在口服脊髓灰质炎病毒疫苗(OPV)停止使用后,在国家免疫计划中重新启动口服脊髓灰质炎病毒疫苗(OPV)的相关方案的复杂性。

Gates Open Research Pub Date : 2023-04-17 eCollection Date: 2023-01-01 DOI:10.12688/gatesopenres.14511.1
Dominika A Kalkowska, Steven Gf Wassilak, Eric Wiesen, Concepcion F Estivariz, Cara C Burns, Kamran Badizadegan, Kimberly M Thompson
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引用次数: 0

摘要

背景:根除脊髓灰质炎工作的复杂性不断增加。 2022 年报告的脊髓灰质炎病例由 1 型野生脊髓灰质炎病毒和所有三种类型(1、2 和 3)的疫苗衍生脊髓灰质炎病毒引起,脊髓灰质炎病毒疫苗的数量、配方和使用给国家免疫计划和疫苗供应商带来了挑战。 之前对全球协调停止口服脊髓灰质炎病毒疫苗(OPV)的特定类型进行的脊髓灰质炎病毒传播建模假定建立了用于紧急情况的 Sabin 单价 OPV(mOPV)储备,并探讨了如果全球在停止 OPV 后病例数达到指定的累计阈值,是否需要重新启动 OPV。方法: 我们记录了 2 型 OPV (OPV2) 停止使用的实际经验,并重新考虑了之前与 OPV 重启相关的模型假设。 考虑到 OPV 重启的不同可能性,我们开发了最新的脊髓灰质炎病毒疫苗国家免疫方案决策树。结果: 虽然 OPV 重启是风险管理和应急规划的一种假设情况,以支持 2013-2018 年全球根除脊髓灰质炎倡议(GPEI)战略计划,但 OPV2 停用以来的实际流行病学经验提出了一些问题,即在常规免疫接种中重启 OPV2 的触发因素(如果有的话)是什么,以及/或 1 型和 3 型 OPV 在各自停用后未来可能重启的计划。 基因稳定的新型 2 型 OPV (nOPV2)的紧急使用清单以及对 1 型和/或 3 型 nOPV 的持续评估增加了重新启动 OPV 的可能 OPV 配方组合,从而进一步增加了复杂性。 结论:在 2019 年关于重启 OPV 的后勤挑战和影响的讨论基础上,我们发现到 2023 年初,与重启 OPV 的决策和政策相关的许多选择和许多问题的结构非常复杂。 由于脊髓灰质炎病毒疫苗选择的潜在组合越来越多,我们预计在脊髓灰质炎终局期间,预测未来疫苗供应需求将面临许多挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Complexity of options related to restarting oral poliovirus vaccine (OPV) in national immunization programs after OPV cessation.

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 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.

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来源期刊
Gates Open Research
Gates Open Research Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
3.60
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