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Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation
Background: The polio eradication endgame continues to increase in complexity. With polio cases caused by wild poliovirus type 1 and circulating vaccine-derived polioviruses of all three types (1, 2 and 3) reported in 2022, the number, formulation, and use of poliovirus vaccines poses challenges fo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403636/ https://www.ncbi.nlm.nih.gov/pubmed/37547300 http://dx.doi.org/10.12688/gatesopenres.14511.1 |
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author | Kalkowska, Dominika A Wassilak, Steven GF Wiesen, Eric F Estivariz, Concepcion Burns, Cara C Badizadegan, Kamran Thompson, Kimberly M |
author_facet | Kalkowska, Dominika A Wassilak, Steven GF Wiesen, Eric F Estivariz, Concepcion Burns, Cara C Badizadegan, Kamran Thompson, Kimberly M |
author_sort | Kalkowska, Dominika A |
collection | PubMed |
description | Background: The polio eradication endgame continues to increase in complexity. With polio cases caused by wild poliovirus type 1 and circulating vaccine-derived polioviruses of all three types (1, 2 and 3) reported in 2022, the number, formulation, and use of poliovirus vaccines poses challenges for national immunization programs and vaccine suppliers. Prior poliovirus transmission modeling of globally-coordinated type-specific cessation of oral poliovirus vaccine (OPV) assumed creation of Sabin monovalent OPV (mOPV) stockpiles for emergencies and explored the potential need to restart OPV if the world reached a specified cumulative threshold number of cases after OPV cessation. Methods: We document the actual experience of type 2 OPV (OPV2) cessation and reconsider prior modeling assumptions related to OPV restart. We develop updated decision trees of national immunization options for poliovirus vaccines considering different possibilities for OPV restart. Results: While OPV restart represented a hypothetical situation for risk management and contingency planning to support the 2013-2018 Global Polio Eradication Initiative (GPEI) Strategic Plan, the actual epidemiological experience since OPV2 cessation raises questions about what, if any, trigger(s) could lead to restarting the use of OPV2 in routine immunization and/or plans for potential future restart of type 1 and 3 OPV after their respective cessation. The emergency use listing of a genetically stabilized novel type 2 OPV (nOPV2) and continued evaluation of nOPV for types 1 and/or 3 add further complexity by increasing the combinations of possible OPV formulations for OPV restart. Conclusions: Expanding on a 2019 discussion of the logistical challenges and implications of restarting OPV, we find a complex structure of the many options and many issues related to OPV restart decisions and policies as of early 2023. We anticipate many challenges for forecasting prospective vaccine supply needs during the polio endgame due to increasing potential combinations of poliovirus vaccine choices. |
format | Online Article Text |
id | pubmed-10403636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-104036362023-08-06 Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation Kalkowska, Dominika A Wassilak, Steven GF Wiesen, Eric F Estivariz, Concepcion Burns, Cara C Badizadegan, Kamran Thompson, Kimberly M Gates Open Res Research Article Background: The polio eradication endgame continues to increase in complexity. With polio cases caused by wild poliovirus type 1 and circulating vaccine-derived polioviruses of all three types (1, 2 and 3) reported in 2022, the number, formulation, and use of poliovirus vaccines poses challenges for national immunization programs and vaccine suppliers. Prior poliovirus transmission modeling of globally-coordinated type-specific cessation of oral poliovirus vaccine (OPV) assumed creation of Sabin monovalent OPV (mOPV) stockpiles for emergencies and explored the potential need to restart OPV if the world reached a specified cumulative threshold number of cases after OPV cessation. Methods: We document the actual experience of type 2 OPV (OPV2) cessation and reconsider prior modeling assumptions related to OPV restart. We develop updated decision trees of national immunization options for poliovirus vaccines considering different possibilities for OPV restart. Results: While OPV restart represented a hypothetical situation for risk management and contingency planning to support the 2013-2018 Global Polio Eradication Initiative (GPEI) Strategic Plan, the actual epidemiological experience since OPV2 cessation raises questions about what, if any, trigger(s) could lead to restarting the use of OPV2 in routine immunization and/or plans for potential future restart of type 1 and 3 OPV after their respective cessation. The emergency use listing of a genetically stabilized novel type 2 OPV (nOPV2) and continued evaluation of nOPV for types 1 and/or 3 add further complexity by increasing the combinations of possible OPV formulations for OPV restart. Conclusions: Expanding on a 2019 discussion of the logistical challenges and implications of restarting OPV, we find a complex structure of the many options and many issues related to OPV restart decisions and policies as of early 2023. We anticipate many challenges for forecasting prospective vaccine supply needs during the polio endgame due to increasing potential combinations of poliovirus vaccine choices. F1000 Research Limited 2023-04-17 /pmc/articles/PMC10403636/ /pubmed/37547300 http://dx.doi.org/10.12688/gatesopenres.14511.1 Text en Copyright: © 2023 Kalkowska DA et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The author(s) is/are employees of the US Government and therefore domestic copyright protection in USA does not apply to this work. The work may be protected under the copyright laws of other jurisdictions when used in those jurisdictions. |
spellingShingle | Research Article Kalkowska, Dominika A Wassilak, Steven GF Wiesen, Eric F Estivariz, Concepcion Burns, Cara C Badizadegan, Kamran Thompson, Kimberly M Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation |
title | Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation |
title_full | Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation |
title_fullStr | Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation |
title_full_unstemmed | Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation |
title_short | Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation |
title_sort | complexity of options related to restarting oral poliovirus vaccine (opv) in national immunization programs after opv cessation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403636/ https://www.ncbi.nlm.nih.gov/pubmed/37547300 http://dx.doi.org/10.12688/gatesopenres.14511.1 |
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