Abstract

We consider a mathematical model that describes the interactions of the HIV virus, CD4 cells and CTLs within host, which is a modification of some existing models by incorporating (i) two distributed kernels reflecting the variance of time for virus to invade into cells and the variance of time for invaded virions to reproduce within cells; (ii) a nonlinear incidence function f for virus infections, and (iii) a nonlinear removal rate function h for infected cells. By constructing Lyapunov functionals and subtle estimates of the derivatives of these Lyapunov functionals, we shown that the model has the threshold dynamics: if the basic reproduction number (BRN) is less than or equal to one, then the infection free equilibrium is globally asymptotically stable, meaning that HIV virus will be cleared; whereas if the BRN is larger than one, then there exist an infected equilibrium which is globally asymptotically stable, implying that the HIV-1 infection will persist in the host and the viral concentration will approach a positive constant level. This together with the dependence/independence of the BRN on f and h reveals the effect of the adoption of these nonlinear functions.

Highlights

  • There has been a substantial effort in the mathematical modeling of virus dynamics, primarily motivated the HIV and AIDS epidemic, see, e.g., [3, 4, 26, 30]

  • We propose a general model describing the interactions of HIV virus, cells and cytotoxic T lymphocytes (CTLs) within host

  • In the model we allow general nonlinear incidence rate and removal rate, as well as two general distributed delays accounting for the variance of time for virions to invade into cells and the variance of time for invade virions to reproduce

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Summary

Introduction

There has been a substantial effort in the mathematical modeling of virus dynamics, primarily motivated the HIV and AIDS epidemic, see, e.g., [3, 4, 26, 30]. Those mathematical models can provide some insights into the dynamics of HIV viral load in vivo and may play a significant role in the development of a better understanding of HIV/AIDs and drug therapies. Cytotoxic T lymphocytes (CTLs) play a critical role in

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