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作为测量甲型流感病毒1组血凝素茎部反应性抗体的候选标准的混合血清的开发与评估

Development and Assessment of a Pooled Serum as Candidate Standard to Measure Influenza A Virus Group 1 Hemagglutinin Stalk-Reactive Antibodies.

作者信息

Carreño Juan Manuel, McDonald Jacqueline U, Hurst Tara, Rigsby Peter, Atkinson Eleanor, Charles Lethia, Nachbagauer Raffael, Behzadi Mohammad Amin, Strohmeier Shirin, Coughlan Lynda, Aydillo Teresa, Brandenburg Boerries, García-Sastre Adolfo, Kaszas Krisztian, Levine Min Z, Manenti Alessandro, McDermott Adrian B, Montomoli Emanuele, Muchene Leacky, Narpala Sandeep R, Perera Ranawaka A P M, Salisch Nadine C, Valkenburg Sophie A, Zhou Fan, Engelhardt Othmar G, Krammer Florian

机构信息

Department of Microbiology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1124, New York, NY 10029, USA.

Division of Virology, National Institute for Biological Standards and Control (NIBSC), South Mimms, Potters Bar EN6 3QG, UK.

出版信息

Vaccines (Basel). 2020 Nov 9;8(4):666. doi: 10.3390/vaccines8040666.

Abstract

The stalk domain of the hemagglutinin has been identified as a target for induction of protective antibody responses due to its high degree of conservation among numerous influenza subtypes and strains. However, current assays to measure stalk-based immunity are not standardized. Hence, harmonization of assay readouts would help to compare experiments conducted in different laboratories and increase confidence in results. Here, serum samples from healthy individuals ( = 110) were screened using a chimeric cH6/1 hemagglutinin enzyme-linked immunosorbent assay (ELISA) that measures stalk-reactive antibodies. We identified samples with moderate to high IgG anti-stalk antibody levels. Likewise, screening of the samples using the mini-hemagglutinin (HA) headless construct #4900 and analysis of the correlation between the two assays confirmed the presence and specificity of anti-stalk antibodies. Additionally, samples were characterized by a cH6/1N5 virus-based neutralization assay, an antibody-dependent cell-mediated cytotoxicity (ADCC) assay, and competition ELISAs, using the stalk-reactive monoclonal antibodies KB2 (mouse) and CR9114 (human). A "pooled serum" (PS) consisting of a mixture of selected serum samples was generated. The PS exhibited high levels of stalk-reactive antibodies, had a cH6/1N5-based neutralization titer of 320, and contained high levels of stalk-specific antibodies with ADCC activity. The PS, along with blinded samples of varying anti-stalk antibody titers, was distributed to multiple collaborators worldwide in a pilot collaborative study. The samples were subjected to different assays available in the different laboratories, to measure either binding or functional properties of the stalk-reactive antibodies contained in the serum. Results from binding and neutralization assays were analyzed to determine whether use of the PS as a standard could lead to better agreement between laboratories. The work presented here points the way towards the development of a serum standard for antibodies to the HA stalk domain of phylogenetic group 1.

摘要

血凝素的柄部结构域已被确定为诱导保护性抗体反应的靶点,因为它在众多流感亚型和毒株中具有高度保守性。然而,目前用于测量基于柄部的免疫力的检测方法尚未标准化。因此,统一检测读数将有助于比较不同实验室进行的实验,并增加对结果的信心。在这里,使用一种嵌合的cH6/1血凝素酶联免疫吸附测定(ELISA)对110名健康个体的血清样本进行筛选,该测定可检测柄部反应性抗体。我们鉴定出了具有中度至高IgG抗柄部抗体水平的样本。同样,使用微型血凝素(HA)无头构建体#4900对样本进行筛选,并分析两种检测方法之间的相关性,证实了抗柄部抗体的存在和特异性。此外,使用基于cH6/1N5病毒的中和试验、抗体依赖性细胞介导的细胞毒性(ADCC)试验以及竞争ELISA对样本进行表征,使用柄部反应性单克隆抗体KB2(小鼠)和CR9114(人)。生成了一种由选定血清样本混合物组成的“混合血清”(PS)。该PS表现出高水平的柄部反应性抗体,基于cH6/1N5的中和滴度为320,并且含有高水平的具有ADCC活性的柄部特异性抗体。在一项试点合作研究中,PS与不同抗柄部抗体滴度的盲法样本一起分发给了全球多个合作者。样本接受了不同实验室可用的不同检测,以测量血清中所含柄部反应性抗体的结合或功能特性。对结合和中和试验的结果进行分析,以确定使用PS作为标准是否能使各实验室之间达成更好的一致性。本文介绍的工作为开发针对第1系统发育组HA柄部结构域抗体的血清标准指明了方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7385/7712758/ccb1cdd443f0/vaccines-08-00666-g001.jpg

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