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Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions

Influenza A virus presents a constant pandemic threat due to the mutagenic nature of the virus and the inadequacy of current vaccines to protect against emerging strains. We have developed a whole-inactivated influenza vaccine using γ-irradiation (γ-Flu) that can protect against both vaccine-include...

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Autores principales: Singleton, Eve Victoria, Gates, Chloe Jayne, David, Shannon Christa, Hirst, Timothy Raymond, Davies, Justin Bryan, Alsharifi, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8652198/
https://www.ncbi.nlm.nih.gov/pubmed/34899711
http://dx.doi.org/10.3389/fimmu.2021.761632
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author Singleton, Eve Victoria
Gates, Chloe Jayne
David, Shannon Christa
Hirst, Timothy Raymond
Davies, Justin Bryan
Alsharifi, Mohammed
author_facet Singleton, Eve Victoria
Gates, Chloe Jayne
David, Shannon Christa
Hirst, Timothy Raymond
Davies, Justin Bryan
Alsharifi, Mohammed
author_sort Singleton, Eve Victoria
collection PubMed
description Influenza A virus presents a constant pandemic threat due to the mutagenic nature of the virus and the inadequacy of current vaccines to protect against emerging strains. We have developed a whole-inactivated influenza vaccine using γ-irradiation (γ-Flu) that can protect against both vaccine-included strains as well as emerging pandemic strains. γ-irradiation is a widely used inactivation method and several γ-irradiated vaccines are currently in clinical or pre-clinical testing. To enhance vaccine efficacy, irradiation conditions should be carefully considered, particularly irradiation temperature. Specifically, while more damage to virus structure is expected when using higher irradiation temperatures, reduced radiation doses will be required to achieve sterility. In this study, we compared immunogenicity of γ-Flu irradiated at room temperature, chilled on ice or frozen on dry ice using different doses of γ-irradiation to meet internationally accepted sterility assurance levels. We found that, when irradiating at sterilising doses, the structural integrity and vaccine efficacy were well maintained in all preparations regardless of irradiation temperature. In fact, using a higher temperature and lower radiation dose appeared to induce higher neutralising antibody responses and more effective cytotoxic T cell responses. This outcome is expected to simplify irradiation protocols for manufacturing of highly effective irradiated vaccines.
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spelling pubmed-86521982021-12-09 Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions Singleton, Eve Victoria Gates, Chloe Jayne David, Shannon Christa Hirst, Timothy Raymond Davies, Justin Bryan Alsharifi, Mohammed Front Immunol Immunology Influenza A virus presents a constant pandemic threat due to the mutagenic nature of the virus and the inadequacy of current vaccines to protect against emerging strains. We have developed a whole-inactivated influenza vaccine using γ-irradiation (γ-Flu) that can protect against both vaccine-included strains as well as emerging pandemic strains. γ-irradiation is a widely used inactivation method and several γ-irradiated vaccines are currently in clinical or pre-clinical testing. To enhance vaccine efficacy, irradiation conditions should be carefully considered, particularly irradiation temperature. Specifically, while more damage to virus structure is expected when using higher irradiation temperatures, reduced radiation doses will be required to achieve sterility. In this study, we compared immunogenicity of γ-Flu irradiated at room temperature, chilled on ice or frozen on dry ice using different doses of γ-irradiation to meet internationally accepted sterility assurance levels. We found that, when irradiating at sterilising doses, the structural integrity and vaccine efficacy were well maintained in all preparations regardless of irradiation temperature. In fact, using a higher temperature and lower radiation dose appeared to induce higher neutralising antibody responses and more effective cytotoxic T cell responses. This outcome is expected to simplify irradiation protocols for manufacturing of highly effective irradiated vaccines. Frontiers Media S.A. 2021-11-24 /pmc/articles/PMC8652198/ /pubmed/34899711 http://dx.doi.org/10.3389/fimmu.2021.761632 Text en Copyright © 2021 Singleton, Gates, David, Hirst, Davies and Alsharifi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Singleton, Eve Victoria
Gates, Chloe Jayne
David, Shannon Christa
Hirst, Timothy Raymond
Davies, Justin Bryan
Alsharifi, Mohammed
Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions
title Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions
title_full Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions
title_fullStr Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions
title_full_unstemmed Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions
title_short Enhanced Immunogenicity of a Whole-Inactivated Influenza A Virus Vaccine Using Optimised Irradiation Conditions
title_sort enhanced immunogenicity of a whole-inactivated influenza a virus vaccine using optimised irradiation conditions
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8652198/
https://www.ncbi.nlm.nih.gov/pubmed/34899711
http://dx.doi.org/10.3389/fimmu.2021.761632
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