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Viral dynamics of an HTLV-I infection model with intracellular delay and CTL immune response delay

机译:具有细胞内延迟和CTL免疫应答延迟的HTLV-I感染模型的病毒动力学

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We have developed a model of HTLV-I infection with two time delays: an intracellular delay, and a CTL immune response delay. The basic reproduction number R-0, which depends on the intracellular delay, is shown to determine stability conditions of the model steady states. If R-0 1, using a suitable Lyapunov function, we show that the infection-free steady state is globally asymptotically stable including both time delays. If R-0 1, the unique infected steady state exists, and we analyze our model in two cases: (a) the model only with the intracellular delay, that has an infected steady state that is globally asymptotically stable for every intracellular delay (shown using suitable Lyapunov functions); (b) the model with the immune response delay only, that experiences a destabilization of the infected steady state leading to Hopf bifurcation and periodic solutions. Furthermore, we employ Latin hypercube sampling (LHS) to investigate the possibility of the occurrence of the Hopf bifurcation and determine the key parameters that affect the stability of the infected steady state, under realistic parameter space. Numerical simulations indicate that an increase of the intracellular delay can cause the infected steady state to stabilize, while an increase of the immune delay can cause it to destabilize. (C) 2017 Elsevier Inc. All rights reserved.
机译:我们已经开发了具有两次延迟的HTLV-I感染模型:细胞内延迟和CTL免疫应答延迟。基本再现数R-0取决于细胞内延迟,显示用于确定模型稳定状态的稳定性条件。如果r-0& 1,使用合适的Lyapunov功能,我们表明无感染稳态是全球渐近状态,包括两个时间延迟。如果r-0& 1,独特的感染稳态存在,我们分析了我们的模型在两种情况下:(a)仅具有细胞内延迟的模型,具有对每个细胞内延迟的全局渐近状态的感染稳定状态(使用合适的Lyapunov功能所示); (b)仅具有免疫应答延迟的模型,经历了感染稳态的稳定化,导致Hopf分叉和周期性解决方案。此外,我们采用拉丁超立方体采样(LHS)来调查HopF分叉发生的可能性,并确定影响感染稳态的稳定性的关键参数,在现实参数空间下。数值模拟表明细胞内延迟的增加会导致感染的稳态稳定,而免疫延迟的增加会导致它变得破坏。 (c)2017年Elsevier Inc.保留所有权利。

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