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出 处:《国际生物制品学杂志》2011年第4期188-190,共3页International Journal of Biologicals
摘 要:目的 比较微量血凝抑制(micro-hemagglutination inhibition,HI)试验与酶联免疫吸附测定(enzyme-linked immunosorbent assay,ELISA)检测血清抗风疹IgG抗体的敏感性和特异性,确定ELISA法检测血清抗风疹IgG抗体的可行性.方法 采集江苏地区506名8~15月龄健康儿童免疫前和麻疹-腮腺炎-风疹联合疫苗免疫后1个月的血清,共1012份血清,分别采用HI法和ELISA法检测血清抗风疹IgG.抗体,并采用卡方检验对两种方法的检测结果进行比较.结果 HI法和ELISA法的血清抗风疹抗体阳性检出率分别为50.30%和47.04%,两种方法的阳性检出率之间的差异无统计学意义(X2=1.780,P=O.182).两种方法检出同为阴性的血清495份,同为阳性的血清476份,两种方法的检测符合率为95.95%.相关与回归分析显示,两种方法具有高度的正相关性(r=O.806,P〈0.001).结论 可用ELISA法替代HI法进行血清抗风疹IgG抗体检测.Objective To compare the sensitivity and specificity for detecting serum anti-rubella IgG antibody between micro-hemagglutination inhibition ( HI) test and enzyme-linked immunosorbent assay ( ELISA) , and define the feasibility of ELISA for detecting serum anti-rubella IgG antibody. Methods Serum samples from 506 healthy children aged 8-15 months in Jiangsu Province were collected before vaccination and one month after vaccination with measles-mumps-rubella combined vaccine, and total 1012 serum samples were obtained. Serum anti-rubella IgG antibodies were detected by HI test and ELISA, respectively, and the detection results between two methods were compared by chi-square test. Results The positive detection rates of HI and ELISA antibodies were 50.30% and 47.04% , respectively, and no statistically significant difference in positive detection rate was found between the two methods (X2 = 1. 780, P =0. 182). Four hundred and ninety-five serum samples were negative and 476 serum samples were positive by both assays. The coincidence rate of detection between two methods was 95.95%. Correlation and regression analysis showed there was high positive correlation between two methods(r=0. 806,P〈0.001). Conclusion ELISA can replace HI test to detecting serum anti-rubella IgG antibody.
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