Krueger Andreas, Fas Stefanie C, Baumann Sven, Krammer Peter H
Tumorimmunology Program,German Cancer Research Center (DKFZ), Heidelberg, Germany.
Immunol Rev. 2003 Jun;193:58-69. doi: 10.1034/j.1600-065x.2003.00047.x.
Apoptosis of activated peripheral T cells during the termination phase of an immune response is critical to maintain T-cell homeostasis. Activated T cells can be removed by two mechanisms: activation-induced cell death (AICD) and death by neglect. AICD is triggered by death receptors, whereas death by neglect is induced by cytokine withdrawal. CD95 (APO-1/Fas) belongs to the subfamily of death receptors and plays a major role in AICD. In this review, we focus on the molecular mechanisms of AICD, in particular those involving the CD95 system. Moreover, we discuss the relative contribution of AICD and death by neglect to terminate a T-cell immune response. In order to become fully activated, T cells require a second signal provided by antigen-presenting cells. We discuss how these costimulatory signals counteract pro-apoptotic signals and, finally, which signals might protect T cells from death to generate a pool of memory T cells.
免疫反应终止阶段活化外周T细胞的凋亡对于维持T细胞稳态至关重要。活化的T细胞可通过两种机制被清除:活化诱导的细胞死亡(AICD)和被忽视死亡。AICD由死亡受体触发,而被忽视死亡则由细胞因子撤离诱导。CD95(APO-1/Fas)属于死亡受体亚家族,在AICD中起主要作用。在本综述中,我们聚焦于AICD的分子机制,尤其是那些涉及CD95系统的机制。此外,我们讨论AICD和被忽视死亡在终止T细胞免疫反应中的相对作用。为了完全活化,T细胞需要抗原呈递细胞提供的第二信号。我们讨论这些共刺激信号如何抵消促凋亡信号,以及最终哪些信号可能保护T细胞免于死亡以产生记忆T细胞池。