Department of Mathematics, University of Louisiana at Lafayette, Lafayette, LA, 70503, USA.
Tongji Zhejiang College, Jiaxing, Zhejiang, China.
Bull Math Biol. 2020 Feb 5;82(2):29. doi: 10.1007/s11538-020-00704-3.
There is a substantial interest in detailed models of viral infection and antiviral drug kinetics in order to optimize the treatment against viruses such as HIV. In this paper, we study within-viral dynamics under general intracellular distributed delays and periodic combination antiviral therapy. The basic reproduction number [Formula: see text] is established as a global threshold determining extinction versus persistence, and spectral methods are utilized for analytical and numerical computations of [Formula: see text]. We derive the critical maturation delay for virus and optimal phase difference between sinusoidally varying drug efficacies under various intracellular delays. Furthermore, numerical simulations are conducted utilizing realistic pharmacokinetics and gamma-distributed viral production delays for HIV. Our results demonstrate that the relative timing of the key viral replication cycle steps and periodic antiviral treatment schedule involving distinct drugs all can interact to critically affect the overall viral dynamics.
人们对详细的病毒感染和抗病毒药物动力学模型有着浓厚的兴趣,以便优化针对 HIV 等病毒的治疗方法。在本文中,我们研究了在一般细胞内分布延迟和周期性联合抗病毒治疗下的病毒内动力学。基本繁殖数 [Formula: see text] 被确立为决定灭绝与持续存在的全局阈值,并且谱方法被用于 [Formula: see text] 的分析和数值计算。我们推导了病毒的临界成熟延迟和在各种细胞内延迟下正弦变化的药物功效之间的最佳相位差。此外,还针对 HIV 利用现实的药代动力学和伽马分布的病毒产生延迟进行了数值模拟。我们的结果表明,关键病毒复制周期步骤的相对时间和涉及不同药物的周期性抗病毒治疗方案都可以相互作用,从而对整体病毒动力学产生关键影响。