Volume 29, Issue 6 923928 pp. 277-286
Article
Open Access

Infectious Agents in the Pathogenesis of Primary Biliary Cirrhosis

Oscar-Danilo Ortega-Hernandez

Oscar-Danilo Ortega-Hernandez

The Zabludowicz Center for Autoimmune Diseases and Department of Medicine B Sheba Medical Center Tel-Aviv, Israel

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Nancy-Agmon Levin

Nancy-Agmon Levin

The Zabludowicz Center for Autoimmune Diseases and Department of Medicine B Sheba Medical Center Tel-Aviv, Israel

Tel-Aviv University Tel-Aviv, Israel , tau.ac.il

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Arie Altman

Arie Altman

The Zabludowicz Center for Autoimmune Diseases and Department of Medicine B Sheba Medical Center Tel-Aviv, Israel

Tel-Aviv University Tel-Aviv, Israel , tau.ac.il

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Yehuda Shoenfeld

Corresponding Author

Yehuda Shoenfeld

The Zabludowicz Center for Autoimmune Diseases and Department of Medicine B Sheba Medical Center Tel-Aviv, Israel

Tel-Aviv University Tel-Aviv, Israel , tau.ac.il

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First published: 21 May 2013
Citations: 1

Abstract

Primary biliary cirrhosis (PBC) is a chronic progressive cholestatic liver disease which is characterized by the breakdown of self-tolerance to the highly conserved pyruvate dehydrogenase complex, specially the pyruvate dehydrogenase E2 complex (PDC-E2). The breakdown of the tolerance to such antigens leads to an autoimmune process characterized by portal inflammation and immune-mediated destruction of the intrahepatic bile ducts. Epidemiological studies have suggested that infections agents can trigger or even exacerbate the disease. Among other gram negative bacteria, Escherichia Coli, and Nosphingobium aromaticivorans are the most associated agents reported hitherto. Epidemiological and molecular evidence points towards molecular mimicry between some components of these microorganisms and specific amino-acid sequences that are present in proteins on normal cells of the biliary tract. In this review, we revisit all reports suggesting that infectious agents might be associated with the autoimmune pathogenesis of PBC. We also retrieve the immune molecular mimicry mechanisms that are likely involved with the autoimmune process in PBC.

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