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Characterizing Poliovirus Transmission and Evolution: Insights from Modeling Experiences with Wild and Vaccine-Related Polioviruses

机译:表征脊髓灰质炎病毒的传播和进化:来自与野生和疫苗相关的脊髓灰质炎病毒建模经验的见解

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摘要

With national and global health policymakers facing numerous complex decisions related to achieving and maintaining polio eradication, we expanded our previously developed dynamic poliovirus transmission model using information from an expert literature review process and including additional immunity states and the evolution of oral poliovirus vaccine (OPV). The model explicitly considers serotype differences and distinguishes fecal-oral and oropharyn-geal transmission. We evaluated the model by simulating diverse historical experiences with polioviruses, including one country that eliminated wild poliovirus using both OPV and inactivated poliovirus vaccine (IPV) (USA), three importation outbreaks of wild poliovirus (Albania, the Netherlands, Tajikistan), one situation in which no circulating vaccine-derived polioviruses (cVDPVs) emerge despite annual OPV use and cessation (Cuba), three cVDPV outbreaks (Haiti, Madura Island in Indonesia, northern Nigeria), one area of current endemic circulation of all three serotypes (northern Nigeria), and one area with recent endemic circulation and subsequent elimination of multiple serotypes (northern India). We find that when sufficient information about the conditions exists, the model can reproduce the general behavior of poliovirus transmission and outbreaks while maintaining consistency in the generic model inputs. The assumption of spatially homogeneous mixing remains a significant limitation that affects the performance of the differential equation-based model when significant heterogeneities in immunity and mixing may exist. Further studies on OPV virus evolution and improved understanding of the mechanisms of mixing and transmission may help to better characterize poliovirus transmission in populations. Broad application of the model promises to offer insights in the context of global and national policy and economic models.
机译:随着国家和全球卫生政策制定者面临着与实现和维持消灭脊髓灰质炎有关的众多复杂决定,我们利用专家文献复审过程中的信息扩展了我们先前开发的动态脊髓灰质炎病毒传播模型,其中包括其他免疫状态和口服脊髓灰质炎病毒疫苗(OPV)的演变。该模型明确考虑血清型差异,并区分粪-口和口咽-基因传播。我们通过模拟脊髓灰质炎病毒的不同历史经验对模型进行了评估,包括一个使用OPV和灭活脊髓灰质炎疫苗(IPV)消除了野生脊髓灰质炎病毒的国家(美国),3次野生脊髓灰质炎病毒进口暴发(阿尔巴尼亚,荷兰,塔吉克斯坦),一种情况尽管每年使用和停止OPV(古巴),3次cVDPV暴发(印度尼西亚的海地,马杜拉岛,尼日利亚北部),所有三种血清型的当前流行区之一(尼日利亚北部),但仍未出现循环的疫苗衍生脊髓灰质炎病毒(cVDPVs) ),以及最近流行的地区和随后消除多种血清型的一个地区(印度北部)。我们发现,当存在有关条件的足够信息时,该模型可以重现脊髓灰质炎病毒传播和爆发的一般行为,同时保持通用模型输入中的一致性。当免疫和混合中可能存在明显的异质性时,空间均匀混合的假设仍然是一个重要的限制,它会影响基于微分方程的模型的性能。对OPV病毒进化的进一步研究以及对混合和传播机制的进一步了解可能有助于更好地表征人群中的脊髓灰质炎病毒传播。该模型的广泛应用有望在全球和国家政策与经济模型的背景下提供见解。

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  • 来源
    《Risk analysis》 |2013年第4期|703-749|共47页
  • 作者单位

    Kid Risk, Inc., 10524 Moss Park Rd., Ste. 204-364, Orlando, FL 32832, USA;

    Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA;

    Kid Risk, Inc., 10524 Moss Park Rd., Ste. 204-364, Orlando, FL 32832, USA,Delft Institute of Applied Mathematics, Delft University of Technology, Mekelweg 4,2628 CD, Delft, Netherlands;

    Global Immunization Division, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, USA;

    Global Immunization Division, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, USA;

    Kid Risk, Inc., 10524 Moss Park Rd., Ste. 204-364, Orlando, FL 32832, USA,University of Central Florida, College of Medicine, Orlando, FL, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    polio eradication; dynamic modeling; disease outbreaks;

    机译:根除脊髓灰质炎动态建模疾病暴发;

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