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乙型肝炎病毒X蛋白单克隆抗体的制备及肝癌组织中相应抗原的检测
引用本文:李君,汤钊猷,刘康达.乙型肝炎病毒X蛋白单克隆抗体的制备及肝癌组织中相应抗原的检测[J].中华医学杂志,1994(9).
作者姓名:李君  汤钊猷  刘康达
作者单位:上海医科大学肝癌研究所
摘    要:应用基因工程技术制备的17000乙型肝炎病毒(HBV)X蛋白(HBxAg)免疫动物,成功地制备了抗-HBx单克降抗体,以此抗体对原发性肝癌(HCC)组织、慢性活动性肝炎(CAN)肝组织行相应抗原检测,并同时进行乙型肝炎表面抗原(HBsAg)及乙型肝炎病毒核心抗原(HBcAg)的检测。在HCC标本中HBxAg在癌内及癌周肝组织中的阳性率分别为56%及48%,HBsAg为16%及74%。HBcAg仅见于癌周,阳性率为18%。在CAH标本中,HBxAg、HBsAg、HBcAg阳性率分别为6.6%、73.3%及0。血清HBsAg阳性HCC标本中,HBxAg的检出率为82.3%、明显高于血清HBsAg阴性标本(54.5%)。结果显示。HBxAg在HCC标本中的表达是HBV标志物中最活跃的。HBxAg的表达不依赖于HBV的复制,可能是HBVX基因同宿主细胞基因整合后的产物,HBxAg在HCC标本中的活跃表达为抗-HBx抗体作为HCC导向治疗载体提供了依据。

关 键 词:肝肿瘤,乙型肝炎病毒,单克隆抗体,基因,免疫应答

Preparation of monoclonal antibody directed againsthepatitis B virus X protein and detection of reactiveantigen in hepatocellular carciuoma
Li Jun,TangZhaoyou, Liu Kangda,et al..Preparation of monoclonal antibody directed againsthepatitis B virus X protein and detection of reactiveantigen in hepatocellular carciuoma[J].National Medical Journal of China,1994(9).
Authors:Li Jun  TangZhaoyou  Liu Kangda  
Institution:Li Jun,TangZhaoyou, Liu Kangda, et al.
Abstract:mouse monoclonal antibody directed againsthepatitis B virus (HBV) X protein (HBxAg) was pre-pared. The antibody was used to sereen byimmunogistochemistry 50 liver tissue sections frompatients with hepatoeellular carcinoma (HCC), and 15patients with chronic active hepatitis (CAH). 28 of50(56%). samples were HBxAg positive in tumor tis-sues. The positive rates of HBxAg only in tumor tis-sues or in adjaeent nontumor tissues were 24% and16%. HBsAg was detected in 16% of cases in tumortissues and 74% in suirounding nontumor tissues. InCAH samples, the positive rates of HBxAg andHBsAg were 6.6% and 73.3%. HBcAg was only de-tected in nontumor suirounding liver tissues, the posi-tive rates being 18% . In CAH samples, no HBcAg wasdetected. The results showed that HBxAg is a commonmarker in liver tissue from patients with HBVrelatedHCC. The findings of HBxAg in the absence ofdeteetable HBsAg and HBcAg in the liver tissues suggested that HBxAg could be independent of HBVreplication and implied that the synthesis of HBxAgmay be directed from integrated HBV DNAtemplates. It is possible to use antiHBx monoclonalantibody as a carrier for the targeting therapy ofHCC.
Keywords:Liver    neoplasms Hepatitis B vi-rus Monoclonal antibody Genes  immuneresponse  
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