Influence of peak viral load on the extent of CD4+ T-cell depletion in simian HIV infection

被引:36
作者
Davenport, MP
Zhang, L
Shiver, JW
Casmiro, DR
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, Kensington, NSW 2033, Australia
[3] Univ New S Wales, Ctr Vasc Res, Kensington, NSW 2033, Australia
[4] Merck Res Labs, West Point, PA USA
关键词
vaccine; pathogenesis; viral load; virus-cell interaction; CD4-positive T lymphocytes; mathematic models;
D O I
10.1097/01.qai.0000199232.31340.d3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Simian HIV (SHIV) infection of macaques with CXCR4 tropic viruses results in early and profound CD4(+) T-cell depletion in the first few weeks of infection. Analyzing data from a large study of vaccination and SHIV-89.6P challenge, we observe a strong correlation between peak viral load and the extent of CD4(+) T-cell depletion in acute infection, consistent with a simple kinetic model of viral infection of CD4(+) T cells. We have modeled the dynamics of the interaction of virus and CD4(+) T cells over time to investigate the rate of CD4(+) T-cell infection and death. This analysis indicates that up to 80% of CD4(+) T cells are infected at peak viremia and that the proportion of CD4(+) T cells destroyed is correlated with the peak viral load. The simple relation between viral load and CD4(+) T-cell depletion allows prediction of the level of viral control required to prevent CD4(+) T-cell depletion in acute SHIV infection. Whether such a simple relation also holds for HIV or simian immunodeficiency virus infections remains to be determined, particularly in the gut and other anatomic sites in which most early T-cell depletion occurs.
引用
收藏
页码:259 / 265
页数:7
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