Global stability analysis of a delay cell-population model of hepatitis B infection with humoral immune response. Issue 4 (2nd October 2021)

• Record Type: Journal Article
• Authors: Tadmon, Calvin; Foko, Severin; Rendall, Alan D.
• Is Part Of: Dynamical systems. Volume 36:Issue 4(2021)
• Page Start: 537
• Page End: 559
• Publication Date: 2021-10-02
• Subjects: HBV infection -- diffusion -- humoral immune response -- time delay -- Lyapunov functional -- global stability; Differentiable dynamical systems -- Periodicals; 515.35205
• DOI: 10.1080/14689367.2021.1940868
• Languages: English
• ISSNs: 1468-9367

Abstract

Abstract : In this work, we propose and investigate a delay cell population model of hepatitis B virus (HBV) infection. We suppose spatial diffusion of free HBV particles, and use a Beddington-DeAngelis incidence function to describe viral infection. The model takes into account the exposed hepatocytes and the usually neglected humoral immune response. Moreover, a time delay is introduced to account for the transformation processes necessary for actual HBV production. We naturally find two threshold parameters, namely the basic reproduction number R 0 and the humoral immune response reproduction number R 1 which completely determine the global stability of the spatially homogeneous equilibria of the model obtained. By constructing appropriate Lyapunov functionals and using LaSalle's invariance principle we show that, if R 0 ≤ 1, the disease-free equilibrium is globally asymptotically stable. Furthermore, we prove that the endemic equilibrium without humoral immune response and the endemic equilibrium with humoral immune response are globally asymptotically stable if R 1 ≤ 1 < R 0 and R 1 > 1, respectively. Finally, in one dimensional space, we perform some numerical simulations to illustrate the theoretical results obtained.