Suppressive effect of reactive oxygen species on CD40-induced B cell activation

Reactive oxygen species (ROS) produced by the innate immune system work as effectors to destroy pathogens and to control cellular responses. However, their role in the adaptive immune response remains unclear. Here we studied the effect of exogenous ROS on CD40-induced B cell activation. H 2O 2 treatment inhibited CD40-induced immunoglobulin production of B cells, DNA binding of NF-κB, IκBα degradation and IKK phosphorylation. On the other hand, H 2O 2 treatment did not induce obvious B cell death after 30 min of stimulation. Although the ligation of anti-CD40 antibody was not disturbed by H 2O 2, TRAF2 recruitment to CD40 was inhibited. These results suggest that exogenous ROS play a negative role in CD40 signaling during B cell activation.