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Detection of anti-branched chain 2-oxo acid dehydrogenase complex (BCOADC)-E2 antibody in primary biliary cirrhosis by ELISA using recombinant fusion protein.

Abstract
Anti-M2 of anti-mitochondrial antibody (AMA) is a serological marker of primary biliary cirrhosis (PBC). Anti-pyruvate dehydrogenase complex-E2 (anti-PDC-E2) is recognized as the most frequently occurring anti-M2, and a routine laboratory test for this antibody has already been established. However, it is also known that there are patients with PBC who are negative for anti-PDC-E2. For the serological diagnosis of these patients, immunoblotting for anti-M2s is indicated. However, the technique currently utilized is too laborious to allow testing of a large number of samples. In this study, we have developed an enzyme-linked immunosorbent assay (ELISA) using a recombinant fusion protein in order to evaluate anti-branched chain 2-oxo-acid dehydrogenase complex-E2 (anti-BCOADC-E2), another frequently occurring anti-M2 in PBC patients. KB cell lines (CCL 17) were utilized as source material, and BCOADC-E2 cDNA (971 bp) including the lipoic acid binding domain was amplified by polymerase chain reaction. The amplified region was subcloned into pEX-3 vectors and expressed, and the resulting fusion protein (beta-galactosidase/BCOADC-E2) was utilized as antigen for an ELISA. We ascertained the specificity of this antigen by inhibition tests with ELISA and immunoblotting. We defined the cut-off optical density (OD) value as the mean + 3 SD (0.146) of sera from 60 normal controls. Anti-BCOADC-E2 could not be detected with this assay in sera from normal controls and from patients with autoimmune hepatitis and chronic viral hepatitis. Anti-BCOADC-E2 was detected in 119 of 210 sera (56.7%) from patients with PBC. In addition, anti-BCOADC-E2 was detected in 48 of 99 (48.5%) sera from PBC patients who were negative for anti-PDC-E2. Here, we have succeeded in developing a new ELISA for detecting anti-BCOADC-E2. This system is antigen-specific and easily performed. This assay should allow routine testing of a large number of serum samples, and should become especially useful for the serodiagnosis of anti-PDC-E2-negative PBC patients.
AuthorsH Miyakawa, K Abe, E Kitazawa, K Kikuchi, H Fujikawa, M Matsushita, N Kawaguchi, M Kako
JournalAutoimmunity (Autoimmunity) Vol. 30 Issue 1 Pg. 11-20 ( 1999) ISSN: 0891-6934 [Print] England
PMID10433090 (Publication Type: Journal Article)
Chemical References
  • Antibodies
  • DNA Primers
  • DNA, Complementary
  • Multienzyme Complexes
  • Pyruvate Dehydrogenase Complex
  • Recombinant Fusion Proteins
  • Ketone Oxidoreductases
  • 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Topics
  • 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
  • Antibodies (immunology)
  • Blotting, Western
  • DNA Primers (chemistry)
  • DNA, Complementary (chemistry)
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme-Linked Immunosorbent Assay (methods)
  • Female
  • Humans
  • Ketone Oxidoreductases (immunology)
  • Liver Cirrhosis, Biliary (diagnosis, immunology)
  • Male
  • Middle Aged
  • Mitochondria, Liver (immunology)
  • Multienzyme Complexes (immunology)
  • Pyruvate Dehydrogenase Complex (immunology)
  • Recombinant Fusion Proteins
  • Reverse Transcriptase Polymerase Chain Reaction

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