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Updated: Oct 12, 2025

A Data-Driven Approach to Quantifying Immune States in Sepsis
Published on: February 7, 2025
Data-driven multi-scale mathematical modeling of SARS-CoV-2 infection reveals heterogeneity among COVID-19 patients
Shun Wang1,2, Mengqian Hao1,2, Zishu Pan3
1School of Mathematics and Statistics, Wuhan University, Wuhan, China.
Insights
A computational model reveals how individual differences in COVID-19 progression occur. Enhancing the host antiviral state and T cell responses can guide personalized treatments for coronavirus disease 2019 (COVID-19) patients.
Area of Science:
- Computational biology
- Immunology
- Infectious disease modeling
Background:
- Coronavirus disease 2019 (COVID-19) presents diverse patient outcomes.
- Understanding heterogeneity in COVID-19 progression is crucial for effective treatment.
Purpose of the Study:
- To develop a multi-scale computational model for quantitatively analyzing COVID-19 progression.
- To identify key factors influencing disease heterogeneity and guide personalized therapeutic strategies.
Main Methods:
- Developed a multi-scale computational model integrating intracellular viral dynamics, multicellular infection, and immune responses.
- Utilized differential equations and stochastic modeling, combined with multi-source clinical data.
- Quantified individual heterogeneity using infected cell ratio and incubation period.
Main Results:
- Increased host antiviral state or type I interferon (IFN) production prolongs incubation and delays symptom onset.
- T cell exhaustion thresholds predict transitions between mild and severe COVID-19.
- Severe COVID-19 patients show a late-stage deficiency in naïve T cells.
Conclusions:
- IFN and T cell responses critically regulate COVID-19 stage transitions.
- Model provides insights into personalized therapy for COVID-19, suggesting single antiviral therapy for moderate cases and combination therapy with T cell exhaustion prevention for severe cases.
Abstract:
Patients with coronavirus disease 2019 (COVID-19) often exhibit diverse disease progressions associated with various infectious ability, symptoms, and clinical treatments. To systematically and thoroughly understand the heterogeneous progression of COVID-19, we developed a multi-scale computational model to quantitatively understand the heterogeneous progression of COVID-19 patients infected with severe acute respiratory syndrome (SARS)-like coronavirus (SARS-CoV-2). The model consists of intracellular viral dynamics, multicellular infection process, and immune responses, and was formulated using a combination of differential equations and stochastic modeling. By integrating multi-source clinical data with model analysis, we quantified individual heterogeneity using two indexes, i.e., the ratio of infected cells and incubation period. Specifically, our simulations revealed that increasing the host antiviral state or virus induced type I interferon (IFN) production rate can prolong the incubation period and postpone the transition from asymptomatic to symptomatic outcomes. We further identified the threshold dynamics of T cell exhaustion in the transition between mild-moderate and severe symptoms, and that patients with severe symptoms exhibited a lack of naïve T cells at a late stage. In addition, we quantified the efficacy of treating COVID-19 patients and investigated the effects of various therapeutic strategies. Simulations results suggested that single antiviral therapy is sufficient for moderate patients, while combination therapies and prevention of T cell exhaustion are needed for severe patients. These results highlight the critical roles of IFN and T cell responses in regulating the stage transition during COVID-19 progression. Our study reveals a quantitative relationship underpinning the heterogeneity of transition stage during COVID-19 progression and can provide a potential guidance for personalized therapy in COVID-19 patients.
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