Control of memory B cell responses by extrinsic and intrinsic mechanisms

Immunol Lett. 2016 Oct:178:27-30. doi: 10.1016/j.imlet.2016.05.010. Epub 2016 Jun 23.

Abstract

Following primary activation, B lymphocytes generate a long-lived memory compartment to harness the organism for future reinfections by the same pathogen species. Only recently the composition and signaling signature of the scarce memory B cell pool could be explored in more detail. This review highlights current concepts of how B cells preserve their antigen experience at the cellular and molecular level.

Keywords: Affinity maturation; B cell antigen receptor; Class-switching; Germinal center; Immunoglobulin tail tyrosine; Memory B lymphocytes.

Publication types

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

MeSH terms

  • Animals
  • Antibody Formation / genetics
  • Antibody Formation / immunology
  • B-Lymphocyte Subsets / cytology
  • B-Lymphocyte Subsets / immunology
  • B-Lymphocyte Subsets / metabolism
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism*
  • Cell Communication
  • Germinal Center / immunology
  • Germinal Center / metabolism
  • Humans
  • Immunoglobulin Class Switching / genetics
  • Immunoglobulin Class Switching / immunology
  • Immunologic Memory* / genetics
  • Immunologic Memory* / immunology
  • Immunomodulation* / genetics
  • Immunomodulation* / immunology
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • Phosphorylation
  • Receptors, Antigen, B-Cell / metabolism
  • Receptors, IgG / metabolism
  • Signal Transduction
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • Tyrosine / metabolism

Substances

  • Receptors, Antigen, B-Cell
  • Receptors, IgG
  • Tyrosine