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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Veröffentlicht in:PLoS pathogens 2021-10, Vol.17 (10), p.e1009704-e1009704
Hauptverfasser: 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
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container_end_page e1009704
container_issue 10
container_start_page e1009704
container_title PLoS pathogens
container_volume 17
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
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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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Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Su, Shih-Chieh</au><au>Yang, Tzu-Jing</au><au>Yu, Pei-Yu</au><au>Liang, Kang-Hao</au><au>Chen, Wan-Yu</au><au>Yang, Chun-Wei</au><au>Lin, Hsiu-Ting</au><au>Wang, Mei-Jung</au><au>Lu, Ruei-Min</au><au>Tso, Hsien-Cheng</au><au>Chung, Meng-Jhe</au><au>Hsieh, Tzung-Yang</au><au>Chang, Yu-Ling</au><au>Lin, Shin-Chang</au><au>Hsu, Fang-Yu</au><au>Ke, Feng-Yi</au><au>Wu, Yi-Hsuan</au><au>Hwang, Yu-Chyi</au><au>Liu, I-Ju</au><au>Liang, Jian-Jong</au><au>Liao, Chun-Che</au><au>Ko, Hui-Ying</au><au>Sun, Cheng-Pu</au><au>Wu, Ping-Yi</au><au>Jan, Jia-Tsrong</au><au>Chang, Yuan-Chih</au><au>Lin, Yi-Ling</au><au>Tao, Mi-Hua</au><au>Hsu, Shang-Te Danny</au><au>Wu, Han-Chung</au><au>Subbarao, Kanta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure-guided antibody cocktail for prevention and treatment of COVID-19</atitle><jtitle>PLoS pathogens</jtitle><date>2021-10-21</date><risdate>2021</risdate><volume>17</volume><issue>10</issue><spage>e1009704</spage><epage>e1009704</epage><pages>e1009704-e1009704</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>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.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>34673836</pmid><doi>10.1371/journal.ppat.1009704</doi><orcidid>https://orcid.org/0000-0002-0289-3768</orcidid><orcidid>https://orcid.org/0000-0002-5185-1169</orcidid><oa>free_for_read</oa></addata></record>
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1553-7374
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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
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