The impact of immune cell interactions on virus quasi-species formation.

The process of viral infection spreading in tissues was influenced by various factors, including virus replication within host cells, transportation, and the immune response. Reaction-diffusion systems provided a suitable framework for examining this process. In this work, we studied a nonlocal reaction-diffusion system of equations that modeled the distribution of viruses based on their genotypes and their interaction with the immune response.

Reaction-diffusion waves in biology: new trends, recent developments.

Reaction-diffusion systems are widely used in the description of propagation phenomena in biological systems, where chemical and biological processes combine to produce spatial and temporal patterns. This paper explores the recent trends and developments in the study of reaction-diffusion waves, highlighting their relevance to diverse biological contexts such as population dynamics, ecology or biomedical applications. Progress in mathematical techniques and computational methods advances our ability to model these systems, providing deeper insights into wave propagation, stability, and bifurcations.

Mathematical model of repressive response to collective action and protest waves.

The intricate interplay between the state and society may foster opposition and prompt collective action as a mode of protest. When the state responds repressively to such collective action, it aims to undermine it escalating its costs. A mathematical model relating the repressive response to collective action, articulated through differential equations, facilitates a thorough analysis of their dynamic interaction.

Phase-shifted tACS can modulate cortical alpha waves in human subjects.

Unlabelled: In the present study, we investigated traveling waves induced by transcranial alternating current stimulation in the alpha frequency band of healthy subjects. Electroencephalographic data were recorded in 12 healthy subjects before, during, and after phase-shifted stimulation with a device combining both electroencephalographic and stimulation capacities. In addition, we analyzed the results of numerical simulations and compared them to the results of identical analysis on real EEG data.

A qualitative analysis of an A-monomer model with inflammation processes for Alzheimer's disease.

We introduce and study a new model for the progression of Alzheimer's disease (AD) incorporating the interactions of A -monomers, oligomers, microglial cells and interleukins with neurons through different mechanisms such as protein polymerization, inflammation processes and neural stress reactions. To understand the complete interactions between these elements, we study a spatially homogeneous simplified model that allows us to determine the effect of key parameters such as degradation rates in the asymptotic behaviour of the system and the stability of equilibrium. We observe that inflammation appears to be a crucial factor in the initiation and progression of AD through a phenomenon of hysteresis with respect to the oligomer degradation rate .

Infection spreading in tissue as a reaction-diffusion wave.

Viral infection develops in the organism due to virus replication inside infected cells and its transmission from infected to uninfected cells through the extracellular matrix or cell junctions. In this work, we model infection spreading in tissue with a delay reaction-diffusion system of equations for the concentrations of uninfected cells, infected cells and virus. We prove the wave existence, determine its speed of propagation and introduce a simplified one-equation model obtained from the complete model using a quasi-stationary approximation.

Delay epidemic models determined by latency, infection, and immunity duration.

We propose new single and two-strain epidemic models represented by systems of delay differential equations and based on the number of newly exposed individuals. Transitions between exposed, infectious, recovered, and back to susceptible compartments are determined by the corresponding time delays. Existence and positiveness of solutions are proved.

On a two-strain epidemic model involving delay equations.

We propose an epidemiological model for the interaction of either two viruses or viral strains with cross-immunity, where the individuals infected by the first virus cannot be infected by the second one, and without cross-immunity, where a secondary infection can occur. The model incorporates distributed recovery and death rates and consists of integro-differential equations governing the dynamics of susceptible, infectious, recovered, and dead compartments. Assuming that the recovery and death rates are uniformly distributed in time throughout the duration of the diseases, we can simplify the model to a conventional ordinary differential equation (ODE) model.

Phenotype-structured model of intra-clonal heterogeneity and drug resistance in multiple myeloma.

Multiple myeloma (MM) is a genetically complex hematological cancer characterized by the abnormal proliferation of malignant plasma cells in the bone marrow. This disease progresses from a premalignant condition known as monoclonal gammopathy of unknown significance (MGUS) through sequential genetic alterations involving various genes. These genetic changes contribute to the uncontrolled growth of multiple clones of plasma cells.

The influence of immune cells on the existence of virus quasi-species.

This article investigate a nonlocal reaction-diffusion system of equations modeling virus distribution with respect to their genotypes in the interaction with the immune response. This study demonstrates the existence of pulse solutions corresponding to virus quasi-species. The proof is based on the Leray-Schauder method, which relies on the topological degree for elliptic operators in unbounded domains and a priori estimates of solutions.

Inflammation propagation modeled as a reaction-diffusion wave.

Inflammation is a physiological process aimed to protect the organism in various diseases and injuries. This work presents a generic inflammation model based on the reaction-diffusion equations for the concentrations of uninflamed cells, inflamed cells, immune cells and the inflammatory cytokines. The analysis of the model shows the existence of three different regimes of inflammation progression depending on the value of a parameter R called the inflammation number.

An epidemic model with time delays determined by the infectivity and disease durations.

We propose an epidemiological model with distributed recovery and death rates. It represents an integrodifferential system of equations for susceptible, exposed, infectious, recovered and dead compartments. This model can be reduced to the conventional ODE model under the assumption that recovery and death rates are uniformly distributed in time during disease duration.

Characterization of spatiotemporal dynamics in EEG data during picture naming with optical flow patterns.

In this study, we investigate the spatiotemporal dynamics of the neural oscillations by analyzing the electric potential that arises from neural activity. We identify two types of dynamics based on the frequency and phase of oscillations: standing waves or as out-of-phase and modulated waves, which represent a combination of standing and moving waves. To characterize these dynamics, we use optical flow patterns such as sources, sinks, spirals and saddles.

Emergence and competition of virus variants in respiratory viral infections.

The emergence of new variants of concern (VOCs) of the SARS-CoV-2 infection is one of the main factors of epidemic progression. Their development can be characterized by three critical stages: virus mutation leading to the appearance of new viable variants; the competition of different variants leading to the production of a sufficiently large number of copies; and infection transmission between individuals and its spreading in the population. The first two stages take place at the individual level (infected individual), while the third one takes place at the population level with possible competition between different variants.

Airway obstruction in respiratory viral infections due to impaired mucociliary clearance.

Respiratory viral infections, such as SARS-CoV-2 or influenza, can lead to impaired mucociliary clearance in the bronchial tree due to increased mucus viscosity and its hyper-secretion. We develop in this work a mathematical model to study the interplay between viral infection and mucus motion. The results of numerical simulations show that infection progression can be characterized by three main stages.

Pharmacokinetic/pharmacodynamic model of a methionine starvation based anti-cancer drug.

A new therapeutic approach against cancer is developed by the firm Erytech. This approach is based on starved cancer cells of an amino acid essential to their growth (the L-methionine). The depletion of plasma methionine level can be induced by an enzyme, the methionine-γ-lyase.

Modelling of the Innate and Adaptive Immune Response to SARS Viral Infection, Cytokine Storm and Vaccination.

In this work, we develop mathematical models of the immune response to respiratory viral infection, taking into account some particular properties of the SARS-CoV infections, cytokine storm and vaccination. Each model consists of a system of ordinary differential equations that describe the interactions of the virus, epithelial cells, immune cells, cytokines, and antibodies. Conventional analysis of the existence and stability of stationary points is completed by numerical simulations in order to study the dynamics of solutions.

An age-dependent immuno-epidemiological model with distributed recovery and death rates.

The work is devoted to a new immuno-epidemiological model with distributed recovery and death rates considered as functions of time after the infection onset. Disease transmission rate depends on the intra-subject viral load determined from the immunological submodel. The age-dependent model includes the viral load, recovery and death rates as functions of age considered as a continuous variable.

Mathematical modeling of respiratory viral infection and applications to SARS-CoV-2 progression.

Viral infection in cell culture and tissue is modeled with delay reaction-diffusion equations. It is shown that progression of viral infection can be characterized by the viral replication number, time-dependent viral load, and the speed of infection spreading. These three characteristics are determined through the original model parameters including the rates of cell infection and of virus production in the infected cells.

Competition of SARS-CoV-2 Variants in Cell Culture and Tissue: Wins the Fastest Viral Autowave.

Replication of viruses in living tissues and cell cultures is a "number game" involving complex biological processes (cell infection, virus replication inside infected cell, cell death, viral degradation) as well as transport processes limiting virus spatial propagation. In epithelial tissues and immovable cell cultures, viral particles are basically transported via Brownian diffusion. Highly non-linear kinetics of viral replication combined with diffusion limitation lead to spatial propagation of infection as a moving front switching from zero to high local viral concentration, the behavior typical of spatially distributed excitable media.

An Epidemic Model with Time-Distributed Recovery and Death Rates.

A compartmental epidemiological model with distributed recovery and death rates is proposed. In some particular cases, the model can be reduced to the conventional SIR model. However, in general, the dynamics of epidemic progression in this model is different.

Virus replication and competition in a cell culture: Application to the SARS-CoV-2 variants.

Viral replication in a cell culture is described by a delay reaction-diffusion system. It is shown that infection spreads in cell culture as a reaction-diffusion wave, for which the speed of propagation and viral load can be determined both analytically and numerically. Competition of two virus variants in the same cell culture is studied, and it is shown that the variant with larger individual wave speed out-competes another one, and eliminates it.