High frequencies of polyfunctional HIV-specific T cells are associated with preservation of mucosal CD4 T cells in bronchoalveolar lavage

被引:63
|
作者
Brenchley, J. M. [1 ]
Knox, K. S. [2 ,3 ]
Asher, A. I. [1 ]
Price, D. A. [1 ,4 ]
Kohli, L. M. [2 ]
Gostick, E. [4 ]
Hill, B. J. [1 ]
Hage, C. A. [2 ,3 ]
Brahmi, Z. [5 ]
Khoruts, A. [6 ]
Twigg, H. L., III [2 ]
Schacker, T. W. [6 ]
Douek, D. C. [1 ]
机构
[1] NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
[2] Indiana Univ, Div Pulm & Crit Care Med, Indianapolis, IN 46204 USA
[3] Richard L Roudebush VA Med Ctr, Indianapolis, IN USA
[4] Univ Oxford, Weatherall Inst Mol Med, Oxford, England
[5] Indiana Univ, Med Ctr, Dept Med, Indianapolis, IN USA
[6] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
基金
英国医学研究理事会;
关键词
D O I
10.1038/mi.2007.5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The mechanisms underlying the massive gastrointestinal tract CD4 T-cell depletion in human immunodeficiency virus (HIV) infection are not well understood nor is it clear whether similar depletion is manifest at other mucosal surfaces. Studies of T-cell and virus dynamics in different anatomical sites have begun to illuminate the pathogenesis of HIV-associated disease. Here, we studied depletion and HIV infection frequencies of CD4 T cells from the gastrointestinal tract, bronchoalveolar lavage (BAL), and blood with the frequencies and functional profiles of HIV-specific T cells in these anatomically distinct sites in HIV-infected individuals. The major findings to emerge were as follows: (i) depletion of gastrointestinal CD4 T cells is associated with high frequencies of infected CD4 T cells; (ii) HIV-specific T cells are present at low frequencies in the gastrointestinal tract compared to blood; (iii) BAL CD4 T cells are not massively depleted during the chronic phase; (iv) infection frequencies of BAL CD4 T cells are similar to those in blood; (v) significantly higher frequencies and increased functionality of HIV-specific T cells were observed in BAL compared to blood. Taken together, these data suggest mechanisms for mucosal CD4 T-cell depletion and interventions that might circumvent global depletion of mucosal CD4 T cells.
引用
收藏
页码:49 / 58
页数:10
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