VARIABLE EXPRESSION OF CD3-ZETA CHAIN IN TUMOR-INFILTRATING LYMPHOCYTES (TIL) DERIVED FROM RENAL-CELL CARCINOMA - RELATIONSHIP WITH TIL PHENOTYPE AND FUNCTION

被引:102
作者
TARTOUR, E
LATOUR, S
MATHIOT, C
THIOUNN, N
MOSSERI, V
JOYEUX, I
DENGHIEN, CD
LEE, RS
DEBRE, B
FRIDMAN, WH
机构
[1] INST CURIE,DEPT BIOL CLIN,PARIS,FRANCE
[2] INST CURIE,INSERM,U255,PARIS,FRANCE
[3] UNIV PARIS 05,PARIS,FRANCE
[4] HOP COCHIN,DEPT UROL,PARIS,FRANCE
[5] INST CURIE,UNITE BIOSTAT,PARIS,FRANCE
关键词
D O I
10.1002/ijc.2910630210
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has been reported that in mice and in humans, tumor-infiltrating lymphocytes (TIL) may exhibit a defect in CD3-zeta-chain expression. Therefore, the level of CD3-zeta was analyzed in TIL derived from patients with renal-cell carcinoma, and its correlation with TIL phenotype and function was assessed. We identified 4 out of 13 tumor-infiltrating lymphocytes derived from renal-cell carcinoma, with a significant decrease in CD3-zeta-chain expression as compared with control peripheral-blood lymphocytes. This defect was never found after culturing TIL with IL2. In one case, the low expression of zeta chain observed in TIL on day 0 was reversed when TIL were cultured with IL2. The zeta-chain level did not seem to predict the growth of TIL. in response to IL2. All the TIL, irrespective of the level of zeta-chain expression, exhibited lower proliferative response when stimulated with PHA or anti-CDS MAb in comparison with normal peripheral-blood mononuclear cells. Nevertheless, in this limited series of patients, a correlation was observed between the level of zeta-chain expression and T-cell infiltration (p = 0.02). After TIL stimulation with PHA or anti-CD3, in contrast to IL2 or IFN gamma production, a trend towards a relationship between TNF alpha induction and the level of zeta-chain expression was observed. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:205 / 212
页数:8
相关论文
共 33 条
[1]  
ALEXANDER JP, 1993, CANCER RES, V53, P1380
[2]  
ANDERSON P, 1989, J IMMUNOL, V143, P1899
[3]   ROLE OF ASSOCIATED GAMMA-CHAIN IN TYROSINE KINASE ACTIVATION VIA MURINE FC-GAMMA-RIII [J].
BONNEROT, C ;
AMIGORENA, S ;
CHOQUET, D ;
PAVLOVICH, R ;
CHOUKROUN, V ;
FRIDMAN, WH .
EMBO JOURNAL, 1992, 11 (07) :2747-2757
[4]   CHRONIC EXPOSURE TO TUMOR-NECROSIS-FACTOR (TNF) IN-VITRO IMPAIRS THE ACTIVATION OF T-CELLS THROUGH THE T-CELL RECEPTOR CD3 COMPLEX - REVERSAL IN-VIVO BY ANTI-TNF ANTIBODIES IN PATIENTS WITH RHEUMATOID-ARTHRITIS [J].
COPE, AP ;
LONDEI, M ;
CHU, NR ;
COHEN, SBA ;
ELLIOTT, MJ ;
BRENNAN, FM ;
MAINI, RN ;
FELDMANN, M .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :749-760
[5]  
FINKE JH, 1993, CANCER RES, V53, P5613
[6]   STRUCTURAL MUTATIONS OF THE T-CELL RECEPTOR ZETA-CHAIN AND ITS ROLE IN T-CELL ACTIVATION [J].
FRANK, SJ ;
NIKLINSKA, BB ;
ORLOFF, DG ;
MERCEP, M ;
ASHWELL, JD ;
KLAUSNER, RD .
SCIENCE, 1990, 249 (4965) :174-177
[7]   DIFFERENT USE OF T-CELL RECEPTOR TRANSDUCING MODULES IN 2 POPULATIONS OF GUT INTRAEPITHELIAL LYMPHOCYTES ARE RELATED TO DISTINCT PATHWAYS OF T-CELL DIFFERENTIATION [J].
GUYGRAND, D ;
ROCHA, B ;
MINTZ, P ;
MALASSISSERIS, M ;
SELZ, F ;
MALISSEN, B ;
VASSALLI, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (02) :673-679
[8]   THE CYTOPLASMIC TAIL OF THE T-CELL RECEPTOR ZETA-CHAIN IS DISPENSABLE FOR ANTIGEN-MEDIATED T-CELL ACTIVATION [J].
HERMANS, MHA ;
MALISSEN, B .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (09) :2257-2262
[9]   THE CYTOPLASMIC DOMAIN OF THE T-CELL RECEPTOR ZETA-CHAIN IS SUFFICIENT TO COUPLE TO RECEPTOR-ASSOCIATED SIGNAL TRANSDUCTION PATHWAYS [J].
IRVING, BA ;
WEISS, A .
CELL, 1991, 64 (05) :891-901
[10]   THE T-CELL ANTIGEN RECEPTOR - INSIGHTS INTO ORGANELLE BIOLOGY [J].
KLAUSNER, RD ;
LIPPINCOTTSCHWARTZ, J ;
BONIFACINO, JS .
ANNUAL REVIEW OF CELL BIOLOGY, 1990, 6 :403-431