PATHFINDER

Mimicking pathogens; an integrated nano-medicine approach to developing intelligent cancer vaccines

 Coordinatore STICHTING KATHOLIEKE UNIVERSITEIT 

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 Nazionalità Coordinatore Netherlands [NL]
 Totale costo 2˙498˙680 €
 EC contributo 2˙498˙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-2010-AdG_20100317
 Funding Scheme ERC-AG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-11-01   -   2017-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    STICHTING KATHOLIEKE UNIVERSITEIT

 Organization address address: GEERT GROOTEPLEIN NOORD 9
city: NIJMEGEN
postcode: 6525 EZ

contact info
Titolo: Mr.
Nome: Wim
Cognome: Van Oijen
Email: send email
Telefono: +31 24 3618937
Fax: +31 24 3540529

NL (NIJMEGEN) hostInstitution 2˙498˙680.00
2    STICHTING KATHOLIEKE UNIVERSITEIT

 Organization address address: GEERT GROOTEPLEIN NOORD 9
city: NIJMEGEN
postcode: 6525 EZ

contact info
Titolo: Prof.
Nome: Carl Gustav
Cognome: Figdor
Email: send email
Telefono: +31 24 3617600
Fax: +31 24 3540339

NL (NIJMEGEN) hostInstitution 2˙498˙680.00

Mappa


 Word cloud

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

immunotherapy    dcs    iquest    cell    patient    carriers    vitro    patients    dendritic    receptors    immune    therapy    polymers    vaccine    cells    cancer    activate    tumour   

 Obiettivo del progetto (Objective)

'Tumour cells survive and grow because they are not effectively recognized by the immune system as ¿foreign¿ and are therefore not attacked and destroyed like most pathogens. We have already demonstrated the clinical value of dendritic cell (DC) vaccines that activate the immune system to fight cancer. Treating more than 300 patients with metastatic melanoma, we achieved extended survival in 40% of patients by maturing dendritic cells from the patient¿s blood in-vitro, loading them with cancer-specific antigens and re-injecting them into the patient. These DCs then activate tumour-specific T cells in the lymph nodes. Our success in this area of research makes us a world leader in dendritic cell immunotherapy. However, despite these encouraging results, more work needs to be done if this type of therapy is to move into routine cancer care.

Therefore the primary objective of the research detailed in this proposal is to significantly enhance cancer treatment efficacy by developing multifunctional nano-sized vaccine carriers that specifically target DCs and T cells in-vivo. If successful, this will also eliminate the costly in-vitro steps associated with current dendritic cell therapy.

The recent discovery of pathogen recognition receptors on dendritic cells opens up the possibility of exploiting these receptors to target dendritic cells within the body. We will therefore develop highly functionalized, slow-release vaccine carriers that target DCs in this way. In order to directly activate tumour-specific T cells, we will develop highly flexible polyisocyanide polymers that mimic naturally occurring DCs. To functionalize these polymers, we aim to develop a revolutionary DNA-based bar-coding technique. I expect this new approach leads to major advances in tumour immunotherapy.'

Altri progetti dello stesso programma (FP7-IDEAS-ERC)

SNLSID (2013)

Data Driven Structured Modelling of Nonlinear Dynamic Systems

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PD-HUMMODEL (2013)

Elucidating early pathogenic mechanisms of neurodegeneration in Parkinson's disease through a humanized dynamic in vitro model

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WDTRACER (2013)

"White Dwarfs as Tracers of Stellar, Binary and Planetary Evolution"

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