A model of HIV-1 infection with two time delays: Mathematical analysis and comparison with patient data

被引:137
作者
Pawelek, Kasia A. [1 ]
Liu, Shengqiang [2 ]
Pahlevani, Faranak [3 ]
Rong, Libin [1 ]
机构
[1] Oakland Univ, Dept Math & Stat, Rochester, MI 48309 USA
[2] Harbin Inst Technol, Acad Fundamental & Interdisciplinary Sci, Harbin 150080, Peoples R China
[3] Penn State Univ, Abington Coll, Div Sci & Engn, Abington, PA 19001 USA
基金
美国国家科学基金会;
关键词
Mathematical model; Virus dynamics; Stability analysis; Delays; Data fitting; INSULIN REGULATORY SYSTEM; SEIR EPIDEMIOLOGIC MODEL; IMMUNE-RESPONSES; LATENT RESERVOIR; GLOBAL DYNAMICS; VIRUS DYNAMICS; VIRAL DYNAMICS; VARYING INFECTIVITY; STABILITY; PLASMA;
D O I
10.1016/j.mbs.2011.11.002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mathematical models have made considerable contributions to our understanding of HIV dynamics. Introducing time delays to HIV models usually brings challenges to both mathematical analysis of the models and comparison of model predictions with patient data. In this paper, we incorporate two delays, one the time needed for infected cells to produce virions after viral entry and the other the time needed for the adaptive immune response to emerge to control viral replication, into an HIV-1 model. We begin model analysis with proving the positivity and boundedness of the solutions, local stability of the infection-free and infected steady states, and uniform persistence of the system. By developing a few Lyapunov functionals, we obtain conditions ensuring global stability of the steady states. We also fit the model including two delays to viral load data from 10 patients during primary HIV-1 infection and estimate parameter values. Although the delay model provides better fits to patient data (achieving a smaller error between data and modeling prediction) than the one without delays, we could not determine which one is better from the statistical standpoint. This highlights the need of more data sets for model verification and selection when we incorporate time delays into mathematical models to study virus dynamics. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:98 / 109
页数:12
相关论文
共 67 条
[11]   Analysis of an SEIRS epidemic model with two delays [J].
Cooke, KL ;
vandenDriessche, P .
JOURNAL OF MATHEMATICAL BIOLOGY, 1996, 35 (02) :240-260
[12]   A delay-differential equation model of HIV infection of CD4+ T-cells [J].
Culshaw, RV ;
Ruan, SG .
MATHEMATICAL BIOSCIENCES, 2000, 165 (01) :27-39
[13]   A mathematical model of cell-to-cell spread of HIV-1 that includes a time delay [J].
Culshaw, RV ;
Ruan, SG ;
Webb, G .
JOURNAL OF MATHEMATICAL BIOLOGY, 2003, 46 (05) :425-444
[14]   TRANSIENT HIGH-LEVELS OF VIREMIA IN PATIENTS WITH PRIMARY HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION [J].
DAAR, ES ;
MOUDGIL, T ;
MEYER, RD ;
HO, DD .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (14) :961-964
[15]   Target cell limited and immune control models of HIV infection: A comparison [J].
De Boer, RJ ;
Perelson, AS .
JOURNAL OF THEORETICAL BIOLOGY, 1998, 190 (03) :201-214
[16]   Virus dynamics: A global analysis [J].
De Leenheer, P ;
Smith, HL .
SIAM JOURNAL ON APPLIED MATHEMATICS, 2003, 63 (04) :1313-1327
[17]   Complex patterns of viral load decay under antiretroviral therapy: influence of pharmacokinetics and intracellular delay [J].
Dixit, NM ;
Perelson, AS .
JOURNAL OF THEORETICAL BIOLOGY, 2004, 226 (01) :95-109
[18]   Identification of a reservoir for HIV-1 in patients on highly active antiretroviral therapy [J].
Finzi, D ;
Hermankova, M ;
Pierson, T ;
Carruth, LM ;
Buck, C ;
Chaisson, RE ;
Quinn, TC ;
Chadwick, K ;
Margolick, J ;
Brookmeyer, R ;
Gallant, J ;
Markowitz, M ;
Ho, DD ;
Richman, DD ;
Siliciano, RF .
SCIENCE, 1997, 278 (5341) :1295-1300
[19]   On stability crossing curves for general systems with two delays [J].
Gu, KQ ;
Niculescu, SI ;
Chen, J .
JOURNAL OF MATHEMATICAL ANALYSIS AND APPLICATIONS, 2005, 311 (01) :231-253
[20]  
Hale J.K., 1993, Introduction to Functional Differntial Equations