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A whole virion vaccine for COVID-19 produced via a novel inactivation method: results from animal challenge model studies

View ORCID ProfileIzabela K Ragan, View ORCID ProfileLindsay M Hartson, Taru S Dutt, View ORCID ProfileAndres Obregon-Henao, View ORCID ProfileRachel M Maison, View ORCID ProfilePaul Gordy, View ORCID ProfileAmy Fox, Burton R Karger, View ORCID ProfileShaun T Cross, Marylee L Kapuscinski, View ORCID ProfileSarah K Cooper, Brendan K Podell, Mark D Stenglein, View ORCID ProfileRichard A Bowen, View ORCID ProfileMarcela Henao-Tamayo, View ORCID ProfileRaymond P Goodrich
doi: https://doi.org/10.1101/2020.11.13.381335
Izabela K Ragan
1Department of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America
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  • ORCID record for Izabela K Ragan
Lindsay M Hartson
2Infectious Disease Research Center, Colorado State University, Fort Collins, Colorado, United States of America
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Taru S Dutt
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Andres Obregon-Henao
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Rachel M Maison
1Department of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America
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Paul Gordy
1Department of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America
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Amy Fox
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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  • ORCID record for Amy Fox
Burton R Karger
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Shaun T Cross
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Marylee L Kapuscinski
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Sarah K Cooper
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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  • ORCID record for Sarah K Cooper
Brendan K Podell
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Mark D Stenglein
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Richard A Bowen
1Department of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America
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Marcela Henao-Tamayo
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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Raymond P Goodrich
2Infectious Disease Research Center, Colorado State University, Fort Collins, Colorado, United States of America
3Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States of America
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  • For correspondence: Ray.Goodrich@colostate.edu
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Abstract

The COVID-19 pandemic has generated intense interest in the rapid development and evaluation of vaccine candidates for this disease and other emerging diseases. Several novel methods for preparing vaccine candidates are currently undergoing clinical evaluation in response to the urgent need to prevent the spread of COVID-19. In many cases, these methods rely on new approaches for vaccine production and immune stimulation. We report on the use of a novel method (SolaVAX™) for production of an inactivated vaccine candidate and the testing of that candidate in a hamster animal model for its ability to prevent infection upon challenge with SARS-CoV-2 virus. The studies employed in this work included an evaluation of the levels of neutralizing antibody produced post-vaccination, levels of specific antibody sub-types to RBD and spike protein that were generated, evaluation of viral shedding post-challenge, flow cytometric and single cell sequencing data on cellular fractions and histopathological evaluation of tissues post-challenge. The results from this study provide insight into the immunological responses occurring as a result of vaccination with the proposed vaccine candidate and the impact that adjuvant formulations, specifically developed to promote Th1 type immune responses, have on vaccine efficacy and protection against infection following challenge with live SARS-CoV-2. This data may have utility in the development of effective vaccine candidates broadly. Furthermore, the results suggest that preparation of a whole virion vaccine for COVID-19 using this specific photochemical method may have utility in the preparation of one such vaccine candidate.

Author Summary We have developed a vaccine for COVID-19 which is prepared by a novel method for inactivation of a whole virion particle and tested it in a hamster animal model for its ability to protect against SARS-CoV-2 infection.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted November 13, 2020.
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A whole virion vaccine for COVID-19 produced via a novel inactivation method: results from animal challenge model studies
Izabela K Ragan, Lindsay M Hartson, Taru S Dutt, Andres Obregon-Henao, Rachel M Maison, Paul Gordy, Amy Fox, Burton R Karger, Shaun T Cross, Marylee L Kapuscinski, Sarah K Cooper, Brendan K Podell, Mark D Stenglein, Richard A Bowen, Marcela Henao-Tamayo, Raymond P Goodrich
bioRxiv 2020.11.13.381335; doi: https://doi.org/10.1101/2020.11.13.381335
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A whole virion vaccine for COVID-19 produced via a novel inactivation method: results from animal challenge model studies
Izabela K Ragan, Lindsay M Hartson, Taru S Dutt, Andres Obregon-Henao, Rachel M Maison, Paul Gordy, Amy Fox, Burton R Karger, Shaun T Cross, Marylee L Kapuscinski, Sarah K Cooper, Brendan K Podell, Mark D Stenglein, Richard A Bowen, Marcela Henao-Tamayo, Raymond P Goodrich
bioRxiv 2020.11.13.381335; doi: https://doi.org/10.1101/2020.11.13.381335

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