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以流感 H5N1 血凝素为特征的慢病毒假型及其在中和试验中的性能。

Characterization of lentiviral pseudotypes with influenza H5N1 hemagglutinin and their performance in neutralization assays.

机构信息

Center for Biologics Evaluation and Research, US Food and Drug Administration, Bethesda, MD 20892, United States.

出版信息

J Virol Methods. 2010 May;165(2):305-10. doi: 10.1016/j.jviromet.2010.02.009. Epub 2010 Feb 11.

Abstract

Pseudotype reporter viruses are being used as safe, quantitative, and high-throughput tools for assessing antibody neutralization for many viruses, including influenza. However, characterization of pseudotypes containing influenza hemagglutinin (HA-pseudotypes) is needed before this system is widely adopted for evaluating neutralizing antibodies in sera following vaccination or infection. In this report HA-pseudotype stocks were analyzed for HA content, stability, and performance in neutralization assays under various conditions. HA-pseudotypes produced with HA genes of H5 strains representing clades 1, 2.2, and 2.3.4 consistently contain similar HA contents, and infectivity was not greatly affected by the purity of the HA-pseudotype preparations or variations in storage conditions. HA-pseudotype neutralization titers using a reference serum panel were also consistent across a wide range of dilutions of HA-pseudotype stocks and correlated well with results from microneutralization assays involving replicating influenza. Concentrated HA-pseudotypes were further shown to work well in hemagglutination inhibition assays. Finally, antisera elicited by genetically modified HA, with changes in the polybasic cleavage site that have been used in some H5 vaccines and reduce pathogenicity, gave identical neutralization titers against HA-pseudotypes with wild type or modified HA. These findings support continued development of HA-pseudotypes as a robust tool for analyzing sera in vaccine and serologic studies.

摘要

假型报告病毒被用作评估多种病毒(包括流感)抗体中和作用的安全、定量和高通量工具。然而,在广泛采用该系统评估疫苗接种或感染后血清中的中和抗体之前,需要对包含流感血凝素(HA-假型)的假型进行特征描述。在本报告中,分析了含有代表 1、2.2 和 2.3.4 分支的 H5 株 HA 基因的 HA-假型病毒株的 HA 含量、稳定性和在各种条件下的中和测定中的性能。HA-假型的制备物的 HA 含量、纯度或储存条件的变化对感染性的影响不大。使用参考血清组进行的 HA-假型中和滴度也在 HA-假型病毒株的广泛稀释范围内保持一致,与涉及复制性流感的微量中和测定结果相关性良好。浓缩的 HA-假型在血凝抑制测定中也能很好地发挥作用。最后,用遗传修饰的 HA 引发的抗血清,其中包括一些 H5 疫苗中使用的改变多碱性切割位点以降低致病性的修饰,对野生型或修饰型 HA 的 HA-假型具有相同的中和滴度。这些发现支持继续开发 HA-假型作为分析疫苗和血清学研究中血清的强大工具。

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