Association of DC-SIGN promoter polymorphism with increased risk for parenteral, but not mucosal, acquisition of human immunodeficiency virus type 1 infection

MP Martin, MM Lederman, HB Hutcheson… - Journal of …, 2004 - Am Soc Microbiol
MP Martin, MM Lederman, HB Hutcheson, JJ Goedert, GW Nelson, Y Van Kooyk, R Detels…
Journal of virology, 2004Am Soc Microbiol
There is considerable debate about the fundamental mechanisms that underlie and restrict
acquisition of human immunodeficiency virus type 1 (HIV-1) infection. In light of recent
studies demonstrating the ability of C type lectins to facilitate infection with HIV-1, we
explored the potential relationship between polymorphisms in the DC-SIGN promoter and
risk for acquisition of HIV-1 according to route of infection. Using samples obtained from
1,611 European-American participants at risk for parenteral (n= 713) or mucosal (n= 898) …
Abstract
There is considerable debate about the fundamental mechanisms that underlie and restrict acquisition of human immunodeficiency virus type 1 (HIV-1) infection. In light of recent studies demonstrating the ability of C type lectins to facilitate infection with HIV-1, we explored the potential relationship between polymorphisms in the DC-SIGN promoter and risk for acquisition of HIV-1 according to route of infection. Using samples obtained from 1,611 European-American participants at risk for parenteral (n = 713) or mucosal (n = 898) infection, we identified single-nucleotide polymorphisms in the DC-SIGN promoter using single-strand conformation polymorphism. Individuals at risk for parenterally acquired infection who had −336C were more susceptible to infection than were persons with −336T (odds ratio = 1.87, P = 0.001). This association was not observed in those at risk for mucosally acquired infection. A potential role for DC-SIGN specific to systemic acquisition and dissemination of infection is suggested.
American Society for Microbiology