VacICoP: Chimpanzee Adenovirus Type 3-Vectored Marburg Glycoprotein (GP)-Expressing Vaccine (ChAd3-MARV)-Induced Correlates of Protection

Grant number: 308739/Z/23/Z

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Key facts

  • Disease

    Marburg virus disease
  • Start & end year

    2025
    2028
  • Known Financial Commitments (USD)

    $0
  • Funder

    Wellcome Trust
  • Principal Investigator

    Dr. Jennifer Serwanga
  • Research Location

    Uganda
  • Lead Research Institution

    Uganda Virus Research Institute
  • Research Priority Alignment

    N/A
  • Research Category

    Vaccines research, development and implementation

  • Research Subcategory

    Pre-clinical studies

  • Special Interest Tags

    Innovation

  • 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

Marburg Virus disease (MVD) outbreaks in Europe and Africa highlight the urgent need for vaccines. This study will increase the breadth of the ICoPs discovery effort, hypothesizing that early, emerging, and sustained Fab- and Fc-mediated effector polyfunctionality are crucial determinants of protection. Objectives include characterizing antibodies, dissecting immunity determinants and developing unbiased ICoPs selection algorithms. With unique access to relevant samples and cutting-edge immunology, we will broaden ICoPs exploration beyond one antigen, generating correlate(s) with broader utility. Our diverse specimen resource includes NHP and clinical samples from the USA, Kenya, and Uganda, survivor and deceased sera with clinical data, and healthy subjects' sera from diverse demographics. Robust validated assays, international standard reagents and protocols will ensure consistency. Through five interlinked work-packages, we will screen specimens for Fab- and Fc- mediated functions, analyze T-cell functions, validate targets of antibody- mediated protection, discover protection-linked biomarkers, and integrate data for ICoPs down-election. Key deliverables include defining ChAd3-MARV ICoPs, scalable screening assays, reference reagents, and licensure guidance. Our proposal aligns with global MVD vaccine efforts to address this critical public health challenge. Capacity building engagements and trainings for key stakeholders like local regulatory bodies, Ministry of Health and the community will be undertaken.