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高通量多重流感抗体检测分析在人类中流感疫苗接种和自然感染后的抗体全景分析。

Antibody Landscape Analysis following Influenza Vaccination and Natural Infection in Humans with a High-Throughput Multiplex Influenza Antibody Detection Assay.

机构信息

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

mBio. 2021 Feb 2;12(1):e02808-20. doi: 10.1128/mBio.02808-20.

DOI:10.1128/mBio.02808-20
PMID:33531397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7858056/
Abstract

To better understand the antibody landscape changes following influenza virus natural infection and vaccination, we developed a high-throughput multiplex influenza antibody detection assay (MIADA) containing 42 recombinant hemagglutinins (rHAs) (ectodomain and/or globular head domain) from pre-2009 A(H1N1), A(H1N1)pdm09, A(H2N2), A(H3N2), A(H5N1), A(H7N7), A(H7N9), A(H7N2), A(H9N2), A(H13N9), and influenza B viruses. Panels of ferret antisera, 227 paired human sera from vaccinees (children and adults) in 5 influenza seasons (2010 to 2018), and 17 paired human sera collected from real-time reverse transcription-PCR (rRT-PCR)-confirmed influenza A(H1N1)pdm09, influenza A(H3N2), or influenza B virus-infected adults were analyzed by the MIADA. Ferret antisera demonstrated clear strain-specific antibody responses to exposed subtype HA. Adults (19 to 49 years old) had broader antibody landscapes than young children (<3 years old) and older children (9 to 17 years old) both at baseline and post-vaccination. Influenza vaccination and infection induced the strongest antibody responses specific to HA(s) of exposed strain/subtype viruses and closely related strains; they also induced cross-reactive antibodies to an unexposed influenza virus subtype(s), including novel viruses. Subsequent serum adsorption confirmed that the cross-reactive antibodies against novel subtype HAs were mainly induced by exposures to A(H1N1)/A(H3N2) influenza A viruses. In contrast, adults infected by influenza B viruses mounted antibody responses mostly specific to two influenza B virus lineage HAs. Median fluorescence intensities (MFIs) and seroconversion in MIADA had good correlations with the titers and seroconversion measured by hemagglutination inhibition and microneutralization assays. Our study demonstrated that antibody landscape analysis by the MIADA can be used for influenza vaccine evaluations and characterization of influenza virus infections. Repeated influenza vaccination and natural infections generate complex immune profiles in humans that require antibody landscape analysis to assess immunity and evaluate vaccines. However, antibody landscape analyses are difficult to perform using traditional assays. Here, we developed a high-throughput, serum-sparing, multiplex influenza antibody detection assay (MIADA) and analyzed the antibody landscapes following influenza vaccination and infection. We showed that adults had broader antibody landscapes than children. Influenza vaccination and infection not only induced the strongest antibody responses to the hemagglutinins of the viruses of exposure, but also induced cross-reactive antibodies to novel influenza viruses that can be removed by serum adsorption. There is a good correlation between the median fluorescence intensity (MFI) measured by MIADA and hemagglutination inhibition/microneutralization titers. Antibody landscape analysis by the MIADA can be used in influenza vaccine evaluations, including the development of universal influenza vaccines and the characterization of influenza virus infections.

摘要

为了更好地了解流感病毒自然感染和接种疫苗后抗体景观的变化,我们开发了一种高通量的多重流感抗体检测分析(MIADA),其中包含来自 2009 年前的 A(H1N1)、A(H1N1)pdm09、A(H2N2)、A(H3N2)、A(H5N1)、A(H7N7)、A(H7N9)、A(H7N2)、A(H9N2)、A(H13N9)和流感 B 病毒的 42 种重组血凝素(rHA)(结构域和/或球形头部结构域)。通过 MIADA 分析了来自 5 个流感季节(2010 年至 2018 年)的 227 对疫苗接种者(儿童和成人)的人血清配对和 17 对从实时逆转录聚合酶链反应(rRT-PCR)确诊的 A(H1N1)pdm09、A(H3N2)或流感 B 病毒感染的成人的配对人血清,以及来自 5 个流感季节(2010 年至 2018 年)的 227 对疫苗接种者(儿童和成人)的人血清配对和 17 对从实时逆转录聚合酶链反应(rRT-PCR)确诊的 A(H1N1)pdm09、A(H3N2)或流感 B 病毒感染的成人的配对人血清。雪貂抗血清对暴露亚型 HA 表现出明显的特异性抗体反应。与幼儿(<3 岁)和年龄较大的儿童(9 至 17 岁)相比,成年人(19 至 49 岁)在基线和接种疫苗后都具有更广泛的抗体景观。流感疫苗接种和感染诱导了针对暴露株/亚型病毒和密切相关株的最强抗体反应;它们还诱导了针对未暴露的流感病毒亚型(包括新型病毒)的交叉反应性抗体。随后的血清吸附证实,针对新型 HA 的交叉反应性抗体主要是由暴露于 A(H1N1)/A(H3N2)流感 A 病毒引起的。相比之下,感染流感 B 病毒的成年人则对两种流感 B 病毒谱系 HA 产生了主要的特异性抗体反应。中位数荧光强度(MFI)和 MIADA 中的血清转化率与血凝抑制和微量中和测定中测量的滴度和血清转化率具有良好的相关性。我们的研究表明,MIADA 的抗体景观分析可用于流感疫苗评估和流感病毒感染的特征描述。重复的流感疫苗接种和自然感染在人体内产生了复杂的免疫特征,需要进行抗体景观分析来评估免疫和评估疫苗。然而,使用传统检测方法很难进行抗体景观分析。在这里,我们开发了一种高通量、节省血清、多重流感抗体检测分析(MIADA),并分析了流感疫苗接种和感染后的抗体景观。我们表明,成年人的抗体景观比儿童更广泛。流感疫苗接种和感染不仅诱导了针对暴露病毒血凝素的最强抗体反应,还诱导了可通过血清吸附去除的新型流感病毒的交叉反应性抗体。MIADA 测量的中位数荧光强度(MFI)与血凝抑制/微量中和滴度之间存在良好的相关性。MIADA 的抗体景观分析可用于流感疫苗评估,包括通用流感疫苗的开发和流感病毒感染的特征描述。

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