DEVELOPMENT OF CELLULAR IMMUNOLOGY · DEVELOPMENT OF CELLULAR IMMUNOLOGY _____ 1880’s: Antibodies...
Transcript of DEVELOPMENT OF CELLULAR IMMUNOLOGY · DEVELOPMENT OF CELLULAR IMMUNOLOGY _____ 1880’s: Antibodies...
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DEVELOPMENT OF CELLULAR IMMUNOLOGY________________________________________________1880’s: Antibodies described
(dominated studies of immunology until 1960’s)
1958: Journal of Immunology (137 papers)“lymphocyte” not listed in indexTwo papers on transfer of lymph node cells were the
only papers dealing with lymphocytes
1960’s: Importance of cellular immunology recognized as mediator of: allograft rejection
protection against transfer of mouse tumors
1970’s: No convincing evidence for human lymphocytes reactive with cancer or the existence of human cancer antigens
No successful immunotherapies for cancer in humans
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“It would be as difficult to reject the right ear and leave the left ear intact as it is to immunize against cancer.”
W. H. WoglumCancer Research
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ADVANTAGES OF CELL TRANSFER THERAPY
1. Administer large numbers of highly selectedcells with high avidity for tumor antigens.
2. Administer cells activated ex-vivo to exhibitanti-tumor effector function.
3. Manipulate host prior to cell transfer to provide altered environment for transferredcells.
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Adoptive transfer of tumor infiltrating lymphocytes (TIL)
+
+
-
-
-
-
Excise tumor
Reinfuse post-lymphodepletion
Plate fragments
Culture with 6000 IU/ml IL-2
Assay for specific tumor
recognition
Select and expand to 1010 cells
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INITIAL RESULTS WITH CELL TRANSFER THERAPY FOLLOWING LYMPHODEPLETING
CHEMOTHERAPY
Six of 13 (46%) patients with metastatic melanoma experienced objective cancer regression.
Four patients had mixed or minor responses.
All had previously been refractory to IL-2 administration and eight had prior chemotherapy.
(Science 298:850-854, 2002)
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Cell Transfer Therapy(10/1/09)
________________________________________________________Treatment Total PR CR OR (%)No TBI 43 16 5 21 (49%)
(84, 36, 29, 28 (85+, 79+, 69+,14, 13, 11, 8 68+, 54+)
8, 7, 4, 3, 3, 2, 2, 2)
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Preparative Regimens for Cell Transfer______________________________________________
Days-7 -6 -5 -4 -3 -2 -1 0 1 2 3
_____________________________________________________________________Non-myeloablative Cy Cy Flu Flu Flu Flu Flu
Cells IL-2 IL-2 IL-2
_____________________________________________________________________Ablative Cy Cy
Flu Flu Flu Flu FluTBI
Cells IL-2 IL-2 IL-2CD34+
_____________________________________________________________________
Cy: Cyclophosphamide 60 μg/kgFlu: Fludarabine 25 mg/m2
IL-2: 720,000 IU/kg q8hCells: Autologous TIL (1-5 x 1010)CD34+: >2 x 106/kgTBI: 200 cGy total body irradiation
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Cell Transfer Therapy(10/1/09)
________________________________________________________Treatment Total PR CR OR (%)No TBI 43 16 5 21 (49%)
(84, 36, 29, 28, (85+, 79+, 69+,14, 13, 11, 8, 68+, 54+)
8, 7, 4, 3, 3, 2, 2, 2)
200 TBI 25 11 2 13 (52%)(54+, 50, 44+, 14, (58+, 47+)10, 6, 5, 5,
4, 3, 3)
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Preparative Regimens for Cell Transfer______________________________________________
Days-7 -6 -5 -4 -3 -2 -1 0 1 2 3
_____________________________________________________________________Non-myeloablative Cy Cy Flu Flu Flu Flu Flu
Cells IL-2 IL-2 IL-2
_____________________________________________________________________Ablative Cy Cy
(200cGy) Flu Flu Flu Flu FluTBI
Cells IL-2 IL-2 IL-2
CD34+_____________________________________________________________________Ablative Cy Cy
(1200cGy) Flu Flu Flu Flu FluTBI TBI TBI
CellsIL-2 IL-2 IL-2 IL-2
CD34+
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Cell Transfer Therapy(10/1/09)
________________________________________________________Treatment Total PR CR OR (%)No TBI 43 16 5 21 (49%)
(84, 36, 29, 28, (85+, 79+, 69+,14, 13, 11, 8, 68+, 54+)
8, 7, 4, 3, 3, 2, 2, 2)
200 TBI 25 11 2 13 (52%)(54+, 50, 44+, 14, (58+, 47+)10, 6, 5, 5,
4, 3, 3)
1200TBI 25 10 8 18(72%)(35+, 28+, 21, 13, (38+, 19, 34+, 34+,
7, 6, 6, 5, 29+, 28+, 28+, 27+) 4 , 3)
(52 responding patients: 42 had prior IL-2, 21 had prior IL-2 + chemotherapy)
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0
10
20
30
40
50
60
70
80
Vaccines IL-2 Anti-CTLA-4 ACT ACT +NMA
ACT +NMA +TBI
% o
bjec
tive
resp
onse
(REC
IST)
n = 541
n = 684n = 139
n = 86
n = 43
n = 25
Objective response rates (RECIST) in metastatic melanoma patients treated in the Surgery Branch, NCI
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R.K. (NMA)
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J.B.
1200 TBI
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Pt. M.H.
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Pt. M.H.
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Pt. R.B.
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Pt. R.B.
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C.K. (200cGy) Pre 12 days
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A.H.: N-M cell transfer
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Pt. A.H. NMA
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P.T.
Young TILCD8
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P.T.Young TIL
CD8
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Hypothesis of Mechanism of Cancer Regression Following Cell Transfer
The lymphophenic environment
1) eliminates T regulatory (suppressor) cells
2) eliminates competition for homeostaticcytokines (IL-7, IL-15) vital forT cell survival
In the lymphopenic host, anti-tumor T cells proliferate, persist, infiltrate organs, recognize cancer antigens and destroy cancer cells.
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pg/m
l IL-
15
0
20
40
60
80
No TBI 200 TBI 1200 TBI
Impact of Lymphodepletion on Serum Levels Of IL-15 and IL-7
pg/m
l IL-
7
0
20
40
60
80
PrePrePre Day 0Day 0Day 0
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Three Factors that Correlate with Cancer Regression Following Cell Transfer Therapy
_______________________________________________
Non-Responders Responders
_______________________________________________________________(mean)
Persistence in PBMC at 18.5 1.0 p<0.0011-2 months (% CD3)
Telomere length in infusion 6.5 5.4 p<0.01TIL (kb)
CD27+CD8+ cells infused 1.5 0.46 p<0.0001(x10-10)
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Simplification of adoptive immunotherapy to make it more widely applicable
_______________________________________________________________
Administer “Young TIL” (new method of cell preparation)
single cell suspension of the entire tumor, grow for 2 weeks REP for 2 weeks and administerno in vitro testing
Advantages:
short time in culture cells are less differentiated with shorter telomeres heterogeneous tumor antigen recognitionless labor intensive (no multiple cultures and no functional tests)more patients qualify for treatment
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Cell Transfer Therapy(10/1/09)
_______________________________________________Treatment Total PR CR OR (%)
________________________________________________________________number of patients (duration in months)
Young TIL 24 4 1(25+,10,5,2) (16+) 5 (21%)
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Cell Transfer Therapy(10/1/09)
_______________________________________________Treatment Total PR CR OR (%)
________________________________________________________________number of patients (duration in months)
Young TIL 24 4 1(25+,10,5,2) (16+) 5 (21%)
CD8 Young TIL 33 15 3 18 (55%)(12+,11+,10+,9+, (10+,8+,6+)9+,8+,6+,6+,4+,9,8,6,5,3,2)
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CONCLUSION
T cell based immunotherapy is capable of mediating the regression of large vascularized, invasive metastatic melanoma in humans
(The widely-held belief that immunotherapy can only affect minimal disease in the adjuvant setting is not the case.)
CHALLENGEDetermine ways to extend this approach to:
1) additional melanoma patients
2) patients with common epithelial cancers
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Antigen recognition by CD4+ and CD8+ T lymphocytes
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IRESAIB LTR
MSGV1martAIB
anti-Mart-1 retroviral vector
TCR TCR
LTR
(Science 314:126,2006)
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Treatment with MART-1 TCR transducedautologous lymphocytes
• Stimulate circulating PBL with OKT-3
• On day 2 and 3 transduce PBL with MART-1 TCR retroviral vector and culture in IL-2
• Infuse transduced cells following lymphodepletion of the host and administer IL-2
(Science 314:126, 2006)
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First Trial of Cell Transfer Therapy using TCR Gene‐Modified Cells
________________________________________________________
17 patients with metastatic melanoma (Science, 314:126, 2006)
2 (12%) with objective regressions
(both disease free over three years later)
14 additional patients treated
2 further objective regressions
Overall: 4/31 (13%) objective regressions
(Science 314:126, 2006)
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DMF4 and DMF5 MART1 andgp100(154) TCR retroviral constructs
gp100(154 ) (high-affinity murine TCR)
5’ LTR TCR IRES TCR 3’ LTR
5’ LTR TCR IRES TCR 3’ LTR
5’ LTR TCR 2A TCR 3’ LTR
DMF4 (previous MART1 clinical trial)
DMF5
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Gene Therapy Using the DMF5 Receptor in Patients with Metastatic Melanoma
________________________________________________________
Cohort Cell# IL-2 ResponseTotal OR
________________________________________________________1 1-3x1010 limited 6 2
2 ~3x109 to tolerance 6 2
3 1-8x1010 to tolerance 8 2
Total 20 6(30%)
(All patients were refractory to prior treatment with IL-2.)
(Blood 114:535-546, 2009)
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D.T. DMF5 TCR
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J.K. F5 TCR
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T.D. F5 TCR
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S.S. 154 TCR
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D.Th. F5 TCR Pretreatment
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Day 0 Day 6
Day 11 Day 20
Sequential tumor biopsies (D.Th.): MART TCR
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day 0 day 5 day 6 day 9
12 day day 16 day 19 day 26
Sequential tumor biopsies (D.Th.): MART TCR (CD8, 40x)
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Two methods to improve the effectiveness of transduced T cell receptors
Reduce mispairing of the transduced alpha and beta chains
Modify the CDR2 and CDR3 regions of the TCR to improve antigen recognition
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Optimizing Expression of the TCR Vector Constructs
Protein engineering of TCR chains
VDJ EX
EX TM CYVDJ
TM CY
SS
TCR Constant Region
SS
originalnew
Substitution of murine for human constant regions enhances pairing of the introduce TCR chains
Introduction of a secondCys disulfide bridge.
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Human Constant Regions
F5-HH
Constant Regions: H
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Human CR+ Cysteines
F5-HH-Cys
Constant Regions: H<H-Cys
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Mouse Constant Regions
F5-HM
Constant Regions: H<H-Cys<M
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Mouse CR + Cysteines
F5-HM-Cys
Constant Regions: H<H-Cys<M<M-Cys
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Method for increasing the affinity of T cell receptors_______________________________________________
CDR2 and CDR3 regions of the T cell receptor are responsible for binding to the peptide/MHC complex.
Selective substitution of individual amino acids in the CDR2 and CDR3 regions can increase the affinity of the TCR.
(J. Immunol. 180:6116-6131, 2008.)
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1G4 CDR395
WT TS
95:L L-
96:L -L
95:LL LL
95:LY LY
GFP
A2 NY-ESO-1+ +
+ +
+ +
+ +
+ -
+ -
1G4 CDR395
WT TS
95:L L-
96:L -L
95:LL LL
95:LY LY
GFP
CD4+ T cells CD8+ T cells
0 2000 4000 6000 8000
3 9 7 A 26 2 4 .3 81 3 0 0M D A 4 3 5 S -A 25 2 68 8 8 A 2
0 5 0 00 1 0 0 00 1 5 0 00 2 0 0 00 2 5 0 0 0IFN- (pg/ml)
Reactivity of Wild-type and Substituted Anti-ESO T Cell Receptor
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CONCLUSION
T cell based immunotherapy is capable of mediating the regression of large vascularized, invasive metastatic melanoma in humans
(The widely-held belief that immunotherapy can only affect minimal disease in the adjuvant setting is not the case.)
CHALLENGEDetermine ways to extend this approach to:
1) additional melanoma patients
2) patients with common epithelial cancers
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T-Cell Receptor Cell Transfer Gene Therapy for Cancers Other than Melanoma
_______________________________________________
NY-ESO-1 Cancer-testes antigen expressed on about one-third of common cancers
CEA Overexpressed on selected colorectal and other G-I cancers
CD19 Expressed on B-cell lymphomas and leukemias and normal B cells
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NY-ESO-1 CANCER ANTIGEN____________________________________________
No expression on adult human tissues except for testis
Expressed on about 25% of common epithelial cancers such as lung, breast, prostate