U.S. patent application number 11/219967 was filed with the patent office on 2006-06-22 for purification of antigen-specific t cells.
This patent application is currently assigned to Ortho Pharmaceutical Corporation. Invention is credited to Michael R. Jackson, Alain T. Luxembourg, Per A. Peterson.
Application Number | 20060134125 11/219967 |
Document ID | / |
Family ID | 21826936 |
Filed Date | 2006-06-22 |
United States Patent
Application |
20060134125 |
Kind Code |
A1 |
Luxembourg; Alain T. ; et
al. |
June 22, 2006 |
Purification of antigen-specific T cells
Abstract
A new method to capture, purify and expand antigen-specific T
lymphocytes has been developed using magnetic beads coated with
recombinant MHC class I molecules. This method was optimized using
homogenous populations of naive T cells purified from mice
transgenic for the 2C T cell receptor (TCR). These T cells were
captured on beads coated with MHC class I molecules and the
relevant antigenic peptides. MHC and peptide specificity was
confirmed by the usage of irrelevant MHC peptide combinations. An
enrichment of 800 to 1600 fold was measured, using 2C T cells mixed
with irrelevant T cells, starting from a 2C T cell frequency of
1/3000. The same approach was used to purify antigen-specific
CD8.sup.+ T cells from total CD8.sup.+ T cells from naive mice. The
recovered cells could be expanded and specifically kill target
cells in vitro; they had a significant effect in vivo as well. We
expect this procedure to be suitable to purify and expand in vitro
tumor- and virus-specific killer T cells for use in cell
therapy.
Inventors: |
Luxembourg; Alain T.; (La
Jolla, CA) ; Jackson; Michael R.; (Del Mar, CA)
; Peterson; Per A.; (Sante Fe, CA) |
Correspondence
Address: |
WOODCOCK WASHBURN LLP
ONE LIBERTY PLACE
46TH FLOOR
PHILADELPHIA
PA
19103
US
|
Assignee: |
Ortho Pharmaceutical
Corporation
Raritan
NJ
08869
|
Family ID: |
21826936 |
Appl. No.: |
11/219967 |
Filed: |
September 6, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10785472 |
Feb 23, 2004 |
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11219967 |
Sep 6, 2005 |
|
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|
09434965 |
Nov 5, 1999 |
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|
10785472 |
Feb 23, 2004 |
|
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|
08909549 |
Aug 12, 1997 |
|
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09434965 |
Nov 5, 1999 |
|
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60025588 |
Sep 6, 1996 |
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Current U.S.
Class: |
424/184.1 |
Current CPC
Class: |
G01N 33/5094 20130101;
A61K 39/39 20130101; G01N 33/54326 20130101; C12N 5/0636 20130101;
G01N 33/56977 20130101; C07K 16/2818 20130101; A61K 2039/5158
20130101; C12N 2501/51 20130101 |
Class at
Publication: |
424/184.1 |
International
Class: |
A61K 39/00 20060101
A61K039/00 |
Claims
1. A method for enriching antigen-specific T lymphocytes comprising
the steps: a) contacting a heterogeneous population of
antigen-specific T-lymphocytes with a matrix comprising MHC-antigen
complexes wherein said MHC-antigen complexes comprise one or more
antigens, for a period of time sufficient to allow the antigen
specific T lymphocytes to interact with the matrix; b) eluting the
antigen-specific T lymphocytes from the matrix to provide an
enriched population of antigen specific T lymphocytes.
2. A method for isolating antigen-specific T lymphocytes from a
heterogeneous population of cells from a patient, comprising the
steps: a) contacting a heterogeneous population of antigen-specific
T-lymphocytes from said patient with a matrix comprising
MHC-antigen complexes wherein said MHC-antigen complexes comprise
one or more antigens, for a period of time sufficient to allow the
antigen-specific T lymphocytes to interact with the matrix; b)
expanding in culture the antigen-specific T lymphocytes on the
matrix to provide an enriched population of said patient's
antigen-specific T lymphocytes.
3. The method of claim 2 wherein the antigen specific T lymphocytes
are eluted from the matrix before expanding in culture.
4. The method of claim 2 wherein the antigen-specific T lymphocytes
are expanded in culture with one or more immobilized costimulatory
molecules selected from the group consisting of anti-CD28 antibody,
B7-1, B7-2, integrins, cell adhesion molecules, IL-2 and IL-4.
5. The method of claim 4 wherein the antigen-specific T lymphocytes
are eluted from the matrix before expanding in culture.
6. A matrix for capturing antigen specific T lymphocytes,
comprising a support having on its surface immobilized Class I
peptide, and a predetermined amount of an antigen.
7. The matrix of claim 6 wherein the matrix is a bead.
8. The matrix of claim 6 wherein the antigen is a peptide.
9. A method for enriching antigen-specific T lymphocytes comprising
the steps: a) contacting a heterogeneous population of
antigen-specific T-lymphocytes with the matrix of claim 4 for a
period of time sufficient to allow the antigen specific T
lymphocytes to interact with the matrix; b) eluting the
antigen-specific T lymphocytes from the matrix to provide an
enriched population of antigen specific T lymphocytes.
10. The method of claim 9 wherein the matrix is a bead.
11. The method of claim 9 wherein the antigen is a peptide.
12. A method for isolating antigen-specific T lymphocytes from a
heterogeneous population of cells from a patient, comprising the
steps: a) contacting a heterogeneous population of antigen-specific
T-lymphocytes from said patient with the matrix of claim 4 for a
period of time sufficient to allow the antigen-specific T
lymphocytes to interact with the matrix; b) expanding in culture
the antigen-specific T lymphocytes on the matrix to provide an
enriched population of said patient's antigen-specific T
lymphocytes.
13. The method of claim 12 wherein the matrix is a bead.
14. The method of claim 12 wherein the antigen is a peptide.
15. The method of claim 12 wherein the antigen-specific T
lymphocytes are eluted from the matrix before expanding in
culture.
16. A matrix for capturing antigens, comprising a support having on
its surface immobilized empty Class I peptide, wherein said Class I
peptide is capable of binding one or more antigens.
17. The matrix of claim 16 wherein the matrix is a bead.
18. The matrix of claim 16 wherein the antigen is a peptide.
19. A method for enriching antigen-specific T lymphocytes
comprising the steps: a) binding one or more antigens to the matrix
of claim 14; b) contacting a heterogeneous population of
antigen-specific T-lymphocytes with the matrix of step a) for a
period of time sufficient to allow the antigen-specific T
lymphocytes to interact with the matrix; c) eluting the
antigen-specific T lymphocytes from the matrix to provide an
enriched population of antigen specific T lymphocytes.
20. The method of claim 19 wherein the matrix is a bead.
21. The method of claim 19 wherein the antigen is a peptide.
22. A method for isolating antigen-specific T lymphocytes from a
heterogeneous population of cells from a patient, comprising the
steps: a) binding one or more antigens to the matrix of claim 14;
b) contacting a heterogeneous population of antigen-specific
T-lymphocytes from said patient with the matrix of step a) for a
period of time sufficient to allow the antigen-specific T
lymphocytes to interact with the matrix; c) expanding in culture
the antigen-specific T lymphocytes on the matrix to provide an
enriched population of said patient's antigen-specific T
lymphocytes.
23. The method of claim 22 wherein the matrix is a bead.
24. The method of claim 22 wherein the antigen is a peptide.
25. The method of claim 22 wherein the antigen-specific T
lymphocytes are eluted from the matrix before expanding in
culture.
26. The method of claim 22 wherein the antigen-specific T
lymphocytes interact with the antigen with low-affinity.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This is a continuation of U.S. application Ser. No.
10/785,472, filed Feb. 23, 2004, which is a continuation of U.S.
application Ser. No. 09/434,965, filed Nov. 5, 1999, which is a
divisional of U.S. application Ser. No. 08/909,549, filed Aug. 12,
1997, which claims the benefit of U.S. Provisional Application No.
60/025,588, filed Sep. 6, 1996.
FIELD OF THE INVENTION
[0002] This invention is drawn to a method to derive
antigen-specific T cell lines from a heterogeneous lymphocyte
population, including total T lymphocyte populations of naive
individuals. This method is based on a step of enrichment for
antigen-specific lymphocytes by capture of the antigen-specific T
lymphocytes on a substrate coated with antigenic peptide-MHC
complexes which serve as ligands for specific T-cell antigen
receptors, followed by a step of expansion using surfaces coated
with antigenic peptide-MHC complexes.
BACKGROUND OF THE INVENTION
[0003] Antigen-specific immune responses are mediated by
antigen-specific effector B and T lymphocytes. These cells
originate from generally low frequency resting precursor cells
expressing receptors for various antigens representing the whole
repertoire and which, upon encounter with specific antigens and
appropriate costimulation, become activated, expand and
differentiate into effector cells.
[0004] Development of ex vivo immunotherapy for conditions such as
cancer or viral infections is limited by the low frequency of
antigen-specific precursor lymphocytes. For instance,
virus-specific CTL precursor (CTLp) frequencies in the peripheral
lymphoid tissues of mice are generally lower than
1/100,000-1/1,000,000 (Lau et al., 1994; Hou et al., 1994).
Isolation of antigen-specific lymphocytes by capture on an
antigen-coated support has been described for mouse spleen resting
B cells specific for TNP (Snow et al, 1983a). The isolation
procedure involved a rosetting step on haptenated horse red blood
cells and allowed the recovery of hapten-specific B cells with a
40% purity. This technique has been useful to study the
requirements for activation (Stein et al, 1986) as well as the
initial signaling events following activation (Snow et al, 1986;
Myers et al, 1987; Grupp et al, 1987; Noelle and Snow, 1990; Gold
and DeFranco, 1994). However, this was a very favorable situation
because of the relatively high frequency of B cells specific for
TNP (about 1%) (Snow et al, 1983a). No study on B cell activation
using resting B cells specific for another antigen with low
precursor frequency has been reported to date (Radbruch and
Recktenwald, 1995).
[0005] Low precursor frequency is also a problem with T cells.
Additionally, while B cells recognize the antigen directly, T cells
recognize a complex structure made of the combination of an
antigenic peptide bound to a major histocompatibility complex (MHC)
molecule. TCR/MHC-peptide interaction has a low to moderate
affinity (10.sup.-4-10.sup.-7 M range: Matsui et al, 1991; Weber et
al, 1992; Sykulev et al, 1994a; Corr et al, 1994; Sykulev et al,
1994b). Antibodies usually exhibit affinities several orders of
magnitude higher and exploit multivalency. New techniques of
isolation of rare cell populations are available now. These are
based on cell sorting and/or magnetic separation (Bellone et al,
1995; Radbruch and Recktenwald, 1995). Also, recombinant ligands
for TCR are now available by combining recombinant empty MHC
molecules (Jackson et al, 1992) and MHC-binding antigenic peptides
(Engelhard, 1994; Ramensee et al, 1995). These synthetic
MHC-peptide complexes can be immobilized on beads to yield
multivalent ligands for the TCR. Theoretically, multivalency should
help to overcome low affinity. The interaction between TCR and
immobilized peptide-MHC complex has been previously shown to lead
to the establishment of stable interactions in certain in vitro
systems. First, MHC class I antigens immobilized on lipid
monolayers (Nakanashi et al, 1983) or on lipid-coated cell-sized
beads (Kane et al, 1988) are sufficient to cause binding of cloned
allogeneic cytotoxic T cells (CTL). Second, syngeneic cloned CTL
bind to MHC-coated beads in a peptide dependent manner (Kane and
Mescher, 1993; Mescher, 1995). Third, a cloned syngeneic CTL can
form aggregates with RMA-S cells, a cell line which expresses large
amounts of empty MHC molecules, in a peptide specific manner (De
Bruijn et al, 1992). In two of these reports, TCR-MHC-peptide
interactions were not the primary mediator of adhesion. They rather
played an initial role in the early events of aggregation,
presumably by transducing signals that led to activation of
adhesion via accessory molecules.
[0006] Here, we describe a method to isolate antigen-specific T
cells using empty MHC class I molecules purified from Drosophila
melanogaster cells (Jackson et al, 1992) immobilized on magnetic
beads and loaded with peptide. This artificial substrate for T
cells is coated with a high density of identical MHC-peptide
complexes. T cell isolation was optimized using populations of
naive T cells purified from mice transgenic for the 2C TCR (Sha et
al, 1988). Ligands of various affinities and specificities for the
2C TCR have been identified (Sykulev et al, 1994a, b). 2C T cells
could be adsorbed on beads bearing peptide-MHC complexes which had
an affinity for the 2C TCR as low as 10.sup.-4 M. Adsorption was
MHC restricted and peptide specific since it occurred only with the
proper MHC-peptide combinations recognized by the 2C TCR.
Additionally, 2C T cells mixed with irrelevant T cells from a naive
animal could be recovered using this adsorption procedure. This
technique was successfully used to recover antigen-specific T cells
from naive animals.
SUMMARY OF THE INVENTION
[0007] The present invention provides a method for the isolation
and expansion in culture of antigen-specific T lymphocytes from a
heterogeneous population of lymphocytes. The present invention also
provides a method for preparing a population of antigen-specific T
lymphocytes from a patient for treatment of the patient's disease
or condition. This invention provides a matrix containing empty
Class I peptides which are functional in that the empty Class I
peptides can accept and bind a variety of antigens. These matrices
can be prepared to contain specific predetermined amounts of one or
more antigens. Such matrices are useful for a variety of purposes
including, but not limited to, use in the methods of the present
invention.
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] FIG. 1 Panels A, B, C and D: Analysis of binding of
biotinylated Ld to avidin-coated magnetic beads using flow
cytofluorometry.
[0009] Panel A shows a dose response curve of the mean fluorescence
values of beads incubated with increasing amounts of L.sup.d, then
stained with fluorescein-labeled anti-L.sup.d antibody 30.5.7.
Panel B shows green fluorescence (FL1) histograms of unlabeled
avidin-coated magnetic beads. Panel C shows green fluorescence
(FL1) histograms of avidin-coated magnetic beads after incubation
with 3 .mu.g of biotinylated L.sup.d/10.sup.6 beads; staining was
performed using fluorescein-labeled anti-L.sup.d antibody 30.5.7.
Panel D shows green fluorescence (FL1) histograms of avidin-coated
magnetic beads after incubation with 3 .mu.g of non-biotinylated
L.sup.d/10.sup.6 beads; staining was performed using
fluorescein-labeled anti-L.sup.d antibody 30.5.7.
[0010] FIG. 2 Panels A, B, C, D, E and F: Assessment of
L.sup.d-coated bead-2C T cell complex formation in the presence of
antigenic peptides using green (FL1) versus red (FL2) fluorescence
dot plots. Cells were stained in green with fluorescein; beads were
stained in red with phycoerythrin. Magnetic beads are
autofluorescent; compensation was set so that phycoerythin stained
beads displayed the same green fluorescence intensity as unstained
beads. Panel A shows beads alone. Panel B shows 2C T cells alone.
Panel C shows L.sup.d-coated beads and 2C T cells incubated in the
presence of QL9. Panel D shows L.sup.d-coated beads and 2C T cells
incubated in the presence of p2Ca. Panel E shows L.sup.d-coated
beads and 2C T cells incubated in the presence of SL9. Panel F
shows L.sup.d-coated beads and 2C T cells incubated in the presence
of LCMV peptide.
[0011] FIG. 3 Panels A, B, C, D, E, F, G and H: Assessment of
MHC-coated bead-2C T cell complex formation in the presence of
antigenic peptides using side scatter (SSC) versus forward scatter
(FSC) dot plots. Panel A: shows boundaries of the regions
containing the cells, the beads, and the cell-beads complexes.
Panel B shows beads alone. Panel C shows 2C T cells alone. Panel D
shows L.sup.d-coated beads and 2C T cells incubated in the presence
of QL9. Panel E shows L.sup.d-coated beads and 2C T cells incubated
in the presence of p2Ca. F: L.sup.d-coated beads and 2C T cells
incubated in the presence of LCMV peptide. Panel G shows
K.sup.bm3-coated beads and 2C T cells incubated in the presence of
dEV-8. Panel H shows K.sup.bm3-coated beads and 2C T cells
incubated in the presence of E1.
[0012] FIG. 4 Panels A, B, C, D, E and F: effect of various
parameters on 2C T cell adsorption onto MHC-coated magnetic beads.
Panel A shows time dependence: purified 2C T cells were mixed with
MHC-coated beads and peptide, and incubated at room temperature for
various amounts of time; cell attachment was then quantified by
flow cytofluorometry. Panel B shows temperature dependence:
purified 2C T cells were mixed with MHC-coated beads and peptide,
and incubated at various temperatures and for various amounts of
time; cell attachment was then quantified by flow cytofluorometry.
Panel C shows CD8 dependence: purified 2C T cells or purified
CD8.sup.- 2C T cells were mixed with MHC-coated beads and peptide,
and incubated at room temperature for 3 hours; cell attachment was
then quantified by flow cytofluorometry.
[0013] FIG. 5 Panels A, B, C, D and E: enrichment in 2C T cells
using capture on K.sup.bm3-coated magnetic beads, starting with a
mixture of 2C T cells and CD8.sup.+ T cells at a ratio of 1:3000.
Panel A shows green fluorescence (FL1) histogram of
fluorescein-labeled purified 2C T cells. Panel B shows green
fluorescence (FL1) histogram of purified CD8.sup.+ T cells from
C57BL/6 mouse. Panel C shows green fluorescence (FL1) histogram of
purified fluorescein-labeled 2C T cells mixed with CD8.sup.+ T
cells from C57BL/6 mouse at a ratio of 1:3000. Panel D shows green
fluorescence (FL1) histogram of cells eluted after incubation with
K.sup.bm3-coated magnetic beads in the presence of dEV-8. Panel E
shows green fluorescence (FL1) histogram of cells eluted after
incubation with K.sup.bm3-coated magnetic beads in the presence of
E1.
[0014] FIG. 6 Panels A, B, C and D: in vitro functional activity of
CTL derived from naive C57BL/6 mouse using adsorption on
K.sup.b-OVA-8 or K.sup.b-VSV-8-coated magnetic beads. Cultured T
cells were tested for cytotoxicity by chromium release assay as
indicated in Example 4. EL4 cells were used as targets. Peptides
were used at a final concentration of 1 .mu.M.
[0015] FIG. 7 Panels A, B, C and D: in vitro functional activity of
CTL derived from naive BALB/c mouse using adsorption on
L.sup.d-LCMV-coated magnetic beads. Cultured T cells were tested in
vitro for cytotoxicity by chromium release assay as indicated in
Example 4. L.sup.d-expressing RMA-S (panel A), BALB/c CL-7 (panel
B), MC57 (panel C) or YAC-1 (panel D) were used as targets.
Peptides were used at a final concentration of 1 .mu.M.
[0016] FIG. 8 Panels A, B, C and D: in vivo functional activity of
CTL derived from naive BALB/c mouse using adsorption on
L.sup.d-LCMV-coated magnetic beads. In vivo activity in mice
acutely infected with LCMV was assayed as indicated in Example 4.
LCMV-infected BALB/c mice were injected with 10.sup.7 CTL anti-LCMV
NP 118-126 at day 1, while 4 BALB/c mice received only PBS. As a
control we used LCMV-C57BL/6 mice injected with either 10.sup.7 CTL
anti-LCMV NP 118-126 or PBS.
DETAILED DESCRIPTION OF THE INVENTION
[0017] The present invention provides a new method to derive in
vitro antigen-specific T cell lines from mixed cell populations,
including total T cells from naive individuals. Deriving T cell
lines in vitro from naive T cell populations poses several types of
problems: first, the precursor frequencies are typically very low,
often lower than 10.sup.-5; second, naive T cells have special
requirements for activation, needing generally stronger stimuli
than previously activated T cells.
[0018] The method of the present invention comprises two steps: one
step of isolation to enrich the cell preparation in
antigen-specific T cells, and one step of in vitro expansion to
derive antigen-specific cell lines from the enriched cell
preparation. It is readily apparent to those skilled in the art
that these steps may be repeated, as desired. The step of isolation
of antigen-specific T cells utilizes MHC-coated substrates, which
upon incubation with antigenic peptide and T cells, enabled
isolation of T cells specific for the antigenic peptide-MHC
complex. It will be readily apparent to those skilled in the art
that a wide variety of MHC molecules are suitable for use in the
method of the present invention, including, but not limited to,
classical and non-classical MHC proteins from any mammalian or
avian species, with human HLA proteins and murine H-2 proteins
being preferred. It will also be readily apparent to those skilled
in the art that MHC molecules from a variety of sources are
suitable for use in the present invention, including, but not
limited to, MHC derived from naturally occurring sources and from
recombinant sources such as MHC proteins expressed in bacteria,
insect cells or mammalian cells, with insect cells being preferred.
In addition, it will be readily apparent to those skilled in the
art that a wide variety of MHC coated substrates are suitable for
use in the present invention, including, but not limited to,
columns (acrylamide, agarose, . . . ), glass beads, latex beads,
membranes (nitrocellulose, nylon, . . . ), plastic (e.g.,
polystyrene) surfaces such as microtitration plates, high molecular
weigh polysaccharides such as dextrans, red blood cells, and
magnetic beads, with magnetic beads being preferred. Finally, it
will be readily apparent to those skilled in the art that a wide
variety of procedures could be used to attach MHC molecules on
substrates for use in the method of the present invention,
including, but not limited to, passive adsorption, use of
cross-linkers, biotinylation of MHC molecules for adsorption on
avidin-coated substrate, introduction of a recognition site by
genetic engineering of MHC molecules or use of natural recognition
site for adsorption on antibody-coated substrate, with
avidin-biotin and antibody recognition being preferred.
[0019] To establish the procedure, combination of several resources
was utilized: first, we used empty recombinant MHC molecules
produced in Drosophila melanogaster cells (Jackson et al, 1992),
which allowed the use of MHC protein homogeneously loaded with the
same peptide; second, naive T cells purified from lymph nodes of
mice transgenic for the 2C TCR (Sha et al, 1988) were used, these
cells homogeneously express the same TCR at the same level. This
allowed analysis at a single cell level. Also several different
peptide-MHC complexes whose affinities for the 2C TCR have been
recently determined (Sykulev et al, 1994a, b) were used. This made
it possible to investigate the procedure using complexes with
various affinities. The MHC class I molecules that were used
included L.sup.d, K.sup.b and K.sup.bm3. Since the 2C cytotoxic T
cell clone was derived from BALB.B (H-2.sup.b) mice (Sha et al,
1988), L.sup.d and K.sup.bm3 are allogeneic restriction elements
for the 2C TCR while K.sup.b is syngeneic. Immobilized biotinylated
L.sup.d, K.sup.b and K.sup.bm3 on avidin-coated magnetic beads were
used. 2C T cells were absorbed on such beads in the presence of
several antigenic peptides. Adsorption was observed in the presence
of peptide-MHC complexes with an affinity for the 2C TCR in a
10.sup.-4-10.sup.-7 M range, using L.sup.d, K.sup.bm3 or K.sup.b as
restriction element. Finally adsorption was specific, since control
peptides did not cause interaction between MHC-coated beads and 2C
T cells.
[0020] The characteristics of adsorption of T cells onto MHC-coated
beads were further studied: adsorption was time dependent, reaching
a plateau between 1 and 4 hours when performed at room temperature.
Adsorption started to decrease beyond that time, which might
reflect the initiation of a de-adhesion process. Adsorption was
also temperature dependent: it was slightly lower at 37.degree. C.
than at room temperature for 3 of the peptide-MHC complexes
examined, and was even dramatically lower than at room temperature
for another one. This is due to the decrease in stability of MHC
molecules at higher temperature. Adsorption at 4.degree. C. was
much lower than at room temperature which was likely a consequence
of the changes in cell membrane fluidity at low temperature which
reduces molecular associations. Additionally, some signaling
events, which occur only at higher temperature, might contribute to
adsorption, as noted in a previous report about the role of CD8 in
adhesion induced by TCR-antigen interaction (Kane and Mescher,
1993). Interestingly, CD8 dependence of cell-bead complex formation
varied according to the antigen used. Among the peptides tested,
the most CD8-dependent were p2Ca and dEV-8, which had been isolated
as naturally occurring at the surface of antigen presenting cells;
QL9 and SIYR, which have not been found on cell surface, were CD8
independent. In any case, CD8 dependence of T cell capture on
MHC-coated beads was not completely correlated with TCR-ligand
affinity. Finally, capture was not completely correlated with
TCR-ligand affinity, since we consistently observed capture with
K.sup.bm3-dEV-8 (1.8.times.10.sup.4 M.sup.-1), K.sup.b-SIYR
(3.1.times.10.sup.4 M.sup.-1) or K.sup.bm3-SIYR (3.4.times.10.sup.4
M.sup.-1), but not with L.sup.d-p2Ca-A3 (2.times.10.sup.4 M.sup.-1)
or K.sup.b-dEV-8 (1.2.times.10.sup.4 M.sup.-1). Capture was
observed or not with L.sup.d-SL9 (1.4.times.10.sup.4 M.sup.-1),
according to L.sup.d batches. This is consistent with the
prediction that knowing the affinity of a single TCR for a given
peptide-MHC complex is probably not enough to make predictions
about interactions at the whole cell level (Agrawal and Linderman,
1996). It is anticipated that MHC-coated beads will be useful as
probes to study the rules of antigen recognition by T cells.
[0021] To investigate the suitability of this technique to recover
a low frequency population of antigen-specific CTL precursors, it
was attempted to recover 2C T cells mixed with irrelevant T cells
from a naive animal. It was shown that the procedure of the present
invention allowed the purification of antigen-specific T cells
about 800 to 1600 fold in one step of purification, starting from a
2C T cell frequency as low as 0.03%. Cell recovery was about 50%
when using peptide-MHC complexes of low affinity for the 2C TCR
such as K.sup.bm3-dEV-8 and K.sup.b-SIYR, and reached 90-100% with
the high affinity L.sup.d-QL9 complex. Final 2C T cell purity was
47.6.+-.2.1% when using K.sup.b, the syngeneic restriction element
for the 2C TCR, and 24.8.+-.6.9% when using L.sup.d, an allogeneic
restriction element. This suggests that this difference could be
accounted for by anti-L.sup.d allogeneic T cells captured using
L.sup.d-coated beads. This would mean that some of the non-2C cells
eluted from the beads had been captured specifically. Taken
together, these results showed that this method was suitable to
purify low frequency T cell precursors from a naive animal,
including cells whose TCR would have a low affinity for an
MHC-peptide complex.
[0022] It was also shown that the isolation procedure of the
present invention, when used in combination with a new in vitro T
cell expansion step, was usable to enrich in CTL precursors from
naive mice. The cell expansion step was based on the culture of
isolated cells in tissue culture plates coated with MHC-peptide
complexes and anti-CD28 antibody. It will be readily apparent to
those skilled in the art that other costimulatory molecules are
suitable for use in the method of the present invention, including,
but not limited to, anti-CD28 antibody, other ligands of CD28 such
as B7-1 and B7-2, or ligands or antibodies to other T cell
costimulatory molecules such as integrins and other cell adhesion
molecules, or cytokines such as interleukin-2 or interleukin-4, or
any combination thereof. It is noteworthy that other classical
expansion protocols, including stimulation with concanavalin A or
with anti-TCR antibody, would not allow antigen-specific CTL to be
derived from naive lymphocyte populations. This is likely because
the cells are not 100% pure after isolation and thus need some
specific stimulation to be recovered. Additionally, a high density
of homogeneous ligands is necessary to activate unprimed T cells,
which is provided by the method of the present invention, as well
as by using MHC-expressing insect cells as antigen-presenting cells
(Cai et al., 1996), but not by using classical antigen presenting
cells which present a heterogeneous population of antigens on their
surface. Additionally, this totally synthetic expansion system of
the present invention does not require use of exogenous
antigen-presenting cells, which eliminates potential complications
such as contamination and cross-priming. Interestingly, it was not
necessary to detach the cells from the MHC-coated magnetic beads
used for isolation prior to expansion, which reduces the time of
manipulation. However, the antigen-specific T lymphocytes may be
eluted or removed from the substrate for culturing or for other
purposes, if desired. The T lymphocytes may be eluted using a
variety of techniques known to those skilled in the art, such as
prolonged incubation and/or addition of an anti-MHC antibody. Using
this method, LCM virus-specific CTL could be derived from
uninfected BALB/c mice using L.sup.d-coated magnetic beads and
LCMV-nucleoprotein peptide. Enrichment certainly had occurred since
at least one cell in the 10.sup.4 cells recovered was
antigen-specific, as compared to a precursor frequency of less than
10.sup.-5 in a naive animal (Oehen et al 1992, Lau et al, 1994).
Additionally, unseparated total CD8.sup.+ T cells from the same
animal cultured in the same conditions did not yield specific CTL
activity. Finally, specific CTL activity was measured after only
one restimulation, which strongly indicates a high frequency of
specific precursor T cells following the enrichment procedure. We
also used the enrichment procedure of the present invention to
recover OVA-8 specific CTL as well as VSV-8 specific CTL from
C57BL/6 mice. Enrichment was specific since no VSV-8-specific CTL
could be grown from cells captured using K.sup.b-OVA-8-coated
beads, and no OVA-8-specific CTL could be grown from cells captured
using K.sup.b-VSV-8-coated beads. The CTL precursor frequency of
OVA-8 specific CTL in the enriched population after capture on
K.sup.b-OVA-8-coated beads was approximately 1/3500. Enrichment
thus certainly had occurred since the precursor frequency for CTL
anti-OVA-8 in naive C57BL/6 mice is 1/30,000 (Dillon et al., 1994).
However, enrichment appeared to be lower than expected from the
experiments using 2C T cells (Table II). This is not surprising
because measurements with 2C T cells reflect directly the
capability of the enrichment step, whereas, in experiments starting
from total CD8.sup.+ T cells, enrichment was likely underestimated:
some CD8.sup.+ cells might have been captured and expanded without
displaying a cytotoxic activity, or might have been captured but
would not grow in culture, or might have a too weak interaction
with MHC-coated beads to be "capturable". It is unlikely that
capture makes T cells unresponsive because 2C T cells can be
expanded into CTL after capture.
[0023] Magnetic separation has proven to be the method of choice to
purify rare cell populations. These include human peripheral blood
hemopoietic progenitor cells (purification from 0.18% to 54.4%, 300
fold enrichment, >39% recovery) (Kato and Radbruch, 1993), human
peripheral blood burst-forming units-erythroid (purification from
0.04% to 56.6%, 1400 fold enrichment, 13% recovery) (Sawada et al,
1990), and peripheral blood IgA.sub.1-expressing B lymphocytes
(purification from 0.1-1.5% to up to 80%, up to 80% recovery)
(Irsch et al, 1994). The method of the present invention for
antigen-specific T cell enrichment is substantially better than
these methods, as judged by the enrichment and recovery numbers.
This is especially significant since the purification methods
mentioned above used antibodies as ligands for the specific cells;
antibodies have affinities for antigens that are much higher than
those of MHC-peptide complexes for TCR. The method of the present
invention is also useful for cell purification via other low
affinity ligands to cell surface molecules, low affinity ligands
meaning molecules that have an affinity too low to remain stably
bound to cell surface when used in soluble form. In contrast, high
affinity ligands, such as antibodies, remain stably bound on cell
surface when used in soluble form.
[0024] Interestingly, although fluorescent labeling of
antigen-specific T cells is possible (Altman et al., 1996), cell
sorting by flow cytometry could not be a substitute for magnetic
separation because T cell precursors are usually too rare to be
detectable in flow cytometry, and the speed of analysis and sorting
remains a limiting factor. In contrast, magnetic separation can be
used to separate rare antigen-specific T cell populations, as well
as to sort large numbers of cells quickly. These features make
magnetic isolation an attractive procedure to derive
antigen-specific T cells for clinical use.
[0025] In conclusion, this is the first report of a method of
purification of antigen-specific T cells that is applicable to
naive individuals. We showed that it could be applied to several
different MHC molecules and a variety of peptides. The method of
the present invention is usable in a variety of situations,
including, but not limited to, the use to derive virus- or
tumor-specific cytotoxic T cell lines from human peripheral blood.
The cells derived using the method of the present invention are
themselves useful for a variety of purposes including, but not
limited to, expansion in culture and reinfusion into a patient,
diagnostic analysis, and other therapeutic applications.
[0026] The following Examples are provided for the purpose of
illustrating the present invention without, however, limiting the
scope of the present invention to the following examples.
EXAMPLE 1
Attachment of Biotinylated MHC Class I Molecules on Avidin-Coated
Magnetic Beads
[0027] Soluble MHC class I molecules L.sup.d, K.sup.b and K.sup.bm3
were expressed in Drosophila melanogaster cells (Jackson et al,
1992) and purified as previously described (Sykulev et al, 1994a).
Biotinylation was performed using biotin-BMCC (Pierce, Rockford,
Ill.) according to the manufacturer instructions.
[0028] Dynabeads M500 (Dynal, Lake Success, N.Y.) were coated with
neutravidin (Pierce, Rockford, Ill.), and subsequently incubated
with biotinylated MHC class I molecules diluted in PBS containing
3% FCS for 2 hours at 4.degree. C. under mild agitation. Beads were
then washed 3 times in DMEM containing 10% FCS and incubated for 1
hour with 20 .mu.M peptide. Beads were then used immediately for
cell adsorption.
[0029] Biotinylated L.sup.d was used as a test model to study
attachment of biotinylated MHC class I to avidin-coated magnetic
beads. Various amounts of this molecule were incubated with beads.
Beads were then stained using fluorescein-labeled conformation
sensitive anti-L.sup.d monoclonal antibody 30.5.7. Attachment of
L.sup.d was assessed by flow cytofluorometry analysis. The mean
fluorescence value increased linearly with the amount of L.sup.d
between 0 and 1.5 .mu.g of L.sup.d/10.sup.6 beads, and reached a
plateau at 3 .mu.g of L.sup.d/10.sup.6 beads as shown in FIG. 1A.
The amount of L.sup.d required to reach saturation was the same
with several batches of beads and of biotinylated L.sup.d.
[0030] To quantitate the number of MHC molecules immobilized per
bead, we measured the concentrations of MHC class I molecules in
solution before and after binding by using a solid phase
immunoassay as follows: MHC class I molecules L.sup.d was adsorbed
on 6.8 .mu.m polystyrene latex sulfate beads (Interfacial Dynamics
Corporation, Portland, Oreg.) that had been coated with 28-14-8S
anti-L.sup.d (ATCC, Rockville, Md.); beads were then stained using
fluorescein-labeled 30-5-7 anti-L.sup.d; mean fluorescence values
(MFV) were measured by flow cytofluorometry. A standard curve was
established with known concentrations of L.sup.d and MFV was
plotted versus concentrations. The amount of immobilized L.sup.d in
saturating conditions was found to be 1.23.+-.0.10.times.10.sup.6
molecules per bead. Fluorescence histograms show fluorescence of
unstained beads (FIG. 1B) and of beads adsorbed with saturating
amounts of L.sup.d (FIG. 1C). Attachment occurred via avidin-biotin
interaction since non-biotinylated molecules did not bind to beads
(FIG. 1D). K.sup.b and K.sup.bm3-coated beads were prepared and
tested using the same technique. Saturation was achieved using the
same range of concentrations as for L.sup.d.
EXAMPLE 2
Capture of Antigen-Specific T Cells onto MHC Class 1-Coated
Magnetic Beads in the Presence of Antigenic Peptides
[0031] Mice and cell lines. BALB/c (H-2.sup.d) and C57BL/6
(H-2.sup.b) mice were from Harlan Sprague Dawley (San Diego,
Calif.). 2C transgenic mice (Sha et al, 1988) were bred in R. W.
Johnson P. R. I. vivarium. All mice were kept under specific
pathogen free conditions. L.sup.d-expressing RMA.S cells (Cai and
Spent, 1996), and EL4 cells (H-2.sup.b, obtained from ATCC,
Rockville, Md.) were used as target cells in CTL assays. The
anti-clonotypic 1B2 hybridoma was previously described (Kranz et
al., 1994).
Purification of CD8.sup.+ T Cells from Normal Mice
[0032] Purification was performed at 4.degree. C. under sterile
conditions. Mouse inguinal, axillary, cervical, iliac and
mesenteric lymph nodes were dissected and separated into single
cell suspension. Avidin-coated magnetic beads (Dynal, Lake Success,
N.Y.) were coated with biotinylated goat anti-mouse Ig (Southern
Biotechnology, Birmingham, Ala.), and then incubated with the cell
suspension to adsorb Ig-expressing cells. Non-adsorbed cells were
then incubated with 2 .mu.g/ml H129.19 (anti-CD4, Gibco BRL,
Gaithersburg, Md.), 1 .mu.g/ml AF6-120.1 (anti-I-A.sup.b,
Pharrningen, San Diego, Calif.), 1 .mu.g/ml KH74 (anti-I-A.sup.b,
Pharmingen, San Diego, Calif.) and 1 .mu.g/ml 34-5-3
(anti-I-A.sup.d,b, Pharmingen, San Diego, Calif.) for mice with an
H-2.sup.b background; or with 2 .mu.g/ml H129.19 and 1 .mu.g/ml
34-5-3 for mice with an H-2.sup.d background. Cells were then
washed 3 times and cells expressing CD4 or MHC-class II were
eliminated by adsorption on sheep anti-rat Ig-coated magnetic beads
(Dynal, Lake Success, N.Y.). Purity reached 90 to 94% of CD8.sup.+
cells as judged by antibody staining and flow cytofluorometry.
Purification of 2C T Cells from 2C Transgenic Mice
[0033] 2C T cells were purified from mouse lymph nodes according to
the procedure described above. Purified cells were 97-98% reactive
with the anti-clonotypic antibody 1B2. Additionally, CD8.sup.-
(CD4.sup.-) cells could also be prepared by removing the CD8.sup.+
cells with the anti-CD8a antibody 53-6.7 (Gibco-BRL, Gaithersburg,
Md.) and magnetic beads coated with sheep-anti-rat Ig.
Peptides
[0034] The L.sup.d- and K.sup.b-binding peptides used in these
studies were synthesized on Applied Biosystem 430A and 431A
instruments by standard solid phase peptide synthesis method (tBoc
chemistry). The peptide sequences were as follows: TABLE-US-00001
QL9: QLSPFPFDL [SEQ. ID. NO.:1] p2Ca: LSPFPFDL [SEQ. ID. NO.:2]
SL9: SPFPFDLLL [SEQ. ID. NO.:3] p2Ca-A3: LSAFPFDL [SEQ. ID. NO.:4]
dEV-8: EQYKFYSV [SEQ. ID. NO.:5] SIYR: SIYRYYGL [SEQ. ID. NO.:6]
LCMV: RPQASGVYM [SEQ. ID. NO.:7] MCMV: YPHFMPTNL [SEQ. ID. NO.:8]
OVA-8: SIINFEKL [SEQ. ID. NO.:9] VSV-8: RGYVYQGL [SEQ. ID. NO.:10]
E1: EIINFEKL [SEQ. ID. NO.:11]
2C T Cell Adsorption on MHC-coated Magnetic Beads
[0035] To test the capacity of MHC class I-coated beads to capture
antigen-specific T cells, we used magnetic beads coated with
L.sup.d, K.sup.bm3 or K.sup.b, and T cells purified from 2C TCR
transgenic mice. The 2C TCR has been extensively characterized and
several antigenic peptides, recognized with various affinities in
association with L.sup.d (Table I), have been reported (Sykulev et
al, 1994 a, b). Moreover, K.sup.bm3 and K.sup.b have recently been
shown to serve as restriction elements for the 2C TCR in
association with the peptides dEV-8 and SIYR (Tallquist and Pease,
1995; Ukada et al, 1996; Tallquist et al., 1996). It has been
recently determined that the affinities of K.sup.bm3-dEV-8 and
K.sup.b-SIYR complexes for the 2C TCR were 1.8.times.10.sup.4
M.sup.-1 and 3.1.times.10.sup.4 M.sup.-1 respectively. Unless
stated otherwise, beads were coated with saturating amounts of
biotinylated L.sup.d, K.sup.bm3 or K.sup.b molecules.
[0036] Cells were suspended with beads to reach a final
concentration of 10.sup.7 beads/ml. Cell concentrations were
10.sup.6/ml in FIGS. 2, 3 and 4, and 10.sup.7/ml in FIGS. 5, 6 and
7. Peptides were added at a concentration of 20 .mu.M. Adsorption
was performed under mild agitation for the time durations and under
the temperatures indicated in the text. Cells adsorbed to beads
were then counted under the microscope. In cases where a definite
rosette (3 beads or more per cell) was not observed, attachment was
tested by gently tapping the coverslip. Upon incubation at room
temperature in the presence of the high affinity peptide QL9,
intermediate affinity peptide p2Ca and low affinity peptide SL9,
the majority of 2C T cells attached to L.sup.d-coated beads, as
judged by micoscopic examination after 4 hours of incubation (Table
I). Similar results (60-80% of cells captured) were obtained in 5
independent experiments. Cell attachment was specific since it did
not occur in the presence of non-2C reactive L.sup.d-LCMV and
L.sup.d-MCMV complexes.
[0037] Adsorption was also quantitated by flow cytofluorometry
using a FACSscan.RTM. (Becton Dickinson & Co., Mountain View,
Calif.) by recording either green versus red fluorescence dot
plots, or forward versus side scatter dot plots. To assess
cell-bead complex formation using green versus red fluorescence dot
plots, the beads were labeled in red with phycoerythrin (FIG. 2A:
beads alone) and the cells were labeled in green with
NHS-fluorescein (Pierce, Rockford, Ill.) (FIG. 2B: cells alone).
Cell-bead complex formation was assessed by the appearance of green
(G) and red (R) events. The percentage of cells complexed to beads,
was calculated as the ratio RG/G+RG, where G is the number of
events in the lower right quadrant and RG is the number of events
in the upper right quadrant. We found that on such green versus red
fluorescence dot plots (FIG. 2), cell-bead complex formation was
quite apparent in the presence of antigenic peptides QL9 (FIG. 2C),
p2Ca (FIG. 2D) and SL9 (FIG. 2E), with over 85% of the cells
shifting to a high red fluorescence value. Some red and green
colored events (2.2%) were detected in the sample incubated with a
control peptide (LCMV) (FIG. 2F). This was most likely due to
non-specific adsorption of a small amount of fluorescein-labeled
cell debris to the beads.
[0038] Side scatter versus forward scatter dot plots were also
usable for this quantitation, thanks to the fact that the cells
(FIG. 3C) and the beads (FIG. 3B) had very different side and
forward scatters, which made it easy to draw clearly distinct
regions (FIG. 3A) containing the populations of events representing
cells and beads respectively. Appearance of an additional
population of events with a higher forward scatter than the beads
and a higher side scatter than the cells, reflected cell-bead
complex formation; this allowed to define complex region, distinct
from the cell and bead regions. The percentage of cells adsorbed to
beads was calculated as the ratio CO/CO+CE, where CO was the number
of events in the complex region and CE was the number of events in
the cell region. Such forward versus side scatter measurements
showed antigen-specific adsorption of the 2C T cells to the beads:
in the experiment shown in FIG. 3, 91.0% and 78.9% of the cells
were adsorbed to L.sup.d-coated beads in the presence of QL9 (FIG.
3D) and p2Ca (FIG. 3E) respectively and 63.8% of the cells were
adsorbed to K.sup.bm3-coated beads in the presence of dEV-8 (FIG.
3G) and 75.7% of the cells were adsorbed to K.sup.b-coated beads in
the presence of SIYR (not shown) after 4 hours of incubation.
Several populations, which differed by their side scatter values,
were visible in the complex region; they were likely to represent
complexes containing different numbers of beads. In the presence of
non-2C reactive L.sup.d-LCMV (FIG. 3F), K.sup.bm3-E1 (FIG. 3H) and
K.sup.b-E1 complexes, respectively 2.6%, 1.1% and 0.2% of events
were found in the complex region.
[0039] We used flow cytofluorometry analysis to quantitate the
influence of various parameters on cell-bead complex formation.
Attachment of cells to beads was time dependent. Binding was
detectable after 5 min of incubation, increased subsequently to
reach a plateau between 1 and 4 hours, and decreased notably after
6 hours (FIG. 4A). Kinetics of adsorption were remarkably parallel
for various peptide-MHC complexes. Attachment was also temperature
dependent, as shown in FIG. 4B. At 4.degree. C., only a small
percentage of cells was captured on beads, even after prolonged
incubation. Adsorption at room temperature was very similar to
adsorption at 37.degree. C. with the exception of L.sup.d-p2Ca, for
which attachment levels at 37.degree. C. were about 25% of the
values measured at room temperature, consistent with the inability
of p2Ca to stabilize L.sup.d at 37.degree. C. (Cai and Sprent,
1996). Finally, CD8 dependence of cell capture varied with the
peptide-MHC complex: for instance, L.sup.d-QL9 and K.sup.bm3-SIYR
captures were largely CD8 independent, whereas L.sup.d-p2Ca and
K.sup.bm3-dEV-8 exhibited CD8 dependence (FIG. 4C).
EXAMPLE 3
Recovery of Antigen-Specific T Cells Mixed with Irrelevant T
Cells
[0040] T cell precursor frequencies in a naive animal are typically
low. Magnetic beads have been found suitable in other systems to
enrich low frequency cell populations (Sawada et al., 1990; Kato
and Radbruch, 1993). To assess whether MHC class I-coated magnetic
beads could be used for T cell precursor enrichment, we mixed
fluorescein-labeled 2C T cells with CD8.sup.+ T cells purified from
naive C57BL/6 mice. After incubation with MHC-coated magnetic beads
in the presence of peptide, adsorbed cells were eluted and counted,
and the percentage of 2C T cells was determined by flow
cytofluorometry. In the experiment shown in FIG. 5, 2C T cells were
undetectable at the initial frequency of 0.03%. Following
adsorption using K.sup.bm3-coated beads and dEV-8 peptide, a
definite peak of green fluorescence was observed, displaying the
same intensity as the original fluorescein-stained 2C T cell
population. This peak represented 65.1% of the eluted cells. No
peak was observed when a control peptide was used instead of dEV-8.
We achieved 800-1600 fold enrichment in 2C T cells in comparable
experiments using beads coated with 3 different MHC-peptide
complexes (table II). In all cases, the non-fluorescent cells in
the eluted population represented only a minor fraction of the
initial cell population (.about.0.2%).
EXAMPLE 4
In Vitro Isolation and Expansion of Antigen-Specific CTL from Naive
Mice
In Vitro Cell-Mediated Cytotoxicity
[0041] L.sup.d-expressing RMA.S cells, EL4 cells (H-2.sup.b), MC57
cells (H-2.sup.b) infected with LCMV Armstrong (48 h.; multiplicity
of infection: 1 PFU per cell) or BALB/c CL-7 cells (H-2.sup.d)
infected with LCMV Armstrong (48 h.; multiplicity of infection: 1
PFU per cell) were used as target cells. Target cells were loaded
with 100 .mu.Ci of Na.sub.2.sup.51CrO.sub.4 (New England Nuclear,
Wilmington, Del.) per 10.sup.6 cells at 37.degree. C. for 60 min,
in the presence of 20% FCS. They were washed three times and
aliquoted in 96 well plates at 4,000 to 10,000 cells per well.
Peptides and effector cells were then added. Final volume was 200
.mu.l/well. Plates were incubated at 37.degree. C. for 5 hours. One
hundred .mu.l of supernatant were collected and counted in a gamma
counter. Percent specific lysis was calculated as previously
reported (Wunderlich and Shearer, 1991).
In Vivo Assay for CTL Activity
[0042] Recipient mice were injected on day 0 with 2.times.10.sup.3
PFU of LCMV Armstrong i.v. and adoptively transferred i.v. with
cells on day 1. On day 2, mice were sacrificed, and the spleens
were assayed for infectious virus titers by plaque assay on Vero
cells as described previously (Byrne and Oldstone, 1984). Virus
titers were expressed as plaque forming units per gram of tissue
(pfu/g).
Cell Culture
[0043] Cells adsorbed onto beads were recovered by washing the
beads 3 times with DMEM containing 10% FCS, and then cultured in 96
well plates coated with the appropriate MHC class I molecule and
anti-CD28 antibody in the presence of 10 .mu.M peptide; these
conditions are sufficient to activate resting 2C T cells. Flat
bottom well plates were used to ensure that every cell be in
contact with the immobilized stimulatory molecules. After 2 days of
culture at 37.degree. C. under humid atmosphere containing 8%
CO.sub.2, half the volume of medium was replaced by fresh medium
containing 20% of culture supernatant from concanavalin A-activated
rat splenocytes (conA supernatant). After 8-12 days, cells were
restimulated with spleen cells pulsed with 1 .mu.M peptide, and
cultured in the presence of 10% conA supernatant and 2 ng/ml of
TGF.beta..sub.1 (Lee and Rich, 1991; Zhang et al, 1995).
Generation of Antigen-Specific CTL Lines from Naive Mouse T Cells
Using Adsorption on MHC-Coated Magnetic Beads; Antigen Specificity
of the Isolation Step
[0044] To investigate whether the capture method would be
applicable to isolate antigen-specific T cells from a naive animal,
we incubated two aliquots of CD8.sup.+ T cells purified from
C57BL/6 mouse (H-2.sup.b haplotype) lymph nodes with K.sup.b-coated
magnetic beads in the presence of either OVA-8 peptide (aliquot 1)
or VSV-8 peptide (aliquot 2) during 4 hours at room temperature.
After 3 washes, cells were put in culture in 12 wells of a 96 well
plate coated with K.sup.b and anti-CD28 mAb, in the presence of 10
.mu.M of OVA-8 or VSV-8 peptide. Cultures were processed as
indicated in the previous paragraph. Cell growth was visible after
7 days in wells containing adsorbed cells. Cells were restimulated
on feeder cells at day 9, and tested for cytotoxic activity at day
18. Cells from aliquot 1 cultured with OVA-8 displayed a CTL
activity specific for OVA-8 peptide (FIG. 6A), and cells from
aliquot 2 cultured with VSV-8 displayed a CTL activity specific for
VSV-8 (FIG. 6C). Controls were provided by the reverse combination:
cells captured using OVA-8 peptide contained no detectable
anti-VSV-8 CTL precursors, since they did not generate anti-VSV-8
CTL when VSV-8 was used rather than OVA-8 to activate them in
culture (FIG. 6B); similarly, cells captured using VSV-8 peptide
contained no detectable anti-OVA-8 CTL precursors (FIG. 6D).
[0045] To obtain an estimate of the CTLp frequencies after
enrichment, we repeated the enrichment experiment using
K.sup.b-coated beads and OVA-8 peptide. In a representative
experiment, the 12,000 cells that were recovered by adsorption to
K.sup.b-OVA8-coated magnetic beads were aliquoted and cultured
separately in 12 wells of 96 well plates immediately after capture.
Specific CTL were recovered from cultured captured cells in 3
wells, indicating that the precursor frequency after capture was
approximately 1/3,500. Similar results were obtained in three
independent experiments.
Generation of Anti-LCMV CTL from Naive Mouse T Cells; In Vitro and
In Vivo Anti-Viral Activity
[0046] We derived anti-LCMV CTL by incubating 10.sup.7 CD8.sup.+ T
cells purified from BALB/c mouse (H-2.sup.d haplotype) lymph nodes
together with L.sup.d-coated magnetic beads in the presence of LCMV
peptide during 4 hours at room temperature. After 3 washes, about
10.sup.4 cells were recovered and put in culture in 12 wells of a
96 well plate coated with L.sup.d and anti-CD28 mAb, in the
presence of 10 .mu.M of LCMV peptide. Cells were cultured as
indicated in the previous paragraph. As shown in FIG. 7A, we
obtained cytotoxic T lymphocytes (CTL) specific for LCMV peptide.
Cells also killed LCMV-infected targets of the H-2.sup.d haplotype,
while displaying only a background activity against uninfected
targets (FIG. 7B). An anti-allotypic activity (FIG. 7C) as well as
some NK/LAK activity were also present (FIG. 7D). All cells
expressed CD8, as judged by flow cytofluorometry. In vivo assay
showed that the cells were able to markedly reduce virus titers in
BALB/c mice (H-2.sup.d) acutely infected with LCMV (FIG. 8). This
reduction was MHC-specific since no significant reduction of the
virus titers were observed in C57/BL6 mice (H-2.sup.b) following
CTL injection.
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TABLE-US-00002 TABLE I Capture of 2C T cells on L.sup.d-coated
magnetic beads in the presence of various peptides as assessed by
microscopic examination 2C TCR affinity Peptide affinity % Cell for
L.sup.d-peptide for L.sup.d Peptide captured (M.sup.-1) (M.sup.-1)
QL9 87% 10.sup.7 2 .times. 10.sup.8 p2Ca 83% 2 .times. 10.sup.6 4
.times. 10.sup.6 SL9 77% 1.4 .times. 10.sup.4 4 .times. 10.sup.7
MCMV <1% <10.sup.3 2 .times. 10.sup.9
[0096] TABLE-US-00003 TABLE II Recovery of 2C T cells mixed with
CD8.sup.+ T cells from naive B6 mouse by adsorption on MHC class
I-coated magnetic beads % 2C T cell % 2C T cell before after 2C T
cell 2C T cell Number of MHC molecule Peptide enrichment enrichment
enrichment recovery experiments L.sup.d QL9 0.03% 24.8 .+-. 6.9%
828 .+-. 230 fold 90.0 .+-. 14.0% 3 K.sup.bm3 dEV-8 0.03% 50.9 .+-.
14.2% 1697 .+-. 473 fold 47.7 .+-. 1.7% 2 K.sup.b SIYR 0.03% 47.6
.+-. 2.1% 1588 .+-. 71 fold 56.8 .+-. 0.6% 2
[0097]
Sequence CWU 1
1
* * * * *