Cytokine augmentation of human immunodeficiency virus type 1 (HIV-1) gp120-specific cellular cytotoxicity.

K C Stine, D Bolognesi, K J Weinhold
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Abstract

Currently available anti-human immunodeficiency virus type 1 (HIV-1) agents such as azidothymidine can prevent de novo virus infection in vitro but lack significant activity against chronically infected cells. Our laboratory has recently described glycoprotein (gp)120-specific cell mediated cytotoxicity (CMC) present in HIV-1-seropositive individuals that is capable of destroying virally infected cells. As a means of potentially eliminating persistent reservoirs of HIV-1, we examined the ability of various cytokines to augment preexisting gp120-specific CMC activity of peripheral blood mononuclear cells obtained from early disease patients. We found that interferon-gamma alone had no effect on gp120 cellular reactivity; however, the combination of interferon-gamma plus IL-2 produced enhancement beyond that of IL-2 alone.

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人类免疫缺陷病毒1型(HIV-1) gp120特异性细胞毒性的细胞因子增强
目前可用的抗人类免疫缺陷病毒1型(HIV-1)药物如叠氮胸苷可以在体外预防新发病毒感染,但对慢性感染细胞缺乏显著活性。我们的实验室最近描述了糖蛋白(gp)120特异性细胞介导的细胞毒性(CMC)存在于hiv -1血清阳性个体中,能够破坏病毒感染的细胞。作为一种潜在消除持久性HIV-1储存库的手段,我们检测了各种细胞因子增强早期疾病患者外周血单个核细胞先前存在的gp120特异性CMC活性的能力。我们发现单独使用干扰素对gp120细胞的反应性没有影响;然而,干扰素- γ和IL-2联合使用产生的增强作用超过单独使用IL-2。
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