Defining the Protective Immune Response to SARS CoV2 Using a Human Challenge Model

Grant number: 222305/Z/21/A

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2021
    2023
  • Known Financial Commitments (USD)

    $2,515,307.26
  • Funder

    Wellcome Trust
  • Principal Investigator

    Prof Helen McShane
  • Research Location

    United Kingdom
  • Lead Research Institution

    University of Oxford
  • 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

    UnspecifiedNot Applicable

  • Vulnerable Population

    UnspecifiedNot applicable

  • Occupations of Interest

    UnspecifiedNot applicable

Abstract

Understanding the nature, effectiveness and durability of the human immune response to SARS CoV2 is crucial for vaccine development and effective public health management. We are beginning to understand the pattern and kinetics of the humoral response to natural infection but are less certain about other aspects of the response. We are unable to establish with certainty whether an individual with a particular titre of antibody, or a particular T cell response, is likely to be protected from reinfection and, if so, for how long. These are central questions for the development of an effective vaccine. A controlled human infection model will provide a more detailed understanding of the protective immune response. It will provide the opportunity to interrogate the full extent of the immune response at the time of exposure and will also allow the evaluation of the durability of immune responses of all kinds and how they correlate with protection. Key goals: - To establish an MHRA-approved SARS CoV2 viral stock for use in a controlled human infection model - To determine a challenge dose which is safe and allows virus to be recoverable from infected subjects