No abstract

These authors contributed equally to the text.

CD20 antibody depletion of B lymphocytes effectively ameliorates multiple T cell-mediated autoimmune diseases through mechanisms that remain unclear. To address this, a mouse CD20 antibody that depletes >95% of mature B cells in mice with otherwise intact immune systems was used to assess the role of B cells in CD4 ؉ and CD8 ؉ T cell activation and expansion in vivo. B cell depletion had no direct effect on T cell subsets or the activation status of CD4 ؉ and CD8 ؉ T cells in naive mice. However, B cell depletion impaired CD4 ؉ T cell activation and clonal expansion in response to protein antigens and pathogen challenge, whereas CD8 ؉ T cell activation was not affected. In vivo dendritic cell ablation, along with CD20 immunotherapy, revealed that optimal antigen-specific CD4 ؉ T cell priming required both B cells and dendritic cells. Most importantly, B cell depletion inhibited antigen-specific CD4 ؉ T cell expansion in both collagen-induced arthritis and autoimmune diabetes mouse models. These results provide direct evidence that B cells contribute to T cell activation and expansion in vivo and offer insights into the mechanism of action for B cell depletion therapy in the treatment of autoimmunity.autoimmune disease ͉ B lymphocyte ͉ immunotherapy ͉ antigen presentation