A Delay Differential Equation Model of HIV Infection, with Therapy and CTL Response

B. E. Boukari, N. Yousfi
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引用次数: 3

Abstract

In this work we investigate a new mathematical model that describes the interactions between CD4+ T cells, human immunodeficiency virus (HIV), immune response and therapy with two drugs. Also an intracellular delay is incorporated into the model to express the lag between the time the virus contacts a target cell and the time the cell becomes actively infected. The model dynamics is completely defined by the basic reproduction number R0 . If R0 ≤ 1 the disease-free equilibrium is globally asymptotically stable, and if R0 > 1, two endemic steady states exist, and their local stability depends on value of R0 . We show that the intracellular delay affects on value of R0 because a larger intracellular delay can reduce the value of R0 to below one. Finally, numerical simulations are presented to illustrate our theoretical results.
HIV感染的延迟微分方程模型,治疗和CTL反应
在这项工作中,我们研究了一个新的数学模型,描述了CD4+ T细胞、人类免疫缺陷病毒(HIV)、免疫反应和两种药物治疗之间的相互作用。此外,在模型中加入了细胞内延迟,以表示病毒接触目标细胞和细胞被积极感染的时间之间的滞后。模型动力学完全由基本再现数R0定义。当R0≤1时,无病平衡是全局渐近稳定的;当R0≤1时,存在两个地方性稳态,它们的局部稳定性取决于R0的值。我们证明了胞内延迟对R0值的影响,因为较大的胞内延迟可以使R0值降低到1以下。最后,通过数值模拟对理论结果进行了验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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