Literature DB >> 2391072

Demonstration of "naturally occurring mitochondrial antibodies" in family members of patients with primary biliary cirrhosis.

R Klein1, P A Berg.   

Abstract

Sera from 81 healthy family members (including husbands) of 13 patients with primary biliary cirrhosis were tested by Western blotting against the antigen fractions M9 and M2 derived respectively from rat liver and beef heart mitochondria. Fifty-eight (70%) were positive and recognized four major (molecular weights 98 kD, 65 kD, 61 kD, 58 kD) and eight minor determinants (85 kD, 81 kD, 78 kD, 54 kD, 48 kD, 45 kD, 40 kD, 30 kD) labeled alpha-my. Each of the 58 sera recognized at least one of the four major polypeptides. In contrast, only 6% of 80 primary biliary cirrhosis patients had antibodies against one of these epitopes. Sera from 25 patients with different infectious disorders previously shown to react with submitochondrial particles by enzyme-linked immunosorbent assay also recognized at least one of the four major determinants. From these findings it was concluded that these antibodies may belong to the family of natural autoantibodies. Since they reacted with submitochondrial fractions, they were defined as "naturally occurring mitochondrial antibodies". The high incidence of "naturally occurring mitochondrial antibodies" in primary biliary cirrhosis-contact persons may be taken as indirect evidence for a contagious immunogenic agent circulating in the blood of primary biliary cirrhosis-patients. In contrast, the absence of "naturally occurring mitochondrial antibodies" in primary biliary cirrhosis-patients themselves implies that an underlying B-cell defect is responsible for this lack of antibody production. Considering the protective role of naturally occurring antibodies in general, this postulated B-cell defect could be a major factor in the etiopathogenesis of primary biliary cirrhosis.

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Year:  1990        PMID: 2391072     DOI: 10.1002/hep.1840120222

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  7 in total

Review 1.  Immunological abnormalities and hepatotropic viral infections.

Authors:  I G McFarlane
Journal:  Clin Exp Immunol       Date:  1992-03       Impact factor: 4.330

2.  Anti-M4 antibodies in primary biliary cirrhosis react with sulphite oxidase, an enzyme of the mitochondrial inter-membrane space.

Authors:  R Klein; P A Berg
Journal:  Clin Exp Immunol       Date:  1991-06       Impact factor: 4.330

Review 3.  Autoantibodies in primary biliary cirrhosis.

Authors:  P A Berg; R Klein
Journal:  Springer Semin Immunopathol       Date:  1990

4.  Sera from patients with tuberculosis recognize the M2a-epitope (E2-subunit of pyruvate dehydrogenase) specific for primary biliary cirrhosis.

Authors:  R Klein; M Wiebel; S Engelhart; P A Berg
Journal:  Clin Exp Immunol       Date:  1993-05       Impact factor: 4.330

5.  Antimitochondrial autoantibodies in anti-glomerular basement membrane disease.

Authors:  J B Marriott; D B Oliveira
Journal:  Clin Exp Immunol       Date:  1993-08       Impact factor: 4.330

6.  Distribution of the PBC-specific- (M2) and the naturally-occurring mitochondrial antigen- (NOMAg) systems in plants.

Authors:  P Lang; R Klein; E W Becker; P A Berg
Journal:  Clin Exp Immunol       Date:  1992-12       Impact factor: 4.330

7.  Anti-mitochondrial autoantibodies in systemic lupus erythematosus and their association with disease manifestations.

Authors:  Yann Becker; Renée-Claude Loignon; Anne-Sophie Julien; Geneviève Marcoux; Isabelle Allaeys; Tania Lévesque; Emmanuelle Rollet-Labelle; Hadrien Benk-Fortin; Nathalie Cloutier; Imène Melki; Lihi Eder; Éric Wagner; Martin Pelletier; Hassan El Hajj; Marie-Ève Tremblay; Clémence Belleannée; Marie-Josée Hébert; Mélanie Dieudé; Joyce Rauch; Paul R Fortin; Eric Boilard
Journal:  Sci Rep       Date:  2019-03-14       Impact factor: 4.379

  7 in total

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