Splenic Dendritic Cells and Macrophages Drive B Cells to Adopt a Plasmablast Cell Fate.
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ABSTRACT: Upon encountering cognate antigen, B cells can differentiate into short-lived plasmablasts, early memory B cells or germinal center B cells. The factors that determine this fate decision are unclear. Past studies have addressed the role of B cell receptor affinity in this process, but the interplay with other cellular compartments for fate determination is less well understood. Moreover, B cell fate decisions have primarily been studied using model antigens rather than complex pathogen systems, which potentially ignore multifaceted interactions from other cells subsets during infection. Here we address this question using a Plasmodium infection model, examining the response of B cells specific for the immunodominant circumsporozoite protein (CSP). We show that B cell fate is determi
SUBMITTER: McNamara HA
PROVIDER: S-EPMC9039241 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
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