Content area

Abstract

Expression of Toll-like receptors (TLRs) in B cells provides a cell-intrinsic mechanism for innate signals regulating adaptive immune responses. In combination with other signaling pathways in B cells, including through the B-cell receptor (BCR), TLR signaling plays multiple roles in B-cell differentiation and activation. The outcome of TLR signaling in B cells is largely context-dependent, which partly explains discrepancies among in vitro and in vivo studies, or studies using different immunogens. We focus on recent findings on how B-cell-intrinsic TLR signaling regulates antibody responses, including germinal center formation and autoantibody production in autoimmune disease models. In addition, TLR signaling also acts on the precursors of B cells, which could influence the immune response of animals by shaping the composition of the immune system. With TLR signaling modulating immune responses at these different levels, much more needs to be understood before we can depict the complete functions of innate signaling in host defense.

Details

Title
TLR signaling in B-cell development and activation
Author
Hua, Zhaolin 1 ; Hou, Baidong 1 

 Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China (GRID:grid.418856.6) (ISNI:0000 0004 1792 5640) 
Pages
103-106
Publication year
2013
Publication date
Mar 2013
Publisher
Nature Publishing Group
ISSN
16727681
e-ISSN
20420226
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2760382189
Copyright
© Chinese Society of Immunology and The University of Science and Technology 2013.