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Delineating antibody escape from Omicron variants
Henning Gruell; Kanika Vanshylla; Michael Korenkov; Pinkus Tober-Lau; Matthias Zehner; Friederike Muenn; Hanna Janicki; Max Augustin; Philipp Schommers; Leif Erik Sander; Florian Kurth; Christoph Kreer; Florian Klein.
Affiliation
  • Henning Gruell; University Hospital Cologne
  • Kanika Vanshylla; University Hospital Cologne
  • Michael Korenkov; University Hospital Cologne
  • Pinkus Tober-Lau; Charite Universitaetsmedizin
  • Matthias Zehner; University Hospital Cologne
  • Friederike Muenn; Charite Universitaetsmedizin
  • Hanna Janicki; University Hospital Cologne
  • Max Augustin; University Hospital Cologne
  • Philipp Schommers; University Hospital Cologne
  • Leif Erik Sander; Charite Universitaetsmedizin
  • Florian Kurth; Charite Universitaetsmedizin
  • Christoph Kreer; University Hospital Cologne
  • Florian Klein; Faculty of Medicine and University Hospital Cologne, University of Cologne
Preprint in English | bioRxiv | ID: ppbiorxiv-487257
ABSTRACT
SARS-CoV-2 neutralizing antibodies play a critical role in prevention and treatment of COVID-19 but are challenged by viral evolution and antibody evasion, exemplified by the highly resistant Omicron BA.1 sublineage.1-12 Importantly, the recently identified Omicron sublineages BA.2.12.1 and BA.4/5 with differing spike mutations are rapidly emerging in various countries. By determining polyclonal serum activity of 50 convalescent or vaccinated individuals against BA.1, BA.1.1, BA.2, BA.2.12.1, and BA.4/5, we reveal a further reduction of BA.4/5 susceptibility to vaccinee sera. Most notably, delineation of the sensitivity to an extended panel of 163 antibodies demonstrates pronounced antigenic differences of individual sublineages with distinct escape patterns and increased antibody resistance of BA.4/5 compared to the most prevalent BA.2 sublineage. These results suggest that the antigenic distance from BA.1 and the increased resistance compared to BA.2 may favor immune escape-mediated expansion of BA.4/5 after the first Omicron wave. Finally, while most monoclonal antibodies in clinical stages are inactive against all Omicron sublineages, we identify promising novel antibodies with high pan-Omicron neutralizing potency. Our study provides a detailed understanding of the antibody escape from the most recently emerging Omicron sublineages that can inform on effective strategies to prevent and treat COVID-19.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2022 Document type: Preprint
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