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Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods
Widespread vaccination using the oral live attenuated polio vaccine (OPV) and Sabin strain inactivated vaccine (sIPV) have greatly reduced the incidence of polio worldwide. In the period post-polio, the virulence of reversion of the Sabin strain makes the use of OPV gradually becoming one of the maj...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944487/ https://www.ncbi.nlm.nih.gov/pubmed/36810542 http://dx.doi.org/10.3390/diseases11010028 |
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author | Wang, Xiyan Ren, Ruirui Ma, Bo Xie, Jing Ma, Yan Luo, Hong Guo, Yu Ding, Ling Zhang, Liang Zhang, Mengyuan Wang, Tianlang Shuang, Zhichao Zhu, Xiujuan |
author_facet | Wang, Xiyan Ren, Ruirui Ma, Bo Xie, Jing Ma, Yan Luo, Hong Guo, Yu Ding, Ling Zhang, Liang Zhang, Mengyuan Wang, Tianlang Shuang, Zhichao Zhu, Xiujuan |
author_sort | Wang, Xiyan |
collection | PubMed |
description | Widespread vaccination using the oral live attenuated polio vaccine (OPV) and Sabin strain inactivated vaccine (sIPV) have greatly reduced the incidence of polio worldwide. In the period post-polio, the virulence of reversion of the Sabin strain makes the use of OPV gradually becoming one of the major safety hazards. The verification and release of OPV has become the top priority. The monkey neurovirulence test (MNVT) is the gold standard for detecting whether OPV meets the criteria, which are recommended by the WHO and Chinese Pharmacopoeia. Therefore, we statistically analyzed the MNVT results of type I and III OPV at different stages: 1996–2002 and 2016–2022. The results show that the upper and lower limits and C value of the qualification standard of type I reference products in 2016–2022 have decreased compared with the corresponding scores in the 1996–2002 period. The upper and lower limit and C value of the qualified standard of type III reference products were basically the same as the corresponding scores in the 1996–2002. We also found significant differences in the pathogenicity of the type I and III in the cervical spine and brain, with the decreasing trend in the diffusion index of the type I and type III in the cervical spine and brain. Finally, two evaluation criteria were used to judge the OPV test vaccines from 2016 to 2022. The vaccines all met the test requirements under the evaluation criteria of the above two stages. Based on the characteristics of OPV, data monitoring was one of the most intuitive methods to judge changes in virulence. |
format | Online Article Text |
id | pubmed-9944487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99444872023-02-23 Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods Wang, Xiyan Ren, Ruirui Ma, Bo Xie, Jing Ma, Yan Luo, Hong Guo, Yu Ding, Ling Zhang, Liang Zhang, Mengyuan Wang, Tianlang Shuang, Zhichao Zhu, Xiujuan Diseases Article Widespread vaccination using the oral live attenuated polio vaccine (OPV) and Sabin strain inactivated vaccine (sIPV) have greatly reduced the incidence of polio worldwide. In the period post-polio, the virulence of reversion of the Sabin strain makes the use of OPV gradually becoming one of the major safety hazards. The verification and release of OPV has become the top priority. The monkey neurovirulence test (MNVT) is the gold standard for detecting whether OPV meets the criteria, which are recommended by the WHO and Chinese Pharmacopoeia. Therefore, we statistically analyzed the MNVT results of type I and III OPV at different stages: 1996–2002 and 2016–2022. The results show that the upper and lower limits and C value of the qualification standard of type I reference products in 2016–2022 have decreased compared with the corresponding scores in the 1996–2002 period. The upper and lower limit and C value of the qualified standard of type III reference products were basically the same as the corresponding scores in the 1996–2002. We also found significant differences in the pathogenicity of the type I and III in the cervical spine and brain, with the decreasing trend in the diffusion index of the type I and type III in the cervical spine and brain. Finally, two evaluation criteria were used to judge the OPV test vaccines from 2016 to 2022. The vaccines all met the test requirements under the evaluation criteria of the above two stages. Based on the characteristics of OPV, data monitoring was one of the most intuitive methods to judge changes in virulence. MDPI 2023-02-08 /pmc/articles/PMC9944487/ /pubmed/36810542 http://dx.doi.org/10.3390/diseases11010028 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Xiyan Ren, Ruirui Ma, Bo Xie, Jing Ma, Yan Luo, Hong Guo, Yu Ding, Ling Zhang, Liang Zhang, Mengyuan Wang, Tianlang Shuang, Zhichao Zhu, Xiujuan Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods |
title | Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods |
title_full | Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods |
title_fullStr | Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods |
title_full_unstemmed | Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods |
title_short | Comparative Study on MNVT of OPV Type I and III Reference Products in Different Periods |
title_sort | comparative study on mnvt of opv type i and iii reference products in different periods |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944487/ https://www.ncbi.nlm.nih.gov/pubmed/36810542 http://dx.doi.org/10.3390/diseases11010028 |
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