Chronic CD4+ T-cell activation and depletion in human immunodeficiency virus type 1 infection:: Type I interferon-mediated disruption of T-cell dynamics

被引:138
作者
Sedaghat, Ahmad R. [1 ]
German, Jennifer [1 ]
Teslovich, Tanya M. [2 ]
Cofrancesco, Joseph, Jr. [1 ]
Jie, Chunfa C. [2 ]
Talbot, C. Conover, Jr. [2 ]
Siliciano, Robert F. [1 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
关键词
D O I
10.1128/JVI.02228-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The mechanism of CD4(+) T-cell depletion during chronic human immunodeficiency virus type 1 (HIV-1) infection remains unknown. Many studies suggest a significant role for chronic CD4(+) T-cell activation. We assumed that the pathogenic process of excessive CD4(+) T-cell activation would be reflected in the transcriptional profiles of activated CD4(+) T cells. Here we demonstrate that the transcriptional programs of in vivo-activated CD4(+) T cells from untreated HIV-positive (HIV+) individuals are clearly different from those of activated CD4(+) T cells from HIV-negative (HIV-) individuals. We observed a dramatic up-regulation of cell cycle-associated and interferon-stimulated transcripts in activated CD4(+) T cells of untreated HIV+ individuals. Furthermore, we find an enrichment of proliferative and type I interferon-responsive transcription factor binding sites in the promoters of genes that are differentially expressed in activated CD4(+) T cells of untreated HIV+ individuals compared to those of HIV- individuals. We confirm these findings by examination of in vivo-activated CD4(+) T cells. Taken together, these results suggest that activated CD4(+) T cells from untreated HIV+ individuals are in a hyperproliferative state that is modulated by type I interferons. From these results, we propose a new model for CD4(+) T-cell depletion during chronic HIV-1 infection.
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收藏
页码:1870 / 1883
页数:14
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