Follicular regulatory T cells control humoral and allergic immunity by restraining early B cell responses

Follicular regulatory T (T FR ) cells have specialized roles in modulating follicular helper T (T FH ) cell activation of B cells. However, the precise role of T FR cells in controlling antibody responses to foreign antigens and autoantigens in vivo is still unclear due to a lack of specific tools. A T FR cell-deleter mouse was developed that selectively deletes T FR cells, facilitating temporal studies. T FR cells were found to regulate early, but not late, germinal center (GC) responses to control antigen-specific antibody and B cell memory. Deletion of T FR cells also resulted in increased self-reactive immunoglobulin (Ig) G and IgE. The increased IgE levels led us to interrogate the role of T FR cells in house dust mite models. T FR cells were found to control T FH 13 cell-induced IgE. In vivo, loss of T FR cells increased house-dust-mite-specific IgE and lung inflammation. Thus, T FR cells control IgG and IgE responses to vaccines, allergens and autoantigens, and exert critical immunoregulatory functions before GC formation. The precise role of follicular regulatory (T FR ) cells in the control of the germinal center (GC) reaction is unclear. Sage and colleagues develop a T FR cell-deleter mouse that allows specific temporal deletion and show that T FR cells primarily control early but not late GC responses.