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芯片上的人群:用于流感血清分型的无标记人源单克隆抗体阵列。

Crowd on a Chip: Label-Free Human Monoclonal Antibody Arrays for Serotyping Influenza.

机构信息

Department of Dermatology , University of Rochester Medical Center , Rochester , New York 14642 , United States.

Materials Science Program , University of Rochester , Rochester , New York 14627 , United States.

出版信息

Anal Chem. 2018 Aug 7;90(15):9583-9590. doi: 10.1021/acs.analchem.8b02479. Epub 2018 Jul 20.

Abstract

Rapid changes in influenza A virus (IAV) antigenicity create challenges in surveillance, disease diagnosis, and vaccine development. Further, serological methods for studying antigenic properties of influenza viruses often rely on animal models and therefore may not fully reflect the dynamics of human immunity. We hypothesized that arrays of human monoclonal antibodies (hmAbs) to influenza could be employed in a pattern-recognition approach to expedite IAV serology and to study the antigenic evolution of newly emerging viruses. Using the multiplex, label-free Arrayed Imaging Reflectometry (AIR) platform, we have demonstrated that such arrays readily discriminated among various subtypes of IAVs, including H1, H3 seasonal strains, and avian-sourced human H7 viruses. Array responses also allowed the first determination of antigenic relationships among IAV strains directly from hmAb responses. Finally, correlation analysis of antibody binding to all tested IAV subtypes allowed efficient identification of broadly reactive clones. In addition to specific applications in the context of understanding influenza biology with potential utility in "universal" flu vaccine development, these studies validate AIR as a platform technology for studying antigenic properties of viruses and also antibody properties in a high-throughput manner. We further anticipate that this approach will facilitate advances in the study of other viral pathogens.

摘要

甲型流感病毒 (IAV) 抗原性的快速变化给监测、疾病诊断和疫苗开发带来了挑战。此外,用于研究流感病毒抗原特性的血清学方法通常依赖于动物模型,因此可能无法完全反映人类免疫的动态。我们假设,可以将针对流感的人源单克隆抗体 (hmAb) 阵列用于模式识别方法,以加快 IAV 血清学检测,并研究新出现病毒的抗原进化。我们使用多重、无标记的 Arrayed Imaging Reflectometry (AIR) 平台,证明了这些阵列可以轻松区分各种亚型的 IAV,包括 H1、H3 季节性菌株和源自禽类的人源 H7 病毒。阵列反应还允许直接从 hmAb 反应中确定 IAV 菌株之间的抗原关系。最后,对所有测试的 IAV 亚型的抗体结合进行相关分析,可有效地识别出广泛反应性的克隆。除了在了解流感生物学方面的特定应用,可能对“通用”流感疫苗开发具有潜在用途外,这些研究还验证了 AIR 作为一种平台技术,可用于高通量地研究病毒的抗原特性以及抗体特性。我们进一步预计,这种方法将促进其他病毒病原体研究的进展。

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