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Concordance of immunological events between intrarectal and intravenous SHIVAD8-EO infection when assessed by Fiebig-equivalent staging

  1. Author:
    Dias, Joana
    Fabozzi, Giulia
    March, Kylie
    Asokan, Mangaiarkarasi
    Almasri, Cassandra G
    Fintzi, Jonathan
    Promsote, Wanwisa
    Nishimura, Yoshiaki
    Todd, John-Paul
    Lifson,Jeffrey
    Martin, Malcolm A
    Gama, Lucio
    Petrovas, Constantinos
    Pegu, Amarendra
    Mascola, John R
    Koup, Richard A
  2. Author Address

    Immunology Laboratory, Vaccine Research Center., Tissue Analysis Core, Vaccine Research Center., Virology Laboratory, Vaccine Research Center., Biostatistics Research Branch., Laboratory of Molecular Biology, and., Translational Research Program, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA., AIDS and Cancer Virus Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA.,
    1. Year: 2021
    2. Date: Sep 01
  1. Journal: The Journal of clinical investigation
    1. 131
    2. 17
  2. Type of Article: Article
  3. Article Number: e151632
  1. Abstract:

    Primary HIV-1 infection can be classified into six Fiebig stages based on virological and serological laboratory testing, whereas simian-HIV (SHIV) infection in nonhuman primates (NHPs) is defined in time post-infection, making it difficult to extrapolate NHP experiments to the clinics. We identified and extensively characterized the Fiebig-equivalent stages in NHPs challenged intrarectally or intravenously with SHIVAD8-EO. During the first month post-challenge, intrarectally challenged monkeys were up to 1 week delayed in progression through stages. However, regardless of the challenge route, stages I-II predominated before, and stages V-VI predominated after, peak viremia. Decrease in lymph node (LN) CD4+ T cell frequency and rise in CD8+ T cells occurred at stage V. LN virus-specific CD8+ T cell responses, dominated by degranulation and TNF, were first detected at stage V and increased at stage VI. A similar late elevation in follicular CXCR5+ CD8+ T cells occurred, consistent with higher plasma CXCL13 levels at these stages. LN SHIVAD8-EO RNA+ cells were present at stage II, but appeared to decline at stage VI when virions accumulated in follicles. Fiebig-equivalent staging of SHIVAD8-EO infection revealed concordance of immunological events between intrarectal and intravenous infection despite different infection progressions, and can inform comparisons of NHP studies with clinical data.

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External Sources

  1. DOI: 10.1172/JCI151632
  2. PMID: 34623326
  3. PII : 151632

Library Notes

  1. Fiscal Year: FY2021-2022
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