AIRSHIP

Acute Inflammation Resolution by Soluble Human Inhibitory Protein

 Coordinatore CEMM - FORSCHUNGSZENTRUM FUER MOLEKULARE MEDIZIN GMBH 

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 Nazionalità Coordinatore Austria [AT]
 Totale costo 150˙000 €
 EC contributo 150˙000 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2011-PoC
 Funding Scheme CSA-SA(POC)
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-12-01   -   2013-11-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    CEMM - FORSCHUNGSZENTRUM FUER MOLEKULARE MEDIZIN GMBH

 Organization address address: Dr. Ignaz Seipel-Platz 2
city: WIEN
postcode: 1010

contact info
Titolo: Ms.
Nome: Sigrid
Cognome: Strodl
Email: send email
Telefono: +43 1 4016070028
Fax: +43 1 40160970000

AT (WIEN) hostInstitution 150˙000.00

Mappa


 Word cloud

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intellectual    property    human    inflammatory    pro    soluble    molecular   

 Obiettivo del progetto (Objective)

'Acute inflammatory processes are associated with infections as well as autoimmune flares at the basis of a variety of human diseases. While the molecular components and the logic of pro-inflammatory program are relatively well understood, less is known about the molecular mechanism of resolution, governing the termination of inflammatory responses. In the course of carrying out the i-FIVE ERC grant project plan, we identified a novel, secreted, soluble enzyme as a negative regulator of pro-inflammatory immunity receptors. Here we propose a defined and focused set of measures aimed at obtaining solid evidence for therapeutic feasibility of this novel biological agent in resolving inflammatory processes as well as for the securing of intellectual property. The AIRSHIP workplan proposes to obtain enough purified, soluble, endotoxin-free, active and glycosylated protein material to execute two critical tests, one monitoring the inflammatory response in human cells, and one addressing beneficiary effects in a lung murine infection model. Armed with such a successful proof of concept package and having strategically positioned and secured our intellectual property rights we would be determined to embark into an ambitious commercialization initiative.'

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