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HIV preferentially infects HIV-specific CD4+ T cells

  • Daniel C. Douek
  • , Jason M. Brenchley
  • , Michael R. Betts
  • , David R. Ambrozak
  • , Brenna J. Hill
  • , Yukari Okamoto
  • , Joseph P. Casazza
  • , Janaki Kuruppu
  • , Kevin Kunstman
  • , Steven Wolinsky
  • , Zvi Grossman
  • , Mark Dybul
  • , Annette Oxenius
  • , David A. Price
  • , Mark Connors
  • , Richard A. Koup
  • Vaccine Research Center
  • National Institutes of Health
  • University of Texas Southwestern Medical Center
  • Northwestern University
  • John Radcliffe Hospital

Research output: Contribution to journalArticlepeer-review

1128 Scopus citations

Abstract

HIV infection is associated with the progressive loss of CD4+T cells through their destruction or decreased production. A central, yet unresolved issue of HIV disease is the mechanism for this loss, and in particular whether HIV-specific CD4+ T cells are preferentially affected. Here we show that HIV-specific memory CD4+ T cells in infected individuals contain more HIV viral DNA than other memory CD4+ T cells, at all stages of HIV disease. Additionally, following viral rebound during interruption of antiretroviral therapy, the frequency of HIV viral DNA in the HIV-specific pool of memory CD4+ T cells increases to a greater extent than in memory CD4+ T cells of other specificities. These findings show that HIV-specific CD4+ T cells are preferentially infected by HIV in vivo. This provides a potential mechanism to explain the loss of HIV-specific CD4+ T-cell responses, and consequently the loss of immunological control of HIV replication. Furthermore, the phenomenon of HIV specifically infecting the very cells that respond to it adds a cautionary note to the practice of structured therapy interruption.

Original languageEnglish
Pages (from-to)95-98
Number of pages4
JournalNature
Volume417
Issue number6884
DOIs
StatePublished - 2 May 2002

Funding

FundersFunder number
National Institute of Allergy and Infectious DiseasesZ01AI005034, ZIAAI000855, Z01AI005014

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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