Towards a long-term model construction for the dynamic simulation of HIV infection
-
1.
Department of Chemical Engineering, University of Cambridge, Pembroke Street, Cambridge, CB2 3RA
-
2.
Escuela de Ingenieria Bioquimica, Pontificia Universidad Catolica de Valparaiso, Av Brasil, Valparaiso, 2147
-
Received:
01 October 2006
Accepted:
29 June 2018
Published:
01 May 2007
-
-
MSC :
92B99.
-
-
This study involves the mathematical modelling of long-term HIV dynamics.
The proposed model is able to predict the entire trajectory of the disease:
initial viremia in the early weeks of the infection, latency, and progression
to AIDS; a range spanning approximately ten years. The model outcomes were compared
to clinical data and significant agreement was achieved. The formulated
model considers all important population compartments including macrophages,
latently-infected CD4+ T-cells, and cytotoxic T-lymphocytes (CTLs),
an attempt which in many respects is novel in the area of HIV modelling.
The ranges of the model parameters and initial conditions were obtained
from literature, and their values were determined in this work directly
by fitting published clinical data. Furthermore, the simulation results
emphasize the importance of macrophages in HIV infection and progression
to AIDS and show a clear correlation between the level of CTLs and
HIV progression. The ability of the model to correlate analytical
data gives credibility to its predictions, a fact that will be
exploited in future research in modelling immunological and pharmacological
avenues of treatment.
Citation: M. Hadjiandreou, Raul Conejeros, Vassilis S. Vassiliadis. Towards a long-term model construction for the dynamic simulation of HIV infection[J]. Mathematical Biosciences and Engineering, 2007, 4(3): 489-504. doi: 10.3934/mbe.2007.4.489
-
Abstract
This study involves the mathematical modelling of long-term HIV dynamics.
The proposed model is able to predict the entire trajectory of the disease:
initial viremia in the early weeks of the infection, latency, and progression
to AIDS; a range spanning approximately ten years. The model outcomes were compared
to clinical data and significant agreement was achieved. The formulated
model considers all important population compartments including macrophages,
latently-infected CD4+ T-cells, and cytotoxic T-lymphocytes (CTLs),
an attempt which in many respects is novel in the area of HIV modelling.
The ranges of the model parameters and initial conditions were obtained
from literature, and their values were determined in this work directly
by fitting published clinical data. Furthermore, the simulation results
emphasize the importance of macrophages in HIV infection and progression
to AIDS and show a clear correlation between the level of CTLs and
HIV progression. The ability of the model to correlate analytical
data gives credibility to its predictions, a fact that will be
exploited in future research in modelling immunological and pharmacological
avenues of treatment.
-
-
-
-