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Targeting the vascular-immune interface to induce anti-tumor immunity

Project description

Targeting tumour vasculature for enhanced immunotherapy

Blood vessels in tumours not only provide nutrients and oxygen but also regulate the movement and activation of immune cells. The interface is crucial because it controls how immune cells, such as T-cells, are recruited to and activated within the tumour environment. The ERC-funded VASC-IMMUNE project seeks to optimise vascular-immune interactions for better immunotherapy since despite advances, many patients still do not benefit. The research team will develop tumour-targeting adeno-associated virus vectors to induce immune hubs around tumour blood vessels, enhancing immune responses. By combining expertise in vascular biology, tumor immunology, and gene therapy, the project aims to make groundbreaking advancements in cancer treatment.

Objective

In this ERC Synergy Grant, we will characterize the vascular-immune interface in melanoma and glioblastoma and explore the perivascular niche as a site for local anti-tumor immune activation.
Cancer immunotherapy has made tremendous progress in the last two decades, but a vast majority of cancer patients do not benefit from this progress yet. Refinement of established immunotherapies will undoubtedly increase response rates. However, conceptually brave new therapies must be developed to make additional breakthroughs.
The tumor vasculature plays a key role in orchestrating anti-tumor immunity by regulating recruitment and activation of T-cell and other immune cells. We propose to make a detailed characterization of vascular immune landscapes in melanoma and glioblastoma and to utilize this to optimize vascular-immune crosstalk and immune response as a new breakthrough immunotherapy.
This proposal builds upon new knowledge on how immune hubs can form around tumor vasculature, which to a large part is based upon novel findings and development by the applicants (1, 2) on the importance of perivascular antigen-presenting niches in activating, sustaining, and executing CD8 and CD4 T-cell-mediated immune attacks on cancer. We will develop tumor vessel targeting AAV vectors that can enable therapeutic induction of immune hubs in cancer. This new form of immunotherapy will be evaluated alone and in combination with established cancer immunotherapies.
Combined, our research teams are in a unique position to achieve this goal. Synergistic advancements will be obtained by joining Dimberg’s expertise in the vascular and immune microenvironment in tumors (especially glioblastoma); Tüting’s expertise in tumor immunology and cell plasticity (especially melanoma); and Essand’s expertise in translational gene therapy and cancer immunotherapy. The project is timely, and if successful can bring immunotherapy to the next level, rendering new hope to millions of cancer patients.

Fields of science (EuroSciVoc)

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Keywords

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Programme(s)

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Topic(s)

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Funding Scheme

Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.

HORIZON-ERC-SYG - HORIZON ERC Synergy Grants

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Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

(opens in new window) ERC-2024-SyG

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Host institution

UPPSALA UNIVERSITET
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 6 290 000,00
Address
VON KRAEMERS ALLE 4
751 05 Uppsala
Sweden

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Region
Östra Sverige Östra Mellansverige Uppsala län
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 6 290 000,00

Beneficiaries (2)

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