Esterases and autoimmunity: the sialic acid acetylesterase pathway and the regulation of peripheral B cell tolerance

Trends Immunol. 2009 Oct;30(10):488-93. doi: 10.1016/j.it.2009.07.006. Epub 2009 Sep 18.

Abstract

The best studied mechanisms of B cell tolerance are receptor editing, clonal deletion and anergy. All of these mechanisms of B cell tolerance depend on the induction of signaling downstream of the B cell receptor by self-antigens. Another important and distinct mechanism of B cell tolerance involves the repression of antigen receptor signaling rather than its induction, utilizes the Lyn Src-family kinase, the SHP-1 tyrosine phosphatase, inhibitory members of the Siglec family, and a carbohydrate-modifying enzyme that is capable of negatively regulating B cell receptor activation known as sialic acid acetylesterase.

Publication types

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

MeSH terms

  • Acetylesterase
  • Animals
  • Autoantigens / immunology
  • Autoimmune Diseases / enzymology*
  • B-Lymphocytes / enzymology
  • B-Lymphocytes / immunology*
  • Carbohydrate Metabolism
  • Carboxylic Ester Hydrolases / metabolism*
  • Clonal Deletion
  • Down-Regulation
  • Humans
  • Immune Tolerance*
  • Lymphocyte Activation
  • Mice
  • N-Acetylneuraminic Acid / metabolism
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6 / metabolism
  • Receptors, Interleukin-4 / metabolism
  • src-Family Kinases / metabolism

Substances

  • Autoantigens
  • Receptors, Interleukin-4
  • src-Family Kinases
  • Carboxylic Ester Hydrolases
  • Acetylesterase
  • sialate O-acetylesterase
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6
  • N-Acetylneuraminic Acid