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基于包膜糖蛋白的多重免疫测定法在埃博拉病毒病幸存者队列中检测埃博拉病毒抗体的性能。

Performance of an envelope glycoprotein-based multiplex immunoassay for Ebola virus antibody detection in a cohort of Ebola virus disease survivors.

作者信息

Roe McKenna D, Hood Grace, Sterling Spencer L, Yan Lianying, Boré Joseph Akoi, Tipton Tom, Thompson Craig, Carroll Miles W, Laing Eric D

机构信息

Department of Microbiology and Immunology, Uniformed Services University, Bethesda, MD, USA.

Centre for Human Genetics & Pandemic Sciences Institute, University of Oxford, Oxford, UK.

出版信息

J Virol Methods. 2025 Jan;331:115057. doi: 10.1016/j.jviromet.2024.115057. Epub 2024 Oct 24.

Abstract

Serological surveillance in animal and human hosts can be a cost-effective strategy for orthoebolavirus detection, but is challenged by accurate estimates of seroprevalence, potential pauci-symptomatic disease presentation, and antigenic cross-reactivity. Here, we describe the use of an envelope glycoprotein (GP)-based multiplex microsphere immunoassay, consisting of nine filovirus GP antigens for the detection of anti-Ebola virus (EBOV) antibodies in a well-characterized cohort of Guinean Ebola virus disease (EVD) survivors and contacts from the 2013 - 2016 West African EVD outbreak. We examined sensitivity and specificity for the detection of anti-EBOV antibodies by GP expressed as recombinant trimeric ectodomains, yielding an assay performance of 95.96 % sensitivity and 98.61 % specificity. Additionally, agreement between the multiplex test and a whole virus ELISA and virus neutralization test showed strong correlations. The results demonstrate that this filovirus multiplex test is a sensitive tool for high-throughput serosurveillance.

摘要

在动物和人类宿主中进行血清学监测可能是检测正ebolavirus的一种具有成本效益的策略,但它受到血清阳性率的准确估计、潜在的轻症疾病表现以及抗原交叉反应性的挑战。在这里,我们描述了一种基于包膜糖蛋白(GP)的多重微球免疫测定法的应用,该方法由九种丝状病毒GP抗原组成,用于在一组特征明确的几内亚埃博拉病毒病(EVD)幸存者以及2013 - 2016年西非EVD疫情中的接触者中检测抗埃博拉病毒(EBOV)抗体。我们通过表达为重组三聚体外结构域的GP检测抗EBOV抗体的敏感性和特异性,该检测方法的检测性能为敏感性95.96%,特异性98.61%。此外,多重检测与全病毒ELISA和病毒中和试验之间的一致性显示出很强的相关性。结果表明,这种丝状病毒多重检测是一种用于高通量血清学监测的灵敏工具。

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