scholarly journals Global Dynamics of HIV Infection of CD4+T Cells and Macrophages

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
A. M. Elaiw ◽  
A. S. Alsheri
Keyword(s):  
T Cells ◽  
Steady State ◽  
Hiv Infection ◽  
Reproduction Number ◽  
Infection Model ◽  
Global Dynamics ◽  
Globally Asymptotically Stable ◽  
Virus Particles ◽  
Hiv Infection Model ◽  
Invariant Principle

We study the global dynamics of an HIV infection model describing the interaction of the HIV with CD4+T cells and macrophages. The incidence rate of virus infection and the growth rate of the uninfected CD4+T cells and macrophages are given by general functions. We have incorporated two types of distributed delays into the model to account for the time delay between the time the uninfected cells are contacted by the virus particle and the time for the emission of infectious (matures) virus particles. We have established a set of conditions which are sufficient for the global stability of the steady states of the model. Using Lyapunov functionals and LaSalle's invariant principle, we have proven that if the basic reproduction numberR0is less than or equal to unity, then the uninfected steady state is globally asymptotically stable (GAS), and if the infected steady state exists, then it is GAS.

scholarly journals Global Dynamics of an HIV Infection Model with Two Classes of Target Cells and Distributed Delays

2012 ◽  
Vol 2012 ◽  
pp. 1-13 ◽  
Author(s):  
A. M. Elaiw
Keyword(s):  
T Cells ◽  
Steady State ◽  
Hiv Infection ◽  
Infection Model ◽  
Target Cells ◽  
Global Dynamics ◽  
Asymptotically Stable ◽  
Globally Asymptotically Stable ◽  
Hiv Infection Model ◽  
Nonlinear Delay

We investigate the global dynamics of an HIV infection model with two classes of target cells and multiple distributed intracellular delays. The model is a 5-dimensional nonlinear delay ODEs that describes the interaction of the HIV with two classes of target cells, CD4+T cells and macrophages. The incidence rate of infection is given by saturation functional response. The model has two types of distributed time delays describing time needed for infection of target cell and virus replication. This model can be seen as a generalization of several models given in the literature describing the interaction of the HIV with one class of target cells, CD4+T cells. Lyapunov functionals are constructed to establish the global asymptotic stability of the uninfected and infected steady states of the model. We have proven that if the basic reproduction numberR0is less than unity then the uninfected steady state is globally asymptotically stable, and ifR0>1then the infected steady state exists and it is globally asymptotically stable.

scholarly journals Global Stability of HIV Infection of CD4+T Cells and Macrophages with CTL Immune Response and Distributed Delays

2013 ◽  
Vol 2013 ◽  
pp. 1-11
Author(s):  
A. M. Elaiw ◽  
R. M. Abukwaik ◽  
E. O. Alzahrani
Keyword(s):  
Immune Response ◽  
T Cells ◽  
Steady State ◽  
Hiv Infection ◽  
Global Stability ◽  
Reproduction Number ◽  
Infection Model ◽  
Target Cells ◽  
Globally Asymptotically Stable ◽  
Ctl Immune Response

We study the global stability of a human immunodeficiency virus (HIV) infection model with Cytotoxic T Lymphocytes (CTL) immune response. The model describes the interaction of the HIV with two classes of target cells, CD4+T cells and macrophages. Two types of distributed time delays are incorporated into the model to describe the time needed for infection of target cell and virus replication. Using the method of Lyapunov functional, we have established that the global stability of the model is determined by two threshold numbers, the basic reproduction numberR0and the immune response reproduction numberR0∗. We have proven that, ifR0≤1, then the uninfected steady state is globally asymptotically stable (GAS), ifR0*≤1<R0, then the infected steady state without CTL immune response is GAS, and, ifR0*>1, then the infected steady state with CTL immune response is GAS.

Global properties of a cell mediated immunity in HIV infection model with two classes of target cells and distributed delays

2014 ◽  
Vol 07 (05) ◽  
pp. 1450055 ◽  
Author(s):  
A. M. Elaiw ◽  
R. M. Abukwaik ◽  
E. O. Alzahrani
Keyword(s):  
Immune Response ◽  
Steady State ◽  
Hiv Infection ◽  
Infection Model ◽  
Target Cells ◽  
Cell Mediated Immunity ◽  
Globally Asymptotically Stable ◽  
Global Properties ◽  
Hiv Infection Model ◽  
Ctl Immune Response

In this paper, we study the global properties of a human immunodeficiency virus (HIV) infection model with cytotoxic T lymphocytes (CTL) immune response. The model is a six-dimensional that describes the interaction of the HIV with two classes of target cells, CD4+ T cells and macrophages. The infection rate is given by saturation functional response. Two types of distributed time delays are incorporated into the model to describe the time needed for infection of target cell and virus replication. Using the method of Lyapunov functional, we have established that the global stability of the model is determined by two threshold numbers, the basic infection reproduction number R0 and the immune response activation number [Formula: see text]. We have proven that if R0 ≤ 1, then the uninfected steady state is globally asymptotically stable (GAS), if [Formula: see text], then the infected steady state without CTL immune response is GAS, and if [Formula: see text], then the infected steady state with CTL immune response is GAS.

scholarly journals Global Dynamics of Virus Infection Model with Antibody Immune Response and Distributed Delays

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
A. M. Elaiw ◽  
A. Alhejelan ◽  
M. A. Alghamdi
Keyword(s):  
Immune Response ◽  
Steady State ◽  
Virus Infection ◽  
Reproduction Number ◽  
Distributed Delays ◽  
Infection Model ◽  
Qualitative Behavior ◽  
Global Dynamics ◽  
Globally Asymptotically Stable ◽  
Virus Infection Model

We present qualitative behavior of virus infection model with antibody immune response. The incidence rate of infection is given by saturation functional response. Two types of distributed delays are incorporated into the model to account for the time delay between the time when uninfected cells are contacted by the virus particle and the time when emission of infectious (matures) virus particles. Using the method of Lyapunov functional, we have established that the global stability of the steady states of the model is determined by two threshold numbers, the basic reproduction numberR0and antibody immune response reproduction numberR1. We have proven that ifR0≤1, then the uninfected steady state is globally asymptotically stable (GAS), ifR1≤1<R0, then the infected steady state without antibody immune response is GAS, and ifR1>1, then the infected steady state with antibody immune response is GAS.

scholarly journals Threshold dynamics and threshold analysis of HIV infection model with treatment

2020 ◽  
Vol 2020 (1) ◽  
Author(s):  
Zhimin Chen ◽  
Xiuxiang Liu ◽  
Liling Zeng
Keyword(s):  
Hiv Infection ◽  
Time Delays ◽  
Dynamical Behavior ◽  
Infection Model ◽  
Threshold Dynamics ◽  
Positive Equilibrium ◽  
Asymptotically Stable ◽  
Globally Asymptotically Stable ◽  
Immunodeficiency Virus ◽  
Hiv Infection Model

Abstract In this paper, a human immunodeficiency virus (HIV) infection model that includes a protease inhibitor (PI), two intracellular delays, and a general incidence function is derived from biologically natural assumptions. The global dynamical behavior of the model in terms of the basic reproduction number $\mathcal{R}_{0}$ R 0 is investigated by the methods of Lyapunov functional and limiting system. The infection-free equilibrium is globally asymptotically stable if $\mathcal{R}_{0}\leq 1$ R 0 ≤ 1 . If $\mathcal{R}_{0}>1$ R 0 > 1 , then the positive equilibrium is globally asymptotically stable. Finally, numerical simulations are performed to illustrate the main results and to analyze thre effects of time delays and the efficacy of the PI on $\mathcal{R}_{0}$ R 0 .

scholarly journals Bifurcation Analysis of an Age Structured HIV Infection Model with Both Virus-to-Cell and Cell-to-Cell Transmissions

2018 ◽  
Vol 28 (09) ◽  
pp. 1850109 ◽  
Author(s):  
Xiangming Zhang ◽  
Zhihua Liu
Keyword(s):  
T Cells ◽  
Hopf Bifurcation ◽  
Hiv Infection ◽  
Bifurcation Analysis ◽  
Dynamical Behavior ◽  
Infection Model ◽  
Positive Equilibrium ◽  
Semilinear Equations ◽  
Age Structured ◽  
Hiv Infection Model

We make a mathematical analysis of an age structured HIV infection model with both virus-to-cell and cell-to-cell transmissions to understand the dynamical behavior of HIV infection in vivo. In the model, we consider the proliferation of uninfected CD[Formula: see text] T cells by a logistic function and the infected CD[Formula: see text] T cells are assumed to have an infection-age structure. Our main results concern the Hopf bifurcation of the model by using the theory of integrated semigroup and the Hopf bifurcation theory for semilinear equations with nondense domain. Bifurcation analysis indicates that there exist some parameter values such that this HIV infection model has a nontrivial periodic solution which bifurcates from the positive equilibrium. The numerical simulations are also carried out.

Quasilinearization-Lagrangian method to solve the HIV infection model of CD4 $$^+$$ + T cells

SeMA Journal ◽  
2017 ◽  
Vol 75 (2) ◽  
pp. 271-283 ◽  
Author(s):  
Kourosh Parand ◽  
Zahra Kalantari ◽  
Mehdi Delkhosh
Keyword(s):  
T Cells ◽  
Hiv Infection ◽  
Cd4 T Cells ◽  
Lagrangian Method ◽  
Infection Model ◽  
Hiv Infection Model

Stochastic numerical technique for solving HIV infection model of CD4+ T cells

2020 ◽  
Vol 135 (5) ◽  
Author(s):  
Muhammad Umar ◽  
Zulqurnain Sabir ◽  
Fazli Amin ◽  
Juan L. G. Guirao ◽  
Muhammad Asif Zahoor Raja
Keyword(s):  
T Cells ◽  
Hiv Infection ◽  
Cd4 T Cells ◽  
Numerical Technique ◽  
Infection Model ◽  
Hiv Infection Model

Parameters estimation of HIV infection model of CD4+T-cells by applying orthonormal Bernstein collocation method

2018 ◽  
Vol 11 (02) ◽  
pp. 1850020 ◽  
Author(s):  
Farshid Mirzaee ◽  
Nasrin Samadyar
Keyword(s):  
T Cells ◽  
Nonlinear System ◽  
Hiv Infection ◽  
Initial Conditions ◽  
Bernstein Polynomials ◽  
Nonlinear Ordinary Differential Equation ◽  
Parameters Estimation ◽  
Infection Model ◽  
Algebraic Equations ◽  
Hiv Infection Model

The HIV infection model of CD4[Formula: see text][Formula: see text]T-cells corresponds to a class of nonlinear ordinary differential equation systems. In this study, we provide the approximate solution of this model by using orthonormal Bernstein polynomials (OBPs). By applying the proposed method, the nonlinear system of ordinary differential equations reduces to a nonlinear system of algebraic equations which can be solved by using a suitable numerical method such as Newton’s method. We prove some useful theorems concerning the convergence and error estimate associated to the present method. Finally, we apply the proposed method to get the numerical solution of this model with the arbitrary initial conditions and values. Furthermore, the numerical results obtained by the suggested method are compared with the results achieved by other previous methods. These results indicate that this method agrees with other previous methods.

Asymptotic Analysis of an Age-Structured HIV Infection Model with Logistic Target-Cell Growth and Two Infecting Routes

2020 ◽  
Vol 30 (04) ◽  
pp. 2050059
Author(s):  
Dongxue Yan ◽  
Xianlong Fu
Keyword(s):  
Steady State ◽  
Hiv Infection ◽  
Logistic Growth ◽  
Infection Model ◽  
Target Cells ◽  
Cell Infection ◽  
Numerical Examples ◽  
Distribution Of Eigenvalues ◽  
Age Structured ◽  
Hiv Infection Model

This paper deals with an age-structured HIV infection model with logistic growth for target cells and both virus-to-cell and cell-to-cell infection routes. Based on the existence of the infection-free and infection equilibria and some rigorous analyses for the considered model, we study the asymptotic stability of these equilibria via determining the distribution of eigenvalues. We also address the persistence of the solution semi-flow by proving the existence of a global attractor. Furthermore, Hopf bifurcation occurring at the positive steady state is exploited. At last, some numerical examples are provided to illustrate the obtained results.

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