Ex vivo staining of metastatic lymph nodes by class I major histocompatibility complex tetramers reveals high numbers of antigen-experienced tumor-specific cytolytic T lymphocytes

被引:440
作者
Romero, P
Dunbar, PR
Valmori, D
Pittet, M
Ogg, GS
Rimoldi, D
Chen, JL
Liénard, D
Cerottini, JC
Cerundolo, V
机构
[1] CHU Vaudois, Ludwig Inst Canc Res, Div Clin Oncoimmunol, Lausanne Branch, CH-1011 Lausanne, Switzerland
[2] CHU Vaudois, Multidisciplinary Oncol Ctr, CH-1011 Lausanne, Switzerland
[3] John Radcliffe Hosp, Inst Mol Med, Nuffield Dept Med, Oxford OX3 9DS, England
关键词
melanoma; Melan-A/MART-1; tyrosinase; immunotherapy; tumor immunity;
D O I
10.1084/jem.188.9.1641
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Characterization of cytolytic T lymphocyte (CTL) responses to tumor antigens has been impeded by a lack of direct assays of CTL activity. We have synthesized reagents ("tetramers") that specifically stain CTLs recognizing melanoma antigens. Tetramer staining of tumor-infiltrated lymph nodes ex vivo revealed high frequencies of tumor-specific CTLs which were antigen-experienced by surface phenotype. In vitro culture of lymph node cells with cytokines resulted in very large expansions of tumor-specific CTLs that were dependent on the presence of tumor cells in the lymph nodes. Tetramer-guided sorting by now cytometer allowed isolation of melanoma-specific CTLs and confirmation of their specificity and their ability to lyse autologous tumor cells. Our results demonstrate the value of these novel reagents for monitoring tumor-specific CTL responses and for generating CTLs for adoptive immunotherapy. These data also indicate that strong CTL responses to melanoma often occur in vivo, and that the reactive CTLs have substantial proliferative and tumoricidal potential.
引用
收藏
页码:1641 / 1650
页数:10
相关论文
共 24 条
[1]   Phenotypic analysis of antigen-specific T lymphocytes [J].
Altman, JD ;
Moss, PAH ;
Goulder, PJR ;
Barouch, DH ;
McHeyzerWilliams, MG ;
Bell, JI ;
McMichael, AJ ;
Davis, MM .
SCIENCE, 1996, 274 (5284) :94-96
[2]  
Cormier JN, 1998, INT J CANCER, V75, P517, DOI 10.1002/(SICI)1097-0215(19980209)75:4<517::AID-IJC5>3.0.CO
[3]  
2-W
[4]  
deVries TJ, 1997, CANCER RES, V57, P3223
[5]   Direct isolation, phenotyping and cloning of low-frequency antigen-specific cytotoxic T lymphocytes from peripheral blood [J].
Dunbar, PR ;
Ogg, GS ;
Chen, J ;
Rust, N ;
van der Bruggen, P ;
Cerundolo, V .
CURRENT BIOLOGY, 1998, 8 (07) :413-416
[6]   LOSS OF HLA CLASS-I ANTIGENS BY MELANOMA-CELLS - MOLECULAR MECHANISMS, FUNCTIONAL-SIGNIFICANCE AND CLINICAL RELEVANCE [J].
FERRONE, S ;
MARINCOLA, FM .
IMMUNOLOGY TODAY, 1995, 16 (10) :487-494
[7]   Melanoma cell expression of Fas(Apo-1/CD95) ligand: Implications for tumor immune escape [J].
Hahne, M ;
Rimoldi, D ;
Schroter, M ;
Romero, P ;
Schreier, M ;
French, LE ;
Schneider, P ;
Bornand, T ;
Fontana, A ;
Lienard, D ;
Cerottini, JC ;
Tschopp, J .
SCIENCE, 1996, 274 (5291) :1363-1366
[8]  
KAWAKAMI Y, 1995, J IMMUNOL, V154, P3961
[9]  
Mazzocchi A, 1996, J IMMUNOL, V157, P3030
[10]   ALTERATIONS IN SIGNAL TRANSDUCTION MOLECULES IN LYMPHOCYTES-T FROM TUMOR-BEARING MICE [J].
MIZOGUCHI, H ;
O'SHEA, JJ ;
LONGO, DL ;
LOEFFLER, CM ;
MCVICAR, DW ;
OCHOA, AC .
SCIENCE, 1992, 258 (5089) :1795-1798