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Conventional Dendritic Cells – Ecology, Diversity, and Function

The project aims to explore the diverse roles of conventional dendritic cell subsets in T cell activation during different immune responses to enhance cancer therapies and vaccine efficacy.

Subsidie
€ 1.796.125
2024

Projectdetails

Introduction

Effective T cell responses are critical for the efficacy of vaccination and cancer immunotherapy; therefore, the manipulation of conventional dendritic cells (cDCs) offers great potential for improved therapies as these cells play a key role in the activation and regulation of T cell function.

Background

However, cDCs are a diverse group of cells whose function is incompletely understood. Previous attempts at targeting cDCs therapeutically have been underwhelming, perhaps as a result of not targeting the right cell subset specifically.

Objectives

The goal of this proposal is to:

  1. Reveal the functional properties of the different cDC lineages during type 1 and type 2 immunity.
  2. Understand how the ecology of cDC subsets is regulated to meet the functional demands of tissues undergoing different types of inflammation.

Research Approach

I propose that studying the cDC subsets that:

  • Enhance cytotoxic T cell responses against viruses in type 1 immunity.
  • Enhance parasite clearance and tissue repair in type 2 immunity against nematodes.

This will help to identify those cDC subsets that need to be either triggered or inhibited to improve tumor control.

Methodology

Therefore, we will:

  • Use well-defined models of type 1 and type 2 immunity to reveal the diversity of these cells during inflammation.
  • Generate new mouse models to target cDC subsets specifically to study their functional properties and to reveal how these functional properties are instructed.

Inter-Organ Communication

In this regard, we will address how subset specification is regulated distally by a novel inter-organ communication axis (lung-bone marrow) that could tune the host immune system to ever-evolving challenges.

Proof of Concept

Finally, as a proof of concept, we will use transplantable and orthotopic cancer models to unravel beneficial and detrimental cDC subsets in the immune response against cancer.

Conclusion

cDCFun will open new avenues for the design of better vaccines and immunotherapies that harness the functional properties of specific subsets of cDCs.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 1.796.125
Totale projectbegroting€ 1.796.125

Tijdlijn

Startdatum1-1-2024
Einddatum31-12-2028
Subsidiejaar2024

Partners & Locaties

Projectpartners

  • FUNDACAO D. ANNA DE SOMMER CHAMPALIMAUD E DR. CARLOS MONTEZ CHAMPALIMAUDpenvoerder

Land(en)

Portugal

Inhoudsopgave

European Research Council

Financiering tot €10 miljoen voor baanbrekend frontier-onderzoek via ERC-grants (Starting, Consolidator, Advanced, Synergy, Proof of Concept).

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