COVID-19: comparison of clinical, virological and immunological features in a SARS-CoV-2 patient cohort and a newly-established mouse model (Freiburg-COVID-19)

  • Funded by Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)
  • Total publications:7 publications

Grant number: 01KI2077

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $646,902.27
  • Funder

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

    Prof. Martin Schwemmle
  • Research Location

    Germany
  • Lead Research Institution

    Universität Freiburg
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Disease models

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Adults (18 and older)

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Although clinicians and researchers have been reporting new insights into SARS-CoV-2 infection at an immense rate, many fundamental questions surrounding the underlying biology of the disease remain unanswered. Owing to its unique geographic location, the Upper Rhine region rapidly emerged as one of the earliest sites of viral transmission in Germany. As the major medical center in the area, the University Medical Center Freiburg has been a focal point of patient care, establishing robust diagnostic workflows very early in the epidemic and treating severely ill patients. This project aims to provide an in-depth characterization of the innate and adaptive immune response to SARS-CoV-2 virus in both humans and animals. To achieve this goal, a tightly-linked consortium will leverage a unique synergy between clinicians in direct care of COVID-19 patients, a diagnostic department with established SARS-CoV-2 workflows, basic research expertise in studying highly-pathogenic zoonotic respiratory viruses in animal models, and technical resources allowing in-depth immunophenotyping. This project will provide urgently needed insights into the immune response to COVID-19 infection, including identification of immune effector cells and clarification of a potential cytokine storm. This information can directly aid clinicians in treatment decisions as well as provide key data for research into treatment and prevention strategies. The project will also establish an animal model of infection which will allow in-depth characterization of the disease as well as drug and vaccine tests.

Publicationslinked via Europe PMC

Last Updated:4 hours ago

View all publications at Europe PMC

Total escape of SARS-CoV-2 from dual monoclonal antibody therapy in an immunocompromised patient.

Impaired immune response drives age-dependent severity of COVID-19.

Passive immunization against COVID-19 by anti-SARS-CoV-2 spike IgG in commercially available immunoglobulin preparations in severe antibody deficiency.

SARS-CoV-2-specific T-cell epitope repertoire in convalescent and mRNA-vaccinated individuals.

Antibody escape and global spread of SARS-CoV-2 lineage A.27.

Within-host evolution of SARS-CoV-2 in an immunosuppressed COVID-19 patient as a source of immune escape variants.

Biparatopic nanobodies protect mice from lethal challenge with SARS-CoV-2 variants of concern.