Author/Authors :
Salkowitz، نويسنده , , Janelle R. and Purvis، نويسنده , , Scott F. and Meyerson، نويسنده , , Howard E. Zimmerman، نويسنده , , Peter and OʹBrien، نويسنده , , Thomas R. and Aledort، نويسنده , , Louis and Eyster، نويسنده , , M.Elaine and Hilgartner، نويسنده , , Margaret and Kessler، نويسنده , , Craig and Konkle، نويسنده , , Barbara A. and White II، نويسنده , , Gilbert C. and Goedert، نويسنده , , Ja، نويسنده ,
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.
Keywords :
?-chemokines , CCR5 , HIV-1 , alloreactive antibodies , HLA , Multicenter Hemophilia Cohort Study