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Integration of B cell responses through Toll-like receptors and antigen receptors

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NATURE REVIEWS IMMUNOLOGY
卷 12, 期 4, 页码 282-294

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NATURE PUBLISHING GROUP
DOI: 10.1038/nri3190

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资金

  1. US National Institutes of Health [HD037091, HL075453, AI084457, AI071163]
  2. Cancer Research Institute
  3. Rheumatology T32 Postdoctoral Training Grant [5T32AR007108]
  4. German Research Foundation (Deutsche Forschungsgemeinschaft) [ME2709/2-1]

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Unlike other immune cells, B cells express both an antigen-specific B cell receptor (BCR) and Toll-like receptors (TLRs). Dual BCR and TLR engagement can fine-tune functional B cell responses, directly linking cell-intrinsic innate and adaptive immune programmes. Although most data regarding B cell-specific functions of the TLR signalling pathway have been obtained in mice, the discovery of patients with a deficiency in this pathway has recently provided an insight into human B cell responses. Here, we highlight the importance of the integration of signalling pathways downstream of BCRs and TLRs in modulating B cell function, focusing when possible on B cell-intrinsic roles.

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