Development of neutralizing antibodies against SARS-CoV-2, using a high-throughput single-B-cell cloning method
© The Author(s) 2023. Published by Oxford University Press on behalf of Antibody Therapeutics. All rights reserved. For permissions, please e-mail: journals.permissionsoup.com..
Background: Rapid and efficient strategies are needed to discover neutralizing antibodies (nAbs) from B cells derived from virus-infected patients.
Methods: Here, we report a high-throughput single-B-cell cloning method for high-throughput isolation of nAbs targeting diverse epitopes on the SARS-CoV-2-RBD (receptor binding domain) from convalescent COVID-19 patients. This method is simple, fast and highly efficient in generating SARS-CoV-2-neutralizing antibodies from COVID-19 patients' B cells.
Results: Using this method, we have developed multiple nAbs against distinct SARS-CoV-2-RBD epitopes. CryoEM and crystallography revealed precisely how they bind RBD. In live virus assay, these nAbs are effective in blocking viral entry to the host cells.
Conclusion: This simple and efficient method may be useful in developing human therapeutic antibodies for other diseases and next pandemic.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:6 |
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Enthalten in: |
Antibody therapeutics - 6(2023), 2 vom: 05. Apr., Seite 76-86 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Dou, Yang [VerfasserIn] |
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Anmerkungen: |
Date Revised 21.04.2023 published: Electronic-eCollection Citation Status PubMed-not-MEDLINE |
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doi: |
10.1093/abt/tbad002 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM355812819 |
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245 | 1 | 0 | |a Development of neutralizing antibodies against SARS-CoV-2, using a high-throughput single-B-cell cloning method |
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520 | |a © The Author(s) 2023. Published by Oxford University Press on behalf of Antibody Therapeutics. All rights reserved. For permissions, please e-mail: journals.permissionsoup.com. | ||
520 | |a Background: Rapid and efficient strategies are needed to discover neutralizing antibodies (nAbs) from B cells derived from virus-infected patients | ||
520 | |a Methods: Here, we report a high-throughput single-B-cell cloning method for high-throughput isolation of nAbs targeting diverse epitopes on the SARS-CoV-2-RBD (receptor binding domain) from convalescent COVID-19 patients. This method is simple, fast and highly efficient in generating SARS-CoV-2-neutralizing antibodies from COVID-19 patients' B cells | ||
520 | |a Results: Using this method, we have developed multiple nAbs against distinct SARS-CoV-2-RBD epitopes. CryoEM and crystallography revealed precisely how they bind RBD. In live virus assay, these nAbs are effective in blocking viral entry to the host cells | ||
520 | |a Conclusion: This simple and efficient method may be useful in developing human therapeutic antibodies for other diseases and next pandemic | ||
650 | 4 | |a Journal Article | |
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700 | 1 | |a Deng, Yong-Qiang |e verfasserin |4 aut | |
700 | 1 | |a Jia, Zijing |e verfasserin |4 aut | |
700 | 1 | |a Lan, Jun |e verfasserin |4 aut | |
700 | 1 | |a Xu, Xiaoyu |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Guorui |e verfasserin |4 aut | |
700 | 1 | |a Cao, Tianshu |e verfasserin |4 aut | |
700 | 1 | |a Liu, Pan |e verfasserin |4 aut | |
700 | 1 | |a Wang, Xiangxi |e verfasserin |4 aut | |
700 | 1 | |a Wang, Xinquan |e verfasserin |4 aut | |
700 | 1 | |a Xu, Lingjie |e verfasserin |4 aut | |
700 | 1 | |a Du, Pan |e verfasserin |4 aut | |
700 | 1 | |a Qin, Cheng-Feng |e verfasserin |4 aut | |
700 | 1 | |a Liu, Hong |e verfasserin |4 aut | |
700 | 1 | |a Li, Yafeng |e verfasserin |4 aut | |
700 | 1 | |a Wu, Guizhen |e verfasserin |4 aut | |
700 | 1 | |a Wang, Kang |e verfasserin |4 aut | |
700 | 1 | |a Lu, Bai |e verfasserin |4 aut | |
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