Weinhold K J, Lyerly H K, Matthews T J, Tyler D S, Ahearne P M, Stine K C, Langlois A J, Durack D T, Bolognesi D P
Department of Surgery, Duke University Medical Center, Durham, North Carolina.
Lancet. 1988 Apr 23;1(8591):902-5. doi: 10.1016/s0140-6736(88)91713-8.
Forty-one patients seropositive for human immunodeficiency virus type 1 (HIV-1) were assessed for cell-mediated cytotoxicity (CMC) against autologous target cells bearing the major envelope glycoprotein of HIV-1, gp120. Effector lymphocytes from over 85% of seropositive patients showed CMC specific for gp120-coated targets, whereas seronegative individuals had no detectable CMC. As a group, symptomless individuals had the highest levels of CMC; patients with AIDS-related complex and AIDS showed progressively diminished reactivity. The gp120-specific CMC was mediated by a population of non-T-cell effectors phenotypically resembling NK/K cells. Cytolysis was not restricted by major histocompatibility complex determinants, as shown by killing of heterologous gp120-adsorbed targets and of HIV-1-infected cell-lines. Gp120-specific CMC was highly augmented in the presence of interleukin 2, so it may be possible to develop therapeutic strategies aimed at destruction of virus-producing cell reservoirs in infected individuals through stimulation of HIV-specific host CMC.
对41名1型人类免疫缺陷病毒(HIV-1)血清反应呈阳性的患者进行了评估,检测其针对携带HIV-1主要包膜糖蛋白gp120的自体靶细胞的细胞介导细胞毒性(CMC)。超过85%的血清反应呈阳性患者的效应淋巴细胞表现出对gp120包被靶标的特异性CMC,而血清反应阴性个体则未检测到CMC。总体而言,无症状个体的CMC水平最高;患有艾滋病相关综合征和艾滋病的患者反应性逐渐降低。gp120特异性CMC由一群表型类似于NK/K细胞的非T细胞效应细胞介导。如对异源gp120吸附靶标和HIV-1感染细胞系的杀伤所示,细胞溶解不受主要组织相容性复合体决定簇的限制。在白细胞介素2存在的情况下,gp120特异性CMC显著增强,因此有可能通过刺激HIV特异性宿主CMC来制定旨在破坏感染个体中产生病毒的细胞库的治疗策略。