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The Omicron variant is highly resistant against antibody-mediated neutralization - implications for control of the COVID-19 pandemic
Markus Hoffmann; Nadine Krüger; Sebastian Schulz; Anne Cossmann; Cheila Rocha; Amy Kempf; Inga Nehlmeier; Luise Graichen; Anna-Sophie Moldenhauer; Martin Sebastian Winkler; Martin Lier; Alexandra Dopfer-Jablonka; Hans-Martin Jäck; Georg Behrens; Stefan Pöhlmann.
Affiliation
  • Markus Hoffmann; Deutsches Primatenzentrum GmbH - Leibniz-Institut für Primatenforschung
  • Nadine Krüger; Deutsches Primatenzentrum - Leibniz Institut für Primatenforschung
  • Sebastian Schulz; Friedrich-Alexander-Universitä Erlangen-Nürnberg
  • Anne Cossmann; Medizinische Hochschule Hannover
  • Cheila Rocha; Deutsches Primatenzentrum - Leibniz Institut fü Primatenforschung
  • Amy Kempf; Deutsches Primatenzentrum - Leibniz Institut für Primatenforschung
  • Inga Nehlmeier; Deutsches Primatenzentrum - Leibniz Institut für Primatenforschung
  • Luise Graichen; Deutsches Primatenzentrum - Leibniz Institut für Primatenforschung
  • Anna-Sophie Moldenhauer; Deutsches Primatenzentrum - Leibniz Institut für Primatenforschung
  • Martin Sebastian Winkler; Universitätsmedizin Göttingen
  • Martin Lier; Universitätsmedizin Göttingen
  • Alexandra Dopfer-Jablonka; Medizinische Hochschule Hannover
  • Hans-Martin Jäck; Friedrich-Alexander-Universität Erlangen-Nürnberg
  • Georg Behrens; Medizinische Hochschule Hannover
  • Stefan Pöhlmann; Deutsches Primatenzentrum GmbH - Leibniz-Institut für Primatenforschung
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-472286
Journal article
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ABSTRACT
The rapid spread of the SARS-CoV-2 Omicron variant suggests that the virus might become globally dominant. Further, the high number of mutations in the viral spike-protein raised concerns that the virus might evade antibodies induced by infection or vaccination. Here, we report that the Omicron spike was resistant against most therapeutic antibodies but remained susceptible to inhibition by Sotrovimab. Similarly, the Omicron spike evaded neutralization by antibodies from convalescent or BNT162b2-vaccinated individuals with 10- to 44-fold higher efficiency than the spike of the Delta variant. Neutralization of the Omicron spike by antibodies induced upon heterologous ChAdOx1/BNT162b2-vaccination or vaccination with three doses of BNT162b2 was more efficient, but the Omicron spike still evaded neutralization more efficiently than the Delta spike. These findings indicate that most therapeutic antibodies will be ineffective against the Omicron variant and that double immunization with BNT162b2 might not adequately protect against severe disease induced by this variant.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2021 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2021 Document type: Preprint