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作 者:张欣[1] 袁丽[2] 智再新[2] 陈秀珠[1] 吴远明[2]
机构地区:[1]同济医科大学病毒学研究中心,武汉430030 [2]中国科学院武汉病毒研究所,武汉430071
出 处:《病毒学杂志》1991年第2期102-106,共5页
摘 要:本文运用抗人巨细胞病毒(HCMV)包膜20KD或/和130KD结构蛋白的单克隆抗体分别建立了4类酶联免疫吸附试验(ELISA)夹心法,共对44人份临床尿标本进行HCMV抗原检测。方法的敏感度可高达10.3—32.8ng HCMV抗原/ml尿,与尿标本中的HSV-Ⅰ、HSV-Ⅱ和EBV抗原无交叉反应,重复性良好,与病毒分离比较,敏感性和特异性在71—83%和88—100%之间;与核酸杂交比较,敏感性和特异性也可分别高达60—100%和83.3—100%。混合使用多种单克隆抗体作为包被抗体会得到较好的技术参数。上述结果提示运用单克隆抗体ELISA将有助于一般临床实验室对HCMV感染的快速诊断。An enzyme-linked immunosorbent assay (ELISA) was developed for the detection of human cytomegalovirus (HCMV) in urine samples There were 4 kinds of method of the ELISA and monoclonal antibody directed against 20 or 130 kilodalton envelope structural polypeptides of HCMV was served as a capture antibody for viral antigen respectively or together,it has also been done positive serum of HCMV specific IgG. The assays were capable of detecting 10—32 ng HCMV antigen/ml and no cross reaction with HSV-Ⅰ, HSV-Ⅱ and EBV antigen in urine sample The assay was found to have sensitivity of 71—83%, 60—100% andspecificities of 88—100%, 83.3—100% in comparison with virus isolantion assay and DNA-DNA hybridization assay respectively when 44 thawed urene specimen were examined.
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