Analysis of Hepatitis C Virus Decline during Treatment with the Protease Inhibitor Danoprevir Using a Multiscale Model
- Oakland Univ., Rochester, MI (United States). Dept. of Mathematics and Statistics. Center for Biomedical Research
- Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Theoretical Biology and Biophysics; Univ. Paris Diderot, Paris (France); National Inst. of Health and Medical Research (INSERM), Paris (France)
- Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Theoretical Biology and Biophysics; Univ. of Illinois, Chicago, IL (United States). Dept. of Medicine; Loyola Univ., Chicago, IL (United States). Dept. of Medicine
- Univ. of Michigan, Flint, MI (United States). Mathematics Dept.
- Roche, Nutley, NJ (United States). Pharma Research and Early Development. Clinical Pharmacology; Novartis Pharmaceuticals Corporation, East Hanover, NJ (United States)
- Roche, Nutley, NJ (United States). Pharma Research and Early Development. Clinical Pharmacology
- Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Theoretical Biology and Biophysics
The current paradigm for studying hepatitis C virus (HCV) dynamics in patients utilizes a standard viral dynamic model that keeps track of uninfected (target) cells, infected cells, and virus. The model does not account for the dynamics of intracellular viral replication, which is the major target of direct-acting antiviral agents (DAAs). In this paper, we describe and study a recently developed multiscale age-structured model that explicitly considers the potential effects of DAAs on intracellular viral RNA production, degradation, and secretion as virus into the circulation. We show that when therapy significantly blocks both intracellular viral RNA production and virus secretion, the serum viral load decline has three phases, with slopes reflecting the rate of serum viral clearance, the rate of loss of intracellular viral RNA, and the rate of loss of intracellular replication templates and infected cells, respectively. We also derive analytical approximations of the multiscale model and use one of them to analyze data from patients treated for 14 days with the HCV protease inhibitor danoprevir. Analysis suggests that danoprevir significantly blocks intracellular viral production (with mean effectiveness 99.2%), enhances intracellular viral RNA degradation about 5-fold, and moderately inhibits viral secretion (with mean effectiveness 56%). Finally, the multiscale model can be used to study viral dynamics in patients treated with other DAAs and explore their mechanisms of action in treatment of hepatitis C.
- Research Organization:
- Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
- Sponsoring Organization:
- USDOE; National Science Foundation (NSF); National Inst. of Health (NIH) (United States); Univ. of Illinois Water Payton Liver Center GUILD (United States); Roche (United States)
- Contributing Organization:
- Oakland Univ., Rochester, MI (United States); Univ. of Michigan, Flint, MI (United States); Roche, Nutley, NJ (United States)
- Grant/Contract Number:
- AC52-06NA25396; DMS-1122290; PHY-1125915; R56/R01-AI078881; P20-GM103452; AI028433; R34-HL109334; OD011095
- OSTI ID:
- 1321717
- Report Number(s):
- LA-UR-12-21815
- Journal Information:
- PLoS Computational Biology (Online), Vol. 9, Issue 3; ISSN 1553-7358
- Publisher:
- Public Library of ScienceCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Web of Science
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