Regulation of B cell functions by Toll-like receptors and complement

Immunol Lett. 2016 Oct:178:37-44. doi: 10.1016/j.imlet.2016.07.015. Epub 2016 Jul 30.

Abstract

B cell functions triggered by the clonally-rearranged antigen-specific B cell receptor (BCR) are regulated by several germ-line encoded receptors - including Toll-like receptors (TLRs) and complement receptors (CRs). Simultaneous or sequential engagement of these structures expressed either on the cell membrane or intracellularly, may fundamentally alter and fine tune activation, antibody and cytokine production of B cells. Here we review the expression and function of TLRs and various C3 fragment binding CRs on B cells, emphasizing their role in different human B cell subsets under physiological and pathological conditions. Studies underlining the importance of the crosstalk between TLRs and CRs in regulating B cell functions are also highlighted.

Keywords: B cells; Complement system; Crosstalk; TLR.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoimmunity
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism*
  • Complement System Proteins / immunology*
  • Complement System Proteins / metabolism*
  • Disease Susceptibility
  • Gene Expression Regulation
  • Humans
  • Immunity, Innate
  • Immunomodulation*
  • Protein Binding
  • Receptors, Complement / metabolism
  • Signal Transduction
  • Toll-Like Receptors / metabolism*

Substances

  • Receptors, Complement
  • Toll-Like Receptors
  • Complement System Proteins