MAVS

Role of the mitochondrial anti-viral signaling protein in sepsis

 Coordinatore UNIVERSITATSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITAT MAINZ 

 Organization address address: Langenbeckstrasse 1
city: Mainz
postcode: 55131

contact info
Titolo: Dr.
Nome: Silvia
Cognome: Tschauder
Email: send email
Telefono: +49 6131 17 9695
Fax: +49 6131 17 9669

 Nazionalità Coordinatore Germany [DE]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2012-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-03-01   -   2017-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITATSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITAT MAINZ

 Organization address address: Langenbeckstrasse 1
city: Mainz
postcode: 55131

contact info
Titolo: Dr.
Nome: Silvia
Cognome: Tschauder
Email: send email
Telefono: +49 6131 17 9695
Fax: +49 6131 17 9669

DE (Mainz) coordinator 100˙000.00

Mappa


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treatment    experimental    mavs    sepsis   

 Obiettivo del progetto (Objective)

'Severe sepsis is an important complication of infections and one of the leading causes of morbidity and mortality. For the countries of the European Union it is estimated that approximately 600,000 cases and more than 150,000 deaths occur from sepsis per year. Currently, no approved treatment options are available for the therapy of septic shock in humans.

This research proposal intends to investigate the acute inflammatory response during experimental sepsis in rodents. Our preliminary data indicate an essential role of the novel ‘mitochondrial anti-viral signaling protein’ (MAVS) during sepsis. Mice with genetic deficiency of MAVS appear to be protected against sepsis. We seek to study, how the effects of MAVS are related to regulation of cytokines, innate and adaptive immune cells, apoptosis, abnormalities in blood coagulation and appearance of cytotoxic factors in the context of experimental sepsis.

Such studies will be useful to identify novel molecular mechanisms during sepsis which could ultimately be utilized for the development of effective treatment strategies for sepsis.'

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