Identification of tyrosine hydroxylase as an autoantigen in autoimmune polyendocrine syndrome type I

Biochem Biophys Res Commun. 2000 Jan 7;267(1):456-61. doi: 10.1006/bbrc.1999.1945.

Abstract

Patients with the autosomal recessively inherited autoimmune polyendocrine syndrome type I (APS I) have autoantibodies directed against several endocrine and nonendocrine organs. In this study a new autoantigen related to this syndrome, tyrosine hydroxylase, was identified in sera from patients with alopecia areata through immunoscreening of a scalp cDNA library. Immunoreactivity against in vitro expressed tyrosine hydroxylase was found in 41 (44%) of the 94 APS I patients studied and this reactivity correlated with the presence of alopecia areata (P = 0.02). These findings further stress the importance of enzymes involved in neurotransmitter biosynthesis as important immune targets in APS I.

Publication types

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

MeSH terms

  • Alopecia Areata / enzymology
  • Alopecia Areata / immunology
  • Autoantibodies / blood*
  • Autoantigens / genetics
  • Autoantigens / immunology*
  • Europe
  • Gene Library
  • Humans
  • Isoenzymes / genetics
  • Isoenzymes / immunology
  • Polyendocrinopathies, Autoimmune / enzymology
  • Polyendocrinopathies, Autoimmune / genetics
  • Polyendocrinopathies, Autoimmune / immunology*
  • Scalp / enzymology
  • Syndrome
  • Tyrosine 3-Monooxygenase / genetics
  • Tyrosine 3-Monooxygenase / immunology*

Substances

  • Autoantibodies
  • Autoantigens
  • Isoenzymes
  • Tyrosine 3-Monooxygenase