Cohen G B, Gandhi R T, Davis D M, Mandelboim O, Chen B K, Strominger J L, Baltimore D
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.
Immunity. 1999 Jun;10(6):661-71. doi: 10.1016/s1074-7613(00)80065-5.
To avoid detection by CTL, HIV encodes mechanisms for removal of class I MHC proteins from the surface of infected cells. However, class I downregulation potentially exposes the virus-infected cell to attack by NK cells. Human lymphoid cells are protected from NK cell cytotoxicity primarily by HLA-C and HLA-E. We present evidence that HIV-1 selectively downregulates HLA-A and HLA-B but does not significantly affect HLA-C or HLA-E. We then identify the residues in HLA-C and HLA-E that protect them from HIV down-regulation. This selective downregulation allows HIV-infected cells to avoid NK cell-mediated lysis and may represent for HIV a balance between escape from CTL and maintenance of protection from NK cells. These results suggest that subpopulations of CTL and NK cells may be uniquely suited for combating HIV.
为了避免被细胞毒性T淋巴细胞(CTL)检测到,HIV编码了从受感染细胞表面去除I类主要组织相容性复合体(MHC)蛋白的机制。然而,I类分子的下调可能使病毒感染细胞暴露于自然杀伤细胞(NK细胞)的攻击之下。人类淋巴细胞主要通过HLA-C和HLA-E免受NK细胞的细胞毒性作用。我们提供的证据表明,HIV-1选择性地下调HLA-A和HLA-B,但对HLA-C或HLA-E没有显著影响。然后,我们确定了HLA-C和HLA-E中保护它们不被HIV下调的残基。这种选择性下调使HIV感染细胞能够避免NK细胞介导的裂解,这可能代表了HIV在逃避CTL和维持免受NK细胞保护之间的一种平衡。这些结果表明,CTL和NK细胞的亚群可能特别适合对抗HIV。