| Literature DB >> 11161976 |
J R Salkowitz1, S F Purvis, H Meyerson, P Zimmerman, T R O'Brien, L Aledort, M E Eyster, M Hilgartner, C Kessler, B A Konkle, G C White, J J Goedert, M M Lederman.
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 Delta32 polymorphism. Among the remainder, neither CCR5 density nor beta-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. Copyright 2000 Academic Press.Entities:
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Year: 2001 PMID: 11161976 DOI: 10.1006/clim.2000.4969
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969