Control of human immunodeficiency virus type 1 is associated with HLA-B*13 and targeting of multiple gag-specific CD8+ T-cell epitopes

被引:127
作者
Honeyborne, Isobella
Prendergast, Andrew
Pereyra, Florencia
Leslie, Alasdair
Crawford, Hayley
Payne, Rebecca
Reddy, Shabashini
Bishop, Karen
Moodley, Eshia
Nair, Kriebashnie
van der Stok, Mary
McCarthy, Noel
Rousseau, Christine M.
Addo, Marylyn
Mullins, James I.
Brander, Christian
Kiepiela, Photini
Walker, Bruce D.
Goulder, Philip J. R.
机构
[1] Dept Paediat, Oxford OX1 3SY, England
[2] Massachusetts Gen Hosp, Partners AIDS Res Ctr, Boston, MA 02129 USA
[3] Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02129 USA
[4] Harvard Univ, Sch Med, Boston, MA 02129 USA
[5] Univ KwaZulu Natal, Doris Duke Med Res Inst, HIV Pathogenesis Programme, ZA-4013 Durban, South Africa
[6] Dept Zool, Oxford OX1 3SY, England
[7] Univ Washington, Sch Med, Dept Microbiol, Seattle, WA 98195 USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1128/JVI.02689-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
To better understand relationships between CD8(+) T-cell specificity and the immune control of human immunodeficiency virus type 1 (HIV-1), we analyzed the role of HLA-B*13, an allele associated with low viremia, in a cohort of 578 C clade-infected individuals in Durban, South Africa. Six novel B*13-restricted cytotoxic T lymphocyte epitopes were defined from analyses of 37 B*13-positive subjects, including three Gag epitopes. These B*13-restricted epitopes contribute to a broad Gag-specific CD8(+) response that is associated with the control of viremia. These data are consistent with data from studies of other HIA-class I alleles associated with HIV control that have shown that the targeting of multiple Gag epitopes is associated with relative suppression of viremia.
引用
收藏
页码:3667 / 3672
页数:6
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