在全球协调停用二价口服脊髓灰质炎病毒疫苗之前,维持和加强二价口服脊髓灰质炎病毒疫苗的使用。

Journal of vaccines & vaccination Pub Date : 2016-10-01 Epub Date: 2016-10-03 DOI:10.4172/2157-7560.1000340
Radboud J Duintjer Tebbens, Lee M Hampton, Steven G F Wassilak, Mark A Pallansch, Stephen L Cochi, Kimberly M Thompson
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引用次数: 0

摘要

目的研究在全球协调停止使用血清 1 型和 3 型口服脊灰病毒疫苗(OPV13 停止使用)前后,不同的二价口服脊灰病毒疫苗(bOPV)补充免疫活动(SIA)策略对血清 1 型和 3 型脊灰病毒传播的人群免疫力以及疫苗衍生脊灰病毒(cVDPV)风险的影响:我们调整了以前在三价口服脊髓灰质炎病毒疫苗向双价口服脊髓灰质炎病毒疫苗转换之前为疫苗选择提供信息的数学模型,以估算在停止接种 OPV13 时为预防随后的 cVDPV 暴发所需的血清 1 型和 3 型脊髓灰质炎病毒传播的人群免疫力。然后,我们研究了在高风险人群中使用 bOPV 进行 SIA 的不同频率对血清 1 型和 3 型传播的人群免疫力、血清 1 型和 3 型 cVDPV 爆发风险以及对任何输入的 bOPV 相关脊灰病毒的易感性的影响:结果:使用 bOPV SIA 保持人群对血清 1 型和 3 型传播的高免疫力可显著降低:1)由输入的血清 1 型和 3 型病毒引起的疫情爆发风险;2)在 OPV13 停止使用之前或之后出现本地 cVDPV;3)在 OPV13 非同步停止使用或在 OPV13 停止使用后无意中使用 bOPV 的情况下易感染与 bOPV 相关的脊髓灰质炎病毒:结论:尽管全球 SIA 频率可以安全地有所降低,但常规免疫覆盖率不理想的国家应继续每年至少使用 bOPV 进行一次 SIA,最好更多,直到全球停止使用 OPV13。要在 OPV13 停止使用后预防 cVDPV 风险,需要从现在到 OPV13 停止使用期间对 bOPV SIA 进行投资。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Maintenance and Intensification of Bivalent Oral Poliovirus Vaccine Use Prior to its Coordinated Global Cessation.

Maintenance and Intensification of Bivalent Oral Poliovirus Vaccine Use Prior to its Coordinated Global Cessation.

Maintenance and Intensification of Bivalent Oral Poliovirus Vaccine Use Prior to its Coordinated Global Cessation.

Maintenance and Intensification of Bivalent Oral Poliovirus Vaccine Use Prior to its Coordinated Global Cessation.

Objective: To examine the impact of different bivalent oral poliovirus vaccine (bOPV) supplemental immunization activity (SIA) strategies on population immunity to serotype 1 and 3 poliovirus transmission and circulating vaccine-derived poliovirus (cVDPV) risks before and after globally-coordinated cessation of serotype 1 and 3 oral poliovirus vaccine (OPV13 cessation).

Methods: We adapt mathematical models that previously informed vaccine choices ahead of the trivalent oral poliovirus vaccine to bOPV switch to estimate the population immunity to serotype 1 and 3 poliovirus transmission needed at the time of OPV13 cessation to prevent subsequent cVDPV outbreaks. We then examine the impact of different frequencies of SIAs using bOPV in high risk populations on population immunity to serotype 1 and 3 transmission, on the risk of serotype 1 and 3 cVDPV outbreaks, and on the vulnerability to any imported bOPV-related polioviruses.

Results: Maintaining high population immunity to serotype 1 and 3 transmission using bOPV SIAs significantly reduces 1) the risk of outbreaks due to imported serotype 1 and 3 viruses, 2) the emergence of indigenous cVDPVs before or after OPV13 cessation, and 3) the vulnerability to bOPV-related polioviruses in the event of non-synchronous OPV13 cessation or inadvertent bOPV use after OPV13 cessation.

Conclusion: Although some reduction in global SIA frequency can safely occur, countries with suboptimal routine immunization coverage should each continue to conduct at least one annual SIA with bOPV, preferably more, until global OPV13 cessation. Preventing cVDPV risks after OPV13 cessation requires investments in bOPV SIAs now through the time of OPV13 cessation.

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