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Characterization of high-risk HIV-1 seronegative hemophiliacs

  • Janelle R. Salkowitz
  • , Scott F. Purvis
  • , Howard Meyerson
  • , Peter Zimmerman
  • , Thomas R. O'Brien
  • , Louis Aledort
  • , M. Elaine Eyster
  • , Margaret Hilgartner
  • , Craig Kessler
  • , Barbara A. Konkle
  • , Gilbert C. White
  • , James J. Goedert
  • , Michael M. Lederman

Research output: Contribution to journalArticlepeer-review

55 Scopus citations

Abstract

Mechanisms that protect most high-risk HIV-1 seronegative (HRSN) persons are not well understood. Among hemophiliacs from the Multicenter Hemophilia Cohort Study who remained HIV-1 seronegative despite a high (94%) risk for acquisition of HIV-1 infection, only 7/43 were homozygous for the protective CCR5 Δ32 polymorphism. Among the remainder, neither CCR5 density nor β-chemokine production, nor in vitro susceptibility to infection with the HIV-1 isolate JR-FL could distinguish HRSN hemophiliacs from healthy controls. When compared to lymphocytes of healthy controls not at risk for HIV-1 infection, diminished spontaneous lymphocyte proliferation was seen in lymphocytes of HRSN hemophiliacs as well as in lymphocytes of hemophiliacs not at risk for HIV-1 infection. Surprisingly sera/plasmas obtained from high-risk HIV-1 seropositve hemophiliacs prior to seroconversion more often contained alloreactive antibodies than date-matched sera/plasmas obtained from HRSN hemophiliacs. Thus alloreactivity may predispose to acquisition of HIV-1 infection after parenteral exposure.

Original languageEnglish
Pages (from-to)200-211
Number of pages12
JournalClinical Immunology
Volume98
Issue number2
DOIs
StatePublished - 2001

Keywords

  • Alloreactive antibodies
  • CCR5
  • HIV-1
  • HLA
  • Multicenter hemophilia cohort study
  • β-chemokines

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