Krammer Peter H, Arnold Rüdiger, Lavrik Inna N
Tumour Immunology Program, German Cancer Research Center, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany.
Nat Rev Immunol. 2007 Jul;7(7):532-42. doi: 10.1038/nri2115.
During the course of an immune response, antigen-reactive T cells clonally expand and then are removed by apoptosis to maintain immune homeostasis. Life and death of T cells is determined by multiple factors, such as T-cell receptor triggering, co-stimulation or cytokine signalling, and by molecules, such as caspase-8 (FLICE)-like inhibitory protein (FLIP) and haematopoietic progenitor kinase 1 (HPK1), which regulate the nuclear factor-kappaB (NF-kappaB) pathway. Here, we discuss the concepts of activation-induced cell death (AICD) and activated cell-autonomous death (ACAD) in the regulation of life and death in T cells.
在免疫反应过程中,抗原反应性T细胞发生克隆性扩增,然后通过凋亡被清除以维持免疫稳态。T细胞的生死由多种因素决定,如T细胞受体触发、共刺激或细胞因子信号传导,以及由调节核因子-κB(NF-κB)途径的分子,如半胱天冬酶-8(FLICE)样抑制蛋白(FLIP)和造血祖细胞激酶1(HPK1)决定。在此,我们讨论激活诱导的细胞死亡(AICD)和激活的细胞自主死亡(ACAD)在T细胞生死调节中的概念。