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通过抗体蛋白微阵列分析鉴别甲型流感病毒(A/2009 H1N1)感染与既往暴露情况。

Discrimination of influenza infection (A/2009 H1N1) from prior exposure by antibody protein microarray analysis.

作者信息

te Beest Dennis, de Bruin Erwin, Imholz Sandra, Wallinga Jacco, Teunis Peter, Koopmans Marion, van Boven Michiel

机构信息

Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.

Centre for Health Protection, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.

出版信息

PLoS One. 2014 Nov 18;9(11):e113021. doi: 10.1371/journal.pone.0113021. eCollection 2014.

DOI:10.1371/journal.pone.0113021
PMID:25405997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4236143/
Abstract

Reliable discrimination of recent influenza A infection from previous exposure using hemagglutination inhibition (HI) or virus neutralization tests is currently not feasible. This is due to low sensitivity of the tests and the interference of antibody responses generated by previous infections. Here we investigate the diagnostic characteristics of a newly developed antibody (HA1) protein microarray using data from cross-sectional serological studies carried out before and after the pandemic of 2009. The data are analysed by mixture models, providing a probabilistic classification of sera (susceptible, prior-exposed, recently infected). Estimated sensitivity and specificity for identifying A/2009 infections are low using HI (66% and 51%), and high when using A/2009 microarray data alone or together with A/1918 microarray data (96% and 95%). As a heuristic, a high A/2009 to A/1918 antibody ratio (>1.05) is indicative of recent infection, while a low ratio is indicative of a pre-existing response, even if the A/2009 titer is high. We conclude that highly sensitive and specific classification of individual sera is possible using the protein microarray, thereby enabling precise estimation of age-specific infection attack rates in the population even if sample sizes are small.

摘要

目前,使用血凝抑制(HI)试验或病毒中和试验可靠地区分近期甲型流感感染与既往暴露情况是不可行的。这是由于这些试验的敏感性较低,以及既往感染产生的抗体反应的干扰。在此,我们利用2009年大流行之前和之后进行的横断面血清学研究数据,调查一种新开发的抗体(HA1)蛋白微阵列的诊断特征。通过混合模型对数据进行分析,对血清(易感、既往暴露、近期感染)进行概率分类。使用HI试验识别2009年甲型流感感染的估计敏感性和特异性较低(分别为66%和51%),而单独使用2009年甲型流感微阵列数据或与1918年甲型流感微阵列数据一起使用时,敏感性和特异性较高(分别为96%和95%)。作为一种启发式方法,高的2009年甲型流感与1918年甲型流感抗体比值(>1.05)表明近期感染,而低比值表明既往存在的反应,即使2009年甲型流感滴度很高。我们得出结论,使用蛋白微阵列对个体血清进行高度敏感和特异的分类是可能的,从而即使样本量较小,也能够精确估计人群中特定年龄的感染发病率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/5ab769554d14/pone.0113021.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/f3bcdf2a2fa7/pone.0113021.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/b2519588005a/pone.0113021.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/c32c18533f14/pone.0113021.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/4995f007ac9f/pone.0113021.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/5ab769554d14/pone.0113021.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/f3bcdf2a2fa7/pone.0113021.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/b2519588005a/pone.0113021.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/c32c18533f14/pone.0113021.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/4995f007ac9f/pone.0113021.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e460/4236143/5ab769554d14/pone.0113021.g005.jpg

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