High-potency human immunodeficiency virus vaccination leads to delayed and reduced CD8+ T-cell expansion but improved virus control

被引:27
作者
Davenport, MP
Zhang, L
Bagchi, A
Fridman, A
Fu, TM
Schleif, W
Shiver, JW
Ribeiro, RM
Perelson, AS
机构
[1] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[2] Univ New S Wales, Prince Wales Hosp, Dept Haematol, Sydney, NSW 2052, Australia
[3] Univ New S Wales, Ctr Vasc Res, Sydney, NSW 2052, Australia
[4] Merck Res Labs, W Point, PA 19486 USA
关键词
D O I
10.1128/JVI.79.15.10059-10062.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
CD8(+) T lymphocytes are thought to play an important role in the control of acute and chronic human immunodeficiency virus infections. However, there is a significant delay between infection and the first observed increase in virus-specific CD8(+) T-cell numbers. Prior to this time, viral kinetics are not significantly different between controls and vaccinees. Surprisingly, higher initial virus-specific CD8(+) T-cell numbers lead to a longer delay prior to initial CD8(+) T-cell expansion, and slower CD8(+) T-cell increases. Nevertheless, higher initial CD8(+) T-cell numbers were associated with reduced peak and chronic viral loads and reduced CD4(+) T-cell depletion.
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收藏
页码:10059 / 10062
页数:4
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