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Anti-SARS-CoV-2 human antibodies retaining neutralizing activity against SARS-CoV-2 B.1.1.529 (omicron)
Maya Imbrechts; Winnie Kerstens; Madina Rasulova; Thomas Vercruysse; Wim Maes; Louanne Ampofo; Karen Ven; Jeroen Lammertyn; Karen Vanhoorelbeke; Nico Callewaert; Johan Neyts; Kai Dallmeier; Paul Declerck; Hendrik Jan Thibaut; Nick Geukens.
Afiliação
  • Maya Imbrechts; KU Leuven
  • Winnie Kerstens; KU Leuven
  • Madina Rasulova; KU Leuven
  • Thomas Vercruysse; KU Leuven
  • Wim Maes; KU Leuven
  • Louanne Ampofo; KU Leuven
  • Karen Ven; KU Leuven
  • Jeroen Lammertyn; KU Leuven
  • Karen Vanhoorelbeke; KU Leuven
  • Nico Callewaert; AZ Groeninge
  • Johan Neyts; KU Leuven
  • Kai Dallmeier; KU Leuven
  • Paul Declerck; KU Leuven
  • Hendrik Jan Thibaut; KU Leuven
  • Nick Geukens; KU Leuven
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-473706
ABSTRACT
SARS-CoV-2 B.1.1.529, designated omicron, was recently identified as a new variant of concern by WHO and is rapidly replacing SARS-CoV-2 delta as the most dominant variant in many countries. Unfortunately, because of the high number of mutations present in the spike of SARS-CoV-2 omicron, most monoclonal antibodies (mAbs) currently approved for treatment of COVID-19 lose their in vitro neutralizing activity against this variant. We recently described a panel of human anti-SARS-CoV-2 mAbs that potently neutralize SARS-CoV-2 Wuhan, D614G and variants alpha, beta, gamma and delta. In this work, we evaluated our mAb panel for potential in vitro activity against SARS-CoV-2 delta and omicron. Three mAbs from our panel retain neutralizing activity against both delta and omicron, with mAb 3B8 still resulting in complete neutralization at a concentration as low as 0.02 g/ml for both variants. Overall, our data indicate that mAb 3B8 may have the potential to become a game-changer in the fight against the continuously evolving SARS-CoV-2.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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