Oligoclonal expansions of CD8+ T cells in chronic HIV infection are antigen specific

被引:147
作者
Wilson, JDK [1 ]
Ogg, GS [1 ]
Allen, RL [1 ]
Goulder, PJR [1 ]
Kelleher, A [1 ]
Sewell, AK [1 ]
O'Callaghan, CA [1 ]
Rowland-Jones, SL [1 ]
Callan, MFC [1 ]
McMichael, AJ [1 ]
机构
[1] John Radcliffe Hosp, Inst Mol Med, Mol Immunol Grp, Oxford OX3 9DS, England
关键词
human immunodeficiency virus; T cell receptor; cytotoxic T lymphocytes; tetramer; expansion;
D O I
10.1084/jem.188.4.785
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acute HIV infection is associated with a vigorous immune response characterized by the proliferation of selected T cell receptor V beta (BV)-expressing CD8(+) T cells. These 'expansions', which are commonly detected in the peripheral blood, can persist during chronic HIV infection and may result in the dominance of particular clones. Such clonal populations are most consistent with antigen-driven expansions of CD8(+) T cells. However, due to the difficulties in studying antigen-specific T cells in vivo, it has been hard to prove that oligoclonal BV expansions are actually HIV specific. The use of tetrameric major histocompatibility complex-peptide complexes has recently enabled direct visualization of antigen-specific T cells ex vivo but has not provided information on their clonal composition. We have now made use of these tetrameric complexes in conjunction with anti-BV chain-specific monoclonal antibodies and analysis of cytotoxic T lymphocyte lines/clones to show that chronically clonally expanded CD8+ T cells are HIV specific in vivo.
引用
收藏
页码:785 / 790
页数:6
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