Rapid progression to disease in African sex workers with human immunodeficiency virus type 1 infection [see comments] [published erratum appears in J InfectDis1996 Jun; 173(6):1529] Anzala OA; Nagelkerke NJ; Bwayo J.; Holton D Moses S; Ngugi EN; Ndinya-Ac

Citation:
JOAB PROFBWAYOJOB, O. PROFANZALAAGGREY. "Rapid progression to disease in African sex workers with human immunodeficiency virus type 1 infection [see comments] [published erratum appears in J InfectDis1996 Jun; 173(6):1529] Anzala OA; Nagelkerke NJ; Bwayo J.; Holton D Moses S; Ngugi EN; Ndinya-Ac.". In: J Infect Dis. 1995 Mar;171(3):686-9. John Benjamins Publishing Company; 1996.

Abstract:

In an effort to identify an immunological basis for natural resistance to HIV-1 infection, we have examined serum antibody responses to HLA class I antigens in female prostitutes of the Nairobi Sex Workers Study. Anti-HLA antibodies are known to block HIV infectivity in vitro and can be protective against SIV challenge in macaques immunized with purified class I HLA. Thus, it was postulated that broadly cross-reactive alloantibodies recognizing common HLA alleles in the client population might contribute to the prevention of heterosexual transmission of HIV. In fact, 12% of the women were found to have serum IgG antibodies against class I alloantigens. However, this alloantibody did not correlate with the HIV status of the women and was found in a similar proportion of HIV-positive and HIV-resistant women. The observed levels of alloantibody did not increase with HIV infection in susceptible individuals, suggesting that potential antigenic mimicry between HIV and host HLA class I antigens does not significantly increase levels of anti-class I antibodies. The lack of correlation between serum anti-allo-class I HLA antibodies and the risk of sexual transmission indicates that this humoral immune response is unlikely to be the natural mechanism behind the HIV-resistance phenotype of persistently HIV-seronegative women. This result, however, does not preclude the further investigation of alloimmunization as an artificial HIV immunization strategy.

Notes:

n/a

Website

UoN Websites Search