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作 者:刘洪[1] 貌盼勇[1] 洪世雯[1] 胡燕[1] 白雁平[1] 鞠连才[1]
机构地区:[1]解放军302医院
出 处:《中华实验和临床病毒学杂志》1999年第1期77-79,共3页Chinese Journal of Experimental and Clinical Virology
摘 要:目的建立一种早期、快速诊断庚型肝炎的血清学检测方法。方法以辣根过氧化物酶标记庚型肝炎病毒(HGV)多肽NS3,NS5区段抗原,建立了捕获酶联免疫吸附试验(ELISA),用于检测血清中HGVIgM抗体。结果本法不受特异性IgG的竞争和类风湿因子的干扰;与其它致肝炎的病毒(HAV、HBV、HCV、HEV、CMV、EBV)无交叉反应。检测46例非甲、乙、丙、戊型肝炎患者血清,抗-HGVIgM阳性14例,阳性率30.43%,其中,6例同时为HGVRNA阳性,阳性符合率为42.86%(6/14),检测12例庚型肝炎病人双份血清,其中,急性期血HGVIgM抗体均为阳性。结论该法检测HGVIgM抗体特异性强,敏感性高,且简便快速,适用于临床对庚型肝炎新近感染的早期诊断,有推广应用价值。Objiective To provide a rapid and early serodiagnostic technique for the patients with hepatitis G virus(HGV). Methods A capture ELISA was developed to detect anti HGV IgM in sera using synthetic peptides of HGV NS3 NS5 gene regions conjugated with horseradish peroxidase.Results This assay was not disturbed by competition of specific IgG or interfered by RF and did not cross react with HAV、HBV、HCV、HEV、CMV and EBV. Among 46 sera of non A E hepatitis,14 were positive for anti HGVIgM, the positive rate was 30.43%,6 was positive for HGV RNA the positive rate was 42.86%. 12 paired sera from acute stage of HGV patients were all positive by capture ELISA. Conclusion This method is sensitive, specific, rapid and stable for detecting anti HGV IgM, and is useful in the early diagnosis of HGV infection.
分 类 号:R373.21[医药卫生—病原生物学] R446.61[医药卫生—基础医学]
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