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Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine

As oral poliovirus vaccine (OPV) causes vaccine-associated paralytic poliomyelitis, the polio endgame strategy introduced by the Global Polio Eradication Initiative calls for a phased withdrawal of OPV and an introduction of inactivated poliovirus vaccine (IPV). The introduction of IPV creates chall...

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Autores principales: Shin, Woo-Jin, Hara, Daiki, Gbormittah, Francisca, Chang, Hana, Chang, Byeong S., Jung, Jae U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282204/
https://www.ncbi.nlm.nih.gov/pubmed/30482835
http://dx.doi.org/10.1128/mBio.02287-18
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author Shin, Woo-Jin
Hara, Daiki
Gbormittah, Francisca
Chang, Hana
Chang, Byeong S.
Jung, Jae U.
author_facet Shin, Woo-Jin
Hara, Daiki
Gbormittah, Francisca
Chang, Hana
Chang, Byeong S.
Jung, Jae U.
author_sort Shin, Woo-Jin
collection PubMed
description As oral poliovirus vaccine (OPV) causes vaccine-associated paralytic poliomyelitis, the polio endgame strategy introduced by the Global Polio Eradication Initiative calls for a phased withdrawal of OPV and an introduction of inactivated poliovirus vaccine (IPV). The introduction of IPV creates challenges in maintaining the cold chain for vaccine storage and distribution. Recent advances in lyophilization have helped in finding a temperature-stable formulation for multiple vaccines; however, poliovirus vaccines have yet to capture a stable, safe formula for lyophilization. In addition, efficient in vitro methods for antigen measurement are needed for screening stable vaccine formulations. Here, we report size exclusion high-performance liquid chromatography (SE-HPLC) as a reliable means to identify the leading lyophilized formulation to generate thermostable Sabin inactivated poliovirus vaccine (sIPV). High-throughput screening and SE-HPLC determined the leading formulation, resulting in 95% D-antigen recovery and low residual moisture content of sIPV following lyophilization. Furthermore, the lyophilized sIPV remained stable after 4 weeks of incubation at ambient temperature and induced strong neutralizing antibodies and full protection of poliovirus receptor transgenic mice against the in vivo challenge of wild-type poliovirus. Overall, this report describes a novel means for the high-throughput evaluation of sIPV antigenicity and a thermostable lyophilized sIPV with in vivo vaccine potency.
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spelling pubmed-62822042018-12-10 Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine Shin, Woo-Jin Hara, Daiki Gbormittah, Francisca Chang, Hana Chang, Byeong S. Jung, Jae U. mBio Research Article As oral poliovirus vaccine (OPV) causes vaccine-associated paralytic poliomyelitis, the polio endgame strategy introduced by the Global Polio Eradication Initiative calls for a phased withdrawal of OPV and an introduction of inactivated poliovirus vaccine (IPV). The introduction of IPV creates challenges in maintaining the cold chain for vaccine storage and distribution. Recent advances in lyophilization have helped in finding a temperature-stable formulation for multiple vaccines; however, poliovirus vaccines have yet to capture a stable, safe formula for lyophilization. In addition, efficient in vitro methods for antigen measurement are needed for screening stable vaccine formulations. Here, we report size exclusion high-performance liquid chromatography (SE-HPLC) as a reliable means to identify the leading lyophilized formulation to generate thermostable Sabin inactivated poliovirus vaccine (sIPV). High-throughput screening and SE-HPLC determined the leading formulation, resulting in 95% D-antigen recovery and low residual moisture content of sIPV following lyophilization. Furthermore, the lyophilized sIPV remained stable after 4 weeks of incubation at ambient temperature and induced strong neutralizing antibodies and full protection of poliovirus receptor transgenic mice against the in vivo challenge of wild-type poliovirus. Overall, this report describes a novel means for the high-throughput evaluation of sIPV antigenicity and a thermostable lyophilized sIPV with in vivo vaccine potency. American Society for Microbiology 2018-11-27 /pmc/articles/PMC6282204/ /pubmed/30482835 http://dx.doi.org/10.1128/mBio.02287-18 Text en Copyright © 2018 Shin et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Shin, Woo-Jin
Hara, Daiki
Gbormittah, Francisca
Chang, Hana
Chang, Byeong S.
Jung, Jae U.
Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine
title Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine
title_full Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine
title_fullStr Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine
title_full_unstemmed Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine
title_short Development of Thermostable Lyophilized Sabin Inactivated Poliovirus Vaccine
title_sort development of thermostable lyophilized sabin inactivated poliovirus vaccine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282204/
https://www.ncbi.nlm.nih.gov/pubmed/30482835
http://dx.doi.org/10.1128/mBio.02287-18
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