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Broadly neutralizing anti-S2 antibodies protect against all three human betacoronaviruses that cause deadly disease
Pan-betacoronavirus neutralizing antibodies may hold the key to developing broadly protective vaccines against novel pandemic coronaviruses and to more effectively respond to SARS-CoV-2 variants. The emergence of Omicron and subvariants of SARS-CoV-2 illustrates the limitations of solely targeting t...
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Published in: | Immunity (Cambridge, Mass.) Mass.), 2023-03, Vol.56 (3), p.669-686.e7 |
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creator | Zhou, Panpan Song, Ge Liu, Hejun Yuan, Meng He, Wan-ting Beutler, Nathan Zhu, Xueyong Tse, Longping V. Martinez, David R. Schäfer, Alexandra Anzanello, Fabio Yong, Peter Peng, Linghang Dueker, Katharina Musharrafieh, Rami Callaghan, Sean Capozzola, Tazio Limbo, Oliver Parren, Mara Garcia, Elijah Rawlings, Stephen A. Smith, Davey M. Nemazee, David Jardine, Joseph G. Safonova, Yana Briney, Bryan Rogers, Thomas F. Wilson, Ian A. Baric, Ralph S. Gralinski, Lisa E. Burton, Dennis R. Andrabi, Raiees |
description | Pan-betacoronavirus neutralizing antibodies may hold the key to developing broadly protective vaccines against novel pandemic coronaviruses and to more effectively respond to SARS-CoV-2 variants. The emergence of Omicron and subvariants of SARS-CoV-2 illustrates the limitations of solely targeting the receptor-binding domain (RBD) of the spike (S) protein. Here, we isolated a large panel of broadly neutralizing antibodies (bnAbs) from SARS-CoV-2 recovered-vaccinated donors, which targets a conserved S2 region in the betacoronavirus spike fusion machinery. Select bnAbs showed broad in vivo protection against all three deadly betacoronaviruses, SARS-CoV-1, SARS-CoV-2, and MERS-CoV, which have spilled over into humans in the past two decades. Structural studies of these bnAbs delineated the molecular basis for their broad reactivity and revealed common antibody features targetable by broad vaccination strategies. These bnAbs provide new insights and opportunities for antibody-based interventions and for developing pan-betacoronavirus vaccines.
[Display omitted]
•Isolated a large panel of stem-helix bnAbs from SARS-CoV-2 recovered-vaccinated humans•Stem-helix bnAbs possess recurrent germline features desired for targeted vaccines•IGHV1-46-encoded stem-helix bnAbs are public clonotypes with two binding modes•Stem-helix bnAbs prophylactically protect against SARS-CoV-1, SARS-CoV-2, and MERS-CoV challenge
Pan-betacoronavirus broadly neutralizing antibodies (bnAbs) may hold the key to developing broadly protective vaccines against pandemic coronaviruses and SARS-CoV-2 variants. Zhou et al. isolate a large panel of S2 stem-helix bnAbs to betacoronaviruses and reveal their public features. Select stem-helix bnAbs protect against all three human betacoronaviruses that cause deadly disease. |
doi_str_mv | 10.1016/j.immuni.2023.02.005 |
format | article |
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[Display omitted]
•Isolated a large panel of stem-helix bnAbs from SARS-CoV-2 recovered-vaccinated humans•Stem-helix bnAbs possess recurrent germline features desired for targeted vaccines•IGHV1-46-encoded stem-helix bnAbs are public clonotypes with two binding modes•Stem-helix bnAbs prophylactically protect against SARS-CoV-1, SARS-CoV-2, and MERS-CoV challenge
Pan-betacoronavirus broadly neutralizing antibodies (bnAbs) may hold the key to developing broadly protective vaccines against pandemic coronaviruses and SARS-CoV-2 variants. Zhou et al. isolate a large panel of S2 stem-helix bnAbs to betacoronaviruses and reveal their public features. Select stem-helix bnAbs protect against all three human betacoronaviruses that cause deadly disease.</description><identifier>ISSN: 1074-7613</identifier><identifier>ISSN: 1097-4180</identifier><identifier>EISSN: 1097-4180</identifier><identifier>DOI: 10.1016/j.immuni.2023.02.005</identifier><identifier>PMID: 36889306</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antibodies, Neutralizing ; Antibodies, Viral ; broad coronavirus protection ; Broadly Neutralizing Antibodies ; coronavirus spike ; coronaviruses ; COVID-19 ; Humans ; Immunology ; pan-betacoronavirus vaccines ; S2 stem-helix site ; SARS-CoV-2 ; SARS-CoV-2 variants of concern</subject><ispartof>Immunity (Cambridge, Mass.), 2023-03, Vol.56 (3), p.669-686.e7</ispartof><rights>2023 The Author(s)</rights><rights>Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-8567a128deb615ced6015be7e51905e3ec9cce47be57bb854859b7db2cc55d413</citedby><cites>FETCH-LOGICAL-c435t-8567a128deb615ced6015be7e51905e3ec9cce47be57bb854859b7db2cc55d413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36889306$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/servlets/purl/2423303$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Panpan</creatorcontrib><creatorcontrib>Song, Ge</creatorcontrib><creatorcontrib>Liu, Hejun</creatorcontrib><creatorcontrib>Yuan, Meng</creatorcontrib><creatorcontrib>He, Wan-ting</creatorcontrib><creatorcontrib>Beutler, Nathan</creatorcontrib><creatorcontrib>Zhu, Xueyong</creatorcontrib><creatorcontrib>Tse, Longping V.</creatorcontrib><creatorcontrib>Martinez, David R.</creatorcontrib><creatorcontrib>Schäfer, Alexandra</creatorcontrib><creatorcontrib>Anzanello, Fabio</creatorcontrib><creatorcontrib>Yong, Peter</creatorcontrib><creatorcontrib>Peng, Linghang</creatorcontrib><creatorcontrib>Dueker, Katharina</creatorcontrib><creatorcontrib>Musharrafieh, Rami</creatorcontrib><creatorcontrib>Callaghan, Sean</creatorcontrib><creatorcontrib>Capozzola, Tazio</creatorcontrib><creatorcontrib>Limbo, Oliver</creatorcontrib><creatorcontrib>Parren, Mara</creatorcontrib><creatorcontrib>Garcia, Elijah</creatorcontrib><creatorcontrib>Rawlings, Stephen A.</creatorcontrib><creatorcontrib>Smith, Davey M.</creatorcontrib><creatorcontrib>Nemazee, David</creatorcontrib><creatorcontrib>Jardine, Joseph G.</creatorcontrib><creatorcontrib>Safonova, Yana</creatorcontrib><creatorcontrib>Briney, Bryan</creatorcontrib><creatorcontrib>Rogers, Thomas F.</creatorcontrib><creatorcontrib>Wilson, Ian A.</creatorcontrib><creatorcontrib>Baric, Ralph S.</creatorcontrib><creatorcontrib>Gralinski, Lisa E.</creatorcontrib><creatorcontrib>Burton, Dennis R.</creatorcontrib><creatorcontrib>Andrabi, Raiees</creatorcontrib><creatorcontrib>Argonne National Laboratory (ANL), Argonne, IL (United States). Advanced Photon Source (APS)</creatorcontrib><title>Broadly neutralizing anti-S2 antibodies protect against all three human betacoronaviruses that cause deadly disease</title><title>Immunity (Cambridge, Mass.)</title><addtitle>Immunity</addtitle><description>Pan-betacoronavirus neutralizing antibodies may hold the key to developing broadly protective vaccines against novel pandemic coronaviruses and to more effectively respond to SARS-CoV-2 variants. The emergence of Omicron and subvariants of SARS-CoV-2 illustrates the limitations of solely targeting the receptor-binding domain (RBD) of the spike (S) protein. Here, we isolated a large panel of broadly neutralizing antibodies (bnAbs) from SARS-CoV-2 recovered-vaccinated donors, which targets a conserved S2 region in the betacoronavirus spike fusion machinery. Select bnAbs showed broad in vivo protection against all three deadly betacoronaviruses, SARS-CoV-1, SARS-CoV-2, and MERS-CoV, which have spilled over into humans in the past two decades. Structural studies of these bnAbs delineated the molecular basis for their broad reactivity and revealed common antibody features targetable by broad vaccination strategies. These bnAbs provide new insights and opportunities for antibody-based interventions and for developing pan-betacoronavirus vaccines.
[Display omitted]
•Isolated a large panel of stem-helix bnAbs from SARS-CoV-2 recovered-vaccinated humans•Stem-helix bnAbs possess recurrent germline features desired for targeted vaccines•IGHV1-46-encoded stem-helix bnAbs are public clonotypes with two binding modes•Stem-helix bnAbs prophylactically protect against SARS-CoV-1, SARS-CoV-2, and MERS-CoV challenge
Pan-betacoronavirus broadly neutralizing antibodies (bnAbs) may hold the key to developing broadly protective vaccines against pandemic coronaviruses and SARS-CoV-2 variants. Zhou et al. isolate a large panel of S2 stem-helix bnAbs to betacoronaviruses and reveal their public features. Select stem-helix bnAbs protect against all three human betacoronaviruses that cause deadly disease.</description><subject>Antibodies, Neutralizing</subject><subject>Antibodies, Viral</subject><subject>broad coronavirus protection</subject><subject>Broadly Neutralizing Antibodies</subject><subject>coronavirus spike</subject><subject>coronaviruses</subject><subject>COVID-19</subject><subject>Humans</subject><subject>Immunology</subject><subject>pan-betacoronavirus vaccines</subject><subject>S2 stem-helix site</subject><subject>SARS-CoV-2</subject><subject>SARS-CoV-2 variants of concern</subject><issn>1074-7613</issn><issn>1097-4180</issn><issn>1097-4180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kctu1jAQhS0EoqXwBghZrNgk-BonGySooCBVYgGsLV-m_f0rsYvtVCpPj9OULlmdWXzjM8cHodeU9JTQ4f2xD8uyxtAzwnhPWE-IfIJOKZlUJ-hInm6zEp0aKD9BL0o5EkKFnMhzdMKHcZw4GU5R-ZST8fMdjrDWbObwJ8RrbGIN3Q92rzb5AAXf5FTBVWyuTYil6TzjesgA-LAuJmIL1biUUzS3Ia-lbdSDqdiZNmMP9x4-FDAFXqJnV2Yu8OpBz9CvL59_nn_tLr9ffDv_eNk5wWXtRjkoQ9nowQ5UOvADodKCAkknIoGDm5wDoSxIZe0oxSgnq7xlzknpBeVn6O3-bio16OJCC3BwKcaWQzPBOCe8Qe92qAX8vUKpegnFwTybCGktmqmx-Q0TVw0VO-pyKiXDlb7JYTH5TlOit070Ue-d6K0TTZhunbS1Nw8Oq13APy79K6EBH3YA2mfcBsjbrRBb4pC3U30K_3f4C54-oUU</recordid><startdate>20230314</startdate><enddate>20230314</enddate><creator>Zhou, Panpan</creator><creator>Song, Ge</creator><creator>Liu, Hejun</creator><creator>Yuan, Meng</creator><creator>He, Wan-ting</creator><creator>Beutler, Nathan</creator><creator>Zhu, Xueyong</creator><creator>Tse, Longping V.</creator><creator>Martinez, David R.</creator><creator>Schäfer, Alexandra</creator><creator>Anzanello, Fabio</creator><creator>Yong, Peter</creator><creator>Peng, Linghang</creator><creator>Dueker, Katharina</creator><creator>Musharrafieh, Rami</creator><creator>Callaghan, Sean</creator><creator>Capozzola, Tazio</creator><creator>Limbo, Oliver</creator><creator>Parren, Mara</creator><creator>Garcia, Elijah</creator><creator>Rawlings, Stephen A.</creator><creator>Smith, Davey M.</creator><creator>Nemazee, David</creator><creator>Jardine, Joseph G.</creator><creator>Safonova, Yana</creator><creator>Briney, Bryan</creator><creator>Rogers, Thomas F.</creator><creator>Wilson, Ian A.</creator><creator>Baric, Ralph S.</creator><creator>Gralinski, Lisa E.</creator><creator>Burton, Dennis R.</creator><creator>Andrabi, Raiees</creator><general>Elsevier Inc</general><general>Cell Press</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>OIOZB</scope><scope>OTOTI</scope></search><sort><creationdate>20230314</creationdate><title>Broadly neutralizing anti-S2 antibodies protect against all three human betacoronaviruses that cause deadly disease</title><author>Zhou, Panpan ; Song, Ge ; Liu, Hejun ; Yuan, Meng ; He, Wan-ting ; Beutler, Nathan ; Zhu, Xueyong ; Tse, Longping V. ; Martinez, David R. ; Schäfer, Alexandra ; Anzanello, Fabio ; Yong, Peter ; Peng, Linghang ; Dueker, Katharina ; Musharrafieh, Rami ; Callaghan, Sean ; Capozzola, Tazio ; Limbo, Oliver ; Parren, Mara ; Garcia, Elijah ; Rawlings, Stephen A. ; Smith, Davey M. ; Nemazee, David ; Jardine, Joseph G. ; Safonova, Yana ; Briney, Bryan ; Rogers, Thomas F. ; Wilson, Ian A. ; Baric, Ralph S. ; Gralinski, Lisa E. ; Burton, Dennis R. ; Andrabi, Raiees</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-8567a128deb615ced6015be7e51905e3ec9cce47be57bb854859b7db2cc55d413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antibodies, Neutralizing</topic><topic>Antibodies, Viral</topic><topic>broad coronavirus protection</topic><topic>Broadly Neutralizing Antibodies</topic><topic>coronavirus spike</topic><topic>coronaviruses</topic><topic>COVID-19</topic><topic>Humans</topic><topic>Immunology</topic><topic>pan-betacoronavirus vaccines</topic><topic>S2 stem-helix site</topic><topic>SARS-CoV-2</topic><topic>SARS-CoV-2 variants of concern</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Panpan</creatorcontrib><creatorcontrib>Song, Ge</creatorcontrib><creatorcontrib>Liu, Hejun</creatorcontrib><creatorcontrib>Yuan, Meng</creatorcontrib><creatorcontrib>He, Wan-ting</creatorcontrib><creatorcontrib>Beutler, Nathan</creatorcontrib><creatorcontrib>Zhu, Xueyong</creatorcontrib><creatorcontrib>Tse, Longping V.</creatorcontrib><creatorcontrib>Martinez, David R.</creatorcontrib><creatorcontrib>Schäfer, Alexandra</creatorcontrib><creatorcontrib>Anzanello, Fabio</creatorcontrib><creatorcontrib>Yong, Peter</creatorcontrib><creatorcontrib>Peng, Linghang</creatorcontrib><creatorcontrib>Dueker, Katharina</creatorcontrib><creatorcontrib>Musharrafieh, Rami</creatorcontrib><creatorcontrib>Callaghan, Sean</creatorcontrib><creatorcontrib>Capozzola, Tazio</creatorcontrib><creatorcontrib>Limbo, Oliver</creatorcontrib><creatorcontrib>Parren, Mara</creatorcontrib><creatorcontrib>Garcia, Elijah</creatorcontrib><creatorcontrib>Rawlings, Stephen A.</creatorcontrib><creatorcontrib>Smith, Davey M.</creatorcontrib><creatorcontrib>Nemazee, David</creatorcontrib><creatorcontrib>Jardine, Joseph G.</creatorcontrib><creatorcontrib>Safonova, Yana</creatorcontrib><creatorcontrib>Briney, Bryan</creatorcontrib><creatorcontrib>Rogers, Thomas F.</creatorcontrib><creatorcontrib>Wilson, Ian A.</creatorcontrib><creatorcontrib>Baric, Ralph S.</creatorcontrib><creatorcontrib>Gralinski, Lisa E.</creatorcontrib><creatorcontrib>Burton, Dennis R.</creatorcontrib><creatorcontrib>Andrabi, Raiees</creatorcontrib><creatorcontrib>Argonne National Laboratory (ANL), Argonne, IL (United States). Advanced Photon Source (APS)</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Immunity (Cambridge, Mass.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Panpan</au><au>Song, Ge</au><au>Liu, Hejun</au><au>Yuan, Meng</au><au>He, Wan-ting</au><au>Beutler, Nathan</au><au>Zhu, Xueyong</au><au>Tse, Longping V.</au><au>Martinez, David R.</au><au>Schäfer, Alexandra</au><au>Anzanello, Fabio</au><au>Yong, Peter</au><au>Peng, Linghang</au><au>Dueker, Katharina</au><au>Musharrafieh, Rami</au><au>Callaghan, Sean</au><au>Capozzola, Tazio</au><au>Limbo, Oliver</au><au>Parren, Mara</au><au>Garcia, Elijah</au><au>Rawlings, Stephen A.</au><au>Smith, Davey M.</au><au>Nemazee, David</au><au>Jardine, Joseph G.</au><au>Safonova, Yana</au><au>Briney, Bryan</au><au>Rogers, Thomas F.</au><au>Wilson, Ian A.</au><au>Baric, Ralph S.</au><au>Gralinski, Lisa E.</au><au>Burton, Dennis R.</au><au>Andrabi, Raiees</au><aucorp>Argonne National Laboratory (ANL), Argonne, IL (United States). Advanced Photon Source (APS)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Broadly neutralizing anti-S2 antibodies protect against all three human betacoronaviruses that cause deadly disease</atitle><jtitle>Immunity (Cambridge, Mass.)</jtitle><addtitle>Immunity</addtitle><date>2023-03-14</date><risdate>2023</risdate><volume>56</volume><issue>3</issue><spage>669</spage><epage>686.e7</epage><pages>669-686.e7</pages><issn>1074-7613</issn><issn>1097-4180</issn><eissn>1097-4180</eissn><abstract>Pan-betacoronavirus neutralizing antibodies may hold the key to developing broadly protective vaccines against novel pandemic coronaviruses and to more effectively respond to SARS-CoV-2 variants. The emergence of Omicron and subvariants of SARS-CoV-2 illustrates the limitations of solely targeting the receptor-binding domain (RBD) of the spike (S) protein. Here, we isolated a large panel of broadly neutralizing antibodies (bnAbs) from SARS-CoV-2 recovered-vaccinated donors, which targets a conserved S2 region in the betacoronavirus spike fusion machinery. Select bnAbs showed broad in vivo protection against all three deadly betacoronaviruses, SARS-CoV-1, SARS-CoV-2, and MERS-CoV, which have spilled over into humans in the past two decades. Structural studies of these bnAbs delineated the molecular basis for their broad reactivity and revealed common antibody features targetable by broad vaccination strategies. These bnAbs provide new insights and opportunities for antibody-based interventions and for developing pan-betacoronavirus vaccines.
[Display omitted]
•Isolated a large panel of stem-helix bnAbs from SARS-CoV-2 recovered-vaccinated humans•Stem-helix bnAbs possess recurrent germline features desired for targeted vaccines•IGHV1-46-encoded stem-helix bnAbs are public clonotypes with two binding modes•Stem-helix bnAbs prophylactically protect against SARS-CoV-1, SARS-CoV-2, and MERS-CoV challenge
Pan-betacoronavirus broadly neutralizing antibodies (bnAbs) may hold the key to developing broadly protective vaccines against pandemic coronaviruses and SARS-CoV-2 variants. Zhou et al. isolate a large panel of S2 stem-helix bnAbs to betacoronaviruses and reveal their public features. Select stem-helix bnAbs protect against all three human betacoronaviruses that cause deadly disease.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36889306</pmid><doi>10.1016/j.immuni.2023.02.005</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1074-7613 |
ispartof | Immunity (Cambridge, Mass.), 2023-03, Vol.56 (3), p.669-686.e7 |
issn | 1074-7613 1097-4180 1097-4180 |
language | eng |
recordid | cdi_osti_scitechconnect_2423303 |
source | BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS |
subjects | Antibodies, Neutralizing Antibodies, Viral broad coronavirus protection Broadly Neutralizing Antibodies coronavirus spike coronaviruses COVID-19 Humans Immunology pan-betacoronavirus vaccines S2 stem-helix site SARS-CoV-2 SARS-CoV-2 variants of concern |
title | Broadly neutralizing anti-S2 antibodies protect against all three human betacoronaviruses that cause deadly disease |
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