B Cells Inhibit CD4 T Cell-Mediated Immunity to Infection in a Major Histocompatibility Complex Class II-Dependent Manner.

spp. are facultative intracellular bacteria notorious for their ability to induce a chronic, and often lifelong, infection known as brucellosis. To date, no licensed vaccine exists for prevention of human disease, and mechanisms underlying chronic illness and immune evasion remain elusive. We and others have observed that B cell-deficient mice challenged with display reduced bacterial burden following infection, but the underlying mechanism has not been clearly defined. Here, we show that at 1 month postinfection, B cell deficiency alone enhanced resistance to splenic infection ∼100-fold; however, combined B and T cell deficiency did not impact bacterial burden, indicating that B cells only enhance susceptibility to infection when T cells are present. Therefore, we investigated whether B cells inhibit T cell-mediated protection against Using B and T cell-deficient Rag1 animals as recipients, we demonstrate that adoptive transfer of CD4 T cells alone confers marked protection against that is abrogated by cotransfer of B cells. Interestingly, depletion of CD4 T cells from B cell-deficient, but not wild-type, mice enhanced susceptibility to infection, further confirming that CD4 T cell-mediated immunity against is inhibited by B cells. In addition, we found that the ability of B cells to suppress CD4 T cell-mediated immunity and modulate CD4 T cell effector responses during infection was major histocompatibility complex class II (MHCII)-dependent. Collectively, these findings indicate that B cells modulate CD4 T cell function through an MHCII-dependent mechanism which enhances susceptibility to infection.