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A novel gamma radiation-inactivated sabin-based polio vaccine

A concerted action on the part of international agencies and national governments has resulted in the near-eradication of poliomyelitis. However, both the oral polio vaccine (OPV) and the inactivated polio vaccine (IPV) have deficiencies which make them suboptimal for use after global eradication. O...

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Autores principales: Tobin, Gregory J., Tobin, John K., Gaidamakova, Elena K., Wiggins, Taralyn J., Bushnell, Ruth V., Lee, Wai-Ming, Matrosova, Vera Y., Dollery, Stephen J., Meeks, Heather N., Kouiavskaia, Diana, Chumakov, Konstantin, Daly, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6991977/
https://www.ncbi.nlm.nih.gov/pubmed/31999745
http://dx.doi.org/10.1371/journal.pone.0228006
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author Tobin, Gregory J.
Tobin, John K.
Gaidamakova, Elena K.
Wiggins, Taralyn J.
Bushnell, Ruth V.
Lee, Wai-Ming
Matrosova, Vera Y.
Dollery, Stephen J.
Meeks, Heather N.
Kouiavskaia, Diana
Chumakov, Konstantin
Daly, Michael J.
author_facet Tobin, Gregory J.
Tobin, John K.
Gaidamakova, Elena K.
Wiggins, Taralyn J.
Bushnell, Ruth V.
Lee, Wai-Ming
Matrosova, Vera Y.
Dollery, Stephen J.
Meeks, Heather N.
Kouiavskaia, Diana
Chumakov, Konstantin
Daly, Michael J.
author_sort Tobin, Gregory J.
collection PubMed
description A concerted action on the part of international agencies and national governments has resulted in the near-eradication of poliomyelitis. However, both the oral polio vaccine (OPV) and the inactivated polio vaccine (IPV) have deficiencies which make them suboptimal for use after global eradication. OPV is composed of attenuated Sabin strains and stimulates robust immunity, but may revert to neurovirulent forms in the intestine which can be shed and infect susceptible contacts. The majority of IPV products are manufactured using pathogenic strains inactivated with formalin. Upon eradication, the production of large quantities of pathogenic virus will present an increased biosecurity hazard. A logical ideal endgame vaccine would be an inactivated form of an attenuated strain that could afford protective immunity while safely producing larger numbers of doses per unit of virus stock than current vaccines. We report here the development of an ionizing radiation (IR)-inactivated Sabin-based vaccine using a reconstituted Mn-decapeptide (MDP) antioxidant complex derived from the radioresistant bacterium Deinococcus radiodurans. In bacteria, Mn(2+)-peptide antioxidants protect proteins from oxidative damage caused by extreme radiation exposure. Here we show for the first time, that MDP can protect immunogenic neutralizing epitopes in picornaviruses. MDP protects epitopes in Polio Virus 1 and 2 Sabin strains (PV1-S and PV2-S, respectively), but viral genomic RNA is not protected during supralethal irradiation. IR-inactivated Sabin viruses stimulated equivalent or improved neutralizing antibody responses in Wistar rats compared to the commercially used IPV products. Our approach reduces the biosecurity risk of the current PV vaccine production method by utilizing the Sabin strains instead of the wild type neurovirulent strains. Additionally, the IR-inactivation approach could provide a simpler, faster and less costly process for producing a more immunogenic IPV. Gamma-irradiation is a well-known method of virus inactivation and this vaccine approach could be adapted to any pathogen of interest.
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spelling pubmed-69919772020-02-04 A novel gamma radiation-inactivated sabin-based polio vaccine Tobin, Gregory J. Tobin, John K. Gaidamakova, Elena K. Wiggins, Taralyn J. Bushnell, Ruth V. Lee, Wai-Ming Matrosova, Vera Y. Dollery, Stephen J. Meeks, Heather N. Kouiavskaia, Diana Chumakov, Konstantin Daly, Michael J. PLoS One Research Article A concerted action on the part of international agencies and national governments has resulted in the near-eradication of poliomyelitis. However, both the oral polio vaccine (OPV) and the inactivated polio vaccine (IPV) have deficiencies which make them suboptimal for use after global eradication. OPV is composed of attenuated Sabin strains and stimulates robust immunity, but may revert to neurovirulent forms in the intestine which can be shed and infect susceptible contacts. The majority of IPV products are manufactured using pathogenic strains inactivated with formalin. Upon eradication, the production of large quantities of pathogenic virus will present an increased biosecurity hazard. A logical ideal endgame vaccine would be an inactivated form of an attenuated strain that could afford protective immunity while safely producing larger numbers of doses per unit of virus stock than current vaccines. We report here the development of an ionizing radiation (IR)-inactivated Sabin-based vaccine using a reconstituted Mn-decapeptide (MDP) antioxidant complex derived from the radioresistant bacterium Deinococcus radiodurans. In bacteria, Mn(2+)-peptide antioxidants protect proteins from oxidative damage caused by extreme radiation exposure. Here we show for the first time, that MDP can protect immunogenic neutralizing epitopes in picornaviruses. MDP protects epitopes in Polio Virus 1 and 2 Sabin strains (PV1-S and PV2-S, respectively), but viral genomic RNA is not protected during supralethal irradiation. IR-inactivated Sabin viruses stimulated equivalent or improved neutralizing antibody responses in Wistar rats compared to the commercially used IPV products. Our approach reduces the biosecurity risk of the current PV vaccine production method by utilizing the Sabin strains instead of the wild type neurovirulent strains. Additionally, the IR-inactivation approach could provide a simpler, faster and less costly process for producing a more immunogenic IPV. Gamma-irradiation is a well-known method of virus inactivation and this vaccine approach could be adapted to any pathogen of interest. Public Library of Science 2020-01-30 /pmc/articles/PMC6991977/ /pubmed/31999745 http://dx.doi.org/10.1371/journal.pone.0228006 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Tobin, Gregory J.
Tobin, John K.
Gaidamakova, Elena K.
Wiggins, Taralyn J.
Bushnell, Ruth V.
Lee, Wai-Ming
Matrosova, Vera Y.
Dollery, Stephen J.
Meeks, Heather N.
Kouiavskaia, Diana
Chumakov, Konstantin
Daly, Michael J.
A novel gamma radiation-inactivated sabin-based polio vaccine
title A novel gamma radiation-inactivated sabin-based polio vaccine
title_full A novel gamma radiation-inactivated sabin-based polio vaccine
title_fullStr A novel gamma radiation-inactivated sabin-based polio vaccine
title_full_unstemmed A novel gamma radiation-inactivated sabin-based polio vaccine
title_short A novel gamma radiation-inactivated sabin-based polio vaccine
title_sort novel gamma radiation-inactivated sabin-based polio vaccine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6991977/
https://www.ncbi.nlm.nih.gov/pubmed/31999745
http://dx.doi.org/10.1371/journal.pone.0228006
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