Structure-guided antibody cocktail for prevention and treatment of COVID-19
Development of effective therapeutics for mitigating the COVID-19 pandemic is a pressing global need. Neutralizing antibodies are known to be effective antivirals, as they can be rapidly deployed to prevent disease progression and can accelerate patient recovery without the need for fully developed...
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creator | Su, Shih-Chieh Yang, Tzu-Jing Yu, Pei-Yu Liang, Kang-Hao Chen, Wan-Yu Yang, Chun-Wei Lin, Hsiu-Ting Wang, Mei-Jung Lu, Ruei-Min Tso, Hsien-Cheng Chung, Meng-Jhe Hsieh, Tzung-Yang Chang, Yu-Ling Lin, Shin-Chang Hsu, Fang-Yu Ke, Feng-Yi Wu, Yi-Hsuan Hwang, Yu-Chyi Liu, I-Ju Liang, Jian-Jong Liao, Chun-Che Ko, Hui-Ying Sun, Cheng-Pu Wu, Ping-Yi Jan, Jia-Tsrong Chang, Yuan-Chih Lin, Yi-Ling Tao, Mi-Hua Hsu, Shang-Te Danny Wu, Han-Chung |
description | Development of effective therapeutics for mitigating the COVID-19 pandemic is a pressing global need. Neutralizing antibodies are known to be effective antivirals, as they can be rapidly deployed to prevent disease progression and can accelerate patient recovery without the need for fully developed host immunity. Here, we report the generation and characterization of a series of chimeric antibodies against the receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Some of these antibodies exhibit exceptionally potent neutralization activities in vitro and in vivo, and the most potent of our antibodies target three distinct non-overlapping epitopes within the RBD. Cryo-electron microscopy analyses of two highly potent antibodies in complex with the SARS-CoV-2 spike protein suggested they may be particularly useful when combined in a cocktail therapy. The efficacy of this antibody cocktail was confirmed in SARS-CoV-2-infected mouse and hamster models as prophylactic and post-infection treatments. With the emergence of more contagious variants of SARS-CoV-2, cocktail antibody therapies hold great promise to control disease and prevent drug resistance. |
doi_str_mv | 10.1371/journal.ppat.1009704 |
format | Article |
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Neutralizing antibodies are known to be effective antivirals, as they can be rapidly deployed to prevent disease progression and can accelerate patient recovery without the need for fully developed host immunity. Here, we report the generation and characterization of a series of chimeric antibodies against the receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Some of these antibodies exhibit exceptionally potent neutralization activities in vitro and in vivo, and the most potent of our antibodies target three distinct non-overlapping epitopes within the RBD. Cryo-electron microscopy analyses of two highly potent antibodies in complex with the SARS-CoV-2 spike protein suggested they may be particularly useful when combined in a cocktail therapy. The efficacy of this antibody cocktail was confirmed in SARS-CoV-2-infected mouse and hamster models as prophylactic and post-infection treatments. With the emergence of more contagious variants of SARS-CoV-2, cocktail antibody therapies hold great promise to control disease and prevent drug resistance.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1009704</identifier><identifier>PMID: 34673836</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Animal models ; Antibodies ; Antiviral agents ; Biology and life sciences ; Cloning ; Composition ; Coronaviruses ; COVID-19 ; Disease control ; Disease resistance ; Drug development ; Drug resistance ; Electron microscopy ; Epitopes ; Health aspects ; Immunological research ; Immunotherapy ; Infections ; Medicine and health sciences ; Middle East respiratory syndrome ; Monoclonal antibodies ; Neutralization ; Pandemics ; Prevention ; Proteins ; Research and Analysis Methods ; Respiratory diseases ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Spike protein ; Viral antibodies ; Viral diseases ; Viral proteins</subject><ispartof>PLoS pathogens, 2021-10, Vol.17 (10), p.e1009704-e1009704</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Su et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Su et al 2021 Su et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c638t-fcbe15c8da97e69f11e8f568cd6d836f1c555a633dce066248d8734b1fecdd483</citedby><cites>FETCH-LOGICAL-c638t-fcbe15c8da97e69f11e8f568cd6d836f1c555a633dce066248d8734b1fecdd483</cites><orcidid>0000-0002-0289-3768 ; 0000-0002-5185-1169</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530329/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530329/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53769,53771,79346,79347</link.rule.ids></links><search><contributor>Subbarao, Kanta</contributor><creatorcontrib>Su, Shih-Chieh</creatorcontrib><creatorcontrib>Yang, Tzu-Jing</creatorcontrib><creatorcontrib>Yu, Pei-Yu</creatorcontrib><creatorcontrib>Liang, Kang-Hao</creatorcontrib><creatorcontrib>Chen, Wan-Yu</creatorcontrib><creatorcontrib>Yang, Chun-Wei</creatorcontrib><creatorcontrib>Lin, Hsiu-Ting</creatorcontrib><creatorcontrib>Wang, Mei-Jung</creatorcontrib><creatorcontrib>Lu, Ruei-Min</creatorcontrib><creatorcontrib>Tso, Hsien-Cheng</creatorcontrib><creatorcontrib>Chung, Meng-Jhe</creatorcontrib><creatorcontrib>Hsieh, Tzung-Yang</creatorcontrib><creatorcontrib>Chang, Yu-Ling</creatorcontrib><creatorcontrib>Lin, Shin-Chang</creatorcontrib><creatorcontrib>Hsu, Fang-Yu</creatorcontrib><creatorcontrib>Ke, Feng-Yi</creatorcontrib><creatorcontrib>Wu, Yi-Hsuan</creatorcontrib><creatorcontrib>Hwang, Yu-Chyi</creatorcontrib><creatorcontrib>Liu, I-Ju</creatorcontrib><creatorcontrib>Liang, Jian-Jong</creatorcontrib><creatorcontrib>Liao, Chun-Che</creatorcontrib><creatorcontrib>Ko, Hui-Ying</creatorcontrib><creatorcontrib>Sun, Cheng-Pu</creatorcontrib><creatorcontrib>Wu, Ping-Yi</creatorcontrib><creatorcontrib>Jan, Jia-Tsrong</creatorcontrib><creatorcontrib>Chang, Yuan-Chih</creatorcontrib><creatorcontrib>Lin, Yi-Ling</creatorcontrib><creatorcontrib>Tao, Mi-Hua</creatorcontrib><creatorcontrib>Hsu, Shang-Te Danny</creatorcontrib><creatorcontrib>Wu, Han-Chung</creatorcontrib><title>Structure-guided antibody cocktail for prevention and treatment of COVID-19</title><title>PLoS pathogens</title><description>Development of effective therapeutics for mitigating the COVID-19 pandemic is a pressing global need. Neutralizing antibodies are known to be effective antivirals, as they can be rapidly deployed to prevent disease progression and can accelerate patient recovery without the need for fully developed host immunity. Here, we report the generation and characterization of a series of chimeric antibodies against the receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Some of these antibodies exhibit exceptionally potent neutralization activities in vitro and in vivo, and the most potent of our antibodies target three distinct non-overlapping epitopes within the RBD. Cryo-electron microscopy analyses of two highly potent antibodies in complex with the SARS-CoV-2 spike protein suggested they may be particularly useful when combined in a cocktail therapy. The efficacy of this antibody cocktail was confirmed in SARS-CoV-2-infected mouse and hamster models as prophylactic and post-infection treatments. With the emergence of more contagious variants of SARS-CoV-2, cocktail antibody therapies hold great promise to control disease and prevent drug resistance.</description><subject>Animal models</subject><subject>Antibodies</subject><subject>Antiviral agents</subject><subject>Biology and life sciences</subject><subject>Cloning</subject><subject>Composition</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Disease control</subject><subject>Disease resistance</subject><subject>Drug development</subject><subject>Drug resistance</subject><subject>Electron microscopy</subject><subject>Epitopes</subject><subject>Health aspects</subject><subject>Immunological research</subject><subject>Immunotherapy</subject><subject>Infections</subject><subject>Medicine and health sciences</subject><subject>Middle East respiratory syndrome</subject><subject>Monoclonal 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Neutralizing antibodies are known to be effective antivirals, as they can be rapidly deployed to prevent disease progression and can accelerate patient recovery without the need for fully developed host immunity. Here, we report the generation and characterization of a series of chimeric antibodies against the receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Some of these antibodies exhibit exceptionally potent neutralization activities in vitro and in vivo, and the most potent of our antibodies target three distinct non-overlapping epitopes within the RBD. Cryo-electron microscopy analyses of two highly potent antibodies in complex with the SARS-CoV-2 spike protein suggested they may be particularly useful when combined in a cocktail therapy. The efficacy of this antibody cocktail was confirmed in SARS-CoV-2-infected mouse and hamster models as prophylactic and post-infection treatments. 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language | eng |
recordid | cdi_plos_journals_2598100919 |
source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Public Library of Science (PLoS); PubMed Central |
subjects | Animal models Antibodies Antiviral agents Biology and life sciences Cloning Composition Coronaviruses COVID-19 Disease control Disease resistance Drug development Drug resistance Electron microscopy Epitopes Health aspects Immunological research Immunotherapy Infections Medicine and health sciences Middle East respiratory syndrome Monoclonal antibodies Neutralization Pandemics Prevention Proteins Research and Analysis Methods Respiratory diseases Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Spike protein Viral antibodies Viral diseases Viral proteins |
title | Structure-guided antibody cocktail for prevention and treatment of COVID-19 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T12%3A35%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structure-guided%20antibody%20cocktail%20for%20prevention%20and%20treatment%20of%20COVID-19&rft.jtitle=PLoS%20pathogens&rft.au=Su,%20Shih-Chieh&rft.date=2021-10-21&rft.volume=17&rft.issue=10&rft.spage=e1009704&rft.epage=e1009704&rft.pages=e1009704-e1009704&rft.issn=1553-7374&rft.eissn=1553-7374&rft_id=info:doi/10.1371/journal.ppat.1009704&rft_dat=%3Cgale_plos_%3EA681018714%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2598100919&rft_id=info:pmid/34673836&rft_galeid=A681018714&rft_doaj_id=oai_doaj_org_article_16354bc5faef45df8f05181199b75656&rfr_iscdi=true |