Kinetics of virus-specific CD8+ T cells and the control of human immunodeficiency virus infection

被引:91
|
作者
Davenport, MP
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 Hematol, Kensington, NSW 2033, Australia
[3] Univ New S Wales, Ctr Vasc Res, Kensington, NSW 2033, Australia
[4] Univ Oxford, Dept Zool, Oxford OX1 3PS, England
关键词
D O I
10.1128/JVI.78.18.10096-10103.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Several primate models indicate that cytotoxic T lymphocyte-inducing vaccines may be unable to prevent human immunodeficiency virus infection but may have a long-term benefit in controlling viral replication and delaying disease progression. Here we show that analysis of the kinetics of antigen-specific CD8(+) T-cell expansion suggests a delay in activation following infection that allows unimpeded early viral replication. Viral kinetics do not differ between controls and vaccinees during this delay phase. An increase in virus-specific CD8(+) T-cell numbers around day 10 postinfection coincides with a slowing in viral replication in vaccinees and reduces peak viral loads by around I log. However, this response is too little too late to prevent establishment of persistent infection.
引用
收藏
页码:10096 / 10103
页数:8
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