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用于流感的假型病毒

Pseudotyped Viruses for Influenza.

作者信息

Del Rosario Joanne Marie M, da Costa Kelly A S, Temperton Nigel J

机构信息

Viral Pseudotype Unit, Medway School of Pharmacy, University of Kent and Greenwich at Medway, Chatham, UK.

出版信息

Adv Exp Med Biol. 2023;1407:153-173. doi: 10.1007/978-981-99-0113-5_8.

Abstract

We have developed an influenza hemagglutinin (HA) pseudotype (PV) library encompassing all influenza A (IAV) subtypes from HA1-HA18, influenza B (IBV) subtypes (both lineages), representative influenza C (ICV), and influenza D (IDV) viruses. These influenza HA (or hemagglutinin-esterase fusion (HEF) for ICV and IDV) pseudotypes have been used in a pseudotype microneutralization assay (pMN), an optimized luciferase reporter assay, that is highly sensitive and specific for detecting neutralizing antibodies against influenza viruses. This has been an invaluable tool in detecting the humoral immune response against specific hemagglutinin or hemagglutinin-esterase fusion proteins for IAV to IDV in serum samples and for screening antibodies for their neutralizing abilities. Additionally, we have also produced influenza neuraminidase (NA) pseudotypes for IAV N1-N9 subtypes and IBV lineages. We have utilized these NA-PV as surrogate antigens in in vitro assays to assess vaccine immunogenicity. These NA PV have been employed as the source of neuraminidase enzyme activity in a pseudotype enzyme-linked lectin assay (pELLA) that is able to measure neuraminidase inhibition (NI) titers of reference antisera, monoclonal antibodies, and postvaccination sera. Here we show the production of influenza HA, HEF, and NA PV and their employment as substitutes for wild-type viruses in influenza serological and neutralization assays. We also introduce AutoPlate, an easily accessible web app that can analyze data from pMN and pELLA quickly and efficiently, plotting inhibition curves and calculating half-maximal concentration (IC) neutralizing antibody titers. These serological techniques coupled with user-friendly analysis tools are faster, safer, inexpensive alternatives to classical influenza assays while also offering the reliability and reproducibility to advance influenza research and make it more accessible to laboratories around the world.

摘要

我们构建了一个流感血凝素(HA)假型(PV)文库,涵盖了甲型流感病毒(IAV)从HA1-HA18的所有亚型、乙型流感病毒(IBV)的两个谱系的亚型、代表性丙型流感病毒(ICV)和丁型流感病毒(IDV)。这些流感HA(ICV和IDV为血凝素-酯酶融合蛋白(HEF))假型已用于假型微量中和试验(pMN),这是一种优化的荧光素酶报告基因检测方法,对检测针对流感病毒的中和抗体具有高度敏感性和特异性。这已成为检测血清样本中针对IAV至IDV的特定血凝素或血凝素-酯酶融合蛋白的体液免疫反应以及筛选抗体中和能力的宝贵工具。此外,我们还制备了IAV N1-N9亚型和IBV谱系的流感神经氨酸酶(NA)假型。我们在体外试验中利用这些NA-PV作为替代抗原评估疫苗免疫原性。这些NA PV已被用作假型酶联凝集素试验(pELLA)中神经氨酸酶活性的来源,该试验能够测量参考抗血清、单克隆抗体和疫苗接种后血清的神经氨酸酶抑制(NI)滴度。在这里,我们展示了流感HA、HEF和NA PV的制备及其在流感血清学和中和试验中作为野生型病毒替代品的应用。我们还介绍了AutoPlate,这是一个易于访问的网络应用程序,可以快速有效地分析来自pMN和pELLA的数据,绘制抑制曲线并计算半数最大浓度(IC)中和抗体滴度。这些血清学技术与用户友好的分析工具相结合,是传统流感检测方法更快、更安全、更便宜的替代方法,同时还提供了可靠性和可重复性,以推动流感研究,并使世界各地的实验室更容易进行研究。

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