GIFT

Graft engineering to improve allogeneic stem cell transplantation

 Coordinatore KAROLINSKA INSTITUTET 

 Organization address address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177

contact info
Titolo: Mr.
Nome: Klas
Cognome: Karlsson
Email: send email
Telefono: +46 8 585 824 34
Fax: +46 8 711 76 84

 Nazionalità Coordinatore Sweden [SE]
 Totale costo 179˙588 €
 EC contributo 179˙588 €
 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-2007-4-2-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-08-01   -   2010-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    KAROLINSKA INSTITUTET

 Organization address address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177

contact info
Titolo: Mr.
Nome: Klas
Cognome: Karlsson
Email: send email
Telefono: +46 8 585 824 34
Fax: +46 8 711 76 84

SE (STOCKHOLM) coordinator 0.00

Mappa


 Word cloud

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

limit    transplantation    treating    exploited    grafts    immune    related    malignancies    wider    trafficking    treatment    minimise    stem    immunity    graft    tumour    infection    therapy    blood    anti    gvhd    versus    matched    cells    donors    asct    cancer    allogeneic    host    disease    fty    protocols    responses    cell   

 Obiettivo del progetto (Objective)

'Allogeneic stem cell transplantation (ASCT) is a curative therapy for various haematological malignancies. Obtaining suitably matched donors, problems with graft versus host disease (GVHD) and infection, however, limit the wider application of this therapy. Knowledge from previous studies has highlighted the need for a more effective and integrated approach to address these issues. This project examines how our knowledge of immune cell trafficking can be exploited in conjunction with haploidentical stem cell transplantation to minimise GVHD, promote immunity and antileukemic responses in ASCT. The knowledge derived from this study will contribute to a greater understanding of how immune cell trafficking can be utilised to improve ASCT and immunotherapies. Its success will lead to new and more effective protocols for the design and development of stem cell grafts for the treatment of cancer.'

Introduzione (Teaser)

Infection is a major problem following cell grafting; it accounts for some 30% to 40% of treatment-related mortality. This continues to limit the positive effects of treating malignancy with stem cell transplantation.

Descrizione progetto (Article)

Allogeneic stem cell transplantation (ASCT) is the transfer of blood-forming stem cells from a similar yet not necessarily related donor. Used as a treatment method for a variety of malignancies, challenges in finding well-matched donors, graft versus host disease (GVHD) and infection often limit its wider application.

The 'Graft engineering to improve allogeneic stem cell transplantation' (GIFT) project endeavoured to see how current knowledge of immune cell transfers can be exploited to minimise the incidence of GVHD, enhance immunity and stave off leukaemic responses in ASCT. A primary task was to investigate if FTY720, an immunosuppressive agent, can be used in donors in the phase of stem cell mobilisation to create a graft with low GVHD potential. At the same time it should offer good anti-tumour and immune rebuilding potential.

Study results showed that FTY720 can be successfully used in donors to selectively weaken certain cells and thus prevent GVHD following ASCT. This is effected without affecting cancer-fighting memory T cells or immune boosting natural killer cells. This means it is possible to improve the immunological features of peripheral blood stem cell grafts and therefore fight the threat of infections, avoid GVHD and even preserve anti-tumour activity.

It is expected that this study's findings will facilitate the design of new and more effective protocols guiding stem cell grafts for treating cancer.

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