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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; Karen Mossman; Samira Mubareka; Robert A Kozak; Michael S Pollanen; Natalia Martin Orozco; Anne-Claude Gingras; Eric G Marcusson; Mario A Ostrowski.
Afiliação
  • Jun Liu; University of Toronto
  • Patrick Budylowski; University of Toronto
  • Reuben Samson; University of Toronto
  • Bryan D Griffin; Sunnybrook Research Institute
  • Giorgi Babuadze; Sunnybrook Research Institute
  • Bhavisha Rathod; Mount Sinai Hospital
  • Karen Colwill; Mount Sinai Hospital
  • Jumai A Abioye; Providence Therapeutics Holdings Inc.
  • Jordan A Schwartz; Providence Therapeutics Holdings Inc.
  • Ryan Law; University of Toronto
  • Lily Yip; Sunnybrook Research Institute
  • Sang Kyun Ahn; University of Toronto
  • Serena Chau; University of Toronto
  • Maedeh Naghibosadat; Sunnybrook Research Institute
  • Yuko Arita; Providence Therapeutics Holding Inc.
  • Queenie Hu; Mount Sinai Hospital
  • Feng Yun Yue; University of Toronto
  • Arinjay Banerjee; University of Saskatchewan
  • Karen Mossman; McMaster University
  • Samira Mubareka; University of Toronto
  • Robert A Kozak; Sunnybrook Research Institute
  • Michael S Pollanen; University of Toronto
  • Natalia Martin Orozco; Providence Therpeutics Holdings Inc.
  • Anne-Claude Gingras; University of Toronto
  • Eric G Marcusson; Providence Therapeutics Holdings Inc.
  • Mario A Ostrowski; University of Toronto
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-443286
ABSTRACT
Safe and effective vaccines are needed to end the COVID-19 pandemic caused by SARS-CoV-2. Here we report the preclinical development of a lipid nanoparticle (LNP) 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 (VOCs), including the B.1.1.7, B.1.351 and P.1 lineages. No adverse effects were induced by PTX-COVID19-B in both mice and hamsters. These preclinical results indicate that PTX-COVID19-B is safe and effective. Based on these results, PTX-COVID19-B was authorized by Health Canada to enter clinical trials in December 2020 with a phase 1 clinical trial ongoing (ClinicalTrials.gov number NCT04765436). One Sentence SummaryPTX-COVID19-B is a SARS-CoV-2 mRNA vaccine that is highly immunogenic, safe, and effective in preventing SARS-CoV-2 infection in mice and hamsters and is currently being evaluated in human clinical trials.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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