Control of autoreactive B cells by IgM and IgD B cell receptors: maintaining a fine balance

Curr Opin Immunol. 2018 Dec:55:67-74. doi: 10.1016/j.coi.2018.09.015. Epub 2018 Oct 5.

Abstract

A substantial fraction of mature naïve B cells recognize endogenous antigens, and this autoreactivity must be controlled to prevent autoantibody secretion. Selective downregulation of the IgM BCR on autoreactive B cells has long been appreciated, and recent findings illustrate how this might impose tolerance. The BCR isotype maintained on autoreactive B cells, IgD, is less sensitive to endogenous antigens than IgM. This reduced sensitivity may be conferred by structural properties of IgD and/or differential association with activating and inhibitory co-receptors. Once activated, autoreactive B cells are normally excluded from rapid plasma cell responses, but they can enter the germinal center and lose their autoreactivity through a mutation-selection process termed clonal redemption.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Autoimmunity / immunology*
  • B-Lymphocytes / immunology*
  • Humans
  • Immunoglobulin D / immunology*
  • Immunoglobulin M / immunology*
  • Lymphocyte Activation / immunology*
  • Receptors, Antigen, B-Cell / immunology*

Substances

  • Immunoglobulin D
  • Immunoglobulin M
  • Receptors, Antigen, B-Cell