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Update on Vaccine-Derived Poliovirus Outbreaks — Worldwide July 2019–February 2020

机译:2019年7月至2020年2月全球疫苗衍生脊髓灰质炎病毒暴发的最新信息

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摘要

Circulating vaccine-derived polioviruses (cVDPVs) can emerge in areas with low poliovirus immunity and cause outbreaks of paralytic polio ( – ). Among the three types of wild poliovirus, type 2 was declared eradicated in 2015 ( , ). The use of trivalent oral poliovirus vaccine (tOPV; types 1, 2, and 3 Sabin strains) ceased in April 2016 via a 1-month–long, global synchronized switch to bivalent OPV (bOPV; types 1 and 3 Sabin strains) in immunization activities ( – ). Monovalent type 2 OPV (mOPV2; type 2 Sabin strain) is available for cVDPV type 2 (cVDPV2) outbreak response immunization ( – ). The number and geographic breadth of post-switch cVDPV2 outbreaks have exceeded forecasts that trended toward zero outbreaks 4 years after the switch and assumed rapid and effective control of any that occurred ( ). New cVDPV2 outbreaks have been seeded by mOPV2 use, by both suboptimal mOPV2 coverage within response zones and recently mOPV2-vaccinated children or contacts traveling outside of response zones, where children born after the global switch are fully susceptible to poliovirus type 2 transmission ( – ). In addition, new emergences can develop by inadvertent exposure to Sabin OPV2-containing vaccine (i.e., residual response mOPV2 or tOPV) ( ). This report updates the January 2018–June 2019 report with information on global cVDPV outbreaks during July 2019–February 2020 (as of March 25, 2020) ( ). Among 33 cVDPV outbreaks reported during July 2019–February 2020, 31 (94%) were cVDPV2; 18 (58%) of these followed new emergences. In mid-2020, the Global Polio Eradication Initiative (GPEI) plans to introduce a genetically stabilized, novel OPV type 2 (nOPV2) that has a lower risk for generating VDPV2 than does Sabin mOPV2; if nOPV2 is successful in limiting new VDPV2 emergences, GPEI foresees the replacement of Sabin mOPV2 with nOPV2 for cVDPV2 outbreak responses during 2021 ( , , ).
机译:脊髓灰质炎病毒免疫力低下的地区可能会出现循环疫苗源性脊髓灰质炎病毒(cVDPV),并导致麻痹性脊髓灰质炎爆发(–)。在这三种野生脊髓灰质炎病毒中,2型在2015年被宣布铲除(,)。三价口服脊髓灰质炎病毒疫苗(tOPV; 1、2和3型萨宾菌株)于2016年4月停止免疫,历时1个月,全球同步切换为二价OPV(bOPV; 1和3型Sabin菌株)活动(–)。单价2型OPV(mOPV2; 2型Sabin株)可用于cVDPV 2型(cVDPV2)暴发应答免疫接种(–)。转换后cVDPV2爆发的数量和地理范围已经超出了预测,该预测在转换后4年趋向于零暴发,并假定对发生的任何事件都进行了快速有效的控制()。新的cVDPV2暴发是通过使用mOPV2,在反应区内的次最佳mOPV2覆盖率和最近接种过mOPV2疫苗的儿童或在反应区外旅行的接触者而播种的,在全球性转换后出生的儿童完全容易感染2型脊髓灰质炎病毒。 。此外,由于意外接触含Sabin OPV2的疫苗(即残留反应mOPV2或tOPV),可能出现新的出现()。本报告使用有关2019年7月至2020年2月(截至2020年3月25日)全球cVDPV爆发的信息更新了2018年1月至2019年6月的报告()。在2019年7月至2020年2月报告的33例cVDPV暴发中,有31例(94%)为cVDPV2;其中有18(58%)个是新出现的。 2020年中期,全球根除脊髓灰质炎行动(GPEI)计划引入一种遗传稳定的新型2型OPV(nOPV2),其产生VDPV2的危险性低于Sabin mOPV2;如果nOPV2成功地限制了新的VDPV2出现,GPEI预计在2021年期间用nOPV2替代Sabin mOPV2以应对cVDPV2爆发。

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