Characterisation of a GMP SARS-CoV-2 Delta variant for human challenge

Grant number: 225170/Z/22/Z

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2022
    2025
  • Known Financial Commitments (USD)

    $8,051,015.84
  • Funder

    Wellcome Trust
  • Principal Investigator

    Prof Christopher Chiu
  • Research Location

    United Kingdom
  • Lead Research Institution

    Imperial College London
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Immunity

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Not applicable

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

SARS-CoV-2 continues to spread in spite of vaccination due in part to the high transmissibility of the prevalent delta variant. The factors predisposing to breakthrough infection are unknown and correlates of protection remain unclear. Human challenge studies are uniquely able to control for differences in virus strain, dose and exposure to investigate these factors. Safety in seronegative participants challenged with a D614G pre-alpha strain was recently shown and a new GMP delta challenge agent is now being manufactured. We therefore aim - To establish an optimised controlled human infection model using a GMP SARS-CoV-2 Delta (B.1.617.2) challenge agent, characterising virological and immunological readouts therein to enable further assessment and development of COVID-19 vaccines - To identify the determinants of vaccine breakthrough infection and correlates of protection in antigenically- experienced individuals These will be achieved by challenging vaccinated individuals with Delta and optimising the attack rate by sero-screening and dose-escalation. Using these optimised conditions, 3 groups will then be compared: - vaccinated, uninfected individuals, Delta-challenged; - vaccinated, previously-infected, Delta-challenged; and - vaccinated, uninfected, pre-Alpha-challenged. Thus, host determinants of differential disease and virological outcome will be identified in the context of pre- existing immunity by vaccination and/or infection to define correlates and mechanisms of homologous and heterologous protection.