Role of inhibitory signaling in peripheral B cell tolerance

Immunol Rev. 2022 May;307(1):27-42. doi: 10.1111/imr.13070. Epub 2022 Feb 6.

Abstract

At least 20% of B cells in the periphery expresses an antigen receptor with a degree of self-reactivity. If activated, these autoreactive B cells pose a risk as they can contribute to the development of autoimmune diseases. To prevent their activation, both B cell-intrinsic and extrinsic tolerance mechanisms are in place in healthy individuals. In this review article, I will focus on B cell-intrinsic mechanisms that prevent the activation of autoreactive B cells in the periphery. I will discuss how inhibitory signaling circuits are established in autoreactive B cells, focusing on the Lyn-SHIP-1-SHP-1 axis, how they contribute to peripheral immune tolerance, and how disruptions of these circuits can contribute to the development of autoimmunity.

Keywords: B cells; autoimmunity; protein kinases/phosphatases; signal transduction; tolerance/suppression/anergy.

Publication types

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

MeSH terms

  • Autoimmune Diseases*
  • Autoimmunity
  • B-Lymphocytes
  • Humans
  • Immune Tolerance
  • Receptors, Antigen, B-Cell*
  • Signal Transduction

Substances

  • Receptors, Antigen, B-Cell