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Targeting mechanisms of Thrombo-inflammation

Objective

The recent Covid-19 pandemic dramatically illustrated (i) the clinical relevance of thrombo-inflammation (the interplay of coagulation and inflammation) and (ii) our limited understanding of molecular mechanisms of thrombo-inflammation. Thrombo-inflammation is a frequent disease-driving mechanism, impairing out-come of viral or bacterial infection, cardiovascular disease, cancer and other diseases. The lack of mechanistic insights hampered the development of specific therapies. My group recently discovered a new molecular link between coagulation and inflammation that addresses this enormous unmet medical need: the initiator of coagulation, tissue factor (TF, F3, CD142), forms a previously unknown heterodimer with the cytokine receptor IFNAR1 (Interferon-alpha/beta receptor alpha chain) on resting cells. In this heterodimer, TF and IFNAR1 are both inactive. Upon stimulation (e.g. fVII/fVIIa, LPS, polyIC) the heterodimer dissociates, activating TF-mediated coagulation, IFNAR1-mediated inflammation, and cellular metabolism. This provides a novel, yet simple molecular switch simultaneously controlling coagulation, inflammation, and metabolism. This switch is expected to provide a new conceptional framework for thrombo-inflammatory diseases. To enable future translation of this novel mechanism, I aim to address the following open questions (i) how is this molecular switch regulated in an organ and context specific fashion (in vitro work; cell-specific inducible TFIFNAR1 deficient mice)? (ii) what are the consequences of this molecular switch for intracellular signaling, inflammation, mitochondrial metabolism (omics with bioinformatic analyses)? and (iii) what are the molecular structures required for the TF-IFNAR1 interaction (cross-linking, crystallography, phage display, computational modeling)? I expect that answering these questions will lead to new diagnostic and therapeutic approaches revolutionizing the way we detect and treat thrombo-inflammatory diseases.

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Keywords

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

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(opens in new window) ERC-2023-ADG

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Host institution

UNIVERSITAET LEIPZIG
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.

€ 2 499 000,00
Address
RITTERSTRASSE 26
04109 Leipzig
Germany

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Region
Sachsen Leipzig Leipzig
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.

€ 2 499 000,00

Beneficiaries (1)

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