Lynch D H, Ramsdell F, Alderson M R
Immunex Corporation, Seattle, WA 98101, USA.
Immunol Today. 1995 Dec;16(12):569-74. doi: 10.1016/0167-5699(95)80079-4.
Studies of the biological effects of Fas signaling, using transformed cell lines as targets, indicate that ligation of the Fas receptor induces an apoptotic death signal. Chronically activated normal human T cells are also susceptible to Fas-mediated apoptosis. However, interactions between Fas and Fas ligand can also yield a costimulatory signal. Here, David Lynch, Fred Ramsdell and Mark Alderson present a model for the role of As and FasL in the homeostatic regulation of normal immune responses. They discuss how dysregulation of the Fas apoptotic pathway may contribute to certain disease states, including autoimmune disease and human immunodeficiency virus (HIV)-induced depletion of CD4+ T cells.
以转化细胞系为靶标的Fas信号传导生物学效应研究表明,Fas受体的连接可诱导凋亡死亡信号。长期活化的正常人T细胞也易受Fas介导的凋亡影响。然而,Fas与Fas配体之间的相互作用也可产生共刺激信号。在此,大卫·林奇、弗雷德·拉姆齐德尔和马克·奥尔德森提出了一个关于Fas和FasL在正常免疫反应稳态调节中作用的模型。他们讨论了Fas凋亡途径的失调如何可能导致某些疾病状态,包括自身免疫性疾病和人类免疫缺陷病毒(HIV)诱导的CD4 + T细胞耗竭。