LIVER IVM

Imaging liver immunopathology by intravital microscopy

 Coordinatore FONDAZIONE CENTRO SAN RAFFAELE DEL MONTE TABOR 

 Organization address address: Via Olgettina 60
city: MILANO
postcode: 20132

contact info
Titolo: Mr.
Nome: Mario
Cognome: Valsecchi
Email: send email
Telefono: +39 02 2643 2729
Fax: +39 02 2643 2752

 Nazionalità Coordinatore Italy [IT]
 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-2010-RG
 Funding Scheme MC-IRG
 Anno di inizio 0
 Periodo (anno-mese-giorno) 0000-00-00   -   0000-00-00

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    FONDAZIONE CENTRO SAN RAFFAELE DEL MONTE TABOR

 Organization address address: Via Olgettina 60
city: MILANO
postcode: 20132

contact info
Titolo: Mr.
Nome: Mario
Cognome: Valsecchi
Email: send email
Telefono: +39 02 2643 2729
Fax: +39 02 2643 2752

IT (MILANO) coordinator 100˙000.00

Mappa


 Word cloud

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hbv    liver    hepatitis    virus    mice    cells    viral    infection    cd    related    pathogenesis   

 Obiettivo del progetto (Objective)

'The objective of this proposal is to take advantage of recently developed technological progresses in the field of live imaging to elucidate the pathogenesis of hepatitis B virus (HBV) infection. CD8 T cells play a major part in the development of liver disease and the resolution of HBV infection. A number of important issues pertaining to HBV pathogenesis remain unresolved and they include the way in which CD8 T cells traffic and recognize antigen within the liver and the way in which the diseased liver influences these processes. Our rationale is based on the notion that - at last - we can address these and other related issues experimentally. Single- and two-photon intravital microscopy will be carried out in un-inflamed or fibrotic/cirrhotic livers from mouse models that include transgenic mice that express all of the viral polypeptides and replicate HBV in the hepatocyte and normal mice infected with HBV-replicating, hepatotropic, fluorescent adenoviruses. The spatial and temporal constraints of naïve or effector HBV-specific CD8 T cells recognizing viral antigens and interacting intrahepatically with platelets, endothelial cells or Kupffer cells will be visualized thanks to experimental systems created specifically for this purpose. These studies will shed new light on previously unknown aspects of HBV pathogenesis, paving the road to new immunotherapeutic strategies aimed at terminating chronic HBV infection. Results from this proposal may also have far-reaching implications, not only in related liver infections (i.e. hepatitis C virus), but also in other T cell-mediated pathological conditions of the liver such as autoimmunity, graft rejection or cancer.'

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