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Emergence and kinetics of simian immunodeficiency virus- specific CD8(+) T cells in the intestines of macaques during primary infection

  1. Author:
    Veazey, R. S.
    Gauduin, M. C.
    Mansfield, K. G.
    Tham, I. C.
    Altman, J. D.
    Lifson, J. D.
    Lackner, A. A.
    Johnson, R. P.
  2. Author Address

    Tulane Univ, Tulane Reg Primate Res Ctr, 18703 3 Rivers Rd, Covington, LA 70433 USA. Tulane Univ, Tulane Reg Primate Res Ctr, Covington, LA 70433 USA. Harvard Univ, Sch Med, New England Reg Primate Res Ctr, Southborough, MA 01772 USA. Emory Univ, Sch Med, Emory Vaccine Ctr Yerkes, Atlanta, GA 30322 USA. NCI, SAIC, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA. Harvard Univ, Sch Med, Massachusetts Gen Hosp, Infect Dis Unit, Charlestown, MA 02129 USA. Harvard Univ, Sch Med, Massachusetts Gen Hosp, Partners AIDS Res Ctr, Charlestown, MA 02129 USA. Veazey RS Tulane Univ, Tulane Reg Primate Res Ctr, 18703 3 Rivers Rd, Covington, LA 70433 USA.
    1. Year: 2001
  1. Journal: Journal of Virology
    1. 75
    2. 21
    3. Pages: 10515-10519
  2. Type of Article: Article
  1. Abstract:

    In this report, three Mamu-A*01(+) rhesus macaques were examined to compare the emergence of simian immunodeficiency virus (SIV)-specific CD8(+) T cells in the intestines and blood in early SIV infection using a major histocompatibility complex class I tetramer complexed with the Gag(181-189) peptide. Fourteen days after intravenous inoculation with SIVmac251, large numbers of SrV Gag(181-189)-specific CD8(+) T cells were detected in the intestinal mucosa (3.1 to 11.5% of CD3(+) CD8(+) lymphocytes) as well as in the blood (3.1 to 13.4%) of all three macaques. By 21 days postinoculation, levels of tetramer-binding cells had dropped in both the intestines and blood. At day 63, however, levels of SIV Gag(181-189)- specific CD8(+) T cells in the intestines had rebounded in all three macaques to levels that were higher (8.6 to 18.7%) than those at day 21. In contrast, percentages of tetramer-binding cells in the peripheral blood remained comparatively stable (2.5 to 4.5%) at this time point. In summary, SFV Gag(181-189)-specific CD8(+) T cells appeared in both the intestinal mucosa and peripheral blood at a comparable rate and magnitude in primary SIV infection. Given that the intestine is a major site of early viral replication as well as the site where most of the total body lymphocyte pool resides, these data indicate that it is also an early and important site of development of antiviral immune responses.

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