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恢复期寨卡病毒病患者抗体免疫谱的功能分析。

Functional Profiling of Antibody Immune Repertoires in Convalescent Zika Virus Disease Patients.

机构信息

Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, KS, United States.

Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, MD, United States.

出版信息

Front Immunol. 2021 Feb 24;12:615102. doi: 10.3389/fimmu.2021.615102. eCollection 2021.

DOI:10.3389/fimmu.2021.615102
PMID:33732238
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7959826/
Abstract

The re-emergence of Zika virus (ZIKV) caused widespread infections that were linked to Guillain-Barré syndrome in adults and congenital malformation in fetuses, and epidemiological data suggest that ZIKV infection can induce protective antibody responses. A more detailed understanding of anti-ZIKV antibody responses may lead to enhanced antibody discovery and improved vaccine designs against ZIKV and related flaviviruses. Here, we applied recently-invented library-scale antibody screening technologies to determine comprehensive functional molecular and genetic profiles of naturally elicited human anti-ZIKV antibodies in three convalescent individuals. We leveraged natively paired antibody yeast display and NGS to predict antibody cross-reactivities and coarse-grain antibody affinities, to perform in-depth immune profiling of IgM, IgG, and IgA antibody repertoires in peripheral blood, and to reveal virus maturation state-dependent antibody interactions. Repertoire-scale comparison of ZIKV VLP-specific and non-specific antibodies in the same individuals also showed that mean antibody somatic hypermutation levels were substantially influenced by donor-intrinsic characteristics. These data provide insights into antiviral antibody responses to ZIKV disease and outline systems-level strategies to track human antibody immune responses to emergent viral infections.

摘要

寨卡病毒(ZIKV)的再次出现导致了广泛的感染,这些感染与成年人的格林-巴利综合征和胎儿的先天畸形有关,流行病学数据表明,ZIKV 感染可以诱导保护性抗体反应。更详细地了解抗 ZIKV 抗体反应可能会导致增强的抗体发现,并改进针对 ZIKV 和相关黄病毒的疫苗设计。在这里,我们应用了最近发明的文库规模的抗体筛选技术,以确定来自三名恢复期个体的天然诱导的人抗 ZIKV 抗体的全面功能分子和遗传特征。我们利用天然配对的抗体酵母展示和 NGS 来预测抗体交叉反应性和粗粒度抗体亲和力,对外周血中的 IgM、IgG 和 IgA 抗体库进行深入的免疫分析,并揭示病毒成熟状态依赖性的抗体相互作用。在同一个体中对 ZIKV VLP 特异性和非特异性抗体的抗体库进行比较,还表明平均抗体体细胞超突变水平受到供体内在特征的显著影响。这些数据为寨卡病毒疾病的抗病毒抗体反应提供了深入的了解,并概述了跟踪人类抗体对新发病毒感染的免疫反应的系统级策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf9/7959826/a8202538ce63/fimmu-12-615102-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf9/7959826/a8202538ce63/fimmu-12-615102-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf9/7959826/461ac654bdfd/fimmu-12-615102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf9/7959826/a86538286cb8/fimmu-12-615102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf9/7959826/8b1e94b8d877/fimmu-12-615102-g003.jpg
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