Academic
Publications
Stochastic cellular automata model and Monte Carlo simulations of CD4 + T cell dynamics with a proposed alternative leukapheresis treatment for HIV/AIDS

Stochastic cellular automata model and Monte Carlo simulations of CD4 + T cell dynamics with a proposed alternative leukapheresis treatment for HIV/AI

Stochastic cellular automata model and Monte Carlo simulations of CD4 + T cell dynamics with a proposed alternative leukapheresis treatment for HIV/AIDS  
BibTex | RIS | RefWorks Download
Acquired Immunodeficiency Syndrome (AIDS) is responsible for millions of deaths worldwide. To date, many drug treatment regimens have been applied to AIDS patients but none has resulted in a successful cure. This is mainly due to the fact that free HIV particles are frequently in mutation, and infected CD4+ T cells normally reside in the lymphoid tissue where they cannot (so far) be eradicated. We present a stochastic cellular automaton (CA) model to computationally study what could be an alternative treatment, namely Leukapheresis (LCAP), to remove HIV infected leukocytes in the lymphoid tissue. We base our investigations on Monte Carlo computer simulations. Our major objective is to investigate how the number of infected CD4+ T cells changes in response to LCAP during the short-time (weeks) and long-time (years) scales of HIV/AIDS progression in an infected individual. To achieve our goal, we analyze the time evolution of the CD4+ T cell population in the lymphoid tissue (i.e., the lymph node) for HIV dynamics in treatment situations with various starting times and frequencies and under a no treatment condition. Our findings suggest that the effectiveness of the treatment depends mainly on the treatment starting time and the frequency of the LCAP. Other factors (e.g., the removal proportion, the treatment duration, and the state of removed cells) that likely influence disease progression are subjects for further investigation.
Journal: Computers in Biology and Medicine - COMPUT BIOL MED , vol. 41, no. 7, pp. 546-558, 2011
Cumulative Annual
View Publication
The following links allow you to view full publications. These links are maintained by other sources not affiliated with Microsoft Academic Search.