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原发性胆汁性肝硬化:关于人类原发性胆汁性肝硬化及自发性原发性胆汁性肝硬化小鼠模型,我们已知的和想要了解的内容。

Primary biliary cirrhosis: what we know and what we want to know about human PBC and spontaneous PBC mouse models.

作者信息

Ueno Yoshiyuki, Moritoki Yuki, Shimosegawa Tooru, Gershwin M Eric

机构信息

Division of Gastroenterology, Tohoku University Graduate School of Medicine, 1-1 Seiryo, Aoba, Sendai, Miyagi, 980-8574, Japan.

出版信息

J Gastroenterol. 2007 Mar;42(3):189-95. doi: 10.1007/s00535-007-2019-y. Epub 2007 Mar 30.

Abstract

Human autoimmune cholangiopathy comprises several intractable liver diseases that ultimately lead to hepatic failure. Primary biliary cirrhosis (PBC), allograft rejection, graft versus host diseases, and, possibly, primary sclerosing cholangitis are representative of immune-mediated cholangiopathies. Among them, PBC is the best-investigated human autoimmune cholangiopathy. The immunological approach to PBC has provided much critical information regarding its pathogenesis. The breakdown of self-tolerance in both B cells and T cells toward E2 components of the pyruvate dehydrogenase complex is evident. However, a number of questions regarding its etiology are unclear, in particular, the mechanisms involved in the selectivity of cholangiocyte destruction. In this brief review, we discuss what we know and we do not know regarding the pathogenesis of PBC.

摘要

人类自身免疫性胆管病包括几种最终会导致肝衰竭的难治性肝病。原发性胆汁性肝硬化(PBC)、同种异体移植排斥反应、移植物抗宿主病以及可能的原发性硬化性胆管炎是免疫介导性胆管病的代表。其中,PBC是研究最为深入的人类自身免疫性胆管病。针对PBC的免疫学研究方法已经提供了许多关于其发病机制的关键信息。B细胞和T细胞对丙酮酸脱氢酶复合体E2成分的自身耐受性破坏是明显的。然而,关于其病因的许多问题仍不明确,特别是胆管细胞破坏选择性所涉及的机制。在这篇简短的综述中,我们讨论了关于PBC发病机制我们已知和未知的内容。

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