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The Omicron variant is highly resistant against antibody-mediated neutralization: Implications for control of the COVID-19 pandemic.
Hoffmann, Markus; Krüger, Nadine; Schulz, Sebastian; Cossmann, Anne; Rocha, Cheila; Kempf, Amy; Nehlmeier, Inga; Graichen, Luise; Moldenhauer, Anna-Sophie; Winkler, Martin S; Lier, Martin; Dopfer-Jablonka, Alexandra; Jäck, Hans-Martin; Behrens, Georg M N; Pöhlmann, Stefan.
  • Hoffmann M; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany; Faculty of Biology and Psychology, Georg-August-University Göttingen, Wilhelmsplatz 1, 37073 Göttingen, Germany. Electronic address: mhoffmann@dpz.eu.
  • Krüger N; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany.
  • Schulz S; Division of Molecular Immunology, Department of Internal Medicine 3, Friedrich-Alexander University of Erlangen-Nürnberg, Glückstraße 6, 91054 Erlangen, Germany.
  • Cossmann A; Department for Rheumatology and Immunology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
  • Rocha C; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany.
  • Kempf A; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany; Faculty of Biology and Psychology, Georg-August-University Göttingen, Wilhelmsplatz 1, 37073 Göttingen, Germany.
  • Nehlmeier I; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany.
  • Graichen L; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany; Faculty of Biology and Psychology, Georg-August-University Göttingen, Wilhelmsplatz 1, 37073 Göttingen, Germany.
  • Moldenhauer AS; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany.
  • Winkler MS; Department of Anesthesiology, University of Göttingen Medical Center, Göttingen, Georg-August University of Göttingen, Robert-Koch-Straße 40, 37075 Göttingen, Germany.
  • Lier M; Department of Anesthesiology, University of Göttingen Medical Center, Göttingen, Georg-August University of Göttingen, Robert-Koch-Straße 40, 37075 Göttingen, Germany.
  • Dopfer-Jablonka A; Department for Rheumatology and Immunology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany; German Centre for Infection Research (DZIF), Partner Site Hannover-Braunschweig, Hannover, Germany.
  • Jäck HM; Division of Molecular Immunology, Department of Internal Medicine 3, Friedrich-Alexander University of Erlangen-Nürnberg, Glückstraße 6, 91054 Erlangen, Germany.
  • Behrens GMN; Department for Rheumatology and Immunology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany; German Centre for Infection Research (DZIF), Partner Site Hannover-Braunschweig, Hannover, Germany.
  • Pöhlmann S; Infection Biology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany; Faculty of Biology and Psychology, Georg-August-University Göttingen, Wilhelmsplatz 1, 37073 Göttingen, Germany. Electronic address: spoehlmann@dpz.eu.
Cell ; 185(3): 447-456.e11, 2022 02 03.
Article in English | MEDLINE | ID: covidwho-1712497
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 patients or individuals vaccinated with the BioNTech-Pfizer vaccine (BNT162b2) with 12- to 44-fold higher efficiency than the spike of the Delta variant. Neutralization of the Omicron spike by antibodies induced upon heterologous ChAdOx1 (Astra Zeneca-Oxford)/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: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / Antibodies, Monoclonal, Humanized / Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Animals / Female / Humans / Male Language: English Journal: Cell Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / Antibodies, Monoclonal, Humanized / Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Animals / Female / Humans / Male Language: English Journal: Cell Year: 2022 Document Type: Article