scholarly journals Hopf bifurcation analysis of nonlinear HIV infection model and the effect of delayed immune response with drug therapies

2020 ◽  
Vol 2020 (1) ◽  
Author(s):  
V. Geetha ◽  
S. Balamuralitharan
2018 ◽  
Vol 28 (09) ◽  
pp. 1850109 ◽  
Author(s):  
Xiangming Zhang ◽  
Zhihua Liu

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.


2013 ◽  
Vol 641-642 ◽  
pp. 808-811
Author(s):  
Xiao Zhang ◽  
Dong Wei Huang ◽  
Yong Feng Guo

In this paper, a class of HIV infection model with delayed immune response has been studied. We analyze the global asymptotic stability of the viral free equilibrium, and the stability and Hopf bifurcation of the infected equilibrium have been studied. Numerical simulations are carried out to explain the results of the analysis, and the change of the immune response of CTLs infects stability of system. These results can explain the complexity of the immune state of AIDs.


2014 ◽  
Vol 07 (05) ◽  
pp. 1450055 ◽  
Author(s):  
A. M. Elaiw ◽  
R. M. Abukwaik ◽  
E. O. Alzahrani

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.


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