DENDROWORLD

Mucosal dendritic cells in intestinal homeostasis and bacteria-related diseases

 Coordinatore ISTITUTO EUROPEO DI ONCOLOGIA SRL 

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 Nazionalità Coordinatore Italy [IT]
 Totale costo 1˙195˙680 €
 EC contributo 1˙195˙680 €
 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-2007-StG
 Funding Scheme ERC-SG
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-07-01   -   2013-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    ISTITUTO EUROPEO DI ONCOLOGIA SRL

 Organization address address: Via Filodrammatici 10
city: MILANO
postcode: 20121

contact info
Titolo: Dr.
Nome: Maria
Cognome: Rescigno
Email: send email
Telefono: 390257000000
Fax: 390257000000

IT (MILANO) hostInstitution 0.00
2    ISTITUTO EUROPEO DI ONCOLOGIA SRL

 Organization address address: Via Filodrammatici 10
city: MILANO
postcode: 20121

contact info
Titolo: Ms.
Nome: Ilaria
Cognome: Foti
Email: send email
Telefono: 390257000000
Fax: 390294000000

IT (MILANO) hostInstitution 0.00

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 Word cloud

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responses    tslp    players    intestinal    host    dendritic    cell    mechanisms    shown    dcs    iga    function    regulatory    commensal    bacterial    maintenance    homeostasis    ec    cells    epithelial    immune   

 Obiettivo del progetto (Objective)

'The bacterial microflora has always been regarded as beneficial for the host but recent studies have shown that this symbiosis has risks as well as benefits. Although active mechanisms allow tolerating the commensal flora, the physiological stress that is associated with the symbionts’ metabolism can exhaust the intestinal barrier resulting in serious effects on the health of the host. Protracted immune deregulations can lead to severe disorders including diabetes, cancer and inflammatory bowel disease (IBD). Several mechanisms and players are involved in the maintenance of intestinal immune homeostasis, including T regulatory cells and Immunoglobulin (Ig)-A. In this proposal we focus our attention on dendritic cells (DCs) for their ability to induce both tolerance and immunity by regulating B and T cell responses. We have recently shown that DC function is controlled by intestinal epithelial cell (EC) derived factors and in particular by Thymic stromal lymphopoietin (TSLP). EC-conditioned DCs acquire a ‘mucosal’ phenotype as they are prone to activate T regulatory cells and IgA responses. Three major issues related to the maintenance and disruption of intestinal immune homeostasis will be explored in this project: 1) What are the mediators and mechanisms that regulate the interaction between intestinal epithelial cells and dendritic cells? What is the function of TSLP? 2) Which are the sites and players for the activation of an IgA response to pathogenic and commensal bacteria? Can we visualize them in vivo? 3) Can prolonged infections or bacterial products promote intestinal tumour development? Are there different bacterial constituents acting as inducers or protectors of carcinogenesis? What is the role of Toll-like receptors?'

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