METAPATH

Integrated study of skin resident Memory T cells and dermal mononuclear phagocytes in the fight against PATHogens

 Coordinatore INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) 

 Organization address address: 101 Rue de Tolbiac
city: PARIS
postcode: 75654

contact info
Titolo: Mrs.
Nome: Véronique
Cognome: Legros
Email: send email
Telefono: +33 491827015
Fax: +33 491827048

 Nazionalità Coordinatore France [FR]
 Totale costo 253˙450 €
 EC contributo 253˙450 €
 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-2013-IOF
 Funding Scheme MC-IOF
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-09-02   -   2016-09-01

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)

 Organization address address: 101 Rue de Tolbiac
city: PARIS
postcode: 75654

contact info
Titolo: Mrs.
Nome: Véronique
Cognome: Legros
Email: send email
Telefono: +33 491827015
Fax: +33 491827048

FR (PARIS) coordinator 253˙450.90

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

memory    dermis    cells    trm    dermal    upon    pathogen    resident    generation    infection    phagocytes    encounter    mononuclear    skin   

 Obiettivo del progetto (Objective)

'Integrated study of skin resident Memory T cells and dermal mononuclear phagocytes in the fight against PATHogens'

Control of pathogen infection requires the generation of a tightly regulated immune response that recognizes the invading pathogen and that limits a potentially harmful host response. Recent work highlighted that resident memory T cells (TRM) form a very potent means of establishing effective immunity against infection. In the skin, I contributed to the extensive characterization of mononuclear phagocytes and unveiled the phenotype and some of the functions of the dermal macrophage subsets as well as the different dendritic cell subsets. In the present proposal, I propose to study the role of those different antigen presenting cells in the generation of TRM cells in the dermis upon a first pathogen encounter and their role in the re-activation of those TRM cells upon a second encounter with the pathogen. Learning the mechanisms by which efficient TRM cells are generated in the dermis will be an important step in the design of rational approaches to achieve the appropriate control of the pathogen at the site of infection.'

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