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作 者:周健[1] 姬光[1] 温嘉纳[1] 李佳[1] 沈伟[1] 郭自全[1] 廖国阳[1] 姜述德[1] 孙明波[1]
机构地区:[1]中国医学科学院北京协和医学院医学生物学研究所,昆明650118
出 处:《中华实验和临床病毒学杂志》2008年第6期488-491,共4页Chinese Journal of Experimental and Clinical Virology
基 金:云南省自然科学基金资助(基金编号20040030Q)
摘 要:目的建立一种快速灵敏特异的甲肝灭活疫苗的灭活验证方法。方法运用细胞培养/链特异性逆转录聚合酶链式反应对甲肝灭活疫苗进行灭活验证,并与传统的ELISA法及巢式RT-PCR检测甲肝全RNA进行比较。结果细胞培养/链特异性逆转录聚合酶链式反应法对甲肝灭活疫苗进行灭活验证,结果全为阴性,与传统的ELISA法结果相同。而采用巢式RT-PCR检测甲肝全RNA的方法对甲肝灭活疫苗进行灭活验证,则出现一些假阳性结果。结论细胞培养,链特异性逆转录聚合酶链式反应法是一种简便、快速、灵敏的甲肝灭活疫苗的灭活验证方法。大大缩短了检测周期,用于疫苗的常规检测有较好前景。Objective To establish an quick, sensitive and specific assay for effective inactivatian test of inactivated hepatitis A vaccine. Methods effective inactivatian test of inactivated hepatitis A vaccine were carried out using integrated cell culture/strand-specific RT-PCR (ICC/strand-specific RT-PCR) assay compared with traditional ELISA and nest RT-PCR assay.Results all the samples were infectious negative detecting by both ICC/ strand-specific RT-PCR and ELISA assay, while some samples appeared false positive detecting by nest RT-PCR. Conclusion ICC/strand-specific RT-PCR assay is a novel, rapid, sensitive and reliable method for effective inactivafian test of inactivated hepatitis A vaccine. Shorting detection period largely, this assay may be used as an alternative method for routine inactivated hepatitis A vaccines test.
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