FFC#12/2025

Studying the Immune System’s Response to Nontuberculous Mycobacterial Infections

AREA 4 Lung inflammation

FFC#12/2025

Analysis of immune cells and lung tissue to develop personalised treatments for people with cystic fibrosis
€ 136.500 still needed
0%
€ 136.500 goal

pRINCIPAL INVESTIGATOR

Nicola Ivan Lorè (Emerging bacterial pathogens, Division of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Hospital, Milan, Italy)

Researchers

9

Category

AREA 4 Lung inflammation

Duration

2 years

Goal

€ 136.500

Funds raised

Objectives

Non-tuberculous mycobacteria (NTMs) are among the most frequent bacterial species in the European population with cystic fibrosis (CF) and can cause chronic lung disease, which currently lacks viable treatment options.

This project, a continuation of previous projects FFC#23/2020 and FFC#7/2022, aims to understand the differences between the immune system’s response to NTMs in people with and without CF. The researchers hypothesise that people with CF have a unique immune response that may influence disease progression.
Furthermore, the researchers will study how CF lung cells react when infected with NTM compared to non-CF lung cells.
Early findings suggest that people with CF have an overactive immune response to NTM infections, which might contribute to lung inflammation and damage.
Researchers will use RNA sequencing techniques to analyse the transcriptome of immune cells from people with and without CF. They will then analyse lung tissue from donors with and without CF who have NMT infections, obtained through FFC Ricerca’s Primary Culture Service, to identify the key differences.

The findings could help to identify markers of infection severity and guide personalised treatments, advancing our knowledge on CF-related lung infections and paving the way for more effective therapies.

OTHER PROJECTS

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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