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原发性胆汁性肝硬化:一种具有多种表现形式的疾病。

Primary biliary cirrhosis: one disease with many faces.

作者信息

Hirschfield Gideon M, Gershwin M Eric

机构信息

Liver Centre, Toronto Western Hospital, University of Toronto, Toronto, Canada.

出版信息

Isr Med Assoc J. 2011 Jan;13(1):55-9.

Abstract

Primary biliary cirrhosis (PBC) is considered a model autoimmune disease because of the similarities between patients, their relative homogeneous presentation and natural history, and the presence of the signature autoantibody, the antimitochondrial antibodies. PBC also illustrates the potential role of genetic and environmental influence and is unique in having several well-defined animal models that recapitulate distinct features of the disease. The pathogenesis of the disease includes genetic predisposition, the production of both innate and adaptive immune responses, and cholangiocyte-specific biology that addresses the specificity of disease. In this review we highlight these features of PBC in comparison to other autoimmune diseases.

摘要

原发性胆汁性肝硬化(PBC)被认为是一种典型的自身免疫性疾病,因为患者之间存在相似性,其临床表现和自然病史相对一致,并且存在标志性自身抗体——抗线粒体抗体。PBC还说明了遗传和环境影响的潜在作用,并且独特之处在于有几种明确的动物模型,这些模型概括了该疾病的不同特征。该疾病的发病机制包括遗传易感性、先天性和适应性免疫反应的产生,以及涉及疾病特异性的胆管细胞特异性生物学特性。在这篇综述中,我们将PBC的这些特征与其他自身免疫性疾病进行了比较。

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