Your browser doesn't support javascript.
loading
Spike mutation resilient scFv76 antibody counteracts SARS-CoV-2 lung damage upon aerosol delivery
Ferdinando Maria Milazzo; Antonio Chaves-Sanjuan; Olga Minenkova; Daniela Santapaola; Anna Maria Anastasi; Gianfranco Battistuzzi; Caterina Chiapparino; Antonio Rosi; Emilio Merlo Pich; Claudio Albertoni; Emanuele Marra; Laura Luberto; Cécile Viollet; Luigi Giusto Spagnoli; Anna Riccio; Antono Rossi; M. Gabriella Santoro; Federico Ballabio; Cristina Paissoni; Carlo Camilloni; Martino Bolognesi; Rita De Santis.
Affiliation
  • Ferdinando Maria Milazzo; Alfasigma
  • Antonio Chaves-Sanjuan; Department of Biosciences and Cryo-EM Lab Pediatric Research Center Fondazione Romeo e Enrica Invernizzi University of Milan
  • Olga Minenkova; Alfasigma
  • Daniela Santapaola; Alfasigma
  • Anna Maria Anastasi; Alfasigma
  • Gianfranco Battistuzzi; Alfasigma
  • Caterina Chiapparino; Alfasigma
  • Antonio Rosi; Alfasigma
  • Emilio Merlo Pich; Alfasigma
  • Claudio Albertoni; Studio E Roma
  • Emanuele Marra; Takis
  • Laura Luberto; Takis
  • Cécile Viollet; Texcell
  • Luigi Giusto Spagnoli; Histo-Cyto Service
  • Anna Riccio; University of Rome Tor Vergata
  • Antono Rossi; CNR
  • M. Gabriella Santoro; University of Rome Tor Vergata and CNR
  • Federico Ballabio; University of Milan
  • Cristina Paissoni; University of Milan
  • Carlo Camilloni; University of Milan
  • Martino Bolognesi; University of Milan
  • Rita De Santis; Alfasigma
Preprint in English | bioRxiv | ID: ppbiorxiv-493569
ABSTRACT
Uneven worldwide vaccination coverage against SARS-CoV-2 and emergence of variants escaping immunity call for broadly-effective and easily-deployable therapeutics. We previously described the human single-chain scFv76 antibody, which recognizes SARS-CoV-2 Alfa, Beta, Gamma and Delta variants. We now show that scFv76 also neutralizes infectivity and fusogenic activity of Omicron BA.1 and BA.2 variants. Cryo-EM analysis reveals that scFv76 binds to a well-conserved SARS-CoV-2 spike epitope, providing the structural basis for its broad-spectrum activity. Moreover, we demonstrate that nebulized scFv76 exhibits therapeutic efficacy in a severe hACE2 transgenic mouse model of COVID-19 pneumonia, as shown by body weight and pulmonary viral load data. Counteraction of infection correlates with the inhibition of lung inflammation observed by histopathology and expression of inflammatory cytokines and chemokines. Biomarkers of pulmonary endothelial damage were also significantly reduced in scFv76-treated mice. Altogether the results support the use of nebulized scFv76 for COVID-19 induced by any SARS-CoV-2 variants emerged so far.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2022 Document type: Preprint
...