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Mosaic RBD nanoparticles protect against multiple sarbecovirus challenges in animal models
Alexander A Cohen; Neeltje A van Doremalen; Allison J. Greaney; Hanne Andersen; Ankur Sharma; Tyler N Starr; Jennifer R Keeffe; Chengcheng Fan; Jonathan E Schulz; Priyanthi N.P. Gnanapragasam; Leesa M Kakutani; Anthony P West Jr.; Greg Saturday; Yu E. Lee; Han Gao; Claudia A Jette; Mark G Lewis; Tiong K Tan; Alain R Townsend; Jesse D Bloom; Vincent J Munster; Pamela J Bjorkman.
Affiliation
  • Alexander A Cohen; California Institute of Technology
  • Neeltje A van Doremalen; National Institute of Allergy and Infectious Diseases, NIH
  • Allison J. Greaney; Fred Hutchinson Cancer Research Center
  • Hanne Andersen; Bioqual Inc.
  • Ankur Sharma; Bioqual Inc.
  • Tyler N Starr; Fred Hutchinson Cancer Research Center
  • Jennifer R Keeffe; California Institute of Technology
  • Chengcheng Fan; California Institute of Technology
  • Jonathan E Schulz; National Institute of Allergy and Infectious Diseases, NIH
  • Priyanthi N.P. Gnanapragasam; California Institute of Technology
  • Leesa M Kakutani; California Institute of Technology
  • Anthony P West Jr.; California Institute of Technology
  • Greg Saturday; National Institute of Allergy and Infectious Diseases, NIH
  • Yu E. Lee; California Institute of Technology
  • Han Gao; California Institute of Technology
  • Claudia A Jette; California Institute of Technology
  • Mark G Lewis; Bioqual Inc
  • Tiong K Tan; University of Oxford
  • Alain R Townsend; University of Oxford
  • Jesse D Bloom; Fred Hutchinson Cancer Research Center
  • Vincent J Munster; National Institute of Allergy and Infectious Diseases, NIH
  • Pamela J Bjorkman; California Institute of Technology
Preprint in English | bioRxiv | ID: ppbiorxiv-485875
ABSTRACT
To combat future SARS-CoV-2 variants and spillovers of SARS-like betacoronaviruses (sarbecoviruses) threatening global health, we designed mosaic nanoparticles presenting randomly-arranged sarbecovirus spike receptor-binding domains (RBDs) to elicit antibodies against conserved/relatively-occluded, rather than variable/immunodominant/exposed, epitopes. We compared immune responses elicited by mosaic-8 (SARS-CoV-2 and seven animal sarbecoviruses) and homotypic (only SARS-CoV-2) RBD-nanoparticles in mice and macaques, observing stronger responses elicited by mosaic-8 to mismatched (not on nanoparticles) strains including SARS-CoV and animal sarbecoviruses. Mosaic-8 immunization showed equivalent neutralization of SARS-CoV-2 variants including Omicron and protected from SARS-CoV-2 and SARS-CoV challenges, whereas homotypic SARS-CoV-2 immunization protected only from SARS-CoV-2 challenge. Epitope mapping demonstrated increased targeting of conserved epitopes after mosaic-8 immunization. Together, these results suggest mosaic-8 RBD-nanoparticles could protect against SARS-CoV-2 variants and future sarbecovirus spillovers.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Experimental_studies / Rct Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Experimental_studies / Rct Language: English Year: 2022 Document type: Preprint
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