Coordinatore | FONDAZIONE HUMANITAS PER LA RICERCA
Organization address
address: Via Manzoni 56 contact info |
Nazionalità Coordinatore | Italy [IT] |
Totale costo | 3˙989˙175 € |
EC contributo | 2˙999˙300 € |
Programma | FP7-HEALTH
Specific Programme "Cooperation": Health |
Code Call | FP7-HEALTH-2011-single-stage |
Funding Scheme | CP-FP |
Anno di inizio | 2012 |
Periodo (anno-mese-giorno) | 2012-01-01 - 2015-12-31 |
# | ||||
---|---|---|---|---|
1 |
FONDAZIONE HUMANITAS PER LA RICERCA
Organization address
address: Via Manzoni 56 contact info |
IT (ROZZANO) | coordinator | 597˙503.54 |
2 |
FONDAZIONE PER L'ISTITUTO DI RICERC A IN BIOMEDICINA
Organization address
address: Via Vincenzo Vela 6 contact info |
CH (BELLINZONA) | participant | 363˙600.00 |
3 |
UNIVERSITY OF GLASGOW
Organization address
address: University Avenue contact info |
UK (GLASGOW) | participant | 357˙600.00 |
4 |
THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN
Organization address
address: College Green - contact info |
IE (DUBLIN) | participant | 297˙600.00 |
5 |
TELORMEDIX SA
Organization address
address: Via della Posta 10 contact info |
CH (Bioggio) | participant | 289˙696.46 |
6 |
UNIVERSIDADE FEDERAL DE MINAS GERAIS
Organization address
address: AV. ANTONIO CARLOS - PAMPULHA 6627 contact info |
BR (BELO HORIZONTE MINAS GERAIS) | participant | 250˙500.00 |
7 |
FUNDACAO OSWALDO CRUZ
Organization address
address: AVENIDA BRASIL 4365 contact info |
BR (RIO DE JANEIRO) | participant | 222˙000.00 |
8 |
UNIVERSIDADE DE SAO PAULO
Organization address
address: RUA DA REITORIA 109 BUTANTA contact info |
BR (SAO PAULO SP) | participant | 220˙800.00 |
9 |
NOVIMMUNE SA
Organization address
address: CHEMIN DES AULX 14 contact info |
CH (PLAN LES OUATES GENEVE) | participant | 163˙037.00 |
10 |
ALTA RICERCA E SVILUPPO IN BIOTECNOLOGIE SRLU
Organization address
address: VIA FIORENTINA 151 contact info |
IT (SIENA) | participant | 100˙000.00 |
11 |
DOMPE FARMACEUTICI SPA
Organization address
address: VIA S MARTINO DELLA BATTAGLIA 12 contact info |
IT (MILANO) | participant | 100˙000.00 |
12 |
MERCK SERONO SA
Organization address
address: Chemin des Mines 9 contact info |
CH (GENEVE) | participant | 36˙963.00 |
13 |
DOMPE SPA
Organization address
address: Via Campo di Pile contact info |
IT (L'Aquila) | participant | 0.00 |
Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.
'Resolution of inflammation is a key determinant of pathology, and an active process which involves diverse pathways and molecules. The general objective of the TIMER Consortium is to identify and validate new molecules involved in the resolution of inflammation as a basis for the development of innovative therapeutic strategies in chronic inflammatory and autoimmune diseases. The project will involve discovery of new natural or synthetic “pro-resolving” molecules for plant and animals and investigation on endogenous inflammation “pro-resolving” mechanisms identified by various partners of the Consortium, including atypical chemokine receptors, decoy receptors, and microRNA. Tapping resources of natural compounds will be a major thrust. Efforts will be mainly focused on the regulation by “pro-resolving” agents on two molecular systems of key relevance in inflammation: the chemokine system, which regulates recruitment, permanence and egress of leukocyte in tissues; and the TLR/IL-1R system, which is central for the activation of infiltrating leukocytes. To this purpose, the project will capitalize on, and bring added value to a strong tradition of the Consortium in the fields of: leukocyte recruitment and activation; negative regulators of inflammation; industrial-academic collaboration; identification and characterization of innovative inhibitors of natural origin; European-Brazilian collaboration.'
Although inflammation is desirable to maintain health, the inability to resolve inflammatory responses can alter tissue homeostasis and cause disease. A group of European researchers is taking advantage of the physiological mechanisms that resolve inflammation to design drugs for treating chronic conditions.
Inflammation is the complex response of our immune system to get rid of harmful stimuli, including pathogens.
Pathological chronic inflammation is known to be associated with many conditions including cancer, neurodegeneration and many autoimmune diseases.
The aim of the EU-funded 'Targeting novel mechanisms of resolution in inflammation' (http://www.eumbrella.org/timer.html (TIMER)) project is to identify and validate new molecules involved in the resolution of inflammation.
By focusing on the cells that sustain inflammation, the consortium hopes to provide the basis for the development of innovative therapeutic strategies.
The concept behind the TIMER study lies on the resolution of inflammation rather than on the passive blockade of pro-inflammatory mediators.
Through natural or synthetic 'pro-resolving' molecules, partners will target two key pathways of inflammation, namely the chemokine and the toll-like receptor (TLR) systems.
Chemokines work to attract leukocytes to sites of inflammation where they become activated by macrophages or dendritic cells through TLRs.
So far, researchers have unveiled three different mechanisms controlling inflammation.
The molecule TIR8 has been shown to promote the resolution of inflammation by blocking both chemokine and TLR pathways.
Resolution of inflammation has also been found to depend on microRNA molecules as well as on metabolic molecules.
Partners have worked on providing solutions to resolve inflammation in the form of synthetic or natural peptides and TLR-binding agonists.
Some of these have shown promising results in pre-clinical models and their efficacy is being further evaluated in a human clinical study.
By shedding light onto the mechanisms that resolve inflammation, the TIMER study proposes to use both endogenous and exogenous molecules that can regulate the inflammatory process.
The generated information could be exploited for the design of novel therapies and pro-resolving drugs that can alleviate the detrimental impact of chronic inflammation.
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