HIV model with intracellular delay — a mathematical study

P. Roy, N. Bairagi, J. Chattopadhyay, B. Chattopadhyay
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引用次数: 2

Abstract

Human Immunodeficiency Virus (HIV) is observed to infect the CD4+T lymphocytes in the human blood. In this article we consider a modification of a basic HIV model introduced by Herz et al. [1] representing the HIV dynamics. We introduce an intracellular delay in the disease transmission term. Our theoretical and numerical analysis show that a HIV infected subject will remain infected irrespective of the initial viral load and CD4+T cells count. However, some crucial system parameters may significantly alter the concentrations of both CD4+T cells and the HIV populations. Systematic control of these model parameters may find potential application towards better management of the disease.
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具有细胞内延迟的HIV模型的数学研究
人类免疫缺陷病毒(HIV)被观察到感染人体血液中的CD4+T淋巴细胞。在本文中,我们考虑对Herz等人[1]引入的代表HIV动态的基本HIV模型进行修改。我们在疾病传播项中引入细胞内延迟。我们的理论和数值分析表明,无论初始病毒载量和CD4+T细胞计数如何,HIV感染的受试者将保持感染。然而,一些关键的系统参数可能会显著改变CD4+T细胞和HIV群体的浓度。系统控制这些模型参数可能会发现潜在的应用,以更好地管理疾病。
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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