SARS-CoV-2: understanding the entry, multi-organ spread, and immune response in the context of vaccination and re-infection

  • Funded by Swiss National Science Foundation (SNSF)
  • Total publications:0 publications

Grant number: 205323

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2022
    2025
  • Known Financial Commitments (USD)

    $641,127.23
  • Funder

    Swiss National Science Foundation (SNSF)
  • Principal Investigator

    Chatelain Pascal
  • Research Location

    Switzerland
  • Lead Research Institution

    Institute for Research in Biomedicine (IRB) Università della Svizzera italiana
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Pathogen morphology, shedding & natural history

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) causing the coronavirus disease (COVID-19) with fatal acute respiratory disease has rapidly spread worldwide. Our knowledge about SARS-CoV-2 is accumulating, but its spread to the entire organisms with deleterious consequences and the immunology responses to virus, vaccination and treatment in the context of reinfections are still scarcely understood. The main goal of the project is to characterize the so far elusive biology of entry and pathological organ-specific consequences of SARS-Cov-2 and its variants via ACE2, Neuropilin 1 and Transferrin receptors and the development of the immune response, including the possibility that antibodies, elicited by natural response to infection, vaccination or immunotherapy, could generate serious adverse effects through Antibody Dependent Enhancement (ADE). This project is based on our successful pre-work, established technologies, and on our recent joint publication designing and characterizing novel anti-SARS-Cov-2 therapeutic antibodies (De Gasparo et al., Nature, 2021).