Active Infection & Immunity Cancer

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

In plain English

AI plain-English summary

A single shot of an experimental chimpanzee adenovirus vaccine aims to teach the immune system to recognise and destroy the Marburg virus before it can cause disease. Marburg virus disease is a severe, often fatal haemorrhagic fever with no licensed vaccine. This project tackles a critical gap: scientists do not yet know exactly which immune responses a successful vaccine must trigger. Without that knowledge, it is impossible to reliably predict whether a candidate vaccine will work in people. The researchers will analyse blood samples from survivors, deceased patients, healthy people, and vaccinated non-human primates to identify the specific antibody and T-cell functions that correlate with protection. They will develop standardised screening assays and reference reagents that can be used globally to evaluate future Marburg vaccines. If successful, this work will provide the immunological benchmarks needed to license a Marburg vaccine, giving regulators and manufacturers a clear target. It will also establish a framework for identifying correlates of protection against other emerging viral threats, strengthening pandemic preparedness infrastructure. The project includes training for local health authorities in Kenya and Uganda, building long-term capacity to respond to outbreaks.

View original technical description
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.

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Researchers

Erica Saphire (EPMC Awardee)Jennifer Serwanga (EPMC Awardee)Joseph Campo (EPMC Awardee)Thomas King (EPMC Awardee)Verena Krähling (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Marburg virus - A first in human clinical trial to deliver a vaccine against Marburg virus Disease
Advancing Vaccine Development: Harnessing Multiple Antigenic Epitopes for Crimean-Congo Hemorrhagic Fever in Humans and Animals
A phase 1, first-in-human safety and immunogenicity study of a Marburg virus vaccine, ChAdOx1 Marburg, in healthy volunteers aged 18 55 years in the UK
A One Health approach to pan-valent morbillivirus vaccines
Emerging Viral Vaccine Antigen Insert Consortium (EVAC)

Original classification

Identifying correlates of protection to support vaccine development

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