Tavakoli Ahmad, Rezaei Farhad, Fatemi Nasab Gazal Sadat, Adjaminezhad-Fard Fatemeh, Noroozbabaei Zahra, Mokhtari-Azad Talat
Dept. of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Iran J Public Health. 2017 Dec;46(12):1690-1696.
The most common serological assay to measure anti-influenza antibodies is hemagglutination inhibition (HI) assay. Recently, neutralizing antibodies against influenza virus infection or vaccination can also be detected using microneutralization assays and occasionally, have greater sensitivity than the standard HI assays. The study aimed to compare the sensitivity and specificity of ELISA-based microneutralization (microNT-ELISA) and conventional HI assays in order to detect influenza H1N1 virus antibodies.
MicroNT-ELISA was set up according to the WHO Manual on Influenza Diagnosis and Surveillance in Virology Department of Tehran University of Medical Sciences for the detection of neutralizing antibodies against H1N1 influenza virus in 2013. Fifty serum samples were analyzed with both HI and microNT-ELISA assays. Correlation between methods was calculated by linear regression analysis.
The linear correlation coefficient squares, R2, of microNT-ELISA and HI test was 0.61 (<0.0001) and we observed a high index of coincidence between the two tests. According to McNemar's test, there was no statistically significant difference between these two assays (>0.05).
The sensitivity and specificity of microNT-ELISA assay were high (87% and 73%, respectively) and closely related to gold standard test results. Therefore, microNT-ELISA is recommended as an alternative or complementary test to conventional HI assay for serological and epidemiological purposes.
用于检测抗流感抗体的最常见血清学检测方法是血凝抑制(HI)试验。最近,也可以使用微量中和试验检测针对流感病毒感染或疫苗接种的中和抗体,偶尔其敏感性高于标准HI试验。本研究旨在比较基于酶联免疫吸附测定的微量中和试验(microNT-ELISA)和传统HI试验检测甲型H1N1流感病毒抗体的敏感性和特异性。
2013年,根据世界卫生组织《流感诊断与监测手册》在德黑兰医科大学病毒学系建立了microNT-ELISA,用于检测针对甲型H1N1流感病毒的中和抗体。对50份血清样本进行了HI试验和microNT-ELISA检测。通过线性回归分析计算两种方法之间的相关性。
microNT-ELISA和HI试验的线性相关系数平方R2为0.61(<0.0001),我们观察到两种检测方法之间的符合率较高。根据McNemar检验,这两种检测方法之间没有统计学显著差异(>0.05)。
microNT-ELISA检测的敏感性和特异性较高(分别为87%和73%),且与金标准检测结果密切相关。因此,推荐将microNT-ELISA作为传统HI试验的替代或补充检测方法用于血清学和流行病学目的。