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Article: An antibody class with a common CDRH3 motif broadly neutralizes sarbecoviruses

TitleAn antibody class with a common CDRH3 motif broadly neutralizes sarbecoviruses
Authors
Issue Date2022
Citation
Science Translational Medicine, 2022, v. 14 How to Cite?
AbstractThe devastation caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has made clear the importance of pandemic preparedness. To address future zoonotic outbreaks due to related viruses in the sarbecovirus subgenus, we identified a human monoclonal antibody, 10-40, that neutralized or bound all sarbecoviruses tested in vitro and protected against SARS-CoV-2 and SARS-CoV in vivo. Comparative studies with other receptor-binding domain (RBD)-directed antibodies showed 10-40 to have the greatest breadth against sarbecoviruses, suggesting that 10-40 is a promising agent for pandemic preparedness. Moreover, structural analyses on 10-40 and similar antibodies not only defined an epitope cluster in the inner face of the RBD that is well conserved among sarbecoviruses but also uncovered a distinct antibody class with a common CDRH3 motif. Our analyses also suggested that elicitation of this class of antibodies may not be overly difficult, an observation that bodes well for the development of a pan-sarbecovirus vaccine.
Persistent Identifierhttp://hdl.handle.net/10722/314428
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, L-
dc.contributor.authorIketani, S-
dc.contributor.authorGuo, Y-
dc.contributor.authorReddem, ER-
dc.contributor.authorCasner, RG-
dc.contributor.authorNair, MS-
dc.contributor.authorYu, J-
dc.contributor.authorChan, JFW-
dc.contributor.authorV, M-
dc.contributor.authorCerutti, G-
dc.contributor.authorLI, Z-
dc.contributor.authorMorano, NC-
dc.contributor.authorCastagna, CD-
dc.contributor.authorCorredor, L-
dc.contributor.authorChu, H-
dc.contributor.authorYuan, S-
dc.contributor.authorPoon, KM-
dc.contributor.authorChan, CS-
dc.contributor.authorChen, Z-
dc.contributor.authorLuo, Y-
dc.contributor.authorCunningham, M-
dc.contributor.authorChavez, A-
dc.contributor.authorYin, MT-
dc.contributor.authorPerlin, DS-
dc.contributor.authorTsuji, M-
dc.contributor.authorYuen, KY-
dc.contributor.authorKwong, PD-
dc.contributor.authorSheng, Z-
dc.contributor.authorHuang, Y-
dc.contributor.authorShapiro, L-
dc.contributor.authorHo, DD-
dc.date.accessioned2022-07-22T05:24:21Z-
dc.date.available2022-07-22T05:24:21Z-
dc.date.issued2022-
dc.identifier.citationScience Translational Medicine, 2022, v. 14-
dc.identifier.urihttp://hdl.handle.net/10722/314428-
dc.description.abstractThe devastation caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has made clear the importance of pandemic preparedness. To address future zoonotic outbreaks due to related viruses in the sarbecovirus subgenus, we identified a human monoclonal antibody, 10-40, that neutralized or bound all sarbecoviruses tested in vitro and protected against SARS-CoV-2 and SARS-CoV in vivo. Comparative studies with other receptor-binding domain (RBD)-directed antibodies showed 10-40 to have the greatest breadth against sarbecoviruses, suggesting that 10-40 is a promising agent for pandemic preparedness. Moreover, structural analyses on 10-40 and similar antibodies not only defined an epitope cluster in the inner face of the RBD that is well conserved among sarbecoviruses but also uncovered a distinct antibody class with a common CDRH3 motif. Our analyses also suggested that elicitation of this class of antibodies may not be overly difficult, an observation that bodes well for the development of a pan-sarbecovirus vaccine.-
dc.languageeng-
dc.relation.ispartofScience Translational Medicine-
dc.titleAn antibody class with a common CDRH3 motif broadly neutralizes sarbecoviruses-
dc.typeArticle-
dc.identifier.emailChan, JFW: jfwchan@hku.hk-
dc.identifier.emailChu, H: hinchu@hku.hk-
dc.identifier.emailYuan, S: yuansf@hku.hk-
dc.identifier.emailPoon, KM: vinpoon@hku.hk-
dc.identifier.emailChan, CS: cschan@hku.hk-
dc.identifier.emailChen, Z: zchenai@hku.hk-
dc.identifier.emailYuen, KY: kyyuen@hkucc.hku.hk-
dc.identifier.authorityChan, JFW=rp01736-
dc.identifier.authorityChu, H=rp02125-
dc.identifier.authorityYuan, S=rp02640-
dc.identifier.authorityChen, Z=rp00243-
dc.identifier.authorityYuen, KY=rp00366-
dc.identifier.doi10.1126/scitranslmed.abn6859-
dc.identifier.hkuros334617-
dc.identifier.volume14-
dc.identifier.isiWOS:000801825800005-

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