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Group-specific, major histocompatibility complex class I-restricted cytotoxic responses to human immunodeficiency virus 1 (HIV-1) envelope proteins by cloned peripheral blood T cells from an HIV-1-infected individual.

机译:通过感染HIV-1的个体克隆的外周血T细胞对人类免疫缺陷病毒1(HIV-1)包膜蛋白的特定于组的主要组织相容性复合体I类限制了细胞毒性反应。

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摘要

Freshly separated unfractionated peripheral blood mononuclear cells (PBMC) and cloned cell lines from a healthy human immunodeficiency virus 1 (HIV-1)-seropositive individual were examined for cytotoxic responses to HIV proteins expressed by recombinant vaccinia viruses. It was found that freshly isolated PBMC recognize variant envelope proteins of HIV-1 but not a more distantly related envelope protein derived from the simian immunodeficiency virus (SIVmac). Although the effector cells were predominantly CD8+, both MHC-matched and -unmatched target cells were lysed. Cytotoxic T lymphocyte (CTL) clones were found to lyse cells expressing HIV-1 envelope or reverse transcriptase. In contrast to the cytotoxic response detected with PBMC, the cloned CTLs were major histocompatibility complex (MHC) class I restricted. Our finding that a cloned CTL line lysed cells expressing highly divergent HIV envelopes strongly suggested that a conserved epitope was recognized. Identification of these shared epitopes may assist in designing a vaccine for HIV-1 that could stimulate MHC-restricted cytotoxic responses.
机译:检查了新鲜分离的未分离的外周血单核细胞(PBMC)和来自健康人类免疫缺陷病毒1(HIV-1)血清反应阳性的个体的克隆细胞系对重组牛痘病毒表达的HIV蛋白的细胞毒性反应。发现新鲜分离的PBMC识别HIV-1的变体包膜蛋白,但不能识别源自猿猴免疫缺陷病毒(SIVmac)的更远相关的包膜蛋白。尽管效应细胞主要是CD8 +,但MHC匹配和非匹配的靶细胞均被裂解。发现细胞毒性T淋巴细胞(CTL)克隆可裂解表达HIV-1包膜或逆转录酶的细胞。与PBMC检测到的细胞毒性反应相反,克隆的CTL受主要的组织相容性复合物(MHC)I类限制。我们的发现表明克隆的CTL裂解了表达高度不同的HIV包膜的细胞,这强烈表明已识别出保守的表位。这些共享表位的鉴定可能有助于设计针对HIV-1的疫苗,该疫苗可以刺激MHC限制的细胞毒性反应。

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