Increased production of IL-7 accompanies HIV-l-mediated T-cell depletion: implications for T-cell homeostasis

被引:439
作者
Napolitano, LA
Grant, RM
Deeks, SG
Schmidt, D
De Rosa, SC
Herzenberg, LA
Herndier, BG
Andersson, J
McCune, JM [1 ]
机构
[1] San Francisco Gen Hosp, Gladstone Inst Virol & Immunol, San Francisco, CA 94110 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94110 USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94110 USA
[4] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94110 USA
[5] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[6] Huddinge Univ Hosp, Karolinska Inst, Dept Infect Dis, Stockholm, Sweden
关键词
D O I
10.1038/83381
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We hypothesized that HIV-1-mediated T-cell loss might induce the production of factors that are capable of stimulating lymphocyte development and expansion. Here we perform cross-sectional (n = 168) and longitudinal (n = 11) analyses showing that increased circulating levels of interleukin (IL)-7 are strongly associated with CD4+ T lymphopenia in HIV-1 disease. Using immunohistochemistry with quantitative image analysis, we demonstrate that IL-7 is produced by dendritic-like cells within peripheral lymphoid tissues and that IL-7 production by these cells is greatly increased in lymphocyte-depleted tissues. We propose that IL-7 production increases as part of a homeostatic response to T-cell depletion.
引用
收藏
页码:73 / 79
页数:7
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