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Cross-talk between platelets and immunity - implications for host homeostasis and defense

Descrizione del progetto

Approfondimenti meccanicistici sull’immunotrombosi

Il riconoscimento dei patogeni da parte di cellule specifiche del sistema immunitario, come ad esempio monociti e neutrofili, attiva il sistema di coagulazione. Questa cooperazione, nota come immunotrombosi, comporta l’intrappolamento dei patogeni, limitandone così la diffusione nel compartimento vascolare ed evitando la lesione di altri organi. L’obiettivo del progetto IMMUNOTHROMBOSIS, finanziato dall’UE, consiste nell’analisi del meccanismo alla base di questo fenomeno, comprendendo come può essere coinvolto nelle malattie cardiovascolari. I ricercatori si concentreranno sulle piastrine, svelandone il ruolo nella sinergia omeostatica e patogena tra trombosi e infiammazione. I risultati spianeranno la strada a nuovi interventi contro la formazione di trombi e l’insorgenza di malattie cardiovascolari.  

Obiettivo

The overall aim of the IMMUNOTHROMBOSIS project is to clarify the mechanisms underlying the recently identified synergism between thrombosis and inflammation. Thrombus formation and inflammation are vital host responses that ensure homeostasis, but can also drive cardiovascular disease, including myocardial infarction and stroke, the major causes of death in Europe. My group and others discovered, that thrombosis and inflammation are not to be considered separate processes. They are tightly interrelated and synergize in immune defence, but also in inflammatory and thrombotic diseases in a process we termed immunothrombosis. Targeting this synergism has great potential to identify innovative and unconventional strategies to more specifically prevent undesired activation of thrombotic and inflammatory pathways. However, this requires a deeper mechanistic understanding of immunothrombosis. I recently identified two ground-breaking novel immunothrombotic principles: I discovered that platelets have the ability to migrate autonomously, which assists immune cells in fighting pathogens. Further, I revealed that immune cells play a central role in controlling the production of platelets from their megakaryocyte precursors. The physiological and pathophysiological relevance of both processes is unclear. This is the starting point and focus of the IMMUNOTHROMBOSIS project. My aim is to define how platelets use their ability to migrate to support immune cells in protection of vascular integrity (objective 1) and to identify the contribution of platelet migration to different cardiovascular diseases involving immunothrombotic tissue damage (objective 2). Finally, I will clarify how inflammatory responses feedback to the production of thrombotic effectors and dissect inflammatory mechanisms that control platelet production (objective 3). IMMUNOTHROMBOSIS will identify new options for specific prevention or treatment of thrombotic and inflammatory cardiovascular diseases.

Meccanismo di finanziamento

ERC-ADG - Advanced Grant

Istituzione ospitante

LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN
Contribution nette de l'UE
€ 2 321 416,00
Indirizzo
GESCHWISTER SCHOLL PLATZ 1
80539 MUNCHEN
Germania

Mostra sulla mappa

Regione
Bayern Oberbayern München, Kreisfreie Stadt
Tipo di attività
Higher or Secondary Education Establishments
Collegamenti
Costo totale
€ 2 321 416,00

Beneficiari (1)