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HIV-1 gp160作为Th1和Th2细胞因子反应的调节剂:在体外,gp160抑制γ干扰素和白细胞介素-2的产生,同时增强白细胞介素-4的产生。

HIV-1 gp160 as a modifier of Th1 and Th2 cytokine response: gp160 suppresses interferon-gamma and interleukin-2 production concomitantly with enhanced interleukin-4 production in vitro.

作者信息

Hu R, Oyaizu N, Kalyanaraman V S, Pahwa S

机构信息

Department of Pediatrics, North Shore University Hospital-Cornell University Medical College, Manhasset, New York, New York 11030.

出版信息

Clin Immunol Immunopathol. 1994 Nov;73(2):245-51. doi: 10.1006/clin.1994.1194.

DOI:10.1006/clin.1994.1194
PMID:7523014
Abstract

Disease progression in HIV-1 infection is reported to be associated with a gradual shift in CD4+ T cell function from a Th type 1 to a Th type 2 of response, but the underlying mechanism remains unclear. In this study, the effect of HIV-1 envelope glycoprotein gp160 on secretion of cytokines IFN-gamma/IL-2 (Th1 type) and IL-4 (Th2 type) was analyzed using freshly isolated unfractioned peripheral blood mononuclear cells (PBMC), CD4+ T cell lines, and PBMC depleted of CD8+ cells (CD8- PBMC) as target cells. Pretreatment of these cells with HIV gp160 significantly reduced PHA-induced secretion of IFN-gamma and IL-2 but augmented IL-4 production. This effect of gp160 was not observed when the target cells consisted of PBMC depleted of either CD4+ cells (CD4- PBMC) or of CD2+ cells (CD2- PBMC). Pretreatment of gp160 with soluble CD4-immunoglobulin chimeric molecules abrogated the observed effects of gp160, suggesting that CD4-gp120 interaction is required for modification of the cytokine secretion profile. Our results suggest that exposure of CD4+ T cells to HIV-1 envelope proteins may modify the responses evoked by additional stimuli in favor of a Th2-type dominant response.

摘要

据报道,HIV-1感染的疾病进展与CD4+ T细胞功能从1型辅助性T细胞(Th1)反应逐渐转变为2型辅助性T细胞(Th2)反应有关,但其潜在机制仍不清楚。在本研究中,使用新鲜分离的未分级外周血单核细胞(PBMC)、CD4+ T细胞系以及去除CD8+细胞的PBMC(CD8- PBMC)作为靶细胞,分析了HIV-1包膜糖蛋白gp160对细胞因子γ干扰素/白细胞介素-2(Th1型)和白细胞介素-4(Th2型)分泌的影响。用HIV gp160预处理这些细胞,可显著降低植物血凝素(PHA)诱导的γ干扰素和白细胞介素-2的分泌,但增加白细胞介素-4的产生。当靶细胞为去除CD4+细胞的PBMC(CD4- PBMC)或去除CD2+细胞的PBMC(CD2- PBMC)时,未观察到gp160的这种作用。用可溶性CD4-免疫球蛋白嵌合分子预处理gp160可消除观察到的gp160的作用,这表明CD4与gp120的相互作用是改变细胞因子分泌谱所必需的。我们的结果表明,CD4+ T细胞暴露于HIV-1包膜蛋白可能会改变由其他刺激引发的反应,从而有利于Th2型主导反应。

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