Groux H, Monte D, Bourrez J M, Capron A, Ameisen J C
C.I.B.P., I.N.S.E.R.M. U167-C.N.R.S. 624, Institut Pasteur, Lille.
C R Acad Sci III. 1991;312(12):599-606.
Activation-induced programmed cell death, or apoptosis, is a physiological cell suicide process involved in the negative thymic selection of the T-cell repertoire. We have proposed that the inappropriate re-emergence in the mature CD4+ T-cell population of such a death program could explain both the early dysfunction and the late depletion of CD4+ T-cells from human immunodeficiency virus (HIV)-infected individuals. We present evidence showing that the selective failure of T-cells from 10 HIV-infected asymptomatic individuals (with normal CD4+ T-cell counts) to proliferate in vitro to pokeweed mitogen and to self-major histocompatibility complex class-II T-cell receptor mobilization by superantigens is due to the induction by these stimuli of CD4+ T-cell death. This death process has characteristic features of apoptosis, including DNA fragmentation into multiples of a 200 base pair unit, and the preventive effect of the protein synthesis inhibitor cycloheximide. These findings suggest that in vivo CD4+ T-cell suicide upon activation might account, independently of any HIV-mediated cytopathic effect, for the progressive depletion of CD4+ T-cells that leads to AIDS.
激活诱导的程序性细胞死亡,即凋亡,是一种生理性细胞自杀过程,参与T细胞库的阴性胸腺选择。我们提出,这种死亡程序在成熟CD4+ T细胞群体中不适当的重新出现,可能解释了人类免疫缺陷病毒(HIV)感染个体中CD4+ T细胞的早期功能障碍和晚期耗竭。我们提供的证据表明,10名HIV感染无症状个体(CD4+ T细胞计数正常)的T细胞在体外对商陆有丝分裂原以及超抗原诱导的自身主要组织相容性复合体II类T细胞受体动员的选择性增殖失败,是由于这些刺激诱导了CD4+ T细胞死亡。这种死亡过程具有凋亡的特征,包括DNA断裂成200碱基对单位的倍数,以及蛋白质合成抑制剂环己酰亚胺的预防作用。这些发现表明,激活后体内CD4+ T细胞自杀可能独立于任何HIV介导的细胞病变效应,导致了导致艾滋病的CD4+ T细胞的逐渐耗竭。