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Expression of CD44 on bile ducts in primary sclerosing cholangitis and primary biliary cirrhosis.

机译:原发性硬化性胆管炎和原发性胆汁性肝硬化的胆管中CD44的表达。

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摘要

AIM: To examine expression of CD44, a transmembrane glycoprotein involved in lymphocyte homing and activation, in inflammatory liver diseases. METHODS: Formalin fixed, paraffin embedded tissues were obtained from normal, uninvolved liver from patients undergoing partial hepatectomy for metastatic carcinoma (9) and transplant hepatectomy specimens from patients with primary biliary cirrhosis (12), primary sclerosing cholangitis (8), autoimmune hepatitis (3), hepatitis C (3), and secondary sclerosing cholangitis (1). Expression of CD44 (using antibodies to three core epitopes), HLA-DR, and lymphocyte phenotypic markers was studied by immunohistochemistry. RESULTS: CD44 expression was not detected in either hepatocytes or biliary epithelial cells in normal livers. In sections from all 27 transplant hepatectomy specimens, CD44 was positive in bile duct epithelial cells but not in hepatocytes. The proportion of CD44+ ducts was much higher in biliary disease than in chronic hepatitis. By contrast, expression of HLA-DR was detected in a relatively small percentage of bile ducts. Activated, memory phenotype CD4+ T lymphocytes were increased in the parenchyma of all diseased livers and an infiltrate of activated CD8+ cells within the biliary epithelium was evident in inflammatory biliary disease. CONCLUSIONS: CD44 appears to play an important role in the development of autoimmune biliary disease by promoting lymphoepithelial interactions, whereas HLA-DR may be involved in the subsequent progression of these conditions.
机译:目的:研究炎症性肝病中涉及淋巴细胞归巢和活化的跨膜糖蛋白CD44的表达。方法:从正常,未累及肝的福尔马林固定的,石蜡包埋的组织取自接受转移性癌部分肝切除术的患者(9)和原发性胆汁性肝硬化(12),原发性硬化性胆管炎(8),自身免疫性肝炎( 3),丙型肝炎(3)和继发性硬化性胆管炎(1)。通过免疫组织化学研究了CD44(使用针对三个核心表位的抗体),HLA-DR和淋巴细胞表型标志物的表达。结果:在正常肝的肝细胞或胆管上皮细胞中均未检测到CD44表达。在所有27个移植肝切除标本中的切片中,CD44在胆管上皮细胞中呈阳性,但在肝细胞中呈阴性。胆道疾病中CD44 +导管的比例远高于慢性肝炎。相比之下,在相对较小的胆管中检测到HLA-DR的表达。在所有患病的肝脏的实质中,活化的记忆表型CD4 + T淋巴细胞均增加,并且在炎性胆道疾病中,胆汁上皮内的活化CD8 +细胞浸润明显。结论:CD44似乎通过促进淋巴上皮相互作用而在自身免疫性胆道疾病的发展中起重要作用,而HLA-DR可能参与这些疾病的后续发展。

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