A competitive, chaos-free, implicit, finite-difference method is developed
and used for a novel deterministic model for the perturbation of HIV by com
bination antiretroviral therapy. The compartmental model monitors the inter
action between HIV and CD4+ T cells, its principal target and site of repli
cation in vivo, in the presence of reverse transcription inhibitors and pro
tease inhibitors. The model exhibits two steady states, an uninfected (triv
ial) steady state (with no virus present) and an endemically infected state
(with virus and infected T cells present). Stability and bifurcation analy
ses together with numerical simulations of the resulting dynamical system a
re reported. (C) 2001 Elsevier Science Ltd. All rights reserved.