Tsuneyama K, Van de Water J, Leung P S, Cha S, Nakanuma Y, Kaplan M, De Lellis R, Coppel R, Ansari A, Gershwin M E
Division of Rheumatology, Allergy and Clinical Immunology, University of California, Davis 95616, USA.
Hepatology. 1995 Apr;21(4):1031-7.
Primary biliary cirrhosis (PBC) is a chronic autoimmune liver disease characterized histologically by nonsuppurative destructive cholangitis. Sera from patients with PBC react with a series of intramitochondrial enzymes with the immunodominant response directed against the E2 component of the pyruvate dehydrogenase complex (PDC-E2). Recently, using tissue sections of late-stage PBC, we showed that there is increased expression in biliary epithelial cells of patients with PDC-E2 or a molecule cross-reactive with PDC-E2. Previous work has shown that biliary epithelial cells of patients with PBC express an increased amount of class II. To address the sequence of events in the evolution of PBC, we have focused our attention in this study on early biliary epithelial lesions. In particular, we have studied the liver of 22 female patients with PBC that was diagnosed as either stage I or stage II using both a mouse monoclonal antibody that has reactivity similar to human autoantibodies as well as a human Fab combinatorial prepared from the lymph node of a PBC patient. Tissues were simultaneously stained using antibodies to PDC-E2, class II, and BB1/B7. As a positive control, tissues from late-stage PBC were studied concurrently. By determining the order of expression among the three molecules, PDC-E2, class II, and BB1/B7, we report that the expression of PDC-E2 or a PDC-E2-like molecule on biliary duct epithelium of patients with PBC precedes the expression of BB1/B7 and major histocompatibility complex (MHC) class II molecules. The alteration of an autoantigen in biliary duct epithelium may be the earliest lesion in PBC.
原发性胆汁性肝硬化(PBC)是一种慢性自身免疫性肝病,组织学特征为非化脓性破坏性胆管炎。PBC患者的血清与一系列线粒体内酶发生反应,免疫优势反应针对丙酮酸脱氢酶复合体(PDC-E2)的E2成分。最近,我们使用晚期PBC的组织切片显示,PDC-E2或与PDC-E2交叉反应的分子在PBC患者的胆管上皮细胞中表达增加。先前的研究表明,PBC患者的胆管上皮细胞表达量增加的II类分子。为了探讨PBC演变过程中的事件顺序,我们在本研究中重点关注早期胆管上皮病变。特别是,我们研究了22例被诊断为I期或II期的女性PBC患者的肝脏,使用了一种与人类自身抗体反应性相似的小鼠单克隆抗体以及从一名PBC患者淋巴结制备的人源Fab组合。组织同时用抗PDC-E2、II类和BB1/B7抗体染色。作为阳性对照,同时研究了晚期PBC的组织。通过确定PDC-E2、II类和BB1/B7这三种分子之间的表达顺序,我们报告PBC患者胆管上皮上PDC-E2或类似PDC-E2分子的表达先于BB1/B7和主要组织相容性复合体(MHC)II类分子的表达。胆管上皮自身抗原的改变可能是PBC最早的病变。