首页> 美国卫生研究院文献>Journal of Virology >Selective Downregulation of Rhesus Macaque and Sooty Mangabey Major Histocompatibility Complex Class I Molecules by Nef Alleles of Simian Immunodeficiency Virus and Human Immunodeficiency Virus Type 2
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Selective Downregulation of Rhesus Macaque and Sooty Mangabey Major Histocompatibility Complex Class I Molecules by Nef Alleles of Simian Immunodeficiency Virus and Human Immunodeficiency Virus Type 2

机译:猿猴免疫缺陷病毒和2型人类免疫缺陷病毒的Nef等位基因选择性下调恒河猴和黑手猴的主要组织相容性复合体I类分子

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摘要

Human immunodeficiency virus type 1 (HIV-1) Nef downregulates HLA-A and -B molecules, but not HLA-C or -E molecules, based on amino acid differences in their cytoplasmic domains to simultaneously evade cytotoxic T lymphocyte (CTL) and natural killer cell surveillance. Rhesus macaques and sooty mangabeys express orthologues of HLA-A, -B, and -E, but not HLA-C, and many of these molecules have unique amino acid differences in their cytoplasmic tails. We found that these differences also resulted in differential downregulation by primary simian immunodeficiency virus (SIV) SIVsmm/mac and HIV-2 Nef alleles. Thus, selective major histocompatibility complex class I downregulation is a conserved mechanism of immune evasion for pathogenic SIV infection of rhesus macaques and nonpathogenic SIV infection of sooty mangabeys.
机译:人类免疫缺陷病毒1型(HIV-1)Nef根据细胞质结构域中的氨基酸差异,下调HLA-A和-B分子,但不下调HLA-C或-E分子,同时逃避细胞毒性T淋巴细胞(CTL)和天然杀伤细胞监视。恒河猴和煤烟黑长尾猴表达HLA-A,-B和-E的直向同源物,但不表达HLA-C,并且这些分子中的许多在其细胞质尾巴中具有独特的氨基酸差异。我们发现这些差异还导致原发猿猴免疫缺陷病毒(SIV)SIVsmm / mac和HIV-2 Nef等位基因的差异下调。因此,选择性的主要组织相容性复合体I类下调是恒河猴猕猴的病原性SIV感染和煤烟性象的非病原性SIV感染的免疫逃避的保守机制。

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