The emerging role of HLA-C in HIV-1 infection

被引:53
|
作者
Kulpa, Deanna A. [1 ]
Collins, Kathleen L. [1 ,2 ]
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI USA
基金
美国国家卫生研究院;
关键词
HLA-C; HIV; MHC-I; -35SNP; KIR; IMMUNODEFICIENCY-VIRUS TYPE-1; CELL-SURFACE EXPRESSION; MHC CLASS-I; NATURAL-KILLER-CELLS; CYTOPLASMIC TAIL; HEPATITIS-C; INHIBITORY RECEPTORS; IMMUNE-RESPONSES; HEAVY-CHAIN; NEF PROTEIN;
D O I
10.1111/j.1365-2567.2011.03474.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recently, genome-wide association studies have identified the major histocompatibility complex class I protein HLA-C as an important molecule that affects HIV disease progression. The association between HLA-C and HIV disease outcome was originally determined through a single nucleotide polymorphism (SNP) 35 kb upstream of the HLA-C locus. More recent work has focused on elucidating the functional significance of the 35 SNP, and several groups now have demonstrated HLA-C surface expression to be a key element in control of HIV viral load, with higher surface expression associating with slower disease progression. Most recently, control of HLA-C surface expression has been correlated with the presence of microRNA binding sites that affect HLA-C expression and control of HIV disease. This review highlights these results and explores the ways in which HLA-C surface expression could affect immune system function in the setting of HIV disease.
引用
收藏
页码:116 / 122
页数:7
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