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Maintenance of large numbers of virus-specific CD8(+) T cells in HIV-infected progressors and long-term nonprogressors

  1. Author:
    Gea-Banacloche, J. C.
    Migueles, S. A.
    Martino, L.
    Shupert, W. L.
    McNeil, A. C.
    Sabbaghian, M. S.
    Ehler, L.
    Prussin, C.
    Stevens, R.
    Lambert, L.
    Altman, J.
    Hallahan, C. W.
    de Quiros, J.
    Connors, M.
  2. Author Address

    Connors M NIAID, Immunoregulat Lab, NIH Bldg 10,Room 11B-09,10 Ctr Dr,MSC 1876 Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, NIH Bethesda, MD 20892 USA NIAID, Lab Allerg Dis, NIH Bethesda, MD 20892 USA Sci Applicat Int Corp, Frederick Canc Res & Dev Ctr Frederick, MD 21702 USA Emory Univ, Vaccine Ctr Yerkes Atlanta, GA 30322 USA Hosp Gen Gregorio Maranon, Microbiol Serv Madrid Spain Univ Autonoma Madrid, Serv Med Interne 1, Clin Puerta de Hierro Madrid Spain
    1. Year: 2000
  1. Journal: Journal of Immunology
    1. 165
    2. 2
    3. Pages: 1082-1092
  2. Type of Article: Article
  1. Abstract:

    The virus-specific CD8(+) T cell responses of 21 HIV-infected patients were studied including a unique cohort of long-term nonprogressors with low levels of plasma viral RNA and strong proliferative responses to HIV Ags, HIV-specific CD8(+) T cell responses were studied by a combination of standard cytotoxic T cell (CTL) assays, MHC tetramers, and TCR repertoire analysis, The frequencies of CD8(+) T cells specific to the majority of HIV gene products were measured by how cytometric detection of intracellular IFN-gamma in response to HIV-vaccinia recombinant-infected autologous B cells. Very high frequencies (0.8-18.0%) of circulating CD8(+) T cells were found to be HIV specific. High frequencies of HIV-specific CD8(+) T cells were not limited to long-tern nonprogressors with restriction of plasma virus. No correlation was found between the frequency of HIV-specific CD8(+) T cells and levels of plasma viremia, In each case, the vast majority of cells (up to 17.2%) responded to gag-pol. Repertoire analysis showed these large numbers of Ag-specific cells were scattered throughout the repertoire and in the majority of cases not contained within large monoclonal expansions. These data demonstrate that high numbers of HIV-specific CD8(+) T cells exist even in patients with high-level viremia and progressive disease. Further, they suggest that other qualitative parameters of the CD8+ T cell response may differentiate some patients with very low levels of plasma virus and nonprogressive disease. [References: 74]

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