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Replication of simian immunodeficiency virus (SIV) in ex vivo lymph nodes as a means to assess susceptibility of macaques in vivo

  1. Author:
    Margolis, L.
    Glushakova, S.
    Chougnet, C.
    Shearer, G.
    Markham, P.
    Robert-Guroff, M.
    Benveniste, R.
    Miller, C. J.
    Cranage, M.
    Hirsch, V.
    Franchini, G.
  2. Author Address

    NCI, Basic Res Lab, NIH, 41 Lib Dr, Bldg 41, Room D804, Bethesda, MD 20892 USA. NCI, Basic Res Lab, NIH, Bethesda, MD 20892 USA. NCI, Frederick Canc Res & Dev Ctr, NIH, Bethesda, MD 20892 USA. NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA. NICHHD, Lab Cellular & Mol Biophys, NIH, Bethesda, MD 20892 USA. Adv BioSci Labs Inc, Kensington, MD 20895 USA. Univ Calif Davis, Calif Reg Primate Res Ctr, Davis, CA 95616 USA. Ctr Appl Microbiol & Res, Salisbury, Wilts, England. NIAID, NIH, Bethesda, MD 20892 USA.
    1. Year: 2000
  1. Journal: Virology
    1. 275
    2. 2
    3. Pages: 391-397
  2. Type of Article: Article
  1. Abstract:

    Six macaques, apparently uninfected, following low-dose exposure to the pathogenic SIVmac251 and SIVSME660 by the mucosal route, were used in a pilot study to investigate whether infectability of ex vivo lymph nodes could predict resistance and/or susceptibility to SIV infection in vivo. Of six macaques exposed to the less-pathogenic virus SIVMNE, four resisted viral infection. Analysis of the susceptibility of the PBMC of these four animals before SIVMNE challenge indicated that all of them were resistant to infection by the SIVBK28 isolate and, in three of them, this resistance was dependent on CD8+ T cells. Blocks of lymph nodes of these four macaques were resistant to SIVMNE infection ex vivo following SIVMNE viral challenge exposure. However, the same blocks from the same animals were permissive to the more virulent SIV251(32H). Accordingly, three of these macaques were readily infected following challenge exposure with SIV251(32H). Lymphoproliferative responses in blood or lymph nodes, local C- C chemokine production in the lymph-node explants, and cytotoxic T-cell activity measured throughout the study did not correlate with ex vivo resistance or susceptibility to in vivo infection. In conclusion, PBMC and lymph-node resistance or susceptibility to infection ex vivo appeared to correlate with in vivo infectivity and, thus, these approaches should be further tested for their predictive value for in vivo infection. (C) 2000 Academic Press.

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