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一种治疗和人口统计学对疟疾再感染影响的混合模型。

A hybrid model for the effects of treatment and demography on malaria superinfection.

机构信息

Institute for Health Metrics and Evaluation, University of Washington, Seattle, Washington, USA.

出版信息

J Theor Biol. 2020 Apr 21;491:110194. doi: 10.1016/j.jtbi.2020.110194. Epub 2020 Feb 8.

DOI:10.1016/j.jtbi.2020.110194
Abstract

As standard mathematical models for the transmission of vector-borne pathogens with weak or no apparent sterilizing immunity, Susceptible-Infected-Susceptible (SIS) systems such as the Ross-Macdonald equations are a useful starting point for modeling the impacts of interventions on prevalence for diseases that cannot superinfect their hosts. In particular, they are parameterizable from quantities we can estimate such as the force of infection (FOI), the rate of natural recovery from a single infection, the treatment rate, and the rate of demographic turnover. However, malaria parasites can superinfect their host which has the effect of increasing the duration of infection before total recovery. Queueing theory has been applied to capture this behavior, but a problem with current queueing models is the exclusion of factors such as demographic turnover and treatment. These factors in particular can affect the entire shape of the distribution of the multiplicity of infection (MOI) generated by the superinfection process, its transient dynamics, and the population mean recovery rate. Here we show the distribution of MOI can be described by an alternative hyper-Poisson distribution. We then couple our resulting equations to a simple vector transmission model, extending previous Ross-Macdonald theory.

摘要

作为带有弱或无明显绝育免疫的病媒传播病原体的标准数学模型,如 Ross-Macdonald 方程的易感-感染-易感 (SIS) 系统,是对无法再次感染宿主的疾病进行干预对流行率影响建模的一个有用起点。特别是,它们可以根据我们可以估计的数量进行参数化,例如感染力 (FOI)、单次感染自然恢复率、治疗率和人口更替率。然而,疟原虫可以再次感染宿主,这会增加感染完全恢复前的持续时间。排队论已被应用于捕捉这种行为,但当前排队模型的一个问题是排除了人口更替和治疗等因素。这些因素尤其会影响由再感染过程产生的感染多重性 (MOI) 的分布、其瞬态动力学和群体平均恢复率的整个形状。在这里,我们展示了 MOI 的分布可以用替代的超泊松分布来描述。然后,我们将得到的方程与一个简单的向量传播模型相结合,扩展了之前的 Ross-Macdonald 理论。

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引用本文的文献

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A hybrid transmission model for Plasmodium vivax accounting for superinfection, immunity and the hypnozoite reservoir.一种考虑重复感染、免疫和潜隐体库的间日疟原虫混合传播模型。
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2
Quantifying the impact of interventions against Plasmodium vivax: A model for country-specific use.量化针对间日疟原虫的干预措施的影响:一种供各国具体使用的模型。
Epidemics. 2024 Mar;46:100747. doi: 10.1016/j.epidem.2024.100747. Epub 2024 Feb 5.
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Superinfection and the hypnozoite reservoir for Plasmodium vivax: a general framework.

本文引用的文献

1
Agent-based models of malaria transmission: a systematic review.基于主体的疟疾传播模型:系统评价。
Malar J. 2018 Aug 17;17(1):299. doi: 10.1186/s12936-018-2442-y.
2
Molecular approaches to determine the multiplicity of Plasmodium infections.分子方法确定疟原虫感染的多重性。
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3
Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015.
疟原虫 vivax 的继发感染和休眠子库:一个通用框架。
J Math Biol. 2023 Dec 1;88(1):7. doi: 10.1007/s00285-023-02014-3.
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Cross-reactive immune responses as primary drivers of malaria chronicity.交叉反应性免疫应答是疟疾慢性化的主要驱动因素。
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Ross, macdonald, and a theory for the dynamics and control of mosquito-transmitted pathogens.罗斯、麦克唐纳和蚊虫传播病原体的动力学与控制理论。
PLoS Pathog. 2012;8(4):e1002588. doi: 10.1371/journal.ppat.1002588. Epub 2012 Apr 5.
8
False-negative rapid diagnostic tests for malaria and deletion of the histidine-rich repeat region of the hrp2 gene.疟原虫快速诊断检测的假阴性和 HRP2 基因组氨酸丰富重复区缺失。
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Superinfection in malaria: Plasmodium shows its iron will.疟疾中的继发感染:疟原虫展现出它的“铁意志”。
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Acquired immunity to malaria.获得性疟疾免疫力。
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