FFC#24/2017

Extracorporeal photopheresis as induction therapy to prevent acute rejection after lung transplantation in cystic fibrosis patients

AREA 5 Clinical and Epidemiological research

FFC#24/2017

Extracorporeal photopheresis as induction therapy to prevent acute rejection after lung transplantation in cystic fibrosis patients
€ 0 still needed
0%
€ 110.000 goal

pRINCIPAL INVESTIGATOR

Mario Nosotti (Università degli Studi di Milano, IRCCS Fondazione Ca’ Granda Ospedale Maggiore di Milano, U. O. di Chirurgia Toracica e Trapianto di Polmone)

Researchers

11

Category

AREA 5 Clinical and Epidemiological research

Duration

2 years

Goal

€ 110.000

Funds raised

€ 110.000

Objectives

Despite the immunosuppressive therapy, acute rejection occurs frequently in the first year after transplantation and determinates the onset of chronic rejection, which is the major cause of graft loss in the long run. The aim of this project is to evaluate the efficacy and safety of Extracorporeal Photopheresis (ECP) for prevention of acute reject in recipients affected by cystic fibrosis in the first year after lung transplantation. The hypothesis is ECP could induce graft immunotolerance regulating T-cells activity and inflammatory responses. CF patients referring for transplant to Milan Transplant Center will be included: 24 patients are expected and included in two years. After transplantation, they will be randomly allocated to current therapies or to ECP besides current therapies.

WHO ADOPTED THE PROJECT

Delegazione FFC di Como Dongo

€ 65.000

Delegazione FFC di Belluno con Rocciatori Fonzaso

€ 35.000

Delegazione FFC di Pesaro con il Gruppo di Sostegno FFC di Fidenza

€ 10.000

OTHER PROJECTS

Discover the other projects

GMRF#1/2026

Exploring the role of PKD1 in promoting CFTR stability and function at the cell surface

FFC#1/2026

Mapping proteins regulating CFTR mRNA stability to identify new therapeutic targets for nonsense mutations

FFC#2/2026

Evaluating the potential of phosphodiesterase inhibitors to enhance the efficacy of CFTR modulators and support personalized therapeutic approaches