Project
Acronym: Yellow4FLAVI
Project title: Deconstructing the protective immunity of yellow fever virus 17D to inform flavivirus vaccine design
Funding source: Horizon Europe, Health, Pandemic preparedness and response: Understanding vaccine induced-immunity
Project duration: 5 years (2024-2028)
EU contribution: 7 951 515,75 €
Grant Agreement Number: 101137459
Coordinator: Dr. Giovanna BARBA-SPAETH (Institut Pasteur, France)
Ambitions
While endemic to the tropics, flaviviruses like Zika, dengue, West Nile or yellow fever virus are re-emerging pathogens of global health concern. Climate change and urbanization have largely contributed to the dissemination of their mosquito vector and Europe has in recent years been regularly confronted with autochthonous cases. Few vaccines are licensed to prevent flavivirus disease, but the yellow fever 17D (YF17D) vaccine has a unique track record of efficiency and safety. Intriguingly, despite its success, how YF17D induces immunity remains poorly understood.
The YELLOW4FLAVI consortium aims to fill the gaps in our understanding of the mechanism of action of this vaccine by linking the structure of the viral particle to the resulting host immune response, in order to learn about optimal vaccine design for flaviviruses in general. Since social acceptance of vaccines is critical for their success, we will also develop optimal communication methods. This will provide us with the tools to tailor vaccine design not only to achieve optimal immune protection, but also to facilitate actual implementation.
To pursue our goal of obtaining a blueprint for determinants of long-lasting immunity for flavivirus vaccine candidates, we will use cutting-edge technologies like cryo-EM, super resolution microscopy, spatial transcriptomics, high-dimensional spectral flow cytometry, single-cell RNA sequencing, advanced cell engineering, small animal models, and clinical studies.
In a unique manner, Yellow4FLAVI follows a thread of events from the early response at the site of vaccine injection to the population perception of vaccination, harnessing an enhanced understanding of one of the most successful vaccines of mankind for the development of novel lines of defense against new and old threats.
Specific Objectives
To define the role of the virus architecture in epitope presentation to understand the link between viral particle intracellular trafficking, antigen presentation, and generation of protective epitopes (WP1).
To increase our knowledge of the factors regulating the host immune response to YF17D vaccine from the early events at the site of injection to the maturation of a long-lasting immunological memory (WP2–WP4).
To develop effective risk communication strategies for novel vaccines, particularly for flaviviruses, that are informed by insights into the perceptions of new vaccine technologies and understanding of vaccine induced immunity in different populations (WP5).
Work Packages
The division of the project activities into Work Packages (WP) is typical in this type of large projects funded by the European Union. Each WP is led by a Partner (WP Lead) and groups activities (Tasks) let by several Partners to achieve a common objective.
WP1
Influence of virus architecture on protective epitope exposure and antigen intracellular trafficking
WP5
Mixed-methods research on perceptions of novel vaccine technologies
and conceptions of (vaccine induced) immunity: lessons for flaviviruses risk communication
WP2
Identification of host factors that predict and influence the vaccine response to YF17D
WP6
Communications, Dissemination and Exploitation
WP3
Long‐term protective memory response after vaccination
WP7
Coordination
WP4
Initiation of the immune response and presentation of viral antigens
WP8
Ethics requirements
Governance and Management
GENERAL ASSEMBLY
Ultimate decision-making body of the consortium, it consists of one representative of each Partner and meets at least every 6 months. The ESAC is invited to the GA meetings to provide their insights.
STEERING COMMITTEE
Operational management body reporting to the General Assembly, it consists of the WPs and Tasks Leads and meets once a month.
EXTERNAL SCIENTIFIC ADVISORY BOARD (ESAC)
Supports the General Assembly for the scientific monitoring of the project, and meets at least twice a year.
SCIENTIFIC COORDINATOR
Dr. Giovanna Barba Spaeth
Institut Pasteur, Paris
PROJECT MANAGER
Marine Hurard
Institut Pasteur, Paris
WORK PACKAGES
Each WP is led by a Partner (WP Lead) and groups activities (Tasks) let by several Partners to achieve a common objective. The WP Leads steer the progress of milestones and deliverables.
Public Deliverables
Stay tuned to read Yellow4FLAVI public deliverables including:
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Data Management Plan
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Dissemination & Communication Plan
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Project Website