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首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Plasma cells and the chronic nonsuppurative destructive cholangitis of primary biliary cirrhosis
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Plasma cells and the chronic nonsuppurative destructive cholangitis of primary biliary cirrhosis

机译:浆细胞与原发性胆汁性肝硬化的慢性非化脓性破坏性胆管炎

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There has been increased interest in the role of B cells in the pathogenesis of primary biliary cirrhosis (PBC). Although the vast majority of patients with this disease have anti-mitochondrial antibodies, there is no correlation of anti-mitochondrial antibody titer and/or presence with disease severity. Furthermore, in murine models of PBC, it has been suggested that depletion of B cells may exacerbate biliary pathology. To address this issue, we focused on a detailed phenotypic characterization of mononuclear cell infiltrates surrounding the intrahepatic bile ducts of patients with PBC, primary sclerosing cholangitis, autoimmune hepatitis, chronic hepatitis C, and graft-versus-host disease, including CD3, CD4, CD8, CD20, CD38, and immunoglobulin classes, as well as double immunohistochemical staining for CD38 and IgM. Interestingly, CD20 B lymphocytes, which are a precursor of plasma cells, were found in scattered locations or occasionally forming follicle-like aggregations but were not noted at the proximal location of chronic nonsuppurative destructive cholangitis. In contrast, there was a unique and distinct coronal arrangement of CD38 cells around the intrahepatic ducts in PBC but not controls; the majority of such cells were considered plasma cells based on their expression of intracellular immunoglobulins, including IgM and IgG, but not IgA. Patients with PBC who manifest this unique coronal arrangement were those with significantly higher titers of anti-mitochondrial antibodies. Conclusion: These data collectively suggest a role for plasma cells in the specific destruction of intrahepatic bile ducts in PBC and confirm the increasing interest in plasma cells and autoimmunity. (HEPATOLOGY 2012)
机译:B细胞在原发性胆汁性肝硬化(PBC)发病机理中的作用越来越引起人们的关注。尽管绝大多数患有这种疾病的患者都具有抗线粒体抗体,但抗线粒体抗体滴度和/或存在与疾病的严重程度没有关联。此外,在PBC的鼠模型中,已经表明B细胞的耗竭可能加剧胆道疾病。为解决这个问题,我们着重研究了PBC,原发性硬化性胆管炎,自身免疫性肝炎,慢性丙型肝炎和移植物抗宿主病,包括CD3,CD4,PBC和PBC患者的肝内胆管周围单核细胞浸润的详细表型特征CD8,CD20,CD38和免疫球蛋白类别,以及CD38和IgM的双重免疫组织化学染色。有趣的是,浆细胞的前体CD20 B淋巴细胞在分散的位置发现或偶尔形成卵泡状聚集,但在慢性非化脓性破坏性胆管炎的近端未发现。相比之下,在PBC的肝内导管周围,CD38细胞有独特而独特的冠状排列,但对照没有。根据细胞内免疫球蛋白(包括IgM和IgG,而非IgA)的表达,大多数此类细胞被视为浆细胞。表现出这种独特的冠状排列的PBC患者是抗线粒体抗体滴度明显更高的患者。结论:这些数据共同表明浆细胞在PBC肝内胆管的特异性破坏中的作用,并证实对浆细胞和自身免疫的兴趣日益增加。 (2012年肝病)

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