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Mycoplasma antigens as a possible trigger for the induction of antimitochondrial antibodies in primary biliary cirrhosis
Author(s) -
Berg Christoph P.,
Kannan Thirumalai R.,
Klein Reinhild,
Gregor Michael,
Baseman Joel B.,
Wesselborg Sebastian,
Lauber Kirsten,
Stein Gerburg M.
Publication year - 2009
Publication title -
liver international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.873
H-Index - 110
eISSN - 1478-3231
pISSN - 1478-3223
DOI - 10.1111/j.1478-3231.2008.01942.x
Subject(s) - molecular mimicry , antibody , primary biliary cirrhosis , antigen , mycoplasma pneumoniae , mycoplasma , immunology , autoantibody , biology , immune system , mycoplasma pneumonia , autoimmune disease , virology , medicine , microbiology and biotechnology , pneumonia
Abstract Background: In primary biliary cirrhosis (PBC), autoreactivity mainly targets members of the pyruvate dehydrogenase complex (PDC). Because PDC subunits are expressed on the surface of mycoplasma and molecular mimicry may be one aetiological factor, we analysed the presence of mammalian and mycoplasma PDC‐specific antibodies in PBC patients. Methods: Antibodies to porcine PDC and Mycoplasma pneumoniae (mp) antigens mpPDH‐C (to be designated mpPDC‐E2 chain), mpPDH‐B (to be designated mpPDC‐E1β chain), mpCARDS TX and mpP1 were investigated in sera from 43 PBC patients, 19 patients with autoimmune hepatitis and 11 healthy controls by an enzyme‐linked immunosorbent assay and Western blotting. To study the rate of acute mycoplasma infection, an adhesin P1‐specific polymerase chain reaction (PCR) was performed. Results: Immune reactivity to the mpPDC‐E2 antigen was significantly enhanced in PBC patients (83.7%) as compared with controls (overall frequency of 36.7%), while antibodies to the porcine PDC‐E2 chain were found only in PBC patients (88%) excluding a simple cross‐reactivity of PDC‐related antibodies. This observation was confirmed by inhibition studies demonstrating that porcine PDC did not inhibit mycoplasma PDC‐specific antibodies and vice versa. The occurrence of antibodies to mpPDC seems to precede the occurrence of antibodies to porcine PDC. Infection with mycoplasma was equally distributed in the groups as evidenced by an antibody frequency comparable to CARDS TX and P1 and PCR reactivity. Conclusion: Because PBC patients show a significantly enhanced frequency of mpPDC‐E2‐related antibodies, besides other factors, molecular mimicry between surface molecules of mycoplasma and epitopes of the autoantigen may play a central role in the aetiopathology of PBC.