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Article: In-Silico Analysis of Monoclonal Antibodies against SARS-CoV-2 Omicron

TitleIn-Silico Analysis of Monoclonal Antibodies against SARS-CoV-2 Omicron
Authors
Issue Date2022
Citation
Viruses, 2022, v. 14, p. 390 How to Cite?
AbstractOmicron was designated by the WHO as a VOC on 26 November 2021, only 4 days after its sequence was first submitted. However, the impact of Omicron on current antibodies and vaccines remains unknown and evaluations are still a few weeks away. We analysed the mutations in the Omicron variant against epitopes. In our database, 132 epitopes of the 120 antibodies are classified into five groups, namely NTD, RBD-1, RBD-2, RBD-3, and RBD-4. The Omicron mutations impact all epitopes in NTD, RBD-1, RBD-2, and RBD-3, with no antibody epitopes spared by these mutations. Only four out of 120 antibodies may confer full resistance to mutations in the Omicron spike, since all antibodies in these three groups contain one or more epitopes that are affected by these mutations. Of all antibodies under EUA, the neutralisation potential of Etesevimab, Bamlanivimab, Casirivimab, Imdevima, Cilgavimab, Tixagevimab, Sotrovimab, and Regdanvimab might be dampened to varying degrees. Our analysis suggests the impact of Omicron on current therapeutic antibodies by the Omicron spike mutations may also apply to current COVID-19 vaccines.
Persistent Identifierhttp://hdl.handle.net/10722/317288
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHu, Y-
dc.contributor.authorHu, J-
dc.contributor.authorChu, H-
dc.contributor.authorYau, TCC-
dc.contributor.authorZhang, B-
dc.contributor.authorHuang, J-
dc.date.accessioned2022-10-07T10:17:48Z-
dc.date.available2022-10-07T10:17:48Z-
dc.date.issued2022-
dc.identifier.citationViruses, 2022, v. 14, p. 390-
dc.identifier.urihttp://hdl.handle.net/10722/317288-
dc.description.abstractOmicron was designated by the WHO as a VOC on 26 November 2021, only 4 days after its sequence was first submitted. However, the impact of Omicron on current antibodies and vaccines remains unknown and evaluations are still a few weeks away. We analysed the mutations in the Omicron variant against epitopes. In our database, 132 epitopes of the 120 antibodies are classified into five groups, namely NTD, RBD-1, RBD-2, RBD-3, and RBD-4. The Omicron mutations impact all epitopes in NTD, RBD-1, RBD-2, and RBD-3, with no antibody epitopes spared by these mutations. Only four out of 120 antibodies may confer full resistance to mutations in the Omicron spike, since all antibodies in these three groups contain one or more epitopes that are affected by these mutations. Of all antibodies under EUA, the neutralisation potential of Etesevimab, Bamlanivimab, Casirivimab, Imdevima, Cilgavimab, Tixagevimab, Sotrovimab, and Regdanvimab might be dampened to varying degrees. Our analysis suggests the impact of Omicron on current therapeutic antibodies by the Omicron spike mutations may also apply to current COVID-19 vaccines.-
dc.languageeng-
dc.relation.ispartofViruses-
dc.titleIn-Silico Analysis of Monoclonal Antibodies against SARS-CoV-2 Omicron-
dc.typeArticle-
dc.identifier.emailChu, H: hinchu@hku.hk-
dc.identifier.emailHuang, J: jdhuang@hku.hk-
dc.identifier.authorityChu, H=rp02125-
dc.identifier.authorityYau, TCC=rp01466-
dc.identifier.authorityHuang, J=rp00451-
dc.identifier.doi10.3390/v14020390-
dc.identifier.hkuros338232-
dc.identifier.volume14-
dc.identifier.spage390-
dc.identifier.epage390-
dc.identifier.isiWOS:000762190100001-

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