HIV-1 Vpu Mediates HLA-C Downregulation

被引:110
作者
Apps, Richard [1 ]
Del Prete, Gregory Q. [2 ]
Chatterjee, Pramita [1 ]
Lara, Abigail [2 ]
Brumme, Zabrina L. [3 ,4 ]
Brockman, Mark A. [3 ,4 ]
Neil, Stuart [5 ]
Pickering, Suzanne [5 ]
Schneider, Douglas K. [2 ]
Piechocka-Trocha, Alicja [6 ,7 ]
Walker, Bruce D. [6 ,7 ]
Thomas, Rasmi [8 ]
Shaw, George M. [9 ,10 ]
Hahn, Beatrice H. [9 ,10 ]
Keele, Brandon F. [2 ]
Lifson, Jeffrey D. [2 ]
Carrington, Mary [1 ,6 ,7 ]
机构
[1] Frederick Natl Lab, Canc & Inflammat Program, Leidos Biomed Res, Frederick, MD 21702 USA
[2] Frederick Natl Lab, AIDS & Canc Virus Program, Leidos Biomed Res, Frederick, MD 21702 USA
[3] Simon Fraser Univ, Fac Hlth Sci, Burnaby, BC V5A 1S6, Canada
[4] British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V67 1Y6, Canada
[5] Guys Hosp, Kings Coll London, Sch Med, Dept Infect Dis, London SE1 9RT, England
[6] MIT, Massachusetts Gen Hosp, Ragon Inst, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[7] Harvard Univ, Cambridge, MA 02139 USA
[8] US Mil HIV Res Program, Host Genet Sect, Silver Spring, MD 20910 USA
[9] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[10] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
CLASS-I MOLECULES; IMMUNODEFICIENCY-VIRUS TYPE-1; COMPLEX CLASS-I; NATURAL-KILLER-CELLS; MONOCLONAL-ANTIBODIES; EXPRESSION LEVELS; INFECTED CELLS; T-LYMPHOCYTES; NEF PROTEIN; CLONES;
D O I
10.1016/j.chom.2016.04.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Many pathogens evade cytotoxic T lymphocytes (CTLs) by downregulating HLA molecules on infected cells, but the loss of HLA can trigger NK cell-mediated lysis. HIV-1 is thought to subvert CTLs while preserving NK cell inhibition by Nef-mediated downregulation of HLA-A and -B but not HLA-C molecules. We find that HLA-C is downregulated by most primary HIV-1 clones, including transmitted founder viruses, in contrast to the laboratory-adapted NL4-3 virus. HLA-C reduction ismediated by viral Vpu and reduces the ability of HLA-C restricted CTLs to suppress viral replication in CD4+ cells in vitro. HLA-A/B are unaffected by Vpu, and primary HIV-1 clones vary in their ability to downregulate HLA-C, possibly in response to whether CTLs or NK cells dominate immune pressure through HLA-C. HIV-2 also suppresses HLA-C expression through distinct mechanisms, underscoring the immune pressure HLA-C exerts on HIV. This viral immune evasion casts new light on the roles of CTLs and NK cells in immune responses against HIV.
引用
收藏
页码:686 / 695
页数:10
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