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流感病毒疫苗接种后的抗体趋同进化和克隆型扩增。

Convergent antibody evolution and clonotype expansion following influenza virus vaccination.

机构信息

Center for Vaccines and Immunology, University of Georgia, Athens, GA, United States of America.

Atreca, Inc., South San Francisco, CA, United States of America.

出版信息

PLoS One. 2021 Feb 22;16(2):e0247253. doi: 10.1371/journal.pone.0247253. eCollection 2021.

DOI:10.1371/journal.pone.0247253
PMID:33617543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7899375/
Abstract

Recent advances in high-throughput single cell sequencing have opened up new avenues into the investigation of B cell receptor (BCR) repertoires. In this study, PBMCs were collected from 17 human participants vaccinated with the split-inactivated influenza virus vaccine during the 2016-2017 influenza season. A combination of Immune Repertoire Capture (IRCTM) technology and IgG sequencing was performed on ~7,800 plasmablast (PB) cells and preferential IgG heavy-light chain pairings were investigated. In some participants, a single expanded clonotype accounted for ~22% of their PB BCR repertoire. Approximately 60% (10/17) of participants experienced convergent evolution, possessing public PBs that were elicited independently in multiple participants. Binding profiles of one private and three public PBs confirmed they were all subtype-specific, cross-reactive hemagglutinin (HA) head-directed antibodies. Collectively, this high-resolution antibody repertoire analysis demonstrated the impact evolution can have on BCRs in response to influenza virus vaccination, which can guide future universal influenza prophylactic approaches.

摘要

高通量单细胞测序的最新进展为研究 B 细胞受体 (BCR) 库开辟了新途径。在这项研究中,从 17 名在 2016-2017 流感季节接种流感病毒裂解疫苗的人类参与者中采集 PBMC。对约 7800 个浆母细胞 (PB) 细胞进行了免疫受体捕获 (IRCTM) 技术和 IgG 测序的组合,并研究了优先 IgG 重轻链配对。在一些参与者中,单一扩展克隆型占其 PB BCR 库的~22%。大约 60%(17 人中的 10 人)经历了趋同进化,具有在多个参与者中独立诱导的公共 PB。一个私有和三个公共 PB 的结合谱证实它们都是亚型特异性的、交叉反应的血凝素 (HA) 头部定向抗体。总的来说,这项高分辨率抗体库分析表明,进化对流感病毒疫苗接种后 BCR 产生的影响,可以指导未来通用流感预防方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/e9de82b944ee/pone.0247253.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/f8e49aa934fd/pone.0247253.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/ef301c43a3e2/pone.0247253.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/7548ca1d75ad/pone.0247253.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/fd0cbc3e03d9/pone.0247253.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/eb895e209b91/pone.0247253.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/e9de82b944ee/pone.0247253.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/f8e49aa934fd/pone.0247253.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/ef301c43a3e2/pone.0247253.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/7548ca1d75ad/pone.0247253.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/fd0cbc3e03d9/pone.0247253.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/eb895e209b91/pone.0247253.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f5/7899375/e9de82b944ee/pone.0247253.g006.jpg

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