanized PD-1 protein
that appears in FIG. 8.
[0153] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invnetion has an amino acid
sequence that is substantially identical to an amino acid sequence
of a humanized PD-1 protein that appears in FIG. 8.
[0154] In various embodiments, a humanized PD-1 protein produced by
a non-human animal of the present invnetion has an amino acid
sequence that is identical to an amino acid sequence of a humanized
PD-1 protein that appears in FIG. 8.
[0155] Compositions and methods for making non-human animals that
express a humanized PD-1 protein, including specific polymorphic
forms, allelic variants (e.g., single amino acid differences) or
alternatively spliced isoforms, are provided, including
compositions and methods for making non-human animals that express
such proteins from a human promoter and a human regulatory
sequence. In some embodiments, compositions and methods for making
non-human animals that express such proteins from an endogenous
promoter and an endogenous regulatory sequence are also provided.
In some certain embodiments, endogenous promoters and endogenous
regulatory sequences are endogenous rodent promoters and endogenous
rodent regulatory sequences. The methods include inserting the
genetic material encoding a human PD-1 protein in whole or in part
at a precise location in the genome of a non-human animal that
corresponds to an endogenous Pdcd1 gene thereby creating a
humanized Pdcd1 gene that expresses a PD-1 protein that is human in
whole or in part. In some embodiments, the methods include
inserting genomic DNA corresponding to exon 2 and exon 3, in whole
or in part, of a human PDCD1 gene into an endogenous Pdcd1 gene of
the non-human animal thereby creating a humanized gene that encodes
a PD-1 protein that contains a human portion containing amino acids
encoded by the inserted exons.
[0156] Where appropriate, the coding region of the genetic material
or polynucleotide sequence(s) encoding a human (or humanized) PD-1
protein in whole or in part may be modified to include codons that
are optimized for expression from cells in the non-human animal
(e.g., see U.S. Pat. No.'s 5,670,356 and 5,874,304). Codon
optimized sequences are synthetic sequences, and preferably encode
the identical polypeptide (or a biologically active fragment of a
full length polypeptide which has substantially the same activity
as the full length polypeptide) encoded by the non-codon optimized
parent polynucleotide. In some embodiments, the coding region of
the genetic material encoding a human (or humanized) PD-1 protein,
in whole or in part, may include an altered sequence to optimize
codon usage for a particular cell type (e.g., a rodent cell). For
example, the codons of the genomic DNA corresponding to exon 2 and
a portion of exon 3 (e.g., 71 bp) of a human PDCD1 gene to be
inserted into an endogenous Pdcd1 gene of a non-human animal (e.g.,
a rodent) may be optimized for expression in a cell of the
non-human animal. Such a sequence may be described as a
codon-optimized sequence.
[0157] A humanized Pdcd1 gene approach employs a relatively minimal
modification of the endogenous gene and results in natural
PD-1-mediated signal transduction in the non-human animal, in
various embodiments, because the genomic sequence of the Pdcd1
sequences are modified in a single fragment and therefore retain
normal functionality by including necessary regulatory sequences.
Thus, in such embodiments, the Pdcd1 gene modification does not
affect other surrounding genes or other endogenous
Pdcd1-interacting genes (e.g., PD-L1, PD-L2, etc.). Further, in
various embodiments, the modification does not affect the assembly
of a functional PD-1 transmembrane protein on the cell membrane and
maintains normal effector functions via binding and subsequent
signal transduction through the cytoplasmic portion of the protein
which is unaffected by the modification.
[0158] A schematic illustration (not to scale) of the genomic
organization of an endogenous murine Pdcd1 gene and a human PDCD1
gene is provided in FIG. 1. An exemplary method for humanizing an
endogenous murine Pdcd1 gene using a genomic fragment containing
exon 2 and a portion of exon 3 of a human PDCD1 gene is provided in
FIG. 2, As illustrated, an 883 by genomic DNA fragment containing
exon 2 and a portion of exon 3 (e.g., the first 71 bp) of a human
PDCD1 gene is inserted into the place of a 900 bp sequence of an
endogenous murine Pdcd1 gene locus by a targeting construct. The
883 by human DNA fragment may be cloned directly from human DNA or
synthesized from a source sequence (e.g., Genbank accession no.
NM_005018.2). This genomic DNA includes the portion of the gene
that encodes substantially all of the extracellular portion (e.g.,
amino acid residues 27-169 or 26-169) of a human PD-1 protein
responsible for ligand binding.
[0159] A non-human animal (e.g., a mouse) having a humanized Pdcd1
gene at the endogenous Pdcd1 locus can be made by any method known
in the art. For example, a targeting vector can be made that
introduces a human Pdcd1 gene in whole or in part with a selectable
marker gene, FIG. 2 illustrates a targeting vector that contains an
endogenous Pdcd1 locus of a mouse genome comprising an insertion of
an 883 bp human DNA fragment that includes exon 2 and the first 71
bp of exon 3 of a human PDCD1 gene. As illustrated, the targeting
construct contains a 5' homology arm containing sequence upstream
of exon 2 of an endogenous murine Pdcd1 gene (-61.7 Kb), followed
by a drug selection cassette (e.g., a neomycin resistance gene
flanked on both sides by loxP sequences; .about.5 Kb), a genomic
DNA fragment containing exon 2 and the first 71 bp of exon 3 of a
human Pdcd1 gene (883 bp), and a 3' homology arm containing the
remaining sequence of an endogenous murine exon 3 (i.e., portion
which encodes a transmembrane portion of a PD-1 protein), exon 4
and exon 5 of an endogenous murine Pdcd1 gene (-84 Kb). The
targeting construct contains a self-deleting drug selection
cassette (e.g., a neomycin resistance gene flanked by loxP
sequences; see U.S. Pat. No.'s 8,697,851, 8,518,392 and 8,354,389,
all of which are herein incorporated by reference). Upon
electroporation in embryonic stem cells, a modified endogenous
Pdcd1 gene is created that exchanges 900 bp of an endogenous
wild-type Pdcd1 gene with 883 bp of a human PDCD1 gene (i.e., exon
2 and the first 71 by of exon 3), which is contained in the
targeting vector. A humanized Pdcd1 gene is created resulting in a
cell or non-human animal that expresses a humanized PD-1 protein
that contains amino acids encoded by the 883 bp human DNA fragment
(i.e., exon 2 and 71 bp of exon 3 of a human PDCD1 gene). The drug
selection cassette is removed in a development-dependent manner,
i.e., progeny derived from mice whose germ line cells containing
the humanized Pdcd1 gene described above will shed the selectable
marker from differentiated cells during development (see bottom of
FIG. 2).
[0160] Although embodiments employing a humanized Pdcd1 gene in a
mouse (i.e., a mouse with a Pdcd1 gene that encodes a PD-1 protein
that includes a human portion and a mouse portion) are extensively
discussed herein, other non-human animals that comprise a humanized
Pdcd1 gene are also provided. In some embodiments, such non-human
animals comprise a humanized Pdcd1 gene operably linked to a rodent
Pdcd1 promoter. In some embodiments, such non-human animals
comprise a humanized Pdcd1 gene operably linked to an endogenous
Pdcd1 promoter; in some embodiments, an endogenous rodent Pdcd1
promoter. In some embodiments, such non-human animals express a
humanized PD-1 protein from an endogenous locus, wherein the
humanized PD-1 protein comprises amino acid residues 21-170 (or
26-169, or 27-169, 27-145 or 35-145) of a human PD-1 protein. Such
non-human animals include any of those which can be genetically
modified to express a PD-1 protein as disclosed herein, including,
e.g., mammals, e.g., mouse, rat, rabbit, pig, bovine (e.g., cow,
bull, buffalo), deer, sheep, goat, chicken, cat, dog, ferret,
primate (e.g., marmoset, rhesus monkey), etc. For example, for
those non-human animals for which suitable genetically modifiable
ES cells are not readily available, other methods are employed to
make a non-human animal comprising the genetic modification. Such
methods include, e.g., modifying a non-ES cell genome (e.g., a
fibroblast or an induced pluripotent cell) and employing somatic
cell nuclear transfer (SCNT) to transfer the genetically modified
genome to a suitable cell, e.g., an enucleated oocyte, and
gestating the modified cell (e.g., the modified oocyte) in a
non-human animal under suitable conditions to form an embryo.
[0161] Methods for modifying a non-human animal genome (e.g., a
pig, cow, rodent, chicken, etc. genome) include, e.g., employing a
zinc finger nuclease (ZFN) or a transcription activator-like
effector nuclease (TALEN) to modify a genome to include a humanized
Pdcd1 gene.
[0162] In some embodiments, a non-human animal of the present
invention is a mammal. In some embodiments, a non-human animal of
the present invention is a small mammal, e.g., of the superfamily
Dipodoidea or Muroidea. In some embodiments, a genetically modified
animal of the present invention is a rodent. In some embodiments, a
rodent of the present invention is selected from a mouse, a rat,
and a hamster. In some embodiments, a rodent of the present
invention is selected from the superfamily Muroidea. In some
embodiments, a genetically modified animal of the present invention
is from a family selected from Calomyscidae (e.g., mouse-like
hamsters), Cricetidae (e.g., hamster, New World rats and mice,
voles), Muridae (true mice and rats, gerbils, spiny mice, crested
rats), Nesomyidae (climbing mice, rock mice, white-tailed rats,
Malagasy rats and mice), Platacanthomyidae (e.g., spiny dormice),
and Spala.cidae (e.g., mole rates, bamboo rats, and zokors). In
sonic certain embodiments, a genetically modified rodent of the
present invention is selected from a true mouse or rat (family
Muridae), a gerbil, a spiny mouse, and a crested rat. In some
certain embodiments, a genetically modified mouse of the present
invention is from a member of the family Muridae. In some
embodiment, a non-human animal of the present invention is a
rodent. In some certain embodiments, a rodent of the present
invention is selected from a mouse and a rat. In some embodiments,
a non-human animal of the present invention is a mouse.
[0163] In some embodiments, a non-human animal of the present
invention is a rodent that is a mouse of a C57BL strain selected
from C57BL/A. C57BL/An, C57BL/GrFa, C57BL/KaLwN, C57BL/6,
C57BL/6,J, C57BL/6ByJ, C57BL/6NJ, C57BL/10, C57BL/10ScSn,
C57BL/10Cr, and C57BL/O1a. In some certain embodiments, a mouse of
the present invention is a 129 strain selected from the group
consisting of a strain that is 129P1, 129P2, 129P3, 129X1, 129S1
(e.g., 129S1/SV, 129S1/SvIm), 129S2, 129S4, 129S5, 129S9/SvEvH,
129/SvJae, 129S6 (129/SvEvTac), 129S7, 129S8, 129T1, 129T2 (see,
e.g., Festing et al., 1999, Mammalian Genome 10:836; Auerbach, W.
et al., 2000, Biotechniques 29(5):1024-1028, 1030, 1032). In some
certain embodiments, a genetically modified mouse of the present
invention is a mix of an aforementioned 12.9 strain and an
aforementioned C57BL/6 strain. In some certain embodiments, a mouse
of the present invention is a mix of aforementioned 129 strains, or
a mix of aforementioned BL/6 strains. In some certain embodiments,
a 129 strain of the mix as described herein is a 129S6
(129/SvEvTac) strain. In some embodiments, a mouse of the present
invention is a BALB strain, e.g., BALB/c strain. In some
embodiments, a mouse of the present invention is a mix of a BALB
strain and another aforementioned strain.
[0164] In some embodiments, a non-human animal of the present
invention is a rat. In some certain embodiments, a rat of the
present invention is selected from a Wistar rat, an LEA strain, a
Sprague Dawley strain, a Fischer strain, F344, F6, and Dark Agouti.
In some certain embodiments, a rat strain as described herein is a
mix of two or more strains selected from the group consisting of
Wistar, LEA, Sprague Dawley, Fischer, F344, F6, and Dark
Agouti.
[0165] Methods Employing Non-Human Animals Having Humanized Pdcd1
Genes
[0166] Investigation into PD-1 function has employed the use of
various Pdcd1 mutant and transgenic non-human animals (e.g., see
Nishimura, H. et al. (1998) Intern. Immunol. 10(10):1563-1572;
Nishimura, H. et al. (1999) Immunity 11:141-151; Nishimura, H. et
al. (2001) Science 291:319-322; Iwai, Y. et al. (2004) Intern.
Immunol. 17(2):133-144; Keir, M. E. et al. (2005) J. Immunol.
175:7372-7379; Keir, M. E. et al. (2007) J. Immunol. 179:5064-5070;
Carter, L. L. et al. (2007) J. Neuroimmunol. 182:124-134; Chen, L.
et al. (2007) Europ. Soc. Organ Transplant. 21:21-29; Okazaki, T.
et al. (2011) J. Exp. Med. 208(2):395-407; U.S. Pat. No. 7,414,171;
and European Patent No. 1 334 659 B1; which references are herein
incorporated by reference). Such mutant and transgenic animals have
been useful in determining the molecular aspects of PD-1
expression.sub.; function and regulation of various cellular
processes. However, they are not without limitation. For example,
PD-1-deficient mice generated by knock-in of a human PD-1 cDNA into
exon 1 of a mouse Pdcd1 gene did not express human PD-1 even after
stimulation with PMA (Carter, L. L. et al., supra). Further,
considerable phenotypic differences among PD-1 mutant animals in
different genetic backgrounds has complicated investigation,
especially when attempting to assign various functions and/or
regulatory activities to PD-1. Still, other transgenic animals have
been created that overexpress PD-1 (Chen, L. et al., supra). Such
animals have displayed different expression patterns of the
transgene, which can reasonably be attributed to construct design.
Further, due to the use of the same source genetic material (i.e.,
mouse), PD-1 overexpression may have corresponded to endogenous
PD-1 rather than transgenic PD-1 due to possible position effects
of the transgene. While PD-1 transgenic mice have proved useful in
elucidating some PD-1-mediated biological function, they have
demonstrated variability in the results obtained, which are based,
at least in part, from the different approaches employed to make
them. Therefore, current in vivo systems exploiting PD-1-mediated
biology are incomplete. The molecular aspects of PD-1-mediated
biological function and signaling pathways has not been exploited
in transgenic mice to its fullest potential.
[0167] Non-human animals of the present invention provide an
improved in vivo system and source of biological materials (e.g.,
cells) expressing human (or humanized) PD-1 that are useful for a
variety of assays. In various embodiments, non-human animals of the
present invention are used to develop therapeutics that target PD-1
and/or modulate PD-1 signaling (e.g., interferring with
interactions with PD-L1 and/or PD-L2). In various embodiments,
non-human animals of the present invention are used to identify,
screen and/or develop candidate therapeutics (e.g., antibodies)
that bind human PD-1. In various embodiments, non-human animals of
the present invention are used to screen and develop candidate
therapeutics (e.g., antibodies) that block interaction of human
PD-1 with human PD-L1 and/or human PD-L2. In various embodiments,
non-human animals of the present invention are used to determine
the binding profile of antagonists and/or agonists of a humanized
PD-1 on the surface of a cell of a non-human animal as described
herein; in some embodiments, non-human animals of the present
invention are used to determine the epitope or epitopes of one or
more candidate therapeutic antibodies that bind human PD-1.
[0168] In various embodiments, non-human animals of the present
invention are used to determine the pharmacokinetic profiles of
anti-PD-1 antibodies. In various embodiments, one or more non-human
animals of the present invention and one or more control or
reference non-human animals are each exposed to one or more
candidate therapeutic anti-PD-1 antibodies at various doses (e.g.,
0.1 mg/kg, 0.2 mg/kg, 0.3 mg/kg, 0.4 m 0.5 mg/kg, 1 mg/kg, 2 mg/kg,
3 mg/kg, 4 mg/kg, 5 mg/mg, 7.5 mg/kg, 10 mg/kg, 15 mg/kg, 20 mg/kg,
25 mg/kg, 30 mg/kg, 40 mg/kg, or 50 mg/kg or more). Candidate
therapeutic antibodies may be dosed via any desired route of
administration including parenteral and non-parenteral routes of
administration. Parenteral routes include, e.g., intravenous,
intraarterial, intraportal, intramuscular, subcutaneous,
intraperitoneal, intraspinal, intrathecal, intracerebro
ventricular, intracranial, intrapleural or other routes of
injection. Non-parenteral routes include, e.g., oral, nasal,
transdermal, pulmonary, rectal, buccal, vaginal, ocular.
Administration may also be by continuous infusion, local
administration, sustained release from implants (gels, membranes or
the like), and/or intravenous injection. Blood is isolated from
non-human animals (humanized and control) at various time points
(e.g., 0 hr, 6 hr, 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7
days, 8 days, 9 days, 10 days, 11 days, or up to 30 or more days).
Various assays may be performed to determine the pharmacokinetic
profiles of administered candidate therapeutic antibodies using
samples obtained from non-human animals as described herein
including, but not limited to, total IgG, anti-therapeutic antibody
response, agglutination, etc.
[0169] In various embodiments, non-human animals of the present
invention are used to measure the therapeutic effect of blocking or
modulating PD-1 signaling and the effect on gene expression as a
result of cellular changes. In various embodiments, a non-human
animal of the present invention or cells isolated therefrom are
exposed to a candidate therapeutic that binds a humanized PD-1
protein (or a human portion of a PD-1 protein) on the surface of a
cell of the non-human animal and, after a subsequent period of
time, analyzed for effects on PD-1-dependent processes, for
example, adhesion, apoptosis, cytokine production, inflammation,
proliferation, self-tolerance and viral infection (or
responses).
[0170] Non-human animals of the present invention express humanized
PD-1 protein, thus cells, cell lines, and cell cultures can be
generated to serve as a source of humanized PD-1 for use in binding
and functional assays, e.g., to assay for binding or function of a
PD-1 antagonist or agonist, particularly where the antagonist or
agonist is specific for a human PD-1 sequence or epitope or,
alternatively, specific for a human PD-1 sequence or epitope that
associates with PD-L1 and/or PD-L2. In various embodiments, PD-1
epitopes bound by candidate therapeutic antibodies can be
determined using cells isolated from non-human animals of the
present invention. In various embodiments, a humanized PD-1 protein
expressed by a non-human animal as described herein may comprise a
variant amino acid sequence. Variant human PD-1 proteins (e.g.,
polymorphisms) associated with autoimmune and infectious diseases
have been reported (e.g., see Lee, Y. H. et al. (2014) L.
Rheumatol. PMID: 24942602; Mansur, A. et al. (2014) J. Investig.
Med. 62(3):638-643; Nasi, M. et al. (2013) Intern, J. Infect. Dis.
17:e845-e850; Piskin, I.E. et al. (2013) Neuropediatrics
44(4):187-190; Carter, L.L. et al. (2007) J. Neuroimmunol.
182(1-2):124-134; Wan, B. et al. (2006) J. Immunol,
1770.2):8844-8850). Exemplary human PD-1 variants include those
listed in the SNP GeneView webpage from NCBI and are summarized in
Table 3. In various embodiments, non-human animals of the present
invention express a humanized PD-1 protein variant. In various
embodiments, the variant is polymorphic at an amino acid position
associated with ligand binding. In various embodiments, non-human
animals of the present invention are used to determine the effect
of ligand binding through interaction with a polymorphic variant of
human PD-1. In some certain embodiments, non-human animals of the
present invention express a human PD-1 variant that appears in
Table 3.
TABLE-US-00003 TABLE 3 Chromo- Amino some mRNA Variant ID Amino
Codon acid position position No. Allele acid position position
241851110 883 rs372765600 A Gln [Q] 2 272 G Arg [R] 2 272 241851118
875 rs368411538 T Asp [D] 3 269 C Asp [D] 3 269 241851121 872
rs2227981 A Ala [A] 3 268 C Ala [A] 3 268 G Ala [A] 3 268 T Ala [A]
3 268 241851135 858 rs14664159 T Cys [C] 1 264 C Arg [R] 1 264
241851138 855 rs143359677 A Thr [T] 1 263 G Ala [A] 1 263 241851160
833 rs141228784 T Ser [S] 3 255 C Ser [S] 3 255 241851163 830
rs200434733 C Pro [P] 3 254 T Pro [P] 3 254 241851171 822
rs201961957 A Ile [I] 1 252 G Val [V] 1 252 241851188 805
rs201540918 T Met [M] 7 246 C Thr [T] 2 246 241851190 803
rs201481671 A Gln [Q] 3 245 G Gln [Q] 3 245 241851210 783
rs137861407 A Met [M] 1 239 G Val [V] 1 239 241851220 773
rs370462869 A Pro [P] 3 235 G Pro [P] 3 235 241851237 756
rs147213978 C Arg [R] 1 230 T Trp [W] 1 230 241851264 729
rs373940258 A Met [M] 1 221 G Val [V] 1 221 241851274 719
rs373831349 G Pro [P] 3 217 T Pro [P] 3 217 241851279 714
rs376257658 A Met [M] 1 216 G Val [V] 1 216 241851281 712 rs2227982
T Val [V] 2 215 C Ala [A] 2 215 241851954 690 rs148456597 A Thr [T]
1 208 C Pro [P] 1 208 241851961 683 rs146821282 G Thr [T] 3 205 T
Thr [T] 3 205 C Thr [T] 3 205 241852204 654 rs144217487 A Thr [T] 1
196 G Ala [A] 1 196 241852205 653 rs141119263 T Ala [A] 3 195 C Ala
[A] 3 195 241852209 649 rs200312345 A Gln [Q] 2 194 G Arg [R] 2 194
241852258 600 rs55667829 T Leu [L] 1 178 C Leu [L] 1 178 241852271
587 rs377191240 T Val [V] 3 173 C Val [V] 3 173 241852310 548
rs370660750 G Pro [P] 3 160 C Pro [P] 3 160 241852644 481
rs138031190 A Gln [Q] 2 138 T Leu [L] 2 138 241852658 467
rs374762232 A Gln [Q] 3 133 G Gln [Q] 3 133 241852661 464
rs41400345 A Ala [A] 3 132 G Ala [A] 3 132 241852691 434
rs367833850 T Leu [L] 3 122 C Leu [L] 3 122 241852697 428
rs186074812 T Thr [T] 3 120 C Thr [T] 3 120 241852715 410
rs141299049 A Arg [R] 3 114 G Arg [R] 3 114 241852716 409
rs55679128 A Gln [Q] 2 114 G Arg [R] 2 114 241852720 405
rs200323895 A Thr [T] 1 113 G Ala [A] 1 113 241852729 396
rs190602950 A Met [M] 1 110 G Val [V] 1 110 241852730 395
rs370268595 T Ser [S] 3 109 C Ser [S] 3 109 241852743 382
rs368009835 G Gly [G] 2 105 A Asp [D] 2 105 241852746 379
rs138016578 A His [H] 2 104 G Arg [R] 2 104 241852750 375
rs56124337 A Arg [R] 1 103 G Gly [G] 1 103 241852751 374 rs55637807
T Asn [N] 3 102 C Asn [N] 3 102 241852755 370 rs371902970 T Leu [L]
2 101 C Pro [P] 2 101 241852788 337 rs144257658 T Val [V] 2 90 G
Gly [G] 2 90 241852808 317 rs55804130 T Pro [P] 3 83 C Pro [P] 3 83
241852817 308 rs373755187 A Ala [A] 3 80 T Ala [A] 3 80 C Ala [A] 3
80 241852860 265 rs28615468 C Thr [T] 2 66 A Asn [N] 2 66 241852866
259 rs142434414 G Gly [G] 2 64 T Val [V] 2 64 241852877 248
rs181904226 A Ser [S] 3 60 G Ser [S] 3 60 241852892 233 rs55993679
T Ser [S] 3 55 C Ser [S] 3 55 241852904 221 rs373582646 G Thr [T] 3
51 C Thr [T] 3 51 241852910 215 rs141718335 T Asn [N] 3 49 C Asn
[N] 3 49 241852922 203 rs374726495 T Thr [T] 3 45 C Thr [T] 3 45
241852928 197 rs147586902 C Val [V] 3 43 G Val [V] 3 43 241852930
195 rs368829632 A Met [M] 1 43 G Val [V] 1 43 241852951 174
rs373081859 G Ala [A] 1 36 A Thr [T] 1 36 741852952 173 rs41444844
G Pro [P] 3 35 C Pro [P] 3 35 241852974 151 rs56234260 T Leu [L] 2
28 C Pro [P] 2 28 241858780 127 rs368550965 A Gln [Q] 2 20 G Arg
[R] 2 20 241858800 107 rs370111035 A Ala [A] 3 13 G Ala [A] 3 13
241858808 99 rs142544044 A Ile [I] 1 11 G Val [V] 1 11
[0171] Cells from non-human animals of the present invention can be
isolated and used on an ad hoc basis, or can be maintained in
culture f.COPYRGT.r many generations. In various embodiments, cells
from a non-human animal of the present invention are immortalized
(e.g., via use of a virus) and maintained in culture indefinitely
(e.g., in serial cultures).
[0172] In various embodiments, cells and/or non-human animals of
the present invention are used in various immunization regimens to
determine the PD-1-mediated functions in the immune response to an
antigen. In some embodiments, candidate therapeutics that bind to,
or block one or more ffinctions of, human (or humanized) PD-1 are
characterized in a non-human animal of the present invention.
Suitable measurements include various cellular assays,
proliferation assays, serum immunoglobulin analysis (e.g., antibody
titer), cytotoxicity assays, characterization of ligand-receptor
interactions (e.g., immunoprecipitation assays). In some
embodiments, non-human animals of the present invention are used to
characterize the PD-1-mediated functions regulating an immune
response to an antigen. In some embodiments, the antigen is
associated with an autoimmune disease, disorder or condition. In
some embodiments, the antigen is associated with an inflammatory
disease, disorder or condition. In some embodiments, the antigen is
a test antigen (e.g., ovalbumin or OVA). In some embodiments, the
antigen is a target associated with a disease or condition suffered
by one or more human patients in need of treatment.
[0173] In various embodiments, non-human animals of the present
invention are used in serum assays for determining titers of
autoantibody production for testing the pharma.co-toxicological
aspects of candidate therapeutics that target human PD-1. In some
embodiments, autoantibody production in non-human animals of the
present invention results from one or more autoimmune diseases,
disorders or conditions induced in the non-human animal.
[0174] In various embodiments, non-human animals of the present
invention are used for challenge with one or more antigens to
determine the therapeutic potential of compounds or biological
agents to modulate PD-1-dependent regulation of an immune response,
including but not limited to, the specific T cell-dependent and B
cell-dependent responses to a given antigen.
[0175] In various embodiments, cells and/or non-human animals of
the present invention are used in a survival and/or proliferation
assay (e.g., employing B or T cells) to screen and develop
candidate therapeutics that modulate human PD-1 signaling.
Activation or loss of PD-1 plays an important role in the
regulation of T cell responses, and regulation of self-tolerance by
PD-1 may result from the activation of specific epitopes of the
extracellular domain of PD-1, therefore, candidate PD-1 modulators
(e.g., antagonists or agonists) may be identified, characterized
and developed using cells of non-human animals of the present
invention and/or a non-human animal as described herein. In some
embodiments, cells and/or non-human animals of the present
invention are used in survival or death assay(s) to determine the
effect on proliferation or apoptosis of a specific cell(s) (e.g.,
cancer cells) in the presence and absence of PD-1.
[0176] In various embodiments, cells and/or non-human animals of
the present invention are used in xenotransplantation of
heterologous (e.g., human) cells or tissue to determine the
PD-1-mediated functions in the physiological (e.g., immune)
response to the transplanted human cells or tissue. In some
embodiments, candidate therapeutics that bind, or block one or more
functions of, human PD-1 are characterized in a non-human animal of
the present invention. Suitable measurements include various
cellular assays, proliferation assays, serum immunoglobulin
analysis (e.g., antibody titer), cytotoxicity assays, and
characterization of ligand-receptor interactions
(immunoprecipitation assays). In some embodiments, non-human
animals of the present invention are used to characterize the
PD-1-mediated functions regulating an immune response to an
antigen. In some embodiments, the antigen is associated with a
neoplasm. In some embodiments, the antigen is associated with an
autoimmune disease, disorder or condition. In some embodiments, the
antigen is associated with an inflammatory disease, disorder or
condition. In some embodiments, the antigen is a target associated
with a disease or condition suffered by one or more human patients
in need of treatment,
[0177] In various embodiments, non-human animals of the present
invention are used in transplantation or adoptive transfer
experiments to determine the therapeutic potential of compounds or
biological agents to modulate PD-1-dependent regulation of new
lymphocytes and their immune function. In various embodiments,
non-human animals of the present invention are transplanted with
human T cells; in some embodiments, naive T cells; in some
embodiments, activated T cells.
[0178] In various embodiments, cells of non-human animals of the
present invention are used to in T cell assays to determine the
therapeutic potential of compounds or biological agents to modulate
PD-1-dependent regulation of T cell-dependent response and
function. Exemplary T cell assays include, but are not limited to,
ELISpot, intracellular cytokine staining, major histocompatibility
complex (MHC) restriction, viral suppression assays, cytotoxicity
assays, proliferation assays and regulatory T cell suppression
assays.
[0179] In various embodiments, cells of non-human animals of the
present invention are used in a cell transmigration assay to screen
and develop candidate therapeutics that modulate human PD-1. Cell
transmigration involves the migration of cells across the
endothelium and transmigration assays permit the measurement of
interactions with, and transmigration of, the endothelium by
leukocytes or tumor cells.
[0180] In various embodiments, cells of non-human animals of the
present invention are used in tumor cell growth (or proliferation)
assays to determine the therapeutic potential of compounds or
biological agents to modulate PD-1-dependent regulation and/or
apoptosis of tumor cells.
[0181] In various embodiments, cells of non-human animals of the
present invention are used in cytokine production assays to
determine the therapeutic potential of compounds or biological
agents to modulate PD-1-dependent regulation of cytokine release
from T cells. In some embodiments, cells of non-human animals of
the present invention are used for detection (and/or measurement)
of intracellular cytokine release resulting from interaction of
humanized PD-1 with a drug targeting human PD-1 or a PD-1 ligand
(e.g., PD-L1 or PD-L2).
[0182] In various embodiments, an autoimmune disease, disorder or
condition is induced in one or more non-human animals of the
present invention to provide an in vivo system for determining the
therapeutic potential of compounds or biological agents to modulate
PD-1-dependent regulation of one or more functions of the
autoimmune disease, disorder or condition. Exemplary autoimmune
diseases, disorders or conditions that may be induced in one or
more non-human animals of the present invention include diabetes,
experimental autoimmune encephalomyelitis (e.g., a model for
multiple sclerosis), rheumatoid arthritis, and systemic lupus
erythematosus.
[0183] Non-human animals of the present invention provide an in
vivo system for the analysis and testing of a drug or vaccine. In
various embodiments, a candidate drug or vaccine may be delivered
to one or more non-human animals of the present invention, followed
by monitoring of the non-human animals to determine one or more of
the immune response to the drug or vaccine, the safety profile of
the drug or vaccine, or the effect on a disease or condition. In
some embodiments, the vaccine targets a virus such as, for example,
human immunodeficiency virus or hepatitis virus (e.g. HCV).
Exemplary methods used to determine the safety profile include
measurements of toxicity, optimal dose concentration, efficacy of
the drug or vaccine, and possible risk factors. Such drugs or
vaccines may be improved and/or developed in such non-human
animals.
[0184] Non-human animals of the present invention provide an in
vivo system for assessing the pharmacokinetic properties of a drug
targeting human PD-1. In various embodiments, a drug targeting
human PD-1 may be delivered or administered to one or more
non-human animals of the present invention, followed by monitoring
of, or performing one or more assays on, the non-human animals (or
cells isolated therefrom) to determine the effect of the drug on
the non-human animal. Pharmacokinetic properties include, but are
not limited to, how an animal processes the drug into various
metabolites (or detection of the presence or absence of one or more
drug metabolites, including, toxic metabolites), drug half-life,
circulating levels of drug after administration (e.g., serum
concentration of drug), anti-drug response (e.g., anti-drug
antibodies), drug absorption and distribution, route of
administration, routes of excretion and/or clearance of the drug.
In some embodiments, pharmacokinetic and pharmacodynamic properties
of drugs (e.g., PD-1 modulators) are monitored in or through the
use of non-human animals of the present invention.
[0185] Non-human animals of the present invention provide an in
vivo system for assessing the on-target toxicity of a drug
targeting human PD-1. In various embodiments, a drug targeting
human PD-1 may be delivered or administered to one or more
non-human animals of the present invention, followed by monitoring
of or performing one or more assays on the non-human animals (or
cells isolated therefrom) to determine the on-target toxic effect
of the drug on the non-human animal. Typically, drugs are intended
to modulate one or more functions of their targets. To give but one
example, a PD-1 modulator is intended to modulate PD-1-mediated
functions (e.g., PD-1 signal transduction) through interacting in
some way with the PD-1 molecule on the surface of one or more
cells. In some embodiments, such a modulator may have an adverse
effect that is an exaggeration of the desired pharmacologic
action(s) of the modulator. Such effects are termed on-target
effects. Exemplary on-target effects include too high of a dose,
chronic activation/inactivation, and correct action in an incorrect
tissue. In some embodiments, on-target effects of a drug targeting
PD-1 identified in or through the use of non-human animals of the
present invention are used to determine a previously unknown
function(s) of PD-1.
[0186] Non-human animals of the present invention provide an in
vivo system for assessing the off-target toxicity of a drug
targeting human PD-1. In various embodiments, a drug targeting
human PD-1 may be delivered or administered to one or more
non-human animals of the present invention, followed by monitoring
of or performing one or more assays on the non-human animals (or
cells isolated therefrom) to determine the off-target toxic effect
of the drug on the non-human animal. Off-target effects can occur
when a drug interacts with an unintended target (e.g.,
cross-reactivity to a common epitope). Such interactions can occur
in an intended or unintended tissue. To give but one example, minor
image isomers (enantiomers) of a drug can lead to off-target toxic
effects. Further, a drug can inappropriately interact with and
unintentionally activate different receptor subtypes. Exemplary
off-target effects include incorrect activation/inhibition of an
incorrect target regardless of the tissue in which the incorrect
target is found. In some embodiments, off-target effects of a drug
targeting human PD-1 are determined by comparing the effects of
administering the drug to non-human animals of the present
invention to one or more reference non-human animals.
[0187] In some embodiments, performing an assay includes
determining the effect on the phenotype and/or genotype of the
non-human animal to which the drug is administered. In some
embodiments, performing an assay includes determining lot-to-lot
variability for a PD-1 modulator (e.g., an antagonist or an
agonist). In some embodiments, performing an assay includes
determining the differences between the effects of a drug targeting
PD-1 administered to a non-human animal of the present invention
and a reference non-human animal. In various embodiments, reference
non-human animals may have a modification as described herein, a
modification that is different as described herein (e.g., one that
has a disruption, deletion or otherwise non-functional Pdcd1 gene)
or no modification a wild-type non-human animal).
[0188] Exemplary parameters that may be measured in non-human
animals (or in and/or using cells isolated therefrom) for assessing
the pharmacokinetic properties, on-target toxicity, and/or
off-target toxicity of a drug targeting human PD-1 include, hut are
not limited to, agglutination, autophagy, cell division, cell
death, complement-mediated hemolysis, DNA integrity, drug-specific
antibody titer, drug metabolism, gene expression arrays, metabolic
activity, mitochondrial activity, oxidative stress, phagocytosis,
protein biosynthesis, protein degradation, protein secretion,
stress response, target tissue drug concentration, non-target
tissue drug concentration, transcriptional activity and the like.
In various embodiments, non-human animals of the present invention
are used to determine a pharmaceutically effective dose of a PD-1
modulator.
[0189] Non-human animals of the present invention provide an
improved in vivo system for the development and characterization of
candidate therapeutics for use in cancer. In various embodiments,
non-human animals of the present invention may be implanted with a
tumor, followed by administration of one or more candidate
therapeutics. In some embodiments, candidate therapeutics may
include a multi-specific antibody (e.g., a bi-specific antibody) or
an antibody cocktail; in some embodiments, candidate therapeutics
include combination therapy such as, for example, administration of
mono-specific antibodies dosed sequentially or simultaneously. The
tumor may be allowed sufficient time to be established in one or
more locations within the non-human animal. Tumor cell
proliferation, growth, survival, etc. may be measured both before
and after administration with the candidate therapeutic(s).
Cytoxicity of candidate therapeutics may also be measured in the
non-human animal as desired.
[0190] Non-human animals of the present invention may be used to
develop one or more disease models to evaluate or assess candidate
therapeutics and/or therapeutic regimens (e.g., monotherapy,
combination therapy, dose range testing, etc.) to effectively treat
diseases, disorders or conditions that affect humans. Various
disease conditions may be established in non-human animals of the
present invention followed by administration of one or more
candidate molecules (e.g., drugs targeting PD-1) so that efficacy
of the one or more candidate molecules in a disease condition can
determined. In some embodiments, disease models include autoimmune,
inflammatory and/or neoplastic diseases, disorders or
conditions.
[0191] To give but one example, non-human animals of the present
invention provide an improved animal model for prophylactic and/or
therapeutic treatment of a tumor or tumor cells. In various
embodiments, non-human animals of the present invention may be
implanted with one or more tumor cells, followed by administration
of one or more candidate therapeutics (e.g., antibodies). In some
embodiments, administration of one or more candidate therapeutics
is performed subsequent to (e.g., minutes or hours but typically on
the same day as) implantation of one or more tumor cells and one or
more candidate therapeutics are evaluated in non-human animals of
the present invention for efficacy in preventing establishment of a
solid tumor and/or growth of tumor cells in said non-human animals.
In some embodiments, administration of one or more candidate
therapeutics is performed subsequent to (e.g., days after)
implantation of one or more tumor cells and, in some certain
embodiments, after a sufficient time such that one or more
implanted tumor cells have reached a predetermined size (e.g.,
volume) in non-human animals of the present invention; and one or
more candidate therapeutics are evaluated for efficacy in treatment
of one or more established tumors. Non-human animals may be placed
into different treatment groups according to dose so that an
optimal dose or dose range that correlates to effective treatment
of an established tumor can be determined.
[0192] Candidate molecules can be administered to non-human animal
disease models using any method of administration including
parenteral and non-parenteral routes of administration. Parenteral
routes include, e.g., intravenous, intraarterial, intraportal,
intramuscular, subcutaneous, intraperitoneal, intraspinal,
intrathecal, intracerebroventricular, intracranial, intrapleural or
other routes of injection. Non-parenteral routes include, e.g.,
oral, nasal, transdertnal, pulmonary, rectal, buccal, vaginal,
ocular. Administration may also be by continuous infusion, local
administration, sustained release from implants (gels, membranes or
the like), and/or intravenous injection. When a combination therapy
is evaluted in non-human animals of the present invention,
candidate molecules can be administered via the same administration
route or via different administration routes. When a dosing regimen
is evaluated in non-human animals of the present invention,
candidate molecules may be administered at bimonthly, monthly,
triweekly, biweekly, weekly, daily, at variable intervals and/or in
escalating concentrations to determine a dosing regimen that
demonstrates a desired therapeutic or prophylactic effect in a
non-human animal in which one or more disease models has been
established.
[0193] Non-human animals of the present invention provide an
improved in vivo system for the development and characterization of
candidate therapeutics for use in infectious diseases. In various
embodiments, non-human animals of the present invention may be
infected by injection with a virus (e.g., MHV, HIV, HCV, etc.) or
pathogen (e.g., bacteria), followed by administration of one or
more candidate therapeutics. In some embodiments, candidate
thereapeutics may include a multi-specific antibody (e.g., a
bi-specific antibody) or an antibody cocktail; in some embodiments,
candidate therapeutics include combination therapy such as, for
example, administration of mono-specific antibodies dosed
sequentially or simultaneously; in some embodiments, candidate
therapeutics may include a vaccine. The virus or pathogen may be
allowed sufficient time to be established in one or more locations
or cells within the non-human animal so that one or more symptoms
associated with infection of the virus or pathogen develop in the
non-human animal. T cell proliferation and growth may be measured
both before and after administration with the candidate
therapeutic(s). Further, survival, serum and/or intracellular
cytokine analysis, liver and/or spleen histopathology may be
measured in non-human animals infected with the virus or pathogen.
In some embodiments, non-human animals of the present invention are
used to determine the extent of organ damage associated with viral
infection. In some embodiments, non-human animals of the present
invention are used to determine the cytokine expression profile in
various organs of non-human animals infected with a particular
virus.
[0194] Non-human animals of the present invention can be employed
to assess the efficacy of a therapeutic drug targeting human cells.
In various embodiments, a non-human animal of the present invention
is transplanted with human cells, and a drug candidate targeting
such human cells is administered to such non-human animal. The
therapeutic efficacy of the drug is then determined by monitoring
the human cells in the non-human animal after the administration of
the drug. Drugs that can be tested in the non-human animals include
both small molecule compounds, i.e., compounds of molecular weights
of less than 1500 kD, 1200 kD, 1000 kD, or 800 daltons, and large
molecular compounds (such as proteins, e.g., antibodies), which
have intended therapeutic effects for the treatment of human
diseases and conditions by targeting (e.g., binding to and/or
acting on) human cells.
[0195] In some embodiments, the drug is an anti-cancer drug, and
the human cells are cancer cells, which can be cells of a primary
cancer or cells of cell lines established from a primary cancer. In
these embodiments, a non-human animal of the present invention is
transplanted with human cancer cells, and an anti-cancer drug is
given to the non-human animal. The efficacy of the drug can be
determined by assessing whether growth or metastasis of the human
cancer cells in the non-human animal is inhibited as a result of
the administration of the drug.
[0196] In specific embodiments, the anti-cancer drug is an antibody
molecule, which binds an antigen on human cancer cells. In
particular embodiments, the anti-cancer drug is a bi-specific
antibody that binds to an antigen on human cancer cells, and to an
antigen on other human cells, for example, cells of the human
immune system (or "human immune cells") such as B cells and T
cells.
EXAMPLES
[0197] The following examples are provided so as to describe to
those of ordinary skill in the art how to make and use methods and
compositions of the invention, and are not intended to limit the
scope of what the inventors regard as their invention. Unless
indicated otherwise, temperature is indicated in Celsius, and
pressure is at or near atmospheric.
Example 1
Humanization of an Endogenous Programmed Cell Death 1 (Pdcd1)
Gene
[0198] This example illustrates exemplary methods of humanizing an
endogenous Pdcd1 gene encoding Programmed cell death protein 1
(PD-1) in a non-human mammal such as a rodent (e.g., a mouse). The
methods described in this example can be employed to humanize an
endogenous Pdcd1 gene of a non-human animal using any human
sequence, or combination of human sequences (or sequence fragments)
as desired. In this example, an .about.883 bp human DNA fragment
containing exon 2, intron 2, and the first 71 bp of exon 3 of a
human PDCD1 gene that appears in GenBank accesion NM_005018.2 (SEQ.
ID NO: 23) is employed for humanizing an endogenous Pdcd1 gene of a
mouse. A targeting vector for humanization of the genetic material
encoding an extracellular N-terminal IgV domain, of an endogenous
Pdcd1 gene was constructed using VELOCIGENE.RTM. technology (see,
e.g., U.S. Pat. No. 6,586,251 and Valenzueia et al., 2003, Nature
Biotech. 21(6):652-659; herein incorporated by reference).
[0199] Briefly, mouse bacterial artificial chromosome (BAC) clone
RP23-93N20 (Invitrogen) was modified to delete the sequence
containing exon 2, intron 2 and part of exon 3 of an endogenous
Pdcd1 gene and insert exon 2, intron 2 and part of exon 3 of a
human PDCD1 gene using an .about.883 by human DNA fragment, which
encodes amino acids 26-169 of a human PD-1 polypeptide. Endogenous
DNA containing exon 1, portion of exon 3 (i.e., that encodes the
transmembrane domain), 4 and 5 as well as the 5' and 3'
untranslated regions (UTRs) were retained. Sequence analysis of the
.about.883 by human DNA fragment confirmed all human PDCD1 exons
(i.e., exon 2 and 71 bp of exon 3) and splicing signals. Sequence
analysis revealed that the sequence matched the reference genome
and PDCD1 transcript NM_005018.2.
[0200] In more detail, first, a small bacterial homologous
recombination donor was constructed from a synthetic DNA fragment
containing the following: [(HindIII)-(mouse upstream 78
bp)-(XhoI/NheI restriction enzyme sites)-(human PDCD1 883
bp)-(mouse downstream 75 bp)-(HindIII)]. This fragment was
synthesized by Genescript Inc. (Piscataway, N.J.) and cloned into
an ampicilin-resistant plasmid vector. The XhoI-NheI sites were
employed to ligate a .about.4,996 bp self-deleting neomycin
cassette flanked by recombinase recognition sites
(loxP-hUb1-em7-Neo-pA-mPrm1-Crei-loxP; see U.S. Pat. No.'s
8,697,851, 8,518,392 and 8,354,389, which are herein incorporated
by reference). Subsequent selection employed neomycin. The flanking
HindIII sites were used to linearize the targeting vector prior to
homologous recombination with mouse BAC clone RP23-93N20. By
design, the junction between the Human PDCD1 883bp fragment and the
mouse downstream 75 by preserved the open reading frame in exon 3
(FIG. 2). The resulting targeting vector contained, from 5' to 3',
a 5' homology arm containing .about.61.7 kb of mouse genomic DNA
from BAC clone RP23-93N20, a self-deleting neomycin cassette
flanked by loxP sites, an 883 bp human genomic DNA fragment
(containing exon 2 through the first 71 by of exon 3 of a human
Pdcd1 gene) and .about.84 kb of mouse genomic DNA from BAC clone
RP23-93N20.
[0201] The modified RP23-93N2.0 BAC clone described above was used
to electroporate mouse embryonic stem (ES) cells to create modified
ES cells comprising an endogenous Pdcd1 gene that is humanized from
exon 2 through to part of exon 3 (i.e., deletion of 900 bp of the
endogenous Pdcd1 gene and insertion of 883 bp of human sequence).
Positively targeted ES cells containing a humanized Pdcd1 gene were
identified by an assay (Val enzuela et al., supra) that detected
the presence of the human PDCD1 sequences (e.g., exon 2 and part of
exon 3) and confirmed the loss and/or retention of mouse Pdcd1
sequences (e.g., exon 2 and part of exon 3, and/or exons 1, 4 and
5). Table 4 sets forth the primers and probes that were used to
confirm humanization of an endogenous Pdcd1 gene as described above
(FIG. 3). The nucleotide sequence across the upstream insertion
point included the following, which indicates endogenous mouse
sequence (contained within the parentheses below with an XhoI
restriction site italicized) upstream of the 5' end of
self-deleting neomycin cassette of the insertion point linked
contiguously to a loxP site (bolded) and cassette sequence present
at the insertion point: (TCAAAGGACA GAATAGTAGC CTCCAGACCC
TAGGTTCAGT TATGCTGAAG GAAGAGCCCT CTCGAG)ATAACTTCGT ATAATGTATG
CTATACGAAG TTATATGCAT GGCCTCCGCG CCGGGTTTTG GCGCCTCCCG CGGGCGCCCC
CCTCCTCACG (SEQ ID NO: 19). The nucleotide sequence across the
downstream insertion point at the 3' end of the self-deleting
neomycin cassette included the following, which indicates cassette
sequence (contained within the parentheses below with loxP sequence
bolded and an NheI restriction site italicized) contiguous with
human Pdcd1 genomic sequence downstream of the insertion point:
(CTGGAATAAC TTCGTATAAT GTATGCTATA CGAAGTTATG CTAGTAACTA TAACGGTCCT
AAGGTAGCGA GCMGC) AAGAGGCTCT GCAGTGGAGG CCAGTGCCCA TCCCCGGGTG
GCAGAGGCCC CAGCAGAGAC TTCTCAATGA CATTCCAGCT GGGGTGGCCC TTCCAGAGCC
CTTGCTGCCC GAGGGATGTG AGCAGGTGGC CGGGGAGGCT TTGTGGGGCC ACCCAGCCCC
(SEQ ID NO: 20). The nucleotide sequence across the downstream
insertion point at the 3' end of the human PDCD1 genomic sequence
included the following, which indicates human PDCD1 sequence
contiguous with mouse Pdcd1 genomic sequence (contained within the
parentheses below): CCCTTCCAGA GAGAAGGGCA GAAGTGCCCA CAGCCCACCC
CAGCCCCTCA CCCAGGCCAG CCGGCCAGTT CCAAACCCTG (GTCATTGGTA TCATGAGTGC
CCTAGTGGGT ATCCCTGTAT TGCTGCTGCT GGCCTGGGCC CTAGCTGTCT TCTGCTCAAC)
(SEQ ID NO: 21). The nucleotide sequence across the upstream
insertion point after deletion of the neomycin cassette (77 bp
remaining) included the following, which indicates mouse and human
genomic sequence juxtaposed with remaining cassette sequence loxP
sequence (contained within the parentheses below with XhoI and NheI
restriction sites italicized and loxP sequence in bold): TCAAAGGACA
GAATAGTAGC CTCCAGACCC TAGGTTCAGT TATGCTGAAG GAAGAGCCCT (CTGAG
ATAACTTCGT ATAATGTATG CTATACGAAG TTATGCTAGT AACTATAACG GTCCTAAGGT
AGCGA GCTAGC) AAGAG GCTCTGCAGT GGAGGCCAGT GCCCATCCCC GGGTGGCAGA
GGCCCCAGCA GAGACTTCTC AATGACATTC CAGCTGGGGT GGCCCTTCCA (SEQ ID NO:
22).
[0202] Positive ES cell clones were then used to implant female
mice using the VELOCIMOUSE.RTM. method (see, e.g., U.S. Pat. No.
7,294,754 and Poueymirou et al., 2007, Nature Biotech. 25(1):91-99)
to generate a litter of pups containing an insertion of human PDCD1
exon 2 and part of human PDCD1 exon 3 into an endogenous Pdcd1 gene
of a mouse. Mice bearing the humanization of exon 2 and 3 in part
(i.e., the 883 bp human DNA fragment) of an endogenous Pdcd1 gene
were again confirmed and identified by genotyping of DNA isolated
from tail snips using a modification of allele assay (Valenzuela et
al., supra) that detected the presence of the human PDCD1 gene
sequences. Pups are genotyped and cohorts of animals heterozygous
for the humanized Pdcd1 gene construct are selected for
characterization.
TABLE-US-00004 TABLE 4 Name Primer Sequence (5'-3') 7106 UTU
Forward CCCAGCAGAGACTTCTCAATGAC (SEQ ID NO: 7) Probe
TGGCCCTTCCAGAGCCCTTG (SEQ ID NO: 8) Reverse CGGCCACCTGCTCACATC (SEQ
ID NO: 9) 7106 hTD Forward GGCATCTCTGTCCTCTAGCTC (SEQ ID NO: 10)
Probe AAGCACCCGAGCCCCTCTAGTCTG (SEQ ID NO: 11) Reverse
GGGCTGTGGGCACTTCTG (SEQ ID NO: 12) 7106 TU Forward
CCTTCCTCACAGCTCTTTGTTC (SEQ ID NO: 13) Probe
TCTGCATTTCAGAGGTCCCCAATGG (SEQ ID NO: 14) Reverse
GAGCCAGGCTGGGTAGAAG (SEQ ID NO: 15) 7106 TD Forward
CGGTGTCCTAGAACTCTATTCTTTG (SEQ ID NO: 16) Probe
TCCTGGAGACCTCAACAAGATATCCCA (SEQ ID NO: 17) Reverse
TGAAACCGGCCTTCTGGTT (SEQ ID NO: 18)
Example 2
Expression of Humanized PD-1 on Activated T Cells
[0203] This Example demonstrates that non-human animals (e.g.,
rodents) modified to contain a humanized Pdcd1 gene according to
Example 1 express a humanized PD-1 protein on the surface of
activated lymphocytes. In this Example, activated T cells from mice
heterozygous for humanization of an endogenous Pdcd1 gene as
described in Example 1 were stained with anti-PD-1 antibodies to
determine the expression of PD-1 in stimulated T cells isolated
from wild-type and humanized mice.
[0204] Briefly, spleens were harvested and processed from a
wild-type mouse and a mouse heterozygous for humanization of an
endogenous Pdcd1 gene as described in Example 1 into single cell
suspensions by mechanical dissociation. Cells were washed in media
(RPMI supplemented with 10% FBS) and re-suspended at
1.times.10.sup.6/mL and 200 .mu.L (200,000 cells) were plated in
96-well plates. Cells in selected wells were stimulated with
anti-CD3 and anti-CD28 antibodies (both at 1 .mu.g/ML) for 72
hours. Cells were stained for FACS according to manufacturer's
specifications with antibodies recognizing CD4, CD8, CD19 and human
(clone MIH4, BD Biosciences) or mouse (clone J43, eBioscience) PD1.
Stained cells were ran on LSRII flow cytometer and data was
analyzed using Flowjo software. CD8.sup.+T cells were gated
(CD19.sup.-CD8.sup.+) for expression of human and mouse PD1.
Exemplary results are shown in FIG. 4.
[0205] As shown in FIG. 4, mice bearing a humanized Pdcd1 gene as
described in Example 1 express a PD-1 polypeptide that comprises a
human portion and an endogenous mouse portion. The human portion is
detectably expressed via recognition by an antibody that recognizes
a fully human PD-1 polypeptide.
Example 3
In vivo Efficacy of PD-1 Modulators
[0206] This Example demonstrates that non-human animals (e.g.,
rodents) modified to contain a humanized Pdcd1 gene according to
Example 1 can be used in an in vivo assay to screen PD-1 modulators
(e.g., anti-PD-1 antibodies) and determine various characterisitics
such as, for example, inhibition of tumor growth and/or killing of
tumor cells. Tn this Example, several anti-PD-1 antibodies are
screened in mice homozygous for humanization of an endogenous Pdcd1
gene as described in Example 1 to determine the optimal antibody
dose that inhibits tumor growth and the extent to which anti-PD-1
antibodies mediate killing of tumor cells.
[0207] Briefly, mice were divided evenly according to body weight
into five treatment or control groups for Study 1 (n=5/group),
eight treatment or control groups for Study 2 (n=5/group), and five
treatment or control groups for Study 3 (n=7/group). At day zero,
mice were anesthetized by isoflurane inhalation and then
subcutaneously injected with MC38.ova cells in suspension of 100
.mu.L of DMEM into the right flank (Study 1: 5.times.10.sup.5;
Study 2/3: 1.times.10.sup.6). MC38.ova (mouse colon adenocarcinoma)
cells were engineered to express chicken ovalbumin in order to
increase tumor immunogenicity. For Study 1, treatment groups were
intraperitoneally injected with 200 .mu.g of either one of three
anti-PD-1 antibodies, or an isotype control antibody with
irrelevant specificity on days 3, 7, 10, 14, and 17 of the
experiment, while one group of mice was left untreated. For Study
2, treatment groups were intraperitoneally injected with either one
of three anti-PD-1 antibodies at 10 mg/kg or 5 mg/kg per/dose, one
anti-PD-1 antibody (Ab B, IgG4) at 10mg/kg per dose, or an isotype
control antibody with irrelevant specificity at 10 mg/kg on days 3,
7, 10, 14, and 17 of the experiment. For Study 3, treatment groups
were intraperitoneally injected with either one of two anti-PD-1
antibodies at 5 mg/kg or 2.5 mg/kg per/dose, or a control antibody
not specific to PD-1 (control) at 5 mg/kg on days 3, 7, 10, 14, and
17 of the experiment. Table 5 sets forth experimental dosing and
treatment protocol for groups of mice.
[0208] For each of the studies, average tumor volumes determined by
caliper measurements and percent survival at Day 14 or 17 and Day
23 or 24 of each experiment for each treatment group were recorded.
The number of tumor-free mice were also assessed at the end of the
study (Day 42 for Study 1 and Day 31 for Study 2 and Study 3). Mean
tumor volume (mm.sup.3)(.+-.SD), percent survival, and number of
tumor-free mice were calculated for each study (Tables 7-9).
Exemplary tumor growth curves are provided in FIG. 5.
[0209] As shown in Table 6 for Study 1, mice treated with Ab A did
not develop any detectable tumors during the course of the study.
Mice treated with Ab C exhibited a sustained reduced tumor volume
as compared to controls at days 17 and 24 of the study; and 3 out
of 5 mice were tumor free by the end of the experiment. In
contrast, treatment with Ab B did not demonstrate significant
efficacy in reducing tumor volume in this study as compared to
controls. By day 23 of the study, 1 out of 5 mice died in the group
that received Ab B, and 2 out of 5 mice died in the isotype control
treatment group. In non-treatment and isotype control groups, some
mice exhibited spontaneous regression of tumors (1 out of 5 mice
and 2 out of 5 mice, respectively).
[0210] As shown in Table 7 for Study 2, mice treated with Ab A at
10 mg/kg did not develop detectable tumors during the course of the
study. Groups of mice treated with 10 mg/kg of either Ab C or Ab D
exhibited substantially reduced tumor volume as compared to
controls at days 17 and 24 of the study. Four out of 5 mice in each
group treated with 10 mg/kg of either Ab C or Ab D were tumor free
at Day 31, whereas in the isotype control treatment group only 1
out of 5 animals was tumor free as a result of spontaneous tumor
regression. Ab B tested at 10 mg/kg demonstrated substantially
reduced tumor volume as compared to controls at days 17 and 24 of
the study, but this antibody was the least efficacious anti-PD1
antibody with only 2 out of 5 mice surviving at the end of the
experiment.
[0211] A dose-dependent response in tumor suppression at the tested
doses (5 mg/kg and 10 mg/kg) was observed in groups treated with Ab
A, Ab C, and Ab D. Ab A or Ab C therapy at 5 mg/kg was less
efficacious, with 4 out of 5 tumor-free mice at the end of
experiment on day 31, whereas 5 out of 5 mice remained tumor-free
in 10 mg/kg dose group of Ab A. Dunett's test in 2 way ANOVA
multiple comparisons revealed that the differences in tumor growth
between the group treated with isotype control antibody at 10 mg/kg
as reference and the groups treated at 10 mg/kg with Ab A, Ab C or
Ab D were statistically significant with p value<0.005. The
differences in tumor growth between the group treated with isotype
control antibody at 10 mg/kg as reference and the groups treated at
5 mg/kg with Ab A, Ab C or Ab D were also statistically significant
with a p value<0.05.
[0212] As shown in Table 8 for Study 3, 6 out or 7 mice treated
with Ab A or Ab C at 5mg/kg were tumor free at the end of the
experiment, whereas there were no tumor free animals in the isotype
control group. One tumor-bearing mouse in the IgG4 control group
died on post-implantation day 17. Only 4 out of 7 mice treated with
Ab C at 2.5 mg/kg remained tumor free at the end of the experiment.
The difference in tumor volumes at day 21 between anti-PD-1
antibodies tested and an isotype control group was statistically
significant as determined by one-way ANOVA with Dunnett's multiple
comparison post-test with p<0.01. All four anti-PD-1 antibodies
tested were equally more efficacious at the 5 mg/kg dose than at
the 2.5 mg/kg dose.
[0213] As shown in FIG. 5, anti-PD-1 antibodies significantly
inhibited tumor growth in a prophylactic MC38.ova tumor growth
model in PD-1 humanized mice made according to Example 1. Anti-PD-1
Ab therapy at 10 mg/kg promoted tumor regression in all mice (5 out
of 5) throughout the course of the experiment, whereas only one out
of five animals remained tumor-free in the control group resulting
from spontaneous tumor regression. Anti-PD-1 therapy at 5 mg/kg was
slightly less efficacious, with four out of five tumor-free mice at
the end of the experiment. One-way ANOVA with Dunnett's multiple
comparison post-test revealed a significant difference in tumor
volumes between anti-PD-1 and control antibody treatments with a p
value<0.05 (5 mg/kg) and p value<0.01 (10 mg/kg).
[0214] In a similar experiment, intact functional PD-1 signaling in
PD-1 humanized mice made according to Example 1 was investigated by
measuring CD8.sup.+ T cells and CD3.sup.+ T cells responses and
IFN.gamma. production in spleens of tumor-bearing mice treated with
anti-PD-1 antibody.
[0215] Briefly, spleen cells were obtained from PD-1 humanized mice
(75% C57BL/6/25% 129) treated with anti-PD-1 or control antibody at
the end of the experiments on Day 21 (described above). Total RNA
was isolated, and real-time PCR was performed on reverse
transcribed cDNA using oligonucleotides and taqman probe mix
specific for mouse CD8b (forward primer: GCTCTGGCTG GTCTTCAGTA TG,
SEQ ID NO: 24; reverse primer: TTGCCGTATG GTTGGTTTGA AC, SEQ ID NO:
25; probe: AGCAGCTCTG CCCTCAT, SEQ ID NO: 26), mouse CD3.zeta.
(Mm00446171_m1, Applied Biosystems), mouse IFN-.gamma.
(Mm01168134.sub.--l m1, Applied. Biosystems), human PD-1 (forward
primer: ACTTCCACAT GAGCGTGG, SEQ ID NO: 27; reverse primer:
GGGCTGTGGG CACTTCTG, SEQ ID NO: 28; probe: GCAGATCAAA GAGAGCCTGC,
SEQ ID NO: 29) and mouse PD-1 (Mm01285676_m1, Applied Biosystems).
Samples were normalized relative to expression of mouse cyclophilin
B. Exemplary results are provided in FIG. 6.
[0216] As shown in FIG. 6, administration of anti-hPD-1 antibody
induced increased production of CD8.sup.+ and CD3.sup.+ T cells in
spleens of humanized mice (made according to Example 1) bearing
MC38.ova tumors. Further, activity of anti-hPD-1 antibody in tumor
bearing PD-1 humanized mice was dependent on IFN.gamma., which
confirmed proper signaling through humanized PD-1 on the cell
surface. Overall, an increase in T cells and IFN.gamma. as compared
to control-treated mice was observed for both treatment groups.
[0217] Human PD-1 mRNA expression was measured with human specific
probes designed for the extracellular portion of the PD-1 protein
and confirmed proper expression of humanized PD-1 protein on the
cell surface. Additionally, measurement of mouse PD-1 mRNA
expression with primers designed to detect the extracellular
portion of mouse PD-1 failed to produce a product.
[0218] Taken together, this Example demonstrates that non-human
animals of the present invention can be used to assess the in vivo
efficacy of drugs (e.g., an antibody) targeting PD-1, and such
animals are useful in discriminating the therapeutic effect of
anti-PD-1 antibodies. Morever, non-human animals described herein
can be used to assess the extent to which drugs targeting PD-1 can
inhibit tumor growth and/or mediate killing of tumor cells.
Non-human animals (e.g., mice) of the present invention demonstrate
functional PD-1-signaling and proper PD-1-dependent immune
responses via humanized PD-1 as evidenced by expansion of T cells
and cytokine expression (e.g., IFN-.gamma.).
TABLE-US-00005 TABLE 5 Study # Antibody Dosage 1 Isotype Control
200 .mu.g No treatment N/A Ab A 200 .mu.g Ab B 200 .mu.g Ab C 200
.mu.g 2 Isotype Control 10 mg/kg Ab A 10 mg/kg Ab A 5 mg/kg Ab B 10
mg/kg Ab C 10 mg/kg Ab C 5 mg/kg Ab D 10 mg/kg Ab D 5 mg/kg 3
Isotype Control 5 mg/kg Ab A 5 mg/kg Ab A 2.5 mg/kg Ab C 5 mg/kg Ab
C 2.5 mg/kg
TABLE-US-00006 TABLE 6 Study 1 Tumor Mean tumor volume free
(mm.sup.3, .+-.SD) Survival (%) mice Treatment Day 17 Day 23 Day 17
Day 23 Day 42 group 200 .mu.g/ 200 .mu.g/ 200 .mu.g/ 200 .mu.g/ 200
.mu.g/ (n = 5) mouse mouse mouse mouse mouse No treatment 189
(.+-.110) 554 (.+-.317) 100% 100% 1/5 Isotype Control 86 (.+-.114)
515 (.+-.859) 100% 60% 2/5 Ab A 0 (0) 0 (0) 100% 100% 5/5 Ab B 89
(.+-.176) 445 (.+-.889) 100% 80% 3/5 Ab C 14 (.+-.19) 205 (.+-.312)
100% 100% 3/5
TABLE-US-00007 TABLE 7 Study 2 Mean tumor volume Tumor free
(mm.sup.3; .+-.SD) Survival (%) Mice Day 17 Day 24 Day 17 Day 24
Day 31 Treatment 5 10 5 10 5 10 5 10 5 10 group (n = 5) mg/kg mg/kg
mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg Isotype N/A 449 N/A
824 N/A 100% N/A 60% N/A 1/5 Control (.+-.434) (.+-.858) Ab A 17 0
(0) 104 0 (0) 100 100 100 100 4/5 4/5 (.+-.38) (.+-.233) Ab B N/A
124 N/A 359 N/A 100 N/A 80 N/A 2/5 (.+-.209) (.+-.657) Ab C 91 12
228 96 100 100 80 100 4/5 4/5 (.+-.204) (.+-.28) (.+-.509)
(.+-.215) Ab D 94 10 328 67 100 100 80 100 3/5 4/5 (.+-.160)
(.+-.21) (.+-.559) (.+-.150)
TABLE-US-00008 TABLE 8 Study 3 Mean tumor volume Tumor free
(mm.sup.3; .+-.SD) Survival (%) Mice Day 14 Day 21 Day 14 Day 21
Day 31 Treatment 2.5 5 2.5 5 2.5 5 2.5 5 2.5 5 group (n = 7) mg/kg
mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg Isotype N/A
94 N/A 405 N/A 100 N/A 86 N/A 0/7 Control (.+-.44) (.+-.326) Ab A 0
(0) 0 (0) 19 13 100 100 100 100 6/7 6/7 (.+-.51) (.+-.35) Ab C 41 7
87 16 100 100 100 100 4/7 6/7 (.+-.68) (.+-.20) (.+-.123)
(.+-.42)
Example 4
Rodent Model of Anti-PD-1 Tumor Therapy
[0219] This Example demonstrates that non-human animals (e.g.,
rodents) modified to contain a humanized Pdcd1 gene according to
Example 1 can be used in a tumor model to determine optimal
therapeutic dose(s) of PD-1 modulators (e.g., anti-PD-1
antibodies). In this Example, an anti-PD-1 antibody is administered
to mice homozygous for humanization of an endogenous Pdcd1 gene as
described in Example 1 to determine the optimal therapeutic dose
for treatment of established tumors.
[0220] Briefly, mice containing a humanized Pdcd1 gene (as
described in Example 1) were subcutaneously implanted with
1.times.10.sup.6MC38.Ova cells (described above) and subsequently
randomized into six treatment groups (n=8-9 per group) once tumor
volumes reached 80-120 mm.sup.3 (day 0). Mice were
intraperitoneally administered anti-hPD-1 antibody in an escalating
dose range of mg/kg (i.e., 0.3, 1, 3, 10 or 25 mg/kg) or an isotype
control antibody at 25 mg/kg. Antibodies were dosed on days 0, 3,
7, 10 and 13. Tumor volumes were monitored by calipered
measurements twice per week for the duration of the experiment (60
days). Exemplary tumor growth curves are provided in FIG. 7,
[0221] As shown in FIG. 7, none of the mice administered the
control antibody were tumor free at the end of the experiment. In
constrast, a dose range of 3-25 mg/kg anti-hPD-1 antibody resulted
in about 44-55% tumor free mice among the different treatment
groups. Taken together, this Example demonstrates that non-human
animals of the present invention can be used as a rodent tumor
model to determine the optimal dose and/or dose range of drugs
(e.g., an antibody) targeting PD-1 to effectively treat established
tumors.
Equivalents
[0222] Having thus described several aspects of at least one
embodiment of this invention, it is to be appreciated by those
skilled in the art that various alterations, modifications, and
improvements will readily occur to those skilled in the art. Such
alterations, modifications, and improvements are intended to be
part of this disclosure, and are intended to be within the spirit
and scope of the invention. Accordingly, the foregoing description
and drawing are by way of example only and the invention is
described in detail by the claims that follow.
[0223] Use of ordinal terms such as "first," "second," "third,"
etc., in the claims to modify a claim element does not by itself
connote any priority, precedence, or order of one claim element
over another or the temporal order in which acts of a method are
performed, but are used merely as labels to distinguish one claim
element having a certain name from another element having a same
name (but for use of the ordinal term) to distinguish the claim
elements.
[0224] The articles "a" and "an" as used herein in the
specification and in the claims, unless clearly indicated to the
contrary, should be understood to include the plural referents.
Claims or descriptions that include "or" between one or more
members of a group are considered satisfied if one, more than one,
or all of the group members are present in, employed in, or
otherwise relevant to a given product or process unless indicated
to the contrary or otherwise evident from the context. The
invention includes embodiments in which exactly one member of the
group is present in, employed in, or otherwise relevant to a given
product or process. The invention also includes embodiments in
which more than one, or the entire group members are present in,
employed in, or otherwise relevant to a given product or process.
Furthermore, it is to be understood that the invention encompasses
all variations, combinations, and permutations in which one or more
limitations, elements, clauses, descriptive terms, etc., from one
or more of the listed claims is introduced into another claim
dependent on the same base claim (or, as relevant, any other claim)
unless otherwise indicated or unless it would be evident to one of
ordinary skill in the art that a contradiction or inconsistency
would arise. Where elements are presented as lists, (e.g., in
Markush group or similar format) it is to be understood that each
subgroup of the elements is also disclosed, and any element(s) can
be removed from the group. It should be understood that, in
general, where the invention, or aspects of the invention, is/are
referred to as comprising particular elements, features, etc.,
certain embodiments of the invention or aspects of the invention
consist, or consist essentially of, such elements, features, etc.
For purposes of simplicity those embodiments have not in every case
been specifically set forth in so many words herein. It should also
be understood that any embodiment or aspect of the invention can be
explicitly excluded from the claims, regardless of whether the
specific exclusion is recited in the specification.
[0225] Those skilled in the art will appreciate typical standards
of deviation or error attributable to values obtained in assays or
other processes described herein. The publications, websites and
other reference materials referenced herein to describe the
background of the invention and to provide additional detail
regarding its practice are hereby incorporated by reference.
Sequence CWU 1
1
2911972DNAMus musculus 1tgagcagcgg ggaggaggaa gaggagactg ctactgaagg
cgacactgcc aggggctctg 60ggcatgtggg tccggcaggt accctggtca ttcacttggg
ctgtgctgca gttgagctgg 120caatcagggt ggcttctaga ggtccccaat
gggccctgga ggtccctcac cttctaccca 180gcctggctca cagtgtcaga
gggagcaaat gccaccttca cctgcagctt gtccaactgg 240tcggaggatc
ttatgctgaa ctggaaccgc ctgagtccca gcaaccagac tgaaaaacag
300gccgccttct gtaatggttt gagccaaccc gtccaggatg cccgcttcca
gatcatacag 360ctgcccaaca ggcatgactt ccacatgaac atccttgaca
cacggcgcaa tgacagtggc 420atctacctct gtggggccat ctccctgcac
cccaaggcaa aaatcgagga gagccctgga 480gcagagctcg tggtaacaga
gagaatcctg gagacctcaa caagatatcc cagcccctcg 540cccaaaccag
aaggccggtt tcaaggcatg gtcattggta tcatgagtgc cctagtgggt
600atccctgtat tgctgctgct ggcctgggcc ctagctgtct tctgctcaac
aagtatgtca 660gaggccagag gagctggaag caaggacgac actctgaagg
aggagccttc agcagcacct 720gtccctagtg tggcctatga ggagctggac
ttccagggac gagagaagac accagagctc 780cctaccgcct gtgtgcacac
agaatatgcc accattgtct tcactgaagg gctgggtgcc 840tcggccatgg
gacgtagggg ctcagctgat ggcctgcagg gtcctcggcc tccaagacat
900gaggatggac attgttcttg gcctctttga ccagattctt cagccattag
catgctgcag 960accctccaca gagagcaccg gtccgtccct cagtcaagag
gagcatgcag gctacagttc 1020agccaaggct cccagggtct gagctagctg
gagtgacagc ccagcgcctg caccaattcc 1080agcacatgca ctgttgagtg
agagctcact tcaggtttac cacaagctgg gagcagcagg 1140cttcccggtt
tcctattgtc acaaggtgca gagctggggc ctaagcctat gtctcctgaa
1200tcctactgtt gggcacttct agggacttga gacactatag ccaatggcct
ctgtgggttc 1260tgtgcctgga aatggagaga tctgagtaca gcctgctttg
aatggccctg tgaggcaacc 1320ccaaagcaag ggggtccagg tatactatgg
gcccagcacc taaagccacc cttgggagat 1380gatactcagg tgggaaattc
gtagactggg ggactgaacc aatcccaaga tctggaaaag 1440ttttgatgaa
gacttgaaaa gctcctagct tcgggggtct gggaagcatg agcacttacc
1500aggcaaaagc tccgtgagcg tatctgctgt ccttctgcat gcccaggtac
ctcagttttt 1560ttcaacagca aggaaactag ggcaataaag ggaaccagca
gagctagagc cacccacaca 1620tccagggggc acttgactct ccctactcct
cctaggaacc aaaaggacaa agtccatgtt 1680gacagcaggg aaggaaaggg
ggatataacc ttgacgcaaa ccaacactgg ggtgttagaa 1740tctcctcatt
cactctgtcc tggagttggg ttctggctct ccttcacacc taggactctg
1800aaatgagcaa gcacttcaga cagtcagggt agcaagagtc tagctgtctg
gtgggcaccc 1860aaaatgacca gggcttaagt ccctttcctt tggtttaagc
ccgttataat taaatggtac 1920caaaagcttt aaaaaaaaaa aaaaaaaaaa
aaaaaaaaaa aaaaaaaaaa aa 19722288PRTMus musculus 2Met Trp Val Arg
Gln Val Pro Trp Ser Phe Thr Trp Ala Val Leu Gln 1 5 10 15 Leu Ser
Trp Gln Ser Gly Trp Leu Leu Glu Val Pro Asn Gly Pro Trp 20 25 30
Arg Ser Leu Thr Phe Tyr Pro Ala Trp Leu Thr Val Ser Glu Gly Ala 35
40 45 Asn Ala Thr Phe Thr Cys Ser Leu Ser Asn Trp Ser Glu Asp Leu
Met 50 55 60 Leu Asn Trp Asn Arg Leu Ser Pro Ser Asn Gln Thr Glu
Lys Gln Ala 65 70 75 80 Ala Phe Cys Asn Gly Leu Ser Gln Pro Val Gln
Asp Ala Arg Phe Gln 85 90 95 Ile Ile Gln Leu Pro Asn Arg His Asp
Phe His Met Asn Ile Leu Asp 100 105 110 Thr Arg Arg Asn Asp Ser Gly
Ile Tyr Leu Cys Gly Ala Ile Ser Leu 115 120 125 His Pro Lys Ala Lys
Ile Glu Glu Ser Pro Gly Ala Glu Leu Val Val 130 135 140 Thr Glu Arg
Ile Leu Glu Thr Ser Thr Arg Tyr Pro Ser Pro Ser Pro 145 150 155 160
Lys Pro Glu Gly Arg Phe Gln Gly Met Val Ile Gly Ile Met Ser Ala 165
170 175 Leu Val Gly Ile Pro Val Leu Leu Leu Leu Ala Trp Ala Leu Ala
Val 180 185 190 Phe Cys Ser Thr Ser Met Ser Glu Ala Arg Gly Ala Gly
Ser Lys Asp 195 200 205 Asp Thr Leu Lys Glu Glu Pro Ser Ala Ala Pro
Val Pro Ser Val Ala 210 215 220 Tyr Glu Glu Leu Asp Phe Gln Gly Arg
Glu Lys Thr Pro Glu Leu Pro 225 230 235 240 Thr Ala Cys Val His Thr
Glu Tyr Ala Thr Ile Val Phe Thr Glu Gly 245 250 255 Leu Gly Ala Ser
Ala Met Gly Arg Arg Gly Ser Ala Asp Gly Leu Gln 260 265 270 Gly Pro
Arg Pro Pro Arg His Glu Asp Gly His Cys Ser Trp Pro Leu 275 280 285
32115DNAHomo sapiens 3agtttccctt ccgctcacct ccgcctgagc agtggagaag
gcggcactct ggtggggctg 60ctccaggcat gcagatccca caggcgccct ggccagtcgt
ctgggcggtg ctacaactgg 120gctggcggcc aggatggttc ttagactccc
cagacaggcc ctggaacccc cccaccttct 180ccccagccct gctcgtggtg
accgaagggg acaacgccac cttcacctgc agcttctcca 240acacatcgga
gagcttcgtg ctaaactggt accgcatgag ccccagcaac cagacggaca
300agctggccgc cttccccgag gaccgcagcc agcccggcca ggactgccgc
ttccgtgtca 360cacaactgcc caacgggcgt gacttccaca tgagcgtggt
cagggcccgg cgcaatgaca 420gcggcaccta cctctgtggg gccatctccc
tggcccccaa ggcgcagatc aaagagagcc 480tgcgggcaga gctcagggtg
acagagagaa gggcagaagt gcccacagcc caccccagcc 540cctcacccag
gccagccggc cagttccaaa ccctggtggt tggtgtcgtg ggcggcctgc
600tgggcagcct ggtgctgcta gtctgggtcc tggccgtcat ctgctcccgg
gccgcacgag 660ggacaatagg agccaggcgc accggccagc ccctgaagga
ggacccctca gccgtgcctg 720tgttctctgt ggactatggg gagctggatt
tccagtggcg agagaagacc ccggagcccc 780ccgtgccctg tgtccctgag
cagacggagt atgccaccat tgtctttcct agcggaatgg 840gcacctcatc
ccccgcccgc aggggctcag ctgacggccc tcggagtgcc cagccactga
900ggcctgagga tggacactgc tcttggcccc tctgaccggc ttccttggcc
accagtgttc 960tgcagaccct ccaccatgag cccgggtcag cgcatttcct
caggagaagc aggcagggtg 1020caggccattg caggccgtcc aggggctgag
ctgcctgggg gcgaccgggg ctccagcctg 1080cacctgcacc aggcacagcc
ccaccacagg actcatgtct caatgcccac agtgagccca 1140ggcagcaggt
gtcaccgtcc cctacaggga gggccagatg cagtcactgc ttcaggtcct
1200gccagcacag agctgcctgc gtccagctcc ctgaatctct gctgctgctg
ctgctgctgc 1260tgctgctgcc tgcggcccgg ggctgaaggc gccgtggccc
tgcctgacgc cccggagcct 1320cctgcctgaa cttgggggct ggttggagat
ggccttggag cagccaaggt gcccctggca 1380gtggcatccc gaaacgccct
ggacgcaggg cccaagactg ggcacaggag tgggaggtac 1440atggggctgg
ggactcccca ggagttatct gctccctgca ggcctagaga agtttcaggg
1500aaggtcagaa gagctcctgg ctgtggtggg cagggcagga aacccctcca
cctttacaca 1560tgcccaggca gcacctcagg ccctttgtgg ggcagggaag
ctgaggcagt aagcgggcag 1620gcagagctgg aggcctttca ggcccagcca
gcactctggc ctcctgccgc cgcattccac 1680cccagcccct cacaccactc
gggagaggga catcctacgg tcccaaggtc aggagggcag 1740ggctggggtt
gactcaggcc cctcccagct gtggccacct gggtgttggg agggcagaag
1800tgcaggcacc tagggccccc catgtgccca ccctgggagc tctccttgga
acccattcct 1860gaaattattt aaaggggttg gccgggctcc caccagggcc
tgggtgggaa ggtacaggcg 1920ttcccccggg gcctagtacc cccgccgtgg
cctatccact cctcacatcc acacactgca 1980cccccactcc tggggcaggg
ccaccagcat ccaggcggcc agcaggcacc tgagtggctg 2040ggacaaggga
tcccccttcc ctgtggttct attatattat aattataatt aaatatgaga
2100gcatgctaag gaaaa 21154288PRTHomo sapiens 4Met Gln Ile Pro Gln
Ala Pro Trp Pro Val Val Trp Ala Val Leu Gln 1 5 10 15 Leu Gly Trp
Arg Pro Gly Trp Phe Leu Asp Ser Pro Asp Arg Pro Trp 20 25 30 Asn
Pro Pro Thr Phe Ser Pro Ala Leu Leu Val Val Thr Glu Gly Asp 35 40
45 Asn Ala Thr Phe Thr Cys Ser Phe Ser Asn Thr Ser Glu Ser Phe Val
50 55 60 Leu Asn Trp Tyr Arg Met Ser Pro Ser Asn Gln Thr Asp Lys
Leu Ala 65 70 75 80 Ala Phe Pro Glu Asp Arg Ser Gln Pro Gly Gln Asp
Cys Arg Phe Arg 85 90 95 Val Thr Gln Leu Pro Asn Gly Arg Asp Phe
His Met Ser Val Val Arg 100 105 110 Ala Arg Arg Asn Asp Ser Gly Thr
Tyr Leu Cys Gly Ala Ile Ser Leu 115 120 125 Ala Pro Lys Ala Gln Ile
Lys Glu Ser Leu Arg Ala Glu Leu Arg Val 130 135 140 Thr Glu Arg Arg
Ala Glu Val Pro Thr Ala His Pro Ser Pro Ser Pro 145 150 155 160 Arg
Pro Ala Gly Gln Phe Gln Thr Leu Val Val Gly Val Val Gly Gly 165 170
175 Leu Leu Gly Ser Leu Val Leu Leu Val Trp Val Leu Ala Val Ile Cys
180 185 190 Ser Arg Ala Ala Arg Gly Thr Ile Gly Ala Arg Arg Thr Gly
Gln Pro 195 200 205 Leu Lys Glu Asp Pro Ser Ala Val Pro Val Phe Ser
Val Asp Tyr Gly 210 215 220 Glu Leu Asp Phe Gln Trp Arg Glu Lys Thr
Pro Glu Pro Pro Val Pro 225 230 235 240 Cys Val Pro Glu Gln Thr Glu
Tyr Ala Thr Ile Val Phe Pro Ser Gly 245 250 255 Met Gly Thr Ser Ser
Pro Ala Arg Arg Gly Ser Ala Asp Gly Pro Arg 260 265 270 Ser Ala Gln
Pro Leu Arg Pro Glu Asp Gly His Cys Ser Trp Pro Leu 275 280 285
51972DNAArtificial SequenceHumanized Pdcd1 5tgagcagcgg ggaggaggaa
gaggagactg ctactgaagg cgacactgcc aggggctctg 60ggcatgtggg tccggcaggt
accctggtca ttcacttggg ctgtgctgca gttgagctgg 120caatcagggt
ggcttctaga ctccccagac aggccctgga acccccccac cttctcccca
180gccctgctcg tggtgaccga aggggacaac gccaccttca cctgcagctt
ctccaacaca 240tcggagagct tcgtgctaaa ctggtaccgc atgagcccca
gcaaccagac ggacaagctg 300gccgccttcc ccgaggaccg cagccagccc
ggccaggact gccgcttccg tgtcacacaa 360ctgcccaacg ggcgtgactt
ccacatgagc gtggtcaggg cccggcgcaa tgacagcggc 420acctacctct
gtggggccat ctccctggcc cccaaggcgc agatcaaaga gagcctgcgg
480gcagagctca gggtgacaga gagaagggca gaagtgccca cagcccaccc
cagcccctca 540cccaggccag ccggccagtt ccaaaccctg gtcattggta
tcatgagtgc cctagtgggt 600atccctgtat tgctgctgct ggcctgggcc
ctagctgtct tctgctcaac aagtatgtca 660gaggccagag gagctggaag
caaggacgac actctgaagg aggagccttc agcagcacct 720gtccctagtg
tggcctatga ggagctggac ttccagggac gagagaagac accagagctc
780cctaccgcct gtgtgcacac agaatatgcc accattgtct tcactgaagg
gctgggtgcc 840tcggccatgg gacgtagggg ctcagctgat ggcctgcagg
gtcctcggcc tccaagacat 900gaggatggac attgttcttg gcctctttga
ccagattctt cagccattag catgctgcag 960accctccaca gagagcaccg
gtccgtccct cagtcaagag gagcatgcag gctacagttc 1020agccaaggct
cccagggtct gagctagctg gagtgacagc ccagcgcctg caccaattcc
1080agcacatgca ctgttgagtg agagctcact tcaggtttac cacaagctgg
gagcagcagg 1140cttcccggtt tcctattgtc acaaggtgca gagctggggc
ctaagcctat gtctcctgaa 1200tcctactgtt gggcacttct agggacttga
gacactatag ccaatggcct ctgtgggttc 1260tgtgcctgga aatggagaga
tctgagtaca gcctgctttg aatggccctg tgaggcaacc 1320ccaaagcaag
ggggtccagg tatactatgg gcccagcacc taaagccacc cttgggagat
1380gatactcagg tgggaaattc gtagactggg ggactgaacc aatcccaaga
tctggaaaag 1440ttttgatgaa gacttgaaaa gctcctagct tcgggggtct
gggaagcatg agcacttacc 1500aggcaaaagc tccgtgagcg tatctgctgt
ccttctgcat gcccaggtac ctcagttttt 1560ttcaacagca aggaaactag
ggcaataaag ggaaccagca gagctagagc cacccacaca 1620tccagggggc
acttgactct ccctactcct cctaggaacc aaaaggacaa agtccatgtt
1680gacagcaggg aaggaaaggg ggatataacc ttgacgcaaa ccaacactgg
ggtgttagaa 1740tctcctcatt cactctgtcc tggagttggg ttctggctct
ccttcacacc taggactctg 1800aaatgagcaa gcacttcaga cagtcagggt
agcaagagtc tagctgtctg gtgggcaccc 1860aaaatgacca gggcttaagt
ccctttcctt tggtttaagc ccgttataat taaatggtac 1920caaaagcttt
aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa
19726288PRTArtificial SequenceHumanized PD-1 6Met Trp Val Arg Gln
Val Pro Trp Ser Phe Thr Trp Ala Val Leu Gln 1 5 10 15 Leu Ser Trp
Gln Ser Gly Trp Leu Leu Asp Ser Pro Asp Arg Pro Trp 20 25 30 Asn
Pro Pro Thr Phe Ser Pro Ala Leu Leu Val Val Thr Glu Gly Asp 35 40
45 Asn Ala Thr Phe Thr Cys Ser Phe Ser Asn Thr Ser Glu Ser Phe Val
50 55 60 Leu Asn Trp Tyr Arg Met Ser Pro Ser Asn Gln Thr Asp Lys
Leu Ala 65 70 75 80 Ala Phe Pro Glu Asp Arg Ser Gln Pro Gly Gln Asp
Cys Arg Phe Arg 85 90 95 Val Thr Gln Leu Pro Asn Gly Arg Asp Phe
His Met Ser Val Val Arg 100 105 110 Ala Arg Arg Asn Asp Ser Gly Thr
Tyr Leu Cys Gly Ala Ile Ser Leu 115 120 125 Ala Pro Lys Ala Gln Ile
Lys Glu Ser Leu Arg Ala Glu Leu Arg Val 130 135 140 Thr Glu Arg Arg
Ala Glu Val Pro Thr Ala His Pro Ser Pro Ser Pro 145 150 155 160 Arg
Pro Ala Gly Gln Phe Gln Thr Leu Val Ile Gly Ile Met Ser Ala 165 170
175 Leu Val Gly Ile Pro Val Leu Leu Leu Leu Ala Trp Ala Leu Ala Val
180 185 190 Phe Cys Ser Thr Ser Met Ser Glu Ala Arg Gly Ala Gly Ser
Lys Asp 195 200 205 Asp Thr Leu Lys Glu Glu Pro Ser Ala Ala Pro Val
Pro Ser Val Ala 210 215 220 Tyr Glu Glu Leu Asp Phe Gln Gly Arg Glu
Lys Thr Pro Glu Leu Pro 225 230 235 240 Thr Ala Cys Val His Thr Glu
Tyr Ala Thr Ile Val Phe Thr Glu Gly 245 250 255 Leu Gly Ala Ser Ala
Met Gly Arg Arg Gly Ser Ala Asp Gly Leu Gln 260 265 270 Gly Pro Arg
Pro Pro Arg His Glu Asp Gly His Cys Ser Trp Pro Leu 275 280 285
723DNAArtificial SequenceSynthetic Oligonucleotide 7106 hTU Forward
7cccagcagag acttctcaat gac 23820DNAArtificial SequenceSynthetic
Oligonucleotide 7106 hTU Probe 8tggcccttcc agagcccttg
20918DNAArtificial SequenceSynthetic Oligonucleotide 7106 hTU
Reverse 9cggccacctg ctcacatc 181021DNAArtificial SequenceSynthetic
Oligonucleotide 7106 hTD Forward 10ggcatctctg tcctctagct c
211124DNAArtificial SequenceSynthetic Oligonucleotide 7106 hTD
Probe 11aagcacccca gcccctctag tctg 241218DNAArtificial
SequenceSynthetic Oligonucleotide 7106 hTD Reverse 12gggctgtggg
cacttctg 181322DNAArtificial SequenceSynthetic Oligonucleotide 7106
TU Forward 13ccttcctcac agctctttgt tc 221425DNAArtificial
SequenceSynthetic Oligonucleotide 7106 TU Probe 14tctgcatttc
agaggtcccc aatgg 251519DNAArtificial SequenceSynthetic
Oligonucleotide 7106 TU Reverse 15gagccaggct gggtagaag
191625DNAArtificial SequenceSynthetic Oligonucleotide 7106 TD
Forward 16cggtgtccta gaactctatt ctttg 251727DNAArtificial
SequenceSynthetic Oligonucleotide 7106 TD Probe 17tcctggagac
ctcaacaaga tatccca 271819DNAArtificial SequenceSynthetic
Oligonucleotide 7106 TD Reverse 18tgaaaccggc cttctggtt
1919156DNAArtificial SequenceSynthetic Oligonucleotide 19tcaaaggaca
gaatagtagc ctccagaccc taggttcagt tatgctgaag gaagagccct 60ctcgagataa
cttcgtataa tgtatgctat acgaagttat atgcatggcc tccgcgccgg
120gttttggcgc ctcccgcggg cgcccccctc ctcacg 15620236DNAArtificial
SequenceSynthetic Oligonucleotide 20ctggaataac ttcgtataat
gtatgctata cgaagttatg ctagtaacta taacggtcct 60aaggtagcga gctagcaaga
ggctctgcag tggaggccag tgcccatccc cgggtggcag 120aggccccagc
agagacttct caatgacatt ccagctgggg tggcccttcc agagcccttg
180ctgcccgagg gatgtgagca ggtggccggg gaggctttgt ggggccaccc agcccc
23621160DNAArtificial SequenceSynthetic Oligonucleotide
21cccttccaga gagaagggca gaagtgccca cagcccaccc cagcccctca cccaggccag
60ccggccagtt ccaaaccctg gtcattggta tcatgagtgc cctagtgggt atccctgtat
120tgctgctgct ggcctgggcc ctagctgtct tctgctcaac
16022232DNAArtificial SequenceSynthetic Oligonucleotide
22tcaaaggaca gaatagtagc ctccagaccc taggttcagt tatgctgaag gaagagccct
60ctcgagataa cttcgtataa tgtatgctat acgaagttat gctagtaact ataacggtcc
120taaggtagcg agctagcaag aggctctgca gtggaggcca gtgcccatcc
ccgggtggca 180gaggccccag cagagacttc tcaatgacat tccagctggg
gtggcccttc ca 23223883DNAArtificial SequenceSynthetic
Oligonucleotide Human 883 bp DNA fragment 23aagaggctct gcagtggagg
ccagtgccca tccccgggtg gcagaggccc cagcagagac 60ttctcaatga cattccagct
ggggtggccc ttccagagcc cttgctgccc gagggatgtg 120agcaggtggc
cggggaggct ttgtggggcc acccagcccc ttcctcacct ctctccatct
180ctcagactcc ccagacaggc cctggaaccc ccccaccttc tccccagccc
tgctcgtggt 240gaccgaaggg gacaacgcca ccttcacctg cagcttctcc
aacacatcgg agagcttcgt 300gctaaactgg taccgcatga gccccagcaa
ccagacggac aagctggccg ccttccccga 360ggaccgcagc cagcccggcc
aggactgccg cttccgtgtc acacaactgc ccaacgggcg 420tgacttccac
atgagcgtgg tcagggcccg gcgcaatgac agcggcacct acctctgtgg
480ggccatctcc ctggccccca aggcgcagat caaagagagc ctgcgggcag
agctcagggt 540gacaggtgcg gcctcggagg ccccggggca ggggtgagct
gagccggtcc tggggtgggt 600gtcccctcct gcacaggatc aggagctcca
gggtcgtagg gcagggaccc cccagctcca 660gtccagggct ctgtcctgca
cctggggaat ggtgaccggc atctctgtcc tctagctctg 720gaagcacccc
agcccctcta gtctgccctc acccctgacc ctgaccctcc accctgaccc
780cgtcctaacc cctgaccttt gtgcccttcc agagagaagg gcagaagtgc
ccacagccca 840ccccagcccc tcacccaggc cagccggcca gttccaaacc ctg
8832422DNAArtificial SequenceSynthetic Oligonucleotide 24gctctggctg
gtcttcagta tg 222522DNAArtificial SequenceSynthetic Oligonucleotide
25ttgccgtatg gttggtttga ac 222617DNAArtificial SequenceSynthetic
Oligonucleotide 26agcagctctg ccctcat 172718DNAArtificial
SequenceSynthetic Oligonucleotide 27acttccacat gagcgtgg
182818DNAArtificial SequenceSynthetic Oligonucleotide 28gggctgtggg
cacttctg 182920DNAArtificial SequenceSynthetic Oligonucleotide
29gcagatcaaa gagagcctgc 20
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