Stability of a diffusive-delayed HCV infection model with general cell-to-cell incidence function incorporating immune response and cell proliferation.

In this work, we analyse the dynamics of a five-dimensional hepatitis C virus infection mathematical model including the spatial mobility of hepatitis C virus particles, the transmission of hepatitis C virus infection by mitosis process of infected hepatocytes with logistic growth, time delays, antibody response and cytotoxic T lymphocyte (CTL) immune response with general incidence functions for both modes of infection transmission, namely virus-to-cell as well as cell-to-cell. Firstly, we prove rigorously the existence, the uniqueness, the positivity and the boundedness of the solution of the initial value and boundary problem associated with the new constructed model. Secondly, we found that the basic reproductive number is the sum of the basic reproduction number determined by cell-free virus infection, determined by cell-to-cell infection and determined by proliferation of infected cells.

A class of diffusive delayed viral infection models with general incidence function and cellular proliferation.

We propose and analyze a new class of three dimensional space models that describes infectious diseases caused by viruses such as hepatitis B virus (HBV) and hepatitis C virus (HCV). This work constructs a Reaction-Diffusion-Ordinary Differential Equation model of virus dynamics, including absorption effect, cell proliferation, time delay, and a generalized incidence rate function. By constructing suitable Lyapunov functionals, we show that the model has threshold dynamics: if the basic reproduction number , then the uninfected equilibrium is globally asymptotically stable, whereas if , and under certain conditions, the infected equilibrium is globally asymptotically stable.