Abstract

As the SARS-CoV-2 pandemic evolves, vaccine evaluation needs to include consideration of both durability and cross-reactivity. This report expands on previously reported results from a Phase 1 trial of an AS03-adjuvanted, plant-based coronavirus-like particle (CoVLP) displaying the spike (S) glycoprotein of the ancestral SARS-CoV-2 virus in healthy adults (NCT04450004). Humoral and cellular responses against the ancestral strain were evaluated 6 months post-second dose (D201) as secondary outcomes. Independent of dose, all vaccinated individuals retain binding antibodies, and ~95% retain neutralizing antibodies (NAb). Interferon gamma and interleukin-4 responses remain detectable in ~94% and ~92% of vaccinees respectively. In post-hoc analyses, variant-specific (Alpha, Beta, Delta, Gamma and Omicron) NAb were assessed at D42 and D201. Using a live virus neutralization assay, broad cross-reactivity is detectable against all variants at D42. At D201, cross-reactive antibodies are detectable in almost all participants against Alpha, Gamma and Delta variants (94%) and the Beta variant (83%) and in a smaller proportion against Omicron (44%). Results are similar with the pseudovirion assay. These data suggest that two doses of 3.75 µg CoVLP+AS03 elicit a durable and cross-reactive response that persists for at least 6 months post-vaccination.

Here, the authors report results from a Phase 1 trial with an AS03-adjuvanted, plant-based virus-like particle displaying the spike protein of the ancestral SARS-CoV-2. Six months post-second dose, they observe good neutralizing antibody titers and T cell responses to ancestral virus and variants of concern in participants.

Details

Title
Durability and cross-reactivity of immune responses induced by a plant-based virus-like particle vaccine for COVID-19
Author
Gobeil, Philipe 1 ; Pillet, Stéphane 1 ; Boulay, Iohann 1 ; Charland, Nathalie 1 ; Lorin, Aurélien 1 ; Cheng, Matthew P. 2 ; Vinh, Donald C. 2   VIAFID ORCID Logo  ; Boutet, Philippe 3 ; Van Der Most, Robbert 4   VIAFID ORCID Logo  ; Roman, François 3 ; Ceregido, Maria Angeles 3 ; Landry, Nathalie 1 ; D’Aoust, Marc-André 1 ; Ward, Brian J. 5 

 Medicago Inc., Québec, Canada (GRID:grid.421219.d) (ISNI:0000 0004 0635 0044) 
 The Research Institute of the McGill University Health Centre, Montreal, Canada (GRID:grid.63984.30) (ISNI:0000 0000 9064 4811) 
 GlaxoSmithKline (Vaccines), Wavre, Belgium (GRID:grid.425090.a) (ISNI:0000 0004 0468 9597) 
 GlaxoSmithKline (Vaccines), Rixensart, Belgium (GRID:grid.425090.a) (ISNI:0000 0004 0468 9597); BioNTech, Mainz, Germany (GRID:grid.434484.b) (ISNI:0000 0004 4692 2203) 
 Medicago Inc., Québec, Canada (GRID:grid.421219.d) (ISNI:0000 0004 0635 0044); The Research Institute of the McGill University Health Centre, Montreal, Canada (GRID:grid.63984.30) (ISNI:0000 0000 9064 4811) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2735576586
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.