共 45 条
Mathematical analysis of multiscale models for hepatitis C virus dynamics under therapy with direct-acting antiviral agents
被引:49
作者:

Rong, Libin
论文数: 0 引用数: 0
h-index: 0
机构:
Oakland Univ, Dept Math & Stat, Rochester, MI 48309 USA Oakland Univ, Dept Math & Stat, Rochester, MI 48309 USA

Perelson, Alan S.
论文数: 0 引用数: 0
h-index: 0
机构:
Los Alamos Natl Lab, Los Alamos, NM 87545 USA Oakland Univ, Dept Math & Stat, Rochester, MI 48309 USA
机构:
[1] Oakland Univ, Dept Math & Stat, Rochester, MI 48309 USA
[2] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
基金:
美国国家科学基金会;
关键词:
Hepatitis C virus;
Multiscale model;
Age-structured model;
Stability;
Intracellular viral RNA;
Antiviral therapy;
Viral kinetics;
VIRAL KINETICS;
NS5A INHIBITOR;
INFECTION;
RIBAVIRIN;
INTERFERON;
COMBINATION;
IFN;
RNA;
REPLICATION;
D O I:
10.1016/j.mbs.2013.04.012
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Chronic hepatitis C virus (HCV) infection remains a world-wide public health problem. Therapy with interferon and ribavirin leads to viral elimination in less than 50% of treated patients. New treatment options aiming at a higher cure rate are focused on direct-acting antiviral agents (DAAs), which directly interfere with different steps in the HCV life cycle. In this paper, we describe and analyze a recently developed multiscale model that predicts HCV dynamics under therapy with DAAs. The model includes both intracellular viral RNA replication and extracellular viral infection. We calculate the steady states of the model and perform a detailed stability analysis. With certain assumptions we obtain analytical approximations of the viral load decline after treatment initiation. One approximation agrees well with the prediction of the model, and can conveniently be used to fit patient data and estimate parameter values. We also discuss other possible ways to incorporate intracellular viral dynamics into the multiscale model. (C) 2013 Elsevier Inc. All rights reserved.
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页码:22 / 30
页数:9
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