Concepts of activated T cell death

被引:116
作者
Brenner, Dirk [1 ]
Krammer, Peter H. [1 ]
Arnold, Ruediger [1 ]
机构
[1] German Canc Res Ctr, Tumor Immunol Program, D-69120 Heidelberg, Germany
关键词
apoptosis; T cells; AICD; ACAD; immune response; HPK1; NF-kappa B;
D O I
10.1016/j.critrevonc.2008.01.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Lymphocytes of the adaptive immune system play a crucial role in defending the organism against pathogens. Initial stimulation via antigen receptors induces activation and proliferation of lymphocytes to generate effector cells that clear the pathogen from the body. During the shut-down of the immune response activated lymphocytes are removed by two mechanisms. T cells that are restimulated during the end of the immune response die by activation-induced cell death (AICD), whereas activated lymphocytes which are not restimulated die by activated cell autonomous death (ACAD). Here, we discuss the regulation of AICD and ACAD in T cells and review the role of cytokines, T cell receptor (TCR) proximal signaling mediators like hematopoietic progenitor kinase 1 (HPK1) and the NF-kappa B pathway. We distinguish between AICD dependent on or independent of death receptor ligation, and discuss caspase-independent death of T cells. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:52 / 64
页数:13
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