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

被引:21
|
作者
DeGottardi, M. Quinn [1 ]
Specht, Anke [2 ]
Metcalf, Benjamin [3 ]
Kaur, Amitinder [3 ]
Kirchhoff, Frank [2 ]
Evans, David T. [1 ]
机构
[1] Harvard Univ, Sch Med, New England Reg Primate Res Ctr, Dept Microbiol & Mol Genet, Southborough, MA 01772 USA
[2] Harvard Univ, Sch Med, New England Reg Primate Res Ctr, Div Immunol, Southborough, MA 01772 USA
[3] Univ Ulm Klinikum, Inst Virol, D-89081 Ulm, Germany
关键词
D O I
10.1128/JVI.02102-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
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.
引用
收藏
页码:3139 / 3146
页数:8
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