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The Extent of Early Viral Replication Is a Critical Determinant of the Natural History of Simian Immunodeficiency Virus Infection

  1. Author:
    Lifson, J. D.
    Nowak, M. A.
    Goldstein, S.
    Rossio, J. L.
    Kinter, A.
    Vasquez, G.
    Wiltrout, T. A.
    Brown, C.
    Schneider, D.
    Wahl, L.
    Lloyd, A. L.
    Williams, J.
    Elkins, W. R.
    Fauci, A. S.
    Hirsch, V. M.
  2. Author Address

    Lifson JD NCI FREDERICK CANC RES & DEV CTR SAIC FREDERICK AIDS VACCINE PROGRAM FREDERICK, MD 21702 USA UNIV OXFORD DEPT ZOOL OXFORD OX1 3PS ENGLAND NIAID INFECT DIS LAB ROCKVILLE, MD 20852 USA NIAID IMMUNOREGULAT LAB BETHESDA, MD 20852 USA MAGAININ PHARMACEUT INC PLYMOUTH MEETING, PA 19462 USA
    1. Year: 1997
  1. Journal: Journal of Virology
    1. 71
    2. 12
    3. Pages: 9508-9514
  2. Type of Article: Article
  1. Abstract:

    Different patterns of viral replication correlate with the natural history of disease progression in humans and macaques infected with human immunodeficiency virus type 1 (HIV-1) and simian immunodeficiency virus (SIV), respectively. However, the viral and host factors influencing these patterns of viral replication in vivo are poorly understood. We intensively studied viral replication in macaques receiving identical inocula of SIV. Marked differences in viral replication patterns were apparent within the first week following inoculation, a time prior to the development of measurable specific immune effector responses to viral antigens. Plasma viral RNA levels measured on day 7 postinoculation correlated with levels measured in the postacute phase of infection. Differences in the susceptibility of host cells from different animals to in vitro SIV infection correlated with the permissiveness of the animals for early in vivo viral replication and hence with the postacute set point level of plasma viremia. These results suggest that host factors that exert their effects prior to full development of specific immune responses are critical in establishing the in vivo viral replication pattern and associated clinical course in subjects infected with SIV and, by extension, with HIV-1. [References: 68]

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