Global stability of a delay differential equation of hepatitis B virus infection with immune response

The global stability for a delayed HBV infection model with CTL immune response is investigated. We show that the global dynamics is determined by two sharp thresholds, basic reproduction number $Re_0$ and CTL immune-response reproduction number $Re_1$. When $Re_0 leq 1$, the infection-free equi...

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Bibliographic Details
Main Authors: Jinliang Wang, Xinxin Tian
Format: Article
Language:English
Published: Texas State University 2013-04-01
Series:Electronic Journal of Differential Equations
Subjects:
Online Access:http://ejde.math.txstate.edu/Volumes/2013/94/abstr.html
Description
Summary:The global stability for a delayed HBV infection model with CTL immune response is investigated. We show that the global dynamics is determined by two sharp thresholds, basic reproduction number $Re_0$ and CTL immune-response reproduction number $Re_1$. When $Re_0 leq 1$, the infection-free equilibrium is globally asymptotically stable, which means that the viruses are cleared and immune is not active; when $Re_1 leq 1 < Re_0$, the CTL-inactivated infection equilibrium exists and is globally asymptotically stable, which means that CTLs immune response would not be activated and viral infection becomes chronic; and when $Re_1 > 1$, the CTL-activated infection equilibrium exists and is globally asymptotically stable, in this case the infection causes a persistent CTLs immune response. Our model is formulated by incorporating a Cytotoxic T lymphocytes (CTLs) immune response to recent work [Gourley, Kuang, Nagy, J. Bio. Dyn., 2(2008), 140-153] to model the role in antiviral by attacking virus infected cells. Our analysis provides a quantitative understandings of HBV replication dynamics in vivo and has implications for the optimal timing of drug treatment and immunotherapy in chronic HBV infection.
ISSN:1072-6691