Miroshnichenko Maxim I, Kolpakov Fedor A, Akberdin Ilya R
Department of Computational Biology, Scientific Center for Genetics and Life Sciences, Sirius University of Science and Technology, 354340 Sochi, Russia.
Viruses. 2025 Apr 22;17(5):589. doi: 10.3390/v17050589.
The COVID-19 pandemic highlighted the importance of mathematical modeling for understanding viral infection dynamics and accelerated its application into immunological research. Collaborative efforts among international research groups yielded a wealth of experimental data, which facilitated model development and validation. This study focuses on developing a modular mathematical model of the immune response, capturing the interactions between innate and adaptive immunity, with an application to SARS-CoV-2 infection. The model was validated using experimental data from middle-aged individuals with moderate COVID-19 progression, including measurements of viral load in the upper and lower airways, serum antibodies, CD4+ and CD8+ T cells, and interleukin-6 levels. Parameter optimization and sensitivity analysis were performed to improve the model accuracy. Additionally, identifiability analysis was conducted to assess whether the data were sufficient for reliable parameter estimation. The verified model simulates the dynamics of moderate, severe, and critical COVID-19 progressions using measured data on lung epithelium damage, viral load, and IL-6 levels as key indicators of disease severity. We also performed a series of validation scenarios to assess whether the model correctly reproduces biologically relevant behaviors under various conditions, such as immunity hyperactivation, co-infection with HIV, and interferon administration as a therapeutic strategy. The model was developed as a component of the Digital Twin project and represents a general immune module that integrates both innate and adaptive immunity. It can be utilized for further COVID-19 research or serve as a foundation for studying other infectious diseases, provided sufficient data are available.
新冠疫情凸显了数学建模对于理解病毒感染动态的重要性,并加速了其在免疫学研究中的应用。国际研究团队的合作努力产生了大量实验数据,这推动了模型的开发和验证。本研究专注于开发一种免疫反应的模块化数学模型,捕捉先天免疫和适应性免疫之间的相互作用,并应用于新冠病毒感染。该模型使用了来自新冠病情进展为中度的中年个体的实验数据进行验证,包括上、下呼吸道病毒载量、血清抗体、CD4+和CD8+ T细胞以及白细胞介素-6水平的测量。进行了参数优化和敏感性分析以提高模型准确性。此外,还进行了可识别性分析,以评估数据是否足以进行可靠的参数估计。经过验证的模型使用肺上皮损伤、病毒载量和IL-6水平的测量数据作为疾病严重程度的关键指标,模拟了中度、重度和危重型新冠病情的动态变化。我们还进行了一系列验证场景,以评估该模型在各种条件下是否能正确重现生物学相关行为,如免疫过度激活、与HIV合并感染以及将干扰素给药作为一种治疗策略。该模型是作为数字孪生项目的一个组成部分开发的,代表了一个整合先天免疫和适应性免疫的通用免疫模块。如果有足够的数据,它可用于进一步的新冠研究,或作为研究其他传染病的基础。