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验证一种基于口腔液样本的抗麻疹病毒特异性 IgG 检测方法,用于孟加拉国的免疫监测。

Validation of an anti-measles virus-specific IgG assay with oral fluid samples for immunization surveillance in Bangladesh.

机构信息

International Vaccine Access Center (IVAC), Department of International Health, Johns Hopkins Bloomberg School of Public Health, 855 N. Wolfe Street, Suite 600, Baltimore, MD 21205, USA.

出版信息

J Virol Methods. 2013 Nov;193(2):512-8. doi: 10.1016/j.jviromet.2013.07.014. Epub 2013 Jul 18.

Abstract

Immune marker surveys may be used as substitutes or in conjunction with traditional surveys to monitor immunization program performance. This study assessed the validity and reliability of the Microimmune anti-measles virus-specific IgG ELISA with oral fluid samples (OF-ELISA) among a random sample of children ages 12-16 months in Bangladesh. Up to two oral fluid samples and one serum sample were analyzed for the presence of protective levels of anti-measles IgG antibodies. Results from the OF-ELISA were compared to the Enzygnost anti-measles IgG ELISA with serum and multivariate logistic regression models were developed to identify risk factors for false negative oral fluid results. Anti-measles IgG antibodies were measured in 330 paired oral fluid and serum samples. Immune marker prevalence of measles IgG antibodies was significantly higher in serum (88.1%, 95% CI: [84.1, 91.5]) than oral fluid (56.1% [50.2, 61.5]). Sensitivity (60.2% [54.1, 66.0]) and specificity (75.7% [58.8, 88.2]) of the OF-ELISA were lower than expected, but sensitivity significantly improved for individuals with higher anti-measles IgG in serum. False negative oral fluid results were associated with month of sample collection and variability between data collectors and assay procedures. Due to poor performance, caution should be exercised when using oral fluid samples to assess population immunity to measles virus, especially in highly vaccinated populations.

摘要

免疫标志物检测可作为传统检测的替代或补充方法,用于监测免疫规划的实施效果。本研究评估了在孟加拉国随机抽取的 12-16 月龄儿童中,使用唾液样本的 Microimmune 抗麻疹病毒特异性 IgG ELISA(OF-ELISA)的有效性和可靠性。对每个儿童的两份唾液样本和一份血清样本进行分析,以确定麻疹 IgG 抗体是否达到保护性水平。将 OF-ELISA 的检测结果与 Enzygnost 抗麻疹 IgG ELISA 检测结果进行比较,并建立多变量逻辑回归模型,以确定导致唾液检测结果假阴性的风险因素。在 330 对唾液和血清样本中测量了抗麻疹 IgG 抗体。血清中的麻疹 IgG 抗体免疫标志物流行率明显高于唾液(88.1%[84.1,91.5])(56.1%[50.2,61.5])。OF-ELISA 的灵敏度(60.2%[54.1,66.0])和特异性(75.7%[58.8,88.2])低于预期,但血清中麻疹 IgG 抗体水平较高的个体的灵敏度显著提高。假阴性的唾液检测结果与样本采集月份以及数据收集者和检测程序之间的变异性有关。由于性能不佳,在使用唾液样本评估麻疹病毒人群免疫水平时应谨慎,特别是在高接种人群中。

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