Cytotoxic T-cell antagonism in HIV-1

被引:12
作者
Klenerman, P
Phillips, R
McMichael, A
机构
[1] Nuffield Dept. of Clinical Medicine, Institute of Molecular Medicine, John Radcliffe Hospital
来源
SEMINARS IN VIROLOGY | 1996年 / 7卷 / 01期
基金
英国医学研究理事会; 英国惠康基金;
关键词
CTL; altered peptide ligand; antagonism; T-cell receptor; HIV-1;
D O I
10.1006/smvy.1996.0005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The cytotoxic T-cell (CTL) response to human immunodeficiency virus Type 1 (HIV-1) is vigorous and sustained, but despite this, the virus persists. Natural variation arising within CTL epitopes may affect CTL recognition of infected targets and allow viral escape. Some of these variant epitopes appear to engage T-cell receptors but fail to activate the CTL normally. This can interfere with recognition of the unmutated epitope - a phenomenon known as T-cell antagonism. We discuss the evidence for this in HN-I using CTL and epitope variants derived from infected donors, and discuss its possible relevance in vivo.
引用
收藏
页码:31 / 39
页数:9
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