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更新 2019-2029 年暴发应对策略的特征描述:使用新型 2 型口服脊髓灰质炎疫苗株的影响。

Updated Characterization of Outbreak Response Strategies for 2019-2029: Impacts of Using a Novel Type 2 Oral Poliovirus Vaccine Strain.

机构信息

Kid Risk, Inc., Orlando, FL, USA.

National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.

出版信息

Risk Anal. 2021 Feb;41(2):329-348. doi: 10.1111/risa.13622. Epub 2020 Nov 10.

Abstract

Delays in achieving the global eradication of wild poliovirus transmission continue to postpone subsequent cessation of all oral poliovirus vaccine (OPV) use. Countries must stop OPV use to end all cases of poliomyelitis, including vaccine-associated paralytic polio (VAPP) and cases caused by vaccine-derived polioviruses (VDPVs). The Global Polio Eradication Initiative (GPEI) coordinated global cessation of all type 2 OPV (OPV2) use in routine immunization in 2016 but did not successfully end the transmission of type 2 VDPVs (VDPV2s), and consequently continues to use type 2 OPV (OPV2) for outbreak response activities. Using an updated global poliovirus transmission and OPV evolution model, we characterize outbreak response options for 2019-2029 related to responding to VDPV2 outbreaks with a genetically stabilized novel OPV (nOPV2) strain or with the currently licensed monovalent OPV2 (mOPV2). Given uncertainties about the properties of nOPV2, we model different assumptions that appear consistent with the evidence on nOPV2 to date. Using nOPV2 to respond to detected cases may reduce the expected VDPV and VAPP cases and the risk of needing to restart OPV2 use in routine immunization compared to mOPV2 use for outbreak response. The actual properties, availability, and use of nOPV2 will determine its effects on type 2 poliovirus transmission in populations. Even with optimal nOPV2 performance, countries and the GPEI would still likely need to restart OPV2 use in routine immunization in OPV-using countries if operational improvements in outbreak response to stop the transmission of cVDPV2s are not implemented effectively.

摘要

延迟实现全球消灭野生脊灰病毒传播的目标,继续推迟随后停止所有口服脊髓灰质炎疫苗(OPV)使用。各国必须停止使用 OPV,以结束所有脊髓灰质炎病例,包括疫苗相关麻痹性脊髓灰质炎(VAPP)和疫苗衍生脊灰病毒(VDPV)引起的病例。全球根除脊髓灰质炎行动(GPEI)协调全球于 2016 年停止在常规免疫中使用所有类型 2 OPV(OPV2),但未能成功终止 2 型 VDPV(VDPV2)的传播,因此继续使用 2 型 OPV(OPV2)开展应对疫情活动。利用更新的全球脊灰病毒传播和 OPV 进化模型,我们对 2019-2029 年的疫情应对选择进行了特征描述,涉及使用基因稳定的新型 OPV(nOPV2)株或目前许可的单价 2 型 OPV(mOPV2)应对 VDPV2 疫情。考虑到 nOPV2 的特性存在不确定性,我们对不同假设进行了建模,这些假设似乎与迄今为止有关 nOPV2 的证据一致。与使用 mOPV2 应对疫情相比,使用 nOPV2 应对已检测到的病例,可能会减少预期的 VDPV 和 VAPP 病例,以及需要重新开始在常规免疫中使用 OPV2 的风险。nOPV2 的实际特性、可用性和使用情况将决定其对人群中 2 型脊灰病毒传播的影响。即使 nOPV2 性能达到最佳,在没有有效实施改善疫情应对以阻止 cVDPV2 传播的运营改进的情况下,OPV 接种国家仍可能需要重新开始在常规免疫中使用 OPV2。

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