Division of Rheumatology, Allergy and Clinical Immunology, School of Medicine, University of California, Davis, California, USA.
Hepatol Res. 2007 Oct;37 Suppl 3:S365-9. doi: 10.1111/j.1872-034X.2007.00226.x.
The absence of suitable mouse models has represented a major drawback in our understanding of early events leading to the development of primary biliary cirrhosis (PBC). The recent report of not one, but three mouse models, each with distinctive features resembling PBC, represents a major advance in PBC research and generates novel experimental perspectives. The dnTGFbetaRII mouse, the IL-2Ralpha(-/-) mouse and the NOD.c3c4 mouse are all characterized by different genetic backgrounds and modifications, nonetheless all develop characteristic lymphocytic biliary infiltrates and specific antimitochondrial antibody response. Each model reflects characteristics of PBC in association with unique phenotypic differences. These three distinct models will allow a better understanding of the specific genetics involved in breaking of tolerance and progression of disease, in association with the possible definition of novel therapeutic approaches.
合适的小鼠模型的缺乏一直是我们理解原发性胆汁性肝硬化(PBC)发展早期事件的主要障碍。最近报道了不仅有一种,而是有三种小鼠模型,每种模型都具有类似于 PBC 的独特特征,这代表了 PBC 研究的重大进展,并产生了新的实验视角。dnTGFbetaRII 小鼠、IL-2Ralpha(-/-)小鼠和 NOD.c3c4 小鼠的遗传背景和修饰均不同,但它们均发展为特征性的淋巴细胞胆管浸润和特定的抗线粒体抗体反应。每种模型均反映了与独特表型差异相关的 PBC 的特征。这三种不同的模型将有助于更好地理解与疾病进展相关的特异性遗传因素,以及可能定义新的治疗方法。