Development of an NHP model of infection and ADE with COVID-19 (SARS-CoV-2)

  • Funded by Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR), UK Research and Innovation (UKRI)
  • Total publications:1 publications

Grant number: MC_PC_19080

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $557,172.5
  • Funder

    Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR), UK Research and Innovation (UKRI)
  • Principal Investigator

    Prof. Miles Carroll
  • Research Location

    United Kingdom
  • Lead Research Institution

    Department of Health and Social Care
  • 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

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

This COVID-19 Rapid Response award is jointly funded (50:50) between the Medical Research Council and the National Institute for Health Research. The figure displayed is the total award amount of the two funders combined, with each partner contributing equally towards the project. PHE Porton's extensive experience in the development of high containment infectious disease models will be applied to set up the UK's first primate model of SARS-CoV-2 infection. This will be achieved by intra-tracheal infection using a virus stock of SARS-CoV-2 acquired through international collaboration. PHE's Victoria stock of virus has been propagated in vitro and has already been used to challenge ferrets at PHE Porton. PHE will also assess the ability of a crude (killed whole virus) vaccine to induce immune mediated disease enhancement. This will be achieved by serially immunising NHPs and then infecting them with live SARS-CoV-2. PHE will assess the clinical signs of infection as well as assessing lung pathology in-life through X-ray and/or CT imaging. In this way, if unusal pathology is observed in the immunised groups, PHE will have set up a "positive control" ADE model to help discriminate vaccines or therapies which assist the host or accidentally enhance the immunopathology of acquired infection.

Publicationslinked via Europe PMC

Last Updated:14 hours ago

View all publications at Europe PMC

Immunological and pathological outcomes of SARS-CoV-2 challenge following formalin-inactivated vaccine in ferrets and rhesus macaques.