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Bystander B cells rapidly acquire antigen receptors from activated B cells by membrane transfer

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Quah, Ben
Barlow, Vaughan
McPhun, Virginia
Matthaei, Klaus
Hulett, Mark
Parish, Christopher

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National Academy of Sciences (USA)

Abstract

The B cell antigen receptor (BCR) efficiently facilitates the capture and processing of a specific antigen for presentation on MHC class II molecules to antigen-specific CD4+ T cells (1). Despite this, the majority of B cells are thought to play only a limited role in CD4+ T cell activation because BCRs are clonotypically expressed. Here, we show, however, that activated B cells can, both in vitro and in vivo, rapidly donate their BCR to bystander B cells, a process that is mediated by directmembranetransfer between adjacent B cells and is amplified by the interaction of the BCR with a specific antigen. This results in a dramatic expansion in the number of antigen-binding B cells in vivo, with the transferred BCR endowing recipient B cells with the ability to present a specific antigen to antigen-specific CD4+ T cells.

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PNAS - Proceedings of the National Academy of Sciences of the United States of America

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Restricted until

2037-12-31
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