Cytotoxic T lymphocyte antigen 4 is induced in the thymus upon in vivo activation and its blockade prevents anti-CD3-mediated depletion of thymocytes

被引:43
作者
Cilio, CM
Daws, MR
Malashicheva, A
Sentman, CL
Holmberg, D [1 ]
机构
[1] Umea Univ, Dept Cell & Mol Biol, S-90187 Umea, Sweden
[2] Umea Univ, Umea Ctr Mol Pathogenesis, S-90187 Umea, Sweden
关键词
cytotoxic T lymphocyte antigen 4 (CD152); CD28; costimulation; T cell development; tyrosine phosphatase SHP-2;
D O I
10.1084/jem.188.7.1239
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The development of a normal T cell repertoire in the thymus is dependent on the interplay between signals mediating cell survival (positive selection) and cell death (negative selection or death by neglect). Although the CD28 costimulatory molecule has been implicated in this process, it has been difficult to establish a role for the other major costimulatory molecule, cytotoxic T lymphocyte antigen (CTLA)-4. Here we report that in vivo stimulation through the T cell receptor (TCR)-CD3 complex induces expression of CTLA-4 in thymocytes and leads to the association of CTLA-4 with the SH2 domain-containing phosphatase (SHP)-2 tyrosine phosphatase. Moreover, intrathymic CTLA-4 blockade dramatically inhibits anti-CD3-mediated depletion of CD4(+)CD8(+) double positive immature thymocytes. Similarly, anti-CD3-mediated depletion of CD4(+)CD8(+) double positive cells in fetal thymic organ cultures could also be inhibited by anti-CTLA-4 antibodies. Thus, our data provide evidence for a role of CTLA-4 in thymic selection and suggest a novel mechanism contributing to the regulation of TCR-mediated selection of T cell repertoires.
引用
收藏
页码:1239 / 1246
页数:8
相关论文
共 41 条
[1]  
Alegre ML, 1996, J IMMUNOL, V157, P4762
[2]   CD28-B7 interactions function to co-stimulate clonal deletion of double-positive thymocytes [J].
Amsen, D ;
Kruisbeek, AM .
INTERNATIONAL IMMUNOLOGY, 1996, 8 (12) :1927-1936
[3]   Genetic markers in diagnosis and prediction of relapse in Graves' disease [J].
Badenhoop, K ;
Donner, H ;
Braun, J ;
Siegmund, T ;
Rau, H ;
Usadel, KH .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 1996, 104 :98-100
[4]   A NEW MEMBER OF THE IMMUNOGLOBULIN SUPERFAMILY - CTLA-4 [J].
BRUNET, JF ;
DENIZOT, F ;
LUCIANI, MF ;
ROUXDOSSETO, M ;
SUZAN, M ;
MATTEI, MG ;
GOLSTEIN, P .
NATURE, 1987, 328 (6127) :267-270
[5]   Co-stimulation in T cell responses [J].
Chambers, CA ;
Allison, JP .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (03) :396-404
[6]   Thymocyte development is normal in CTLA-4-deficient mice [J].
Chambers, CA ;
Cado, D ;
Truong, T ;
Allison, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) :9296-9301
[7]  
DEGERMANN S, 1994, J IMMUNOL, V152, P3254
[8]   CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus [J].
Donner, H ;
Rau, H ;
Walfish, PG ;
Braun, J ;
Siegmund, T ;
Finke, R ;
Herwig, J ;
Usadel, KH ;
Badenhoop, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (01) :143-146
[9]   IDENTIFICATION AND MAPPING TO CHROMOSOME-1 OF A SUSCEPTIBILITY LOCUS FOR PERIINSULITIS IN NONOBESE DIABETIC MICE [J].
GARCHON, HJ ;
BEDOSSA, P ;
ELOY, L ;
BACH, JF .
NATURE, 1991, 353 (6341) :260-262
[10]  
GROSS JA, 1992, J IMMUNOL, V149, P380