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作 者:李妙羡[1] 王香玲[1] 吴晓康[1] 卢洁[1] 王小利[1] 尹佳峰[1] 孟昊[1]
机构地区:[1]西安交通大学医学院第二附属医院检验科,西安710004
出 处:《现代检验医学杂志》2012年第4期55-57,共3页Journal of Modern Laboratory Medicine
摘 要:目的评价丙型肝炎病毒核心抗原(HCV抗原)、丙型肝炎病毒抗体(HCV抗体)及丙型肝炎病毒RNA(HCV—RNA)三种检测方法在丙型肝炎实验室诊断中的作用。方法HCV抗原采用双抗体夹心法;HCV-RNA采用实时荧光定量PCR技术(RT—PCR),HCV抗体采用酶联免疫技术(间接法),对44例HCV抗体阳性标本进行HCV抗原和HCV-RNA检测。结果在HCV抗体阳性标本中,HCV抗原阳性检出率为43.2%,HCV-RNA阳性检出率为82.5%;在HCV—RNA阳性标本中,HCV抗原阳性检出率为45.5%。结论三种丙肝标志物中,实时荧光定量PCR技术检测HCV-RNA是判断丙肝感染最可靠的方法而HCV抗原诊断丙肝,仍有54.5%的漏检率,其应用于临床还有距离。所以在没有条件应用实时荧光定量PCR技术检测HCV-RNA的医院,在用HCV抗原对HcV抗体阳性标本进行确认,来判断HCV既往感染或现症感染时,应结合肝功能指标及临床表现以明确诊断。Objective To study the value of measurement of HCV antigen, HCV antibody and HCV-RNA in the clinical diag- nosis of Hepatitis. Methods HCV antigen would adopt double antibody Sandwiched method; HCV-RNA would employ the real-time fluorescence quantitative PCR technique, I-ICV antibody would use the technology of Enzyme-Linked Immunosor- bent Assay (ELISA) ,44 specimens of positive HCV antibody would be detected with HCV antigen and HCV-RNA meas- urement. Results Among the specimens of positive HCV antibody, the rate of positive HCV antigen was measured as 43.2% ;the rate of positive HCV-RNA was measured as 82.5%. Among the specimens of positive HCV-RNA, the rate of positive HCV antigen was measured as 45.5 %. Conclusion In the three kinds of Hepatitis markers,it was the most reliable method to judge whether infected with Hepatitis by using the real-time fluorescence quantitative PCR technique to measure HCV-RNA. If HCV antigen was used to diagnose Hepatitis, there was still 54. 5% rate of missed detection. Hence, there ex- ists a long distance from the application in the clinical practice. In the hospitals where it was impossible to employ the real- time fluorescence quantitative PCR technique to measure HCV-RNA,when confirming the specimens of positive HCV anti- body with HCV antigen and judging past exposure or present exposure to HCV,index of liver function and clinical manifestation should be combined to make a clear and definite diagnosis.
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