Preclinical evaluation of a SARS-CoV-2 mRNA vaccine PTX-COVID19-B

  • Jun Liu
  • , Patrick Budylowski
  • , Reuben Samson
  • , Bryan D. Griffin
  • , Giorgi Babuadze
  • , Bhavisha Rathod
  • , Karen Colwill
  • , Jumai A. Abioye
  • , Jordan A. Schwartz
  • , Ryan Law
  • , Lily Yip
  • , Sang Kyun Ahn
  • , Serena Chau
  • , Maedeh Naghibosadat
  • , Yuko Arita
  • , Queenie Hu
  • , Feng Yun Yue
  • , Arinjay Banerjee
  • , W. Rod Hardy
  • , Karen Mossman
  • Samira Mubareka, Robert A. Kozak, Michael S. Pollanen, Natalia Martin Orozco, Anne Claude Gingras, Eric G. Marcusson, Mario A. Ostrowski

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Safe and effective vaccines are needed to end the COVID-19 pandemic. Here, we report the preclinical development of a lipid nanoparticle-formulated SARS-CoV-2 mRNA vaccine, PTX-COVID19-B. PTX-COVID19-B was chosen among three candidates after the initial mouse vaccination results showed that it elicited the strongest neutralizing antibody response against SARS-CoV-2. Further tests in mice and hamsters indicated that PTX-COVID19-B induced robust humoral and cellular immune responses and completely protected the vaccinated animals from SARS-CoV-2 infection in the lung. Studies in hamsters also showed that PTX-COVID19-B protected the upper respiratory tract from SARS-CoV-2 infection. Mouse immune sera elicited by PTX-COVID19-B vaccination were able to neutralize SARS-CoV-2 variants of concern, including the Alpha, Beta, Gamma, and Delta lineages. No adverse effects were induced by PTX-COVID19-B in either mice or hamsters. Based on these results, PTX-COVID19-B was authorized by Health Canada to enter clinical trials in December 2020 with a phase 2 clinical trial ongoing.

Original languageEnglish (US)
Article numbereabj9815
JournalScience Advances
Volume8
Issue number3
DOIs
StatePublished - Jan 2022
Externally publishedYes

ASJC Scopus subject areas

  • General

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