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作 者:谭德明[1] 聂东宋 彭小虎 杨锡琴 李凯 赵秀英[4] 欧阳奕[1] 曾立明[1] 周松辉 张贺秋[3] 周见远
机构地区:[1]中南大学湘雅医院感染病科,湖南长沙410008 [2]湖南景达生物工程有限公司 [3]军事医学科学院基础医学研究所 [4]北京佑安医院 [5]湖南省岳阳市一医院
出 处:《中国医师杂志》2009年第5期591-593,共3页Journal of Chinese Physician
基 金:国家863重点项目(2006AA020907)
摘 要:目的建立丙型肝炎病毒总核心抗原(总HCV-cAg)酶联免疫测定方法,并对相关的临床样品进行测定。方法通过对样品进行裂解处理,采用酶联免疫试剂盒(ELISA)检测总HCV-cAg,对201名抗-HCV阳性者血清进行总HCV—cAg检测,同时进一步作HCV-RNA检测,其中176例采用荧光定量PCR(FQ—PCR),25例采用逆转录PCR(RT—PCR)检测HCV.RNA。结果共检测201份血清标本,其中经PCR测定HCVRNA阳性88人份,阳性率43.8%;总HCV—cAg阳性71份,阳性率35.3%。经统计学分析,总HCV—cAg检测和HCVRNA检测的阳性率的差异无统计学意义。结论建立的总HCV—cAg酶联免疫测定方法适合临床应用,尤其适合在缺少RT-PCR或荧光定量PCR的中小医院使用。Objective To develop the technique to detect total core antigen of HCV(Total HCV-cAg) by Enzyme-Linked Immunosorbent Assay (ELISA) and apply it for clinical diagnosis. Methods 201 serum samples with anti-HCV antibody were detected total HCV-cAg after pre -treating the samples, then the sensitivity of results were compared with HCV RNA tests. Among them, 176 cases was determined by FQ-PCR, and 25 cases by RT-PCR for HCV-RNA. Results HCV RNA was found in sera from 88 of 201 samples (43.8 % ). Total HCV-cAg was positive in 71 (35.3%) of 201 samples . There was no significant difference between the detection rate of HCV RNA by PCR and total HCV-cAg by ELISA. Conclusion Detection of total core antigen of HCV is suitable to be used as to diagnose HCV in clinic.
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