Grant M D, Smail F M, Rosenthal K L
Department of Pathology, McMaster University, Hamilton, Ontario, Canada.
J Acquir Immune Defic Syndr (1988). 1994 Jun;7(6):571-9.
Human immunodeficiency virus type 1 (HIV-1)-infected individuals, but not HIV-seronegative controls, have non-HLA-restricted T-cell receptor alpha beta+ CD8+ cytotoxic T-lymphocytes (CTL) that kill activated uninfected CD4+ lymphocytes. In vitro stimulation of peripheral blood mononuclear cells from HIV-1-infected individuals with concanavalin A (Con A) or by coculture with phytohemagglutinin-activated autologous lymphoblasts induced CTL that killed autologous and heterologous CD4+ lymphocytes, but not Con A-activated CD8+ lymphocytes or Epstein-Barr virus (EBV)-transformed B lymphocytes. EBV did not stimulate such CTL in two subjects tested, although stimulation with Con A or autologous lymphoblasts induced CTL activity against CD4+ lymphocytes in both subjects. CTL activity against autologous CD4+ lymphocytes varied over time; killing of heterologous CD4+ lymphocytes was often higher than that of autologous CD4+ lymphocytes. HIV-infected individuals with Con A-inducible CTL against autologous CD4+ lymphocytes lost more CD4+ lymphocytes within 6 months of testing than HIV-infected individuals with no such CTL (p < .01). The mean (+/- SD) decrease in CD4+ lymphocyte counts in a group of HIV-infected individuals with CTL activity against autologous CD4+ lymphocytes was 121 +/- 84, or 36%, of total CD4+ lymphocytes over 6 months. In contrast, there was no significant change in mean CD4+ lymphocyte count over 6 months in a group of HIV-infected individuals without CTL activity against autologous CD4+ lymphocytes. In some HIV-infected individuals, CTL activity against autologous CD4+ lymphocytes fell coincident with a drop in CD4+ lymphocyte number in vivo.(ABSTRACT TRUNCATED AT 250 WORDS)
1型人类免疫缺陷病毒(HIV - 1)感染个体而非HIV血清阴性对照者,具有非HLA限制性的T细胞受体αβ + CD8 + 细胞毒性T淋巴细胞(CTL),可杀伤活化的未感染CD4 + 淋巴细胞。用伴刀豆球蛋白A(Con A)体外刺激HIV - 1感染个体的外周血单个核细胞,或与植物血凝素活化的自体淋巴母细胞共培养,可诱导CTL杀伤自体和异源CD4 + 淋巴细胞,但不杀伤Con A活化的CD8 + 淋巴细胞或爱泼斯坦 - 巴尔病毒(EBV)转化的B淋巴细胞。在两名受试对象中,EBV未刺激产生此类CTL,尽管用Con A或自体淋巴母细胞刺激均诱导了针对两名受试对象CD4 + 淋巴细胞的CTL活性。针对自体CD4 + 淋巴细胞的CTL活性随时间变化;对异源CD4 + 淋巴细胞的杀伤通常高于对自体CD4 + 淋巴细胞的杀伤。具有针对自体CD4 + 淋巴细胞的Con A诱导性CTL的HIV感染个体,在检测后的6个月内比无此类CTL的HIV感染个体丢失更多CD4 + 淋巴细胞(p <.01)。一组具有针对自体CD4 + 淋巴细胞CTL活性的HIV感染个体,其CD4 + 淋巴细胞计数的平均(±标准差)下降为121±84,占6个月内总CD4 + 淋巴细胞的36%。相比之下,一组无针对自体CD4 + 淋巴细胞CTL活性的HIV感染个体,其6个月内CD4 + 淋巴细胞平均计数无显著变化。在一些HIV感染个体中,针对自体CD4 + 淋巴细胞的CTL活性下降与体内CD4 + 淋巴细胞数量下降同时发生。(摘要截断于250字)