The HIV-1 envelope protein gp120 impairs B cell proliferation by inducing TGF-?1 production and FcRL4 expression.

ABSTRACT: The humoral immune response after acute infection with HIV-1 is delayed and ineffective. The HIV-1 envelope protein gp120 binds to and signals through integrin ?4?7 on T cells. We found that gp120 also bound to and signaled through ?4?7 on naive B cells, which resulted in an abortive proliferative response. In primary B cells, signaling by gp120 through ?4?7 resulted in increased expression of the immunosuppressive cytokine TGF-?1 and FcRL4, an inhibitory receptor expressed on B cells. Coculture of B cells with HIV-1-infected autologous CD4(+) T cells also increased the expression of FcRL4 by B cells. Our findings indicated that in addition to mediating chronic activation of the immune system, viral proteins contributed directly to HIV-1-associated B cell dysfunction. Our studies identify a mechanism whereby the virus may subvert the early HIV-1-specific humoral immune response.

SUBMITTER: Jelicic K 

PROVIDER: S-EPMC3870659 | biostudies-literature | 2013 Dec

REPOSITORIES: biostudies-literature