Badizadegan Nima D, Wassilak Steven G F, Estívariz Concepción F, Wiesen Eric, Burns Cara C, Bolu Omotayo, Thompson Kimberly M
Kid Risk, Inc., Orlando, FL 32819, USA.
Global Immunization Division, Global Health Center, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Pathogens. 2024 Sep 17;13(9):804. doi: 10.3390/pathogens13090804.
In 2022, global poliovirus modeling suggested that coordinated cessation of bivalent oral poliovirus vaccine (bOPV, containing Sabin-strain types 1 and 3) in 2027 would likely increase the risks of outbreaks and expected paralytic cases caused by circulating vaccine-derived polioviruses (cVDPVs), particularly type 1. The analysis did not include the implementation of planned, preventive supplemental immunization activities (pSIAs) with bOPV to achieve and maintain higher population immunity for types 1 and 3 prior to bOPV cessation. We reviewed prior published OPV cessation modeling studies to support bOPV cessation planning. We applied an integrated global poliovirus transmission and OPV evolution model after updating assumptions to reflect the epidemiology, immunization, and polio eradication plans through the end of 2023. We explored the effects of bOPV cessation in 2027 with and without additional bOPV pSIAs prior to 2027. Increasing population immunity for types 1 and 3 with bOPV pSIAs (i.e., intensification) could substantially reduce the expected global risks of experiencing cVDPV outbreaks and the number of expected polio cases both before and after bOPV cessation. We identified the need for substantial increases in overall bOPV coverage prior to bOPV cessation to achieve a high probability of successful bOPV cessation.
2022年,全球脊髓灰质炎病毒模型显示,2027年二价口服脊髓灰质炎病毒疫苗(bOPV,含1型和3型萨宾株)的协同停用可能会增加由疫苗衍生脊髓灰质炎病毒(cVDPV),尤其是1型cVDPV引起的疫情爆发风险和预期麻痹病例数。该分析未包括在停用bOPV之前开展计划中的预防性补充免疫活动(pSIA)以使用bOPV实现并维持更高的1型和3型人群免疫力。我们回顾了先前发表的关于停用OPV的模型研究,以支持bOPV停用计划。在更新假设以反映截至2023年底的流行病学、免疫接种和脊髓灰质炎根除计划后,我们应用了一个综合的全球脊髓灰质炎病毒传播和OPV进化模型。我们探讨了在2027年停用bOPV且在2027年之前有无额外bOPV pSIA的影响。通过bOPV pSIA提高1型和3型的人群免疫力(即强化免疫)可大幅降低在停用bOPV前后出现cVDPV疫情的预期全球风险以及预期脊髓灰质炎病例数。我们确定在停用bOPV之前需要大幅提高bOPV的总体覆盖率,以实现成功停用bOPV的高概率。