Research article

Parameter analysis of an extended immuno-epidemiological model using sensitivity and elasticity methods

  • Published: 24 August 2026
  • Immuno-epidemiological modeling has been widely studied for understanding disease spread and supporting global control efforts. Mathematical and computational methods are important tools to study interactions between the immune system and infectious diseases. This work presented an extended immuno-epidemiological model that describes the dynamics of the model transmission rates. This study includes some key outputs. First, we calculated the basic reproduction number, R0, which is used to assess disease transmissibility, design control strategies, and evaluate intervention effectiveness. Second, the local sensitivity analysis was numerically evaluated using non-normalization, half normalization, and full normalization techniques between the model states and parameters; it provides an important step forward in identifying the model critical parameters in the spreading of disease. Another model output was calculating the elasticity index between R0 and the model parameters to identify the most critical parameters. Interestingly, numerical results showed the impact of the virus transmission rate, virus clearance rate, killing rate of infected cells, interferon degradation rate, and antibody production rate and discussed some model compartments for different parameter values. The findings help the local and international efforts in suggesting control strategies, optimizing interventions, and guiding public health decisions.

    Citation: Sarbaz H. A. Khoshnaw. Parameter analysis of an extended immuno-epidemiological model using sensitivity and elasticity methods[J]. AIMS Bioengineering, 2026, 13(3): 347-365. doi: 10.3934/bioeng.2026017

    Related Papers:

  • Immuno-epidemiological modeling has been widely studied for understanding disease spread and supporting global control efforts. Mathematical and computational methods are important tools to study interactions between the immune system and infectious diseases. This work presented an extended immuno-epidemiological model that describes the dynamics of the model transmission rates. This study includes some key outputs. First, we calculated the basic reproduction number, R0, which is used to assess disease transmissibility, design control strategies, and evaluate intervention effectiveness. Second, the local sensitivity analysis was numerically evaluated using non-normalization, half normalization, and full normalization techniques between the model states and parameters; it provides an important step forward in identifying the model critical parameters in the spreading of disease. Another model output was calculating the elasticity index between R0 and the model parameters to identify the most critical parameters. Interestingly, numerical results showed the impact of the virus transmission rate, virus clearance rate, killing rate of infected cells, interferon degradation rate, and antibody production rate and discussed some model compartments for different parameter values. The findings help the local and international efforts in suggesting control strategies, optimizing interventions, and guiding public health decisions.



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    Acknowledgments



    This research was partially supported by the University of Raparin. The author is thankful to the University for providing wonderful facilities. This support is greatly appreciated.

    Conflict of interest



    The author declares no conflicts of interest in this paper.

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