Blocking the common γ-chain of cytokine receptors induces T cell apoptosis and long-term islet allograft survival

被引:62
作者
Li, XC
Ima, A
Li, YS
Zheng, XX
Malek, TR
Strom, TB
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Med,Div Immunol, Boston, MA 02215 USA
[2] Univ Miami, Dept Microbiol & Immunol, Miami, FL 33101 USA
关键词
D O I
10.4049/jimmunol.164.3.1193
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 common gamma c-chain is an essential signaling component shared by all known T cell growth factor (TCGF) receptors (i.e., IL-2, IL-4, IL-7, IL-9, and IL-15). In the present study, we have studied the effect of gamma c-chain blockade on T cell activation and allograft rejection. Treatment of B6AF(1) (H-2(b/d.k)) recipient mice with anti-gamma c mAbs induced long-term survival of DBA/2 (H-2(d)) islet allografts (>150 days, n = 8), whereas control Ab-treated mice rejected the islet allografts within 17 days (n = 6), The state of engraftment induced by the anti-gamma c mAbs was remarkably stable, as recipient mice bearing the primary islet allografts accepted a second DBA/2 islet allograft without further immunosuppression and systemic administration of high doses of IL-2Ig fusion protein failed to provoke rejection. Blocking the gamma c-chain inhibited T cell proliferation and induced T cell apoptosis by repressing expression of Bcl-2, Our data suggest that one means of inducing T cell apoptosis and stable allograft survival can be achieved via gamma c-chain blockade.
引用
收藏
页码:1193 / 1199
页数:7
相关论文
共 33 条
[1]  
Barouch DH, 1998, J IMMUNOL, V161, P1875
[2]   Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor [J].
Brunet, A ;
Bonni, A ;
Zigmond, MJ ;
Lin, MZ ;
Juo, P ;
Hu, LS ;
Anderson, MJ ;
Arden, KC ;
Blenis, J ;
Greenberg, ME .
CELL, 1999, 96 (06) :857-868
[3]   DEFECTIVE LYMPHOID DEVELOPMENT IN MICE LACKING EXPRESSION OF THE COMMON CYTOKINE RECEPTOR-GAMMA CHAIN [J].
CAO, XQ ;
SHORES, EW ;
HULI, J ;
ANVER, MR ;
KELSALL, BL ;
RUSSELL, SM ;
DRAGO, J ;
NOGUCHI, M ;
GRINBERG, A ;
BLOOM, ET ;
PAUL, WE ;
KATZ, SI ;
LOVE, PE ;
LEONARD, WJ .
IMMUNITY, 1995, 2 (03) :223-238
[4]   Regulation of cell death protease caspase-9 by phosphorylation [J].
Cardone, MH ;
Roy, N ;
Stennicke, HR ;
Salvesen, GS ;
Franke, TF ;
Stanbridge, E ;
Frisch, S ;
Reed, JC .
SCIENCE, 1998, 282 (5392) :1318-1321
[5]  
Dai ZH, 1999, J IMMUNOL, V163, P3131
[6]   Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241
[7]  
DENDORFER U, 1993, TRANSPLANT SCI, V3, P83
[8]   LYMPHOID DEVELOPMENT IN MICE WITH A TARGETED DELETION OF THE INTERLEUKIN-2 RECEPTOR-GAMMA CHAIN [J].
DISANTO, JP ;
MULLER, W ;
GUYGRAND, D ;
FISCHER, A ;
RAJEWSKY, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (02) :377-381
[9]   Regulation of neuronal survival by the serine-threonine protein kinase Akt [J].
Dudek, H ;
Datta, SR ;
Franke, TF ;
Birnbaum, MJ ;
Yao, RJ ;
Cooper, GM ;
Segal, RA ;
Kaplan, DR ;
Greenberg, ME .
SCIENCE, 1997, 275 (5300) :661-665
[10]   IDENTIFICATION AND CLONING OF A NOVEL IL-15 BINDING-PROTEIN THAT IS STRUCTURALLY RELATED TO THE ALPHA-CHAIN OF THE IL-2 RECEPTOR [J].
GIRI, JG ;
KUMAKI, S ;
AHDIEH, M ;
FRIEND, DJ ;
LOOMIS, A ;
SHANEBECK, K ;
DUBOSE, R ;
COSMAN, D ;
PARK, LS ;
ANDERSON, DM .
EMBO JOURNAL, 1995, 14 (15) :3654-3663