Demonstration of PDC-E1 subunits as major antigens in the complement-fixing fraction M4 and re-evaluation of PDC-E1-specific antibodies in PBC patients

Liver Int. 2006 Sep;26(7):846-55. doi: 10.1111/j.1478-3231.2006.01303.x.

Abstract

Background: Primary biliary cirrhosis (PBC) is characterized by the presence of antimitochondrial antibodies (AMA). Autoantibodies specific for the mitochondrial M4 antigen can be detected by a complement fixation test (CFT) but not by immunoblotting. The aim of this study was to elucidate the identity of the M4 antigen.

Patients and methods: M4 proteins were purified by affinity chromatography using IgG fractions of PBC marker sera being CFT positive (n=5) or negative (n=5) and identified by Western blotting, silver staining and sequence analysis. Further, a cohort of 57 PBC patients was tested for the reactivity to M4 and pyruvate dehydrogenase complex (PDC).

Results: Two AMA patterns of the marker sera were visualized: CFT-positive sera were defined as PDC-E2(+)/E1(+) and the CFT-negative sera as PDC-E2(+)/E1(-). The major proteins in the M4 fraction could be related to the PDC-E1 subunits. A clear-cut association between anti-M4 reactivity in the CFT and the reactivity to both PDC subunits could also be documented in the cohort of 57 PBC patients showing anti-PDC-E1alpha and E1beta antibodies at a frequency of 74% and 67%.

Conclusions: CFT reactivity against M4 antigens could be preferentially identified as a reaction against PDC-E1. As PDC-E1 subunits as compared with PDC-E2 lack lipoyl-binding sites, they probably have to be considered as an independent and important target.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Animals
  • Autoantibodies / blood
  • Autoantibodies / immunology
  • Autoantigens / immunology*
  • Cohort Studies
  • Complement Fixation Tests
  • Female
  • Humans
  • Immunodominant Epitopes / immunology
  • Liver Cirrhosis, Biliary / blood
  • Liver Cirrhosis, Biliary / immunology*
  • Male
  • Middle Aged
  • Mitochondria / immunology
  • Pyruvate Dehydrogenase (Lipoamide) / immunology*
  • Pyruvate Dehydrogenase Complex / immunology
  • Rats

Substances

  • Autoantibodies
  • Autoantigens
  • Immunodominant Epitopes
  • Pyruvate Dehydrogenase Complex
  • Pyruvate Dehydrogenase (Lipoamide)