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.

Plos Computational Biology
|November 24, 2021
PubMed

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.

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