scholarly journals Global stability for an HIV-1 infection model including an eclipse stage of infected cells

2012 ◽  
Vol 385 (2) ◽  
pp. 709-720 ◽  
Author(s):  
Bruno Buonomo ◽  
Cruz Vargas-De-León
2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
M. Higazy ◽  
Sudhanshu Aggarwal ◽  
Y. S. Hamed

In this paper, the authors determine the number of infected cells and concentration of infected (viral) particles in plasma during HIV-1 (human immunodeficiency virus type one) infections using Shehu transformation. For this, the authors first defined some useful properties of Shehu transformation with proof and then applied Shehu transformation on the mathematical representation of the HIV-1 infection model. The mathematical model of HIV-1 infections contains a system of two simultaneous ordinary linear differential equations with initial conditions. Results depict that Shehu transformation is very effective integral transformation for determining the number of infected cells and concentration of viral particles in plasma during HIV-1 infections.


2019 ◽  
Vol 2019 ◽  
pp. 1-18 ◽  
Author(s):  
A. M. Elaiw ◽  
A. A. Almatrafi ◽  
A. D. Hobiny ◽  
K. Hattaf

This paper studies the global dynamics of a general pathogenic infection model with two ways of infections. The effect of antibody immune response is analyzed. We incorporate three discrete time delays and both latently infected cells and actively infected cells. The infection rate and production and clearance/death rates of the cells and pathogens are given by general functions. We determine two threshold parameters to investigate the global stability of three equilibria. We use Lyapunov method to establish the global stability. We support our theoretical results by numerical simulations.


BIOMATH ◽  
2020 ◽  
Vol 9 (2) ◽  
pp. 2012297
Author(s):  
Debadatta Adak ◽  
Nandadulal Bairagi ◽  
Robert Hakl

Biological models inherently contain delay. Mathematical analysis of a delay-induced model is, however, more difficult compare to its non-delayed counterpart. Difficulties multiply if the model contains multiple delays. In this paper, we analyze a realistic HIV-1 infection model in the presence and absence of multiple delays. We consider self-proliferation of CD4+T cells, nonlinear saturated infection rate and recovery of infected cells due to incomplete reverse transcription in a basic HIV-1 in-host model and incorporate multiple delays to account for successful viral entry and subsequent virus reproduction from the infected cell. Both of delayed and non-delayed system becomes disease-free if the basic reproduction number is less than unity. In the absence of delays, the infected equilibrium is shown to be locally asymptotically stable under some parametric space and unstable otherwise. The system may show unstable oscillatory behaviour in the presence of either delay even when the non-delayed system is stable. The second delay further enhances the instability of the endemic equilibrium which is otherwise stable in the presence of a single delay. Numerical results are shown to be in agreement with the analytical results and reflect quite realistic dynamics observed in HIV-1 infected individuals.


2020 ◽  
Vol 2020 ◽  
pp. 1-26
Author(s):  
M. A. Alshaikh ◽  
A. M. Elaiw

This paper studies the global stability of a discrete-time pathogen dynamic model with both cell-mediated and antibody immune responses. Both latently and actively infected cells are incorporated into the model. We discretize the continuous-time model by using the nonstandard finite difference (NSFD) method. We establish that NSFD preserves the nonnegativity and boundedness of the solutions of the model. We derive four threshold parameters which govern the existence and stability of the steady states. We establish by using the Lyapunov method, the global stability of the five steady states of the model. We illustrate our theoretical results by using numerical simulations.


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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