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作 者:黄德庄[1] 闫惠平[1] 郎振为[1] 贺丽香[1] 齐文杰[1] 张建成[1] 文厚洲
机构地区:[1]北京市肝炎研究所,北京佑安医院
出 处:《中华肝脏病杂志》1996年第1期12-15,共4页Chinese Journal of Hepatology
摘 要:以单克隆抗-HCV-NS3直接酶标法对石蜡包埋肝组织中丙型肝炎病毒抗原(HCAg-NS3)进行测定,该抗体系应用基因重组表达丙肝抗原(HCV-NS3区-C33-C)免疫小鼠并通过细胞融合术后获得。49例病毒性肝炎患者肝组织测定结果,抗-HCV阳性组的HCAs-NS3检出率为51.9%(14/27),抗-HCV阴性组为13.6%(3/22),两组有显著性差异(P<0.01),以慢性重症肝炎和肝硬化患者检出率最高,HCAg-NS3阳性物在肝细胞的胞核或胞浆中均可见,呈棕黄色细小颗粒状,以核型居多。直接酶标法测定HCAg与原位杂交法测定HCVRNA的比较,其符合率为81.6%(40/49)。本项技术具有简便、快捷、特异性、敏感性佳、图象清晰等优点,易于推广应用,为HCV感染的临床和发病机理研究提供重要检测手段。We developed a direct enzyme immuno-assay for the detection of HCV antigen-NS3 in formalin-paraffin-embedded liver tissue from 49 viral hepatitis patients. The monoclonal anti-HCV-NS3 was obtained from recombinant HCAg-NS3-C33-C. It has been proved that this is a rapid, simple,specific and sensitive method.In all of 49 cases with viral hepatitis, the detective rate of HCV-NS3 antigen was 34.7% (17/49),51.9%(14/27) in anti-HCV positve patients, and 13.6%(3/22) in anti-HCV negative patients. The positive stain was found more on the nucleus than that in cytoplasm, Hepatocytes with positive staining distributed sporadically within the lobule. Confirmation tests of this method showed that this technique was quite specific. This result was compared with in situ hybridization detection of HCV RNA and the corresponsible rate was 81.6%(P>0.05). The influence of HBV replication during HCV/HBV double infection was disscused.
分 类 号:R512.630.3[医药卫生—内科学]
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