7 research outputs found

    Modelling and optimal control of multi strain epidemics, with application to COVID-19

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    Reinfection and multiple viral strains are among the latest challenges in the current COVID-19 pandemic. In contrast, epidemic models often consider a single strain and perennial immunity. To bridge this gap, we present a new epidemic model that simultaneously considers multiple viral strains and reinfection due to waning immunity. The model is general, applies to any viral disease and includes an optimal control formulation to seek a trade-off between the societal and economic costs of mitigation. We validate the model, with and without mitigation, in the light of the COVID-19 epidemic in England and in the state of Amazonas, Brazil. The model can derive optimal mitigation strategies for any number of viral strains, whilst also evaluating the effect of distinct mitigation costs on the infection levels. The results show that relaxations in the mitigation measures cause a rapid increase in the number of cases, and therefore demand more restrictive measures in the future

    Modelling and optimal control of multi strain epidemics, with application to COVID-19

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    This work introduces a novel epidemiological model that simultaneously considers multiple viral strains, reinfections due to waning immunity response over time and an optimal control formulation. This enables us to derive optimal mitigation strategies over a prescribed time horizon under a more realistic framework that does not imply perennial immunity and a single strain, although these can also be derived as particular cases of our formulation. The model also allows estimation of the number of infections over time in the absence of mitigation strategies under any number of viral strains. We validate our approach in the light of the COVID-19 epidemic and present a number of experiments to shed light on the overall behaviour under one or two strains in the absence of sufficient mitigation measures. We also derive optimal control strategies for distinct mitigation costs and evaluate the effect of these costs on the optimal mitigation measures over a two-year horizon. The results show that relaxations in the mitigation measures cause a rapid increase in the number of cases, which then demand more restrictive measures in the future

    Reinfection and low cross-immunity as drivers of epidemic resurgence under high seroprevalence: a model-based approach with application to Amazonas, Brazil

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    This paper introduces a new multi-strain epidemic model with reinfection and cross-immunity to provide insights into the resurgence of the COVID-19 epidemic in an area with reportedly high seroprevalence due to a largely unmitigated outbreak: the state of Amazonas, Brazil. Although high seroprevalence could have been expected to trigger herd immunity and prevent further waves in the state, we have observed persistent levels of infection after the first wave and eventually the emergence of a second viral strain just before an augmented second wave. Our experiments suggest that the persistent levels of infection after the first wave may be due to reinfection, whereas the higher peak at the second wave can be explained by the emergence of the second variant and a low level of cross-immunity between the original and the second variant. Finally, the proposed model provides insights into the effect of reinfection and cross-immunity on the long-term spread of an unmitigated epidemic

    A model for interactions between immune cells and HIV considering drug treatments

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    In this work, we analyze the capacity of the human body to combat HIV. The model here treated takes into consideration four types of defense of an organism infected by HIV: susceptible defense cells, the infected immune cells, killer T cells, and the HIV-specific killer T cells. This model, therefore, analyzes the interactions between the responses of killer T cells and HIV infections, evidencing how the immune system is attacked and how it defends. An optimal control problem is proposed to derive an optimal sequence of dosages in the standard drug treatment, in such a way as to minimize the side effects.</p
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