ExComPat-Covid19 - Experimental and computational analysis of infection dynamics and lung pathology in COVID-19 - Subproject B

  • Funded by Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)
  • Total publications:4 publications

Grant number: 01KI20239B

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $105,602.99
  • Funder

    Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)
  • Principal Investigator

    N/A

  • Research Location

    Germany
  • Lead Research Institution

    Universität Heidelberg
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Disease pathogenesis

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    UnspecifiedNot Applicable

  • Vulnerable Population

    UnspecifiedNot applicable

  • Occupations of Interest

    UnspecifiedNot applicable

Abstract

The infection dynamics of SARS-CoV-2 within the lung and its association with disease progression is still incompletely understood. To which extent viral replication kinetics and virus-associated tissue pathology determine patient outcome remains an open question that is of urgent importance to advise effective treatment strategies. In this project, we will combine experimental data of lung organoids with detailed mathematical and computational models to assess SARS-CoV-2 infection kinetics under physiologically relevant conditions. By integrating spatially-resolved microscopy images with time course infection data of SARS-CoV-2 in lung organoids by mathematical analyses we will be able to quantify key parameters governing viral replication and spread, and their association with pathological changes. Extending the computational model to extrapolate infection dynamics within a human lung, we will be able to relate observed viral load kinetics in SARS-CoV-2 infected patients to expected tissue pathology and disease progression. This will help to assess the significance of viral load levels for associated lung pathology during infection. Our interdisciplinary approach will improve our understanding of SARS-CoV-2 replication and spread within lung tissue and its association with disease progression. Furthermore, the inferred computational model provides a tool to test the efficacy of antiviral therapies and represents a first step towards a mechanistic model of infection progression within tissue that could improve our understanding of individual patient outcome.

Publicationslinked via Europe PMC

Last Updated:41 minutes ago

View all publications at Europe PMC

Influence of cell type specific infectivity and tissue composition on SARS-CoV-2 infection dynamics within human airway epithelium.

USP22 controls type III interferon signaling and SARS-CoV-2 infection through activation of STING.

Increased Sensitivity of SARS-CoV-2 to Type III Interferon in Human Intestinal Epithelial Cells.

Single-cell analyses reveal SARS-CoV-2 interference with intrinsic immune response in the human gut.