Cutting edge: CD95 maintains effector T cell homeostasis in chronic immune activation

被引:28
作者
Arens, R
Baars, PA
Jak, M
Tesselaar, K
van der Valk, M
van Oers, MHJ
van Lier, RAW
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Expt Immunol, NL-1100 DD Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Hematol, NL-1100 DD Amsterdam, Netherlands
[3] Netherlands Canc Inst, Dept Immunol, Amsterdam, Netherlands
[4] Netherlands Canc Inst, Lab Expt Anim Pathol, Amsterdam, Netherlands
关键词
D O I
10.4049/jimmunol.174.10.5915
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 elimination of activated T cells is important to maintain homeostasis and avoid immunopathology. CD95 (TaslAPO-1) has been identified as a death mediator for activated T cells in vitro but the function of CD95 in death of mature T cells in vivo is still controversial Here we show that triggering of the costimulatory TNF receptor family member CD27 sensitized T cells for CD95-induced apoptosis. CD95-deficient (lpr/lpr) T cells massively expanded and differentiated into IFN-gamma-secreting effector cells in transgenic mice that constitutively express the CD27 ligand, CD70. Concomitantly, CD95-deficient CD70 transgenic mice became moribund by 4 wk of age with severe liver pathology and bone marrow failure. These findings establish that CD95 is a critical regulator of effector T cell homeostasis in chronic immune activation.
引用
收藏
页码:5915 / 5920
页数:6
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