Maternal infection causes dysfunctional BCR signaling in male offspring due to aberrant Xist expression

Abstract

AbstractInfections during pregnancy with pathogens such as helminths correlate with altered immune responses to common childhood immunizations. However, the molecular mechanisms that underlie this remain unknown. Using our murine model of maternal schistosomiasis, when immunized, males from infected mothers had a lower frequency of antigen-specific germinal center B cells and downregulation of transcripts downstream of BCR signaling compared to males from uninfected mothers. This is driven by a reduction in developing B cell populations within the bone marrow of pups from infected mothers. Males from infected mothers were impacted to a greater extent than their female littermate counterparts. We found this defect to be caused by aberrant expression of the long non-coding RNAXistin males leading to dysregulated Igα expression on developing B cells. This, for the first time, links dysfunctional BCR signaling withXistexpression, while also proposing a detrimental function forXistexpression in males.One sentence summaryXistexpression in males decreases BCR reactivity.