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Stability of a general discrete-time viral infection model with humoral immunity and cellular infection

机译:具有体液免疫和细胞感染的一般离散时间病毒感染模型的稳定性

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This paper studies the global stability of a general discrete-time viral infection model with virus-to-cell and cell-to-cell transmissions and with humoral immune response. We consider both latently and actively infected cells. The model incorporates three types of intracellular time delays. The production and clearance rates of all compartments as well as incidence rates of infection are modeled by general nonlinear functions. We use the nonstandard finite difference method to discretize the continuous-time model. We show that the solutions of the discrete-time model are positive and ultimately bounded. We derive two threshold parameters, the basic reproduction number R 0 and the humoral immune response activation number R 1 , which completely determine the existence and stability of the model’s equilibria. By using Lyapunov functions, we have proven that if R 0 ≤ 1 , then the virus-free equilibrium Q 0 is globally asymptotically stable; if R 1 ≤ 1 1 , then the persistent infection equilibrium with immune response Q ˉ is globally asymptotically stable. We illustrate our theoretical results by using numerical simulations. The effects of antiretroviral drug therapy and time delay on the virus dynamics are also studied. We have shown that the time delay has a similar effect as the antiretroviral drug therapy.
机译:本文研究了具有病毒 - 细胞和细胞传输和体液免疫应答的通用离散时间病毒感染模型的全球稳定性。我们考虑潜伏和积极的感染细胞。该模型包含三种类型的细胞内时间延迟。所有隔室的生产和清除率以及感染发生率的速率是通过一般非线性功能的模拟。我们使用非标准的有限差分方法来离散连续时间模型。我们表明离散时间模型的解决方案是积极的和最终界限。我们得出了两个阈值参数,基本再现数R 0和体液免疫反应激活号R 1,其完全确定了模型的均衡的存在和稳定性。通过使用Lyapunov功能,我们已经证明,如果R0≤1,则无病毒平衡Q 0是全球渐近稳定的;如果r1≤11,则具有免疫应答Q≥的持续感染平衡是全球渐近的稳定性。我们通过使用数值模拟来说明我们的理论结果。还研究了抗逆转录病毒药物治疗和时间延迟对病毒动力学的影响。我们已经表明,时间延迟具有与抗逆转录病毒药物治疗类似的效果。

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