Abstract
This study proposes a modified human immunodeficiency virus (HIV) infection differential equation model with a saturated infection rate. This model has an infection-free equilibrium point and an endemic infection equilibrium point. Using Lyapunov functions and LaSalle's invariance principle shows that if the model's basic reproductive number R0 < 1, the infection-free equilibrium point is globally asymptotically stable, otherwise the endemic infection equilibrium point is globally asymptotically stable. It is shown that a forward bifurcation will occur when R0 = 1. The basic reproductive number R0 of the modified model is independent of plasma total CD4+ T cell counts and thus the modified model is more reasonable than the original model proposed by Buonomo and Vargas-De-León. Based on the clinical data from HIV drug resistance database of Stanford University, using the proposed model simulates the dynamics of two group patients' anti-HIV infection treatments. The simulation results have shown that the first 4 weeks' treatments made the two group patients' R'0 < 1, respectively. After the period, drug resistance made the two group patients' R'0 > 1. The results explain why the two group patients' mean CD4+ T cell counts raised and mean HIV RNA levels declined in the first period, but contrary in the following weeks.
Original language | English (US) |
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Pages (from-to) | 95-103 |
Number of pages | 9 |
Journal | IET Systems Biology |
Volume | 9 |
Issue number | 3 |
DOIs | |
State | Published - Jun 1 2015 |
ASJC Scopus subject areas
- Biotechnology
- Modeling and Simulation
- Molecular Biology
- Genetics
- Cell Biology