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Oncolytic virotherapy (OVT) is a promising treatment for cancer which can replace or support the traditional treatments like chemotherapy and radiotherapy. Mathematical models have been considered as a powerful tool to develop oncolytic viral treatments and predict the possible outcomes. We study a spatial model for OVT with cytotoxic T lymphocyte immune response and distributed delays. This model is an extended version of the model studied by Wang et al. (Math Biosci 276:19–27, 2016). We study the basic properties of the model including the existence, nonnegativity, and boundedness of solutions. We carefully analyze all equilibrium points and determine the conditions for their existence. We show the global stability of each one of these points by constructing suitable Lyapunov functionals. We use the characteristic equations to confirm the corresponding instability conditions. We carry out some numerical simulations to support the theoretical results and draw some important conclusions. The results show that the distributed delay can have a large impact on the efficacy and amount of OVT. When the immune response is present, the concentration of oncolytic viruses is decreased and the efficiency of treatment is reduced. Changing the diffusion coefficients does not affect the long-time behavior of solutions.

This paper studies the global dynamics of a general diffusive hepatitis B virus (HBV) infection model. The model includes both enveloped viruses and DNA containing capsids. Two immune responses are recruited to attack the virus and infected hepatocytes. These are the cytotoxic T-lymphocytes (CTL) which kill the infected liver cells, and B cells which send antibodies to attack the virus. The non-negativity and boundedness of the solutions are discussed. The existence of spatially homogeneous equilibrium points is examined. The global stability of all possible equilibrium points is proved by choosing suitable Lyapunov functionals. Some numerical simulations are performed to enhance the theoretical results and present the behavior of solutions in space and time.

Oncolytic virotherapy (OVT) is a promising therapeutic approach that uses replication-competent viruses to target and kill tumor cells. Alphavirus M1 is a selective oncolytic virus which showed high efficacy against tumor cells. Wang et al. (2016) studied an ordinary differential equation (ODE) model to verify the potent efficacy of M1 virus. Our purpose is to extend their model to include the effect of time delays and anti-tumor immune response. Also, we assume that all elements of the extended model undergo diffusion in a bounded domain. We study the existence, non-negativity and boundedness of solutions in order to verify the well-posedness of the model. We calculate all possible equilibrium points and determine the threshold conditions required for their existence and stability. These points reflect three different fates for OVT: partial success, complete success, or complete failure. We prove the global asymptotic stability of all equilibrium points by constructing suitable Lyapunov functionals, and verify the corresponding instability conditions. We conduct some numerical simulations to confirm the analytical results and show the crucial role of time delays and immune response in the success of OVT.

Malaria is one of the most dangerous diseases that threatens people’s lives around the world. In this paper, we study a reaction-diffusion model for the within-host dynamics of malaria infection with an antibody immune response. The model is given by a system of partial differential equations (PDEs) to describe the blood-stage of malaria life cycle. It addresses the interactions between uninfected red blood cells, antibodies, and three types of infected red blood cells, namely ring-infected red blood cells, trophozoite-infected red blood cells and schizont-infected red blood cells. Moreover, the model contains a parameter to measure the efficacy of isoleucine starvation and its effect on the growth of malaria parasites. We show the basic properties of the model. We compute all equilibria and derive the thresholds from the conditions of existence of malaria equilibrium points. We prove the global stability of all equilibrium points based on choosing suitable Lyapunov functionals. We use the characteristic equations to verify the local instability of equilibrium points. We finally execute numerical simulations to validate the theoretical results and highlight some important observations. The results indicate that isoleucine starvation can have a critical impact on the stability of equilibrium points. When the efficacy of isoleucine starvation is high, it switches the system from the infection state to the malaria-free state. The presence of an antibody immune response does not lead to the elimination of malaria infection, but it suppresses the growth of malaria parasites and increases the amount of healthy red blood cells.