Tebbens Radboud J Duintjer, Hampton Lee M, Wassilak Steven G F, Pallansch Mark A, Cochi Stephen L, Thompson Kimberly M
Kid Risk, Inc., 10524 Moss Park Rd., Ste. 204-364, Orlando, FL 32832, USA.
Global Immunization Division, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, USA.
J Vaccines Vaccin. 2016 Oct;7(5). doi: 10.4172/2157-7560.1000340. Epub 2016 Oct 3.
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).
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.
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.
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.
研究在全球协调停止1型和3型口服脊髓灰质炎疫苗(OPV13停止)前后,不同的二价口服脊髓灰质炎疫苗(bOPV)补充免疫活动(SIA)策略对人群针对1型和3型脊髓灰质炎病毒传播的免疫力以及循环疫苗衍生脊髓灰质炎病毒(cVDPV)风险的影响。
我们采用先前在三价口服脊髓灰质炎疫苗转换为bOPV之前为疫苗选择提供依据的数学模型,来估计在OPV13停止时预防随后cVDPV暴发所需的针对1型和3型脊髓灰质炎病毒传播的人群免疫力。然后,我们研究在高风险人群中使用bOPV进行不同频率SIA对针对1型和3型传播的人群免疫力、1型和3型cVDPV暴发风险以及对任何输入性bOPV相关脊髓灰质炎病毒的易感性的影响。
使用bOPV SIA维持人群对1型和3型传播的高免疫力可显著降低:1)因输入1型和3型病毒导致的暴发风险;2)在OPV13停止之前或之后本土cVDPV的出现;3)在OPV13停止不同步或OPV13停止后意外使用bOPV的情况下对bOPV相关脊髓灰质炎病毒的易感性。
虽然全球SIA频率可以安全地有所降低,但常规免疫接种覆盖率欠佳的国家应各自继续每年至少开展一次bOPV SIA,最好更多,直至全球OPV13停止。在OPV13停止后预防cVDPV风险需要从现在起到OPV13停止期间对bOPV SIA进行投资。