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dc.creatorSmyk, D.en
dc.creatorRigopoulou, E. I.en
dc.creatorZen, Y.en
dc.creatorKoutsoumpas, A.en
dc.creatorBaum, H.en
dc.creatorBogdanos, D. P.en
dc.date.accessioned2015-11-23T10:47:35Z
dc.date.available2015-11-23T10:47:35Z
dc.date.issued2011
dc.identifier.issn9724567
dc.identifier.urihttp://hdl.handle.net/11615/33112
dc.description.abstractPrimary biliary cirrhosis (PBC) is an immune mediated liver disease directed against the biliary epithelial cells of the small bile ducts. The disease is characterised by circulating antimitochondrial antibodies (AMA), as well as antinuclear antibodies (ANA). AMA is considered pathognomonic for PBC, with AMA positivity predicting disease development in asymptomatic individuals. Middle aged females are most commonly affected, with increased incidence in families. Sisters and daughters of PBC patients are especially at risk. Epidemiological and twin studies have demonstrated that genetic predisposition, combined with environmental factors likely act together in the disease initiation. Among the environmental risk factors, infectious agents have been implicated. The mechanism by which infectious agents contribute to the pathogenesis of PBC appears to be through molecular-mimicry, and cross reactivity to antigenic epitopes of mitochondrial antigens. Although several bacterial and viral pathogens have been identified with PBC, Escherichia coli, Novosphingobium aromaticivorans, and Lactobacillus delbrueckii subspecies bulgaricus have been considered the most significant infectious triggers, and have also been the most studied. The pathogenic significance of these bacteria may be reflective of their relationship with other identified risk factors, such as recurrent urinary tract infections and alterations in oestrogen metabolism. This review will examine the literature surrounding the epidemiological and molecular studies which have characterised the role of these bacteria in the pathogenesis of PBC.en
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-80051558614&partnerID=40&md5=fc35f1f7a0a3e90619495e0b269c1a0f
dc.subjectAutoimmune diseaseen
dc.subjectAutoimmunityen
dc.subjectBile ductsen
dc.subjectCholestasisen
dc.subjectCross-reactivityen
dc.subjectE. colien
dc.subjectImmunityen
dc.subjectLactobacillus delbrueckii subspecies bulgaricusen
dc.subjectLiveren
dc.subjectMimicryen
dc.subjectNovosphingobium aromaticivoransen
dc.subjectToleranceen
dc.subjectUrinary tract infectionen
dc.subject2 oxoisovalerate dehydrogenase (lipoamide)en
dc.subjectantinuclear antibodyen
dc.subjectcell nucleus antigenen
dc.subjectcytokeratin 19en
dc.subjectendopeptidase Clpen
dc.subjectepitopeen
dc.subjectestrogen receptor alphaen
dc.subjectestrogen receptor betaen
dc.subjectFas antigenen
dc.subjectmitochondrion antibodyen
dc.subjectoxoglutarate dehydrogenaseen
dc.subjectperipheral cellular nuclear antigenen
dc.subjectpyruvate dehydrogenase complexen
dc.subjectunclassified drugen
dc.subjectCD4+ T lymphocyteen
dc.subjectChlamydophila pneumoniaeen
dc.subjectcross reactionen
dc.subjectenvironmental factoren
dc.subjectepigeneticsen
dc.subjectEscherichia colien
dc.subjectestrogen metabolismen
dc.subjectgenetic predispositionen
dc.subjectGram negative bacteriumen
dc.subjectHelicobacter pylorien
dc.subjecthumanen
dc.subjectimmune responseen
dc.subjectimmunological toleranceen
dc.subjectLactobacillus delbrueckiien
dc.subjectmolecular mimicryen
dc.subjectMycobacterium gordonaeen
dc.subjectnatural killer T cellen
dc.subjectnonhumanen
dc.subjectpathogenesisen
dc.subjectprimary biliary cirrhosisen
dc.subjectrecurrent diseaseen
dc.subjectreviewen
dc.subjectrisk factoren
dc.titleInfectious triggers of primary biliary cirrhosis: Do we know enough?en
dc.typejournalArticleen


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