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.
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NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Brenchley, J. M.
[1
]
Knox, K. S.
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机构:
Indiana Univ, Div Pulm & Crit Care Med, Indianapolis, IN 46204 USA
Richard L Roudebush VA Med Ctr, Indianapolis, IN USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Knox, K. S.
[2
,3
]
Asher, A. I.
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NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Asher, A. I.
[1
]
Price, D. A.
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机构:
NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Univ Oxford, Weatherall Inst Mol Med, Oxford, EnglandNIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Price, D. A.
[1
,4
]
Kohli, L. M.
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机构:
Indiana Univ, Div Pulm & Crit Care Med, Indianapolis, IN 46204 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Kohli, L. M.
[2
]
Gostick, E.
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Univ Oxford, Weatherall Inst Mol Med, Oxford, EnglandNIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Gostick, E.
[4
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Hill, B. J.
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NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Hill, B. J.
[1
]
Hage, C. A.
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机构:
Indiana Univ, Div Pulm & Crit Care Med, Indianapolis, IN 46204 USA
Richard L Roudebush VA Med Ctr, Indianapolis, IN USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Hage, C. A.
[2
,3
]
Brahmi, Z.
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机构:
Indiana Univ, Med Ctr, Dept Med, Indianapolis, IN USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Brahmi, Z.
[5
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Khoruts, A.
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Univ Minnesota, Dept Med, Minneapolis, MN 55455 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Khoruts, A.
[6
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Twigg, H. L., III
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机构:
Indiana Univ, Div Pulm & Crit Care Med, Indianapolis, IN 46204 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Twigg, H. L., III
[2
]
Schacker, T. W.
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机构:
Univ Minnesota, Dept Med, Minneapolis, MN 55455 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
Schacker, T. W.
[6
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Douek, D. C.
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NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USANIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
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
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.