Laboratory of Viral Hepatitis, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.
J Clin Lab Anal. 2011;25(2):134-41. doi: 10.1002/jcla.20447.
In this study, a modified enzyme immunoassay (EIA) was evaluated for the Hepatitis B surface antigen (HBsAg) among whole saliva and oral fluid samples. Specimens were collected from 115 individuals who gave serum and oral fluid using Salivette (Sarstedt, Nümbrecht, Germany) and whole saliva. Saliva specimens were tested following a modified ELISA, and the results were compared with paired serum specimens that were tested according to the supplier's instructions. Transport buffer for the oral fluids, sample volume for assay, incubation period of sample with conjugate as well as cut-off values were evaluated to optimize the assay. The highest sensitivity and specificity were obtained by increasing the incubation of sample and conjugate to 16 hr and using the area under the receiver operating characteristic curve to calculate cut-off values. HBsAg was detected in 40 oral fluids and 44 whole saliva samples out of 47 paired positive serum specimens and not detected in 64 oral fluids and 63 whole saliva samples out of 68 matched negative sera samples by the ELISA assay. There was excellent agreement between the results for the serum and saliva specimens kappa value (κ): 0.80 for oral fluid and κ: 0.87 for whole saliva and there was excellent reproducibility. Using an optimized protocol, the sensitivities of whole saliva and oral fluid were 93.6 and 85.1%, respectively, whereas specificities of whole saliva and oral fluid were 92.6 and 94.1%, respectively. Our data showed a significant promise for the use of whole saliva and oral fluid together with the modified commercial EIA for Hepatitis B virus infection surveillance.
本研究评估了改良酶免疫分析法(EIA)在全唾液和口腔液样本中乙型肝炎表面抗原(HBsAg)的检测效果。采集了 115 名个体的血清和唾液样本,唾液样本使用 Sarstedt(德国努姆布赖特)的 Salivette 采集,全唾液样本直接采集。对唾液样本进行改良 ELISA 检测,将结果与按供应商说明检测的配对血清样本进行比较。对检测的缓冲液、样本体积、样本与结合物的孵育时间和截断值进行了评估,以优化检测方法。通过增加样本和结合物的孵育时间至 16 小时,并使用受试者工作特征曲线下的面积来计算截断值,可获得最高的灵敏度和特异性。改良 EIA 检测到 47 份配对阳性血清样本中的 40 份口腔液样本和 44 份全唾液样本中存在 HBsAg,而在 68 份配对阴性血清样本中未检测到 64 份口腔液样本和 63 份全唾液样本中的 HBsAg。血清和唾液样本的检测结果一致性非常好,kappa 值(κ):口腔液为 0.80,全唾液为 0.87,且具有很好的重现性。使用优化方案,全唾液和口腔液的灵敏度分别为 93.6%和 85.1%,特异性分别为 92.6%和 94.1%。我们的数据表明,使用改良的商业 EIA 结合全唾液和口腔液检测乙型肝炎病毒感染监测具有很大的应用潜力。