Gastroenterology and Metabology, Ehime University, Graduate School of Medicine, Ehime, Japan.
Dis Markers. 2010;29(6):313-21. doi: 10.3233/DMA-2010-0747.
Primary biliary cirrhosis (PBC) is a chronic and slowly progressive cholestatic liver disease of autoimmune etiology, characterized by injury of the intrahepatic bile ducts that may eventually lead to cirrhosis and liver failure. Evidence suggests cardinal roles for both environmental factors and genetic susceptibility. Nevertheless, the absolute etiology of PBC is unclear, despite recent well-designed case-control studies that reported environmental risk factors, including infectious agents, for PBC. Of the reported infectious agents, some of them are not reproducible and remain controversial. However, infection is no doubt one of the major risks among the environmental factors. This is supported by the fact that infectious agents in autoimmune diseases express antigens resulting in molecular mimicry and xenobiotics that play a role in breaking tolerance. Taken together, recent findings from genome wide assays as well as novel animal models may enable us to better understand the mechanism of pathogenesis responsible for this disease.
原发性胆汁性肝硬化(PBC)是一种慢性、进行性胆汁淤积性自身免疫性肝病,其特征为肝内胆管损伤,最终可能导致肝硬化和肝功能衰竭。有证据表明,环境因素和遗传易感性都起着重要作用。尽管最近进行了精心设计的病例对照研究,报告了 PBC 的环境危险因素,包括感染因子,但 PBC 的绝对病因仍不清楚。在报告的感染因子中,有些是不可复制的,仍然存在争议。然而,感染无疑是环境因素中的主要危险因素之一。这一事实得到了以下事实的支持:自身免疫性疾病中的感染因子表达抗原,导致分子模拟,以及外源性物质在打破耐受中发挥作用。总之,全基因组分析和新型动物模型的最新发现可能使我们能够更好地理解导致这种疾病的发病机制。