The progress of postapproval clinical studies on Sabin IPV

As one of the powerful vaccines for completely eradicating all types of poliovirus in the polio endgame period, the novel IPV, which is prepared from attenuated polio Sabin strains (sIPV) and is expected to reduce the overall biosafety risk, was licensed in Japan (sIPV-containing diphtheria-tetanus-...

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Main Authors: Li Shi, Mingbo Sun
Format: Article
Language:English
Published: Taylor & Francis Group 2022-01-01
Series:Human Vaccines & Immunotherapeutics
Subjects:
Online Access:http://dx.doi.org/10.1080/21645515.2021.1940653
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author Li Shi
Mingbo Sun
author_facet Li Shi
Mingbo Sun
author_sort Li Shi
collection DOAJ
description As one of the powerful vaccines for completely eradicating all types of poliovirus in the polio endgame period, the novel IPV, which is prepared from attenuated polio Sabin strains (sIPV) and is expected to reduce the overall biosafety risk, was licensed in Japan (sIPV-containing diphtheria-tetanus-acellular pertussis combination vaccines, DTP-sIPV) and China (sIPV) in November 2012 and January 2015, respectively. Limited by the development progress and the manufactured sIPV ability, it has to date only been used in Chinese Expanded Programme on Immunization (EPI) by sequential scheduling with bOPV and in Japan with DTP-sIPV vaccination. We herein summarize postapproval clinical studies of sIPV in both full-dose schedules and sequential schedules, focusing on China, to evaluate sIPV safety and immunogenicity in large populations to provide important data for its broad application in developing countries worldwide.
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spelling doaj.art-c2256451dddd41748b20165d84a335192023-09-26T08:59:30ZengTaylor & Francis GroupHuman Vaccines & Immunotherapeutics2164-55152164-554X2022-01-011811410.1080/21645515.2021.19406531940653The progress of postapproval clinical studies on Sabin IPVLi Shi0Mingbo Sun1Chinese Academy of Medical Sciences & Peking Union Medical CollegeChinese Academy of Medical Sciences & Peking Union Medical CollegeAs one of the powerful vaccines for completely eradicating all types of poliovirus in the polio endgame period, the novel IPV, which is prepared from attenuated polio Sabin strains (sIPV) and is expected to reduce the overall biosafety risk, was licensed in Japan (sIPV-containing diphtheria-tetanus-acellular pertussis combination vaccines, DTP-sIPV) and China (sIPV) in November 2012 and January 2015, respectively. Limited by the development progress and the manufactured sIPV ability, it has to date only been used in Chinese Expanded Programme on Immunization (EPI) by sequential scheduling with bOPV and in Japan with DTP-sIPV vaccination. We herein summarize postapproval clinical studies of sIPV in both full-dose schedules and sequential schedules, focusing on China, to evaluate sIPV safety and immunogenicity in large populations to provide important data for its broad application in developing countries worldwide.http://dx.doi.org/10.1080/21645515.2021.1940653sipvpostapproval clinical studiesfull-dose and sequential vaccinationsafetyimmunogenicity
spellingShingle Li Shi
Mingbo Sun
The progress of postapproval clinical studies on Sabin IPV
Human Vaccines & Immunotherapeutics
sipv
postapproval clinical studies
full-dose and sequential vaccination
safety
immunogenicity
title The progress of postapproval clinical studies on Sabin IPV
title_full The progress of postapproval clinical studies on Sabin IPV
title_fullStr The progress of postapproval clinical studies on Sabin IPV
title_full_unstemmed The progress of postapproval clinical studies on Sabin IPV
title_short The progress of postapproval clinical studies on Sabin IPV
title_sort progress of postapproval clinical studies on sabin ipv
topic sipv
postapproval clinical studies
full-dose and sequential vaccination
safety
immunogenicity
url http://dx.doi.org/10.1080/21645515.2021.1940653
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