Global stability for an HIV-1 infection model with Beddington–DeAngelis incidence rate and CTL immune response

2014 ◽  
Vol 19 (1) ◽  
pp. 121-127 ◽  
Author(s):  
Cuifang Lv ◽  
Lihong Huang ◽  
Zhaohui Yuan
2016 ◽  
Vol 2016 ◽  
pp. 1-21 ◽  
Author(s):  
Hui Miao ◽  
Zhidong Teng ◽  
Zhiming Li

The dynamical behaviors for a five-dimensional viral infection model with three delays which describes the interactions of antibody, cytotoxic T-lymphocyte (CTL) immune responses, and nonlinear incidence rate are investigated. The threshold values for viral infection, antibody response, CTL immune response, CTL immune competition, and antibody competition, respectively, are established. Under certain assumptions, the threshold value conditions on the global stability of the infection-free, immune-free, antibody response, CTL immune response, and interior equilibria are proved by using the Lyapunov functionals method, respectively. Immune delay as a bifurcation parameter is further investigated. The numerical simulations are performed in order to illustrate the dynamical behavior of the model.


2011 ◽  
Vol 2011 ◽  
pp. 1-13 ◽  
Author(s):  
Yunfei Li ◽  
Rui Xu ◽  
Zhe Li ◽  
Shuxue Mao

A delayed HIV-1 infection model with CTL immune response is investigated. By using suitable Lyapunov functionals, it is proved that the infection-free equilibrium is globally asymptotically stable if the basic reproduction ratio for viral infection is less than or equal to unity; if the basic reproduction ratio for CTL immune response is less than or equal to unity and the basic reproduction ratio for viral infection is greater than unity, the CTL-inactivated infection equilibrium is globally asymptotically stable; if the basic reproduction ratio for CTL immune response is greater than unity, the CTL-activated infection equilibrium is globally asymptotically stable.


2018 ◽  
Vol 16 (1) ◽  
pp. 1374-1389
Author(s):  
Eric Ávila-Vales ◽  
Abraham Canul-Pech ◽  
Erika Rivero-Esquivel

AbstractIn this paper, we discussed a infinitely distributed delayed viral infection model with nonlinear immune response and general incidence rate. We proved the existence and uniqueness of the equilibria. By using the Lyapunov functional and LaSalle invariance principle, we obtained the conditions of global stabilities of the infection-free equilibrium, the immune-exhausted equilibrium and the endemic equilibrium. Numerical simulations are given to verify the analytical results.


2013 ◽  
Vol 2013 ◽  
pp. 1-11
Author(s):  
A. M. Elaiw ◽  
R. M. Abukwaik ◽  
E. O. Alzahrani

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.


2013 ◽  
Vol 2013 ◽  
pp. 1-12
Author(s):  
Haibin Wang ◽  
Rui Xu

An HIV-1 infection model with latently infected cells and delayed immune response is investigated. By analyzing the corresponding characteristic equations, the local stability of each of feasible equilibria is established and the existence of Hopf bifurcations at the CTL-activated infection equilibrium is also studied. By means of suitable Lyapunov functionals and LaSalle’s invariance principle, it is proved that the infection-free equilibrium is globally asymptotically stable if the basic reproduction ratio for viral infectionR0≤1; if the basic reproduction ratio for viral infectionR0>1and the basic reproduction ratio for CTL immune responseR1≤1, the CTL-inactivated infection equilibrium is globally asymptotically stable. If the basic reproduction ratio for CTL immune responseR1>1, the global stability of the CTL-activated infection equilibrium is also derived when the time delayτ=0. Numerical simulations are carried out to illustrate the main results.


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