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首页> 外文期刊>Communications in Nonlinear Science and Numerical Simulation >Mathematical model for HIV dynamics in HIV-specific helper cells
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Mathematical model for HIV dynamics in HIV-specific helper cells

机译:HIV特异性辅助细胞中HIV动态的数学模型

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摘要

In this paper we study a delay mathematical model for the dynamics of HIV in HIV-specific CD4 + T helper cells. We modify the model presented by Roy and Wodarz in 2012, where the HIV dynamics is studied, considering a single CD4 + T cell population. Non-specific helper cells are included as alternative target cell population, to account for macrophages and dendritic cells. In this paper, we include two types of delay: (1) a latent period between the time target cells are contacted by the virus particles and the time the virions enter the cells and; (2) virus production period for new virions to be produced within and released from the infected cells. We compute the reproduction number of the model, Ro, and the local stability of the disease free equilibrium and of the endemic equilibrium. We find that for values of R_0 < 1, the model approaches asymptotically the disease free equilibrium. For values of R_0 > 1, the model approximates asymptotically the endemic equilibrium. We observe numerically the phenomenon of backward bifurcation for values of R_0(≤)1. This statement will be proved in future work. We also vary the values of the latent period and the production period of infected cells and free virus. We conclude that increasing these values translates in a decrease of the reproduction number. Thus, a good strategy to control the HIV virus should focus on drugs to prolong the latent period and/or slow down the virus production. These results suggest that the model is mathematically and epidemiologically well-posed.
机译:在本文中,我们研究了HIV特异性CD4 + T辅助细胞中HIV动态的延迟数学模型。我们修改了Roy和Wodarz在2012年提出的模型,其中考虑了单个CD4 + T细胞群体,研究了HIV动力学。非特异性辅助细胞作为替代靶细胞群被包括在内,以说明巨噬细胞和树突状细胞。在本文中,我们包括两种类型的延迟:(1)病毒颗粒与靶细胞接触的时间与病毒体进入细胞的时间之间的潜伏期;以及(2)在受感染细胞内产生并释放出新病毒体的病毒生产期。我们计算模型的复制数Ro,以及无病平衡和地方平衡的局部稳定性。我们发现,对于R_0 <1的值,该模型渐近逼近无病平衡。对于R_0> 1的值,模型渐近地近似地方性均衡。我们在数值上观察到R_0(≤)1值向后分叉的现象。该声明将在以后的工作中得到证明。我们还改变了感染细胞和游离病毒的潜伏期和生产期的值。我们得出结论,增加这些值将导致复制数量减少。因此,控制HIV病毒的良好策略应集中于延长潜伏期和/或减慢病毒产生的药物。这些结果表明该模型在数学和流行病学上都具有良好的条件。

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  • 作者

    Carla M.A. Pinto; Ana Carvalho;

  • 作者单位

    School of Engineering, Polytechnic of Porto and Center of Mathematics of the University of Porto, Rua Dr Antonio Bernardino de Almeida, 431, 4200-072 Porto, Portugal,GECAD - Knowledge Engineering and Decision Support Research Center, Rua Dr Antonio Bernardino de Almeida, 431, 4200-072 Porto, Portugal;

    Faculty of Sciences, University of Porto, Rua do Campo Alegre s, 4440-452 Porto, Portugal;

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

    HIV/AIDS; Specific helper cells; Delay mathematical models;

    机译:HIV爱滋病;特定的辅助细胞;延迟数学模型;

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