Publication

Early regeneration of thymic progenitors in rhesus macaques infected with simian immunodeficiency virus

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Last modified
  • 09/19/2025
Type of Material
Authors
    Joanna J. Wykrzykowska, Harvard Medical SchoolMichael Rosenzweig, Harvard Medical SchoolRonald S. Veazey, Harvard Medical SchoolMeredith A. Simon, Harvard Medical SchoolKatherine Halvorsen, Smith CollegeRonald C. Desrosiers, Harvard Medical SchoolR. Paul Johnson, Emory UniversityAndrew A. Lackner, Harvard Medical School
Language
  • English
Date
  • 1998-06-01
Publisher
  • ROCKEFELLER UNIV PRESS
Publication Version
Copyright Statement
  • © The Rockefeller University Pres
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 187
Issue
  • 11
Start Page
  • 1767
End Page
  • 1778
Grant/Funding Information
  • This work was supported by Public Health Service grants NS-30769, AI-38559, AI-39423, RR-07000, and RR-00168. A.A. Lackner is the recipient of an Elizabeth Glaser Scientist Award.
Abstract
  • The thymus plays a critical role in the maturation and production of T lymphocytes and is a target oF infection by human immunodeficiency virus (HIV) and the related simian immunodeficiency virus (SIV). Using the SIV/macaque model of AIDS, we examined the early effects of SIV on the thymus. We found that thymic infection by SIV resulted in increased apoptosis 7-14 d after infection, Followed by depletion of thymocyte progenitors by day 21. A marked rebound in thymocyte progenitors occurred by day 50 and was accompanied by increased levels of cell proliferation in the thymus. Our results demonstrate a marked increase in thymic progenitor activity very early in the course of SIV infection, long before marked declines in peripheral CD4+ T cell counts.
Author Notes
  • Andrew A. Lackner, New England Regional Primate Research Center, Harvard Medical School, 1 Pine Hill Dr., PO Box 9102, Southborough, MA 01772. Phone: 508-624-8018; Fax: 508-624-8181; E mail: alackner@warren.med.harvard.edu
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