| Literature DB >> 29164395 |
Ana Lleo1,2, Simona Marzorati1, Juan-Manuel Anaya3, M Eric Gershwin4.
Abstract
Primary biliary cholangitis (PBC) is an autoimmune liver disease characterized by biliary destruction, progressive cholestasis, and potentially liver cirrhosis. Patients develop a well-orchestrated immune reaction, both innate and adaptive, against mitochondrial antigens that specifically targets intrahepatic biliary cells. A puzzling feature of PBC is that the immune attack is predominantly organ specific, although the mitochondrial autoantigens are found in all nucleated cells. The disease results from a combination of genetic and environmental risk factors; however, the exact pathogenesis remains unclear. Serologically, PBC is characterized by presence of antimitochondrial antibodies, which are present in 90-95 % of patients and are often detectable years before clinical signs appear. Like other complex disorders, PBC is heterogeneous in its presentation, symptomatology, disease progression, and response to therapy. A significant number of patients develop end-stage liver disease and eventually require liver transplantation. Recent studies from large international cohorts have better identified prognostic factors, suggesting a change in patient management based on risk stratification. Therapeutic options are changing. In this review we discuss data on the autoimmune responses and treatment of the disease.Entities:
Keywords: Antimitochondrial antibodies; Biliary epithelial cells; Epigenetics; Genetics; Obeticholic acid; Primary biliary cholangitis; Prognostic factors; UDCA
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Year: 2017 PMID: 29164395 DOI: 10.1007/s12072-017-9830-1
Source DB: PubMed Journal: Hepatol Int ISSN: 1936-0533 Impact factor: 6.047