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

Ben J.C. Quah, Vaughan P. Barlow, Virginia McPhun, Klaus I. Matthaei, Mark D. Hulett, Christopher R. Parish

    Research output: Contribution to journalArticlepeer-review

    50 Citations (Scopus)

    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.

    Original languageEnglish
    Pages (from-to)4259-4264
    Number of pages6
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume105
    Issue number11
    DOIs
    Publication statusPublished - 18 Mar 2008

    Fingerprint

    Dive into the research topics of 'Bystander B cells rapidly acquire antigen receptors from activated B cells by membrane transfer'. Together they form a unique fingerprint.

    Cite this