Peter M E, Ehret A, Berndt C, Krammer P H
Tumorimmunology Program, German Cancer Research Center, Heidelberg, Germany.
Br Med Bull. 1997;53(3):604-16. doi: 10.1093/oxfordjournals.bmb.a011633.
Activation-induced cell death (AICD) of T cells involves the CD95 receptor/ligand system. T cell activation through the T cell receptor results in expression of the CD95 ligand (CD95L) that acts on CD95+ cells by direct binding and in a paracrine or autocrine fashion. In AIDS, upregulation of CD95L in T cells is accelerated by two viral gene products, HIV-1 Tat and gp120. The CD95 signaling pathway is, therefore, likely to represent an important road to cell death of the CD4+ T cells in AIDS. Recently, the early events in the CD95 signaling pathway have been identified. A key role hereby plays a receptor-interacting member of the interleukin 1 beta-converting enzymes (ICE), FLICE, that could be a target for therapeutic intervention. In addition to CD95, the role of other members of the TNF receptor superfamily in AIDS is discussed.
T细胞的活化诱导细胞死亡(AICD)涉及CD95受体/配体系统。通过T细胞受体激活T细胞会导致CD95配体(CD95L)的表达,该配体通过直接结合以及旁分泌或自分泌方式作用于CD95+细胞。在艾滋病中,T细胞中CD95L的上调会被两种病毒基因产物HIV-1 Tat和gp120加速。因此,CD95信号通路很可能是艾滋病中CD4+ T细胞死亡的一条重要途径。最近,已经确定了CD95信号通路中的早期事件。白细胞介素1β转换酶(ICE)的受体相互作用成员FLICE在此发挥关键作用,它可能是治疗干预的靶点。除了CD95,还讨论了肿瘤坏死因子受体超家族其他成员在艾滋病中的作用。