Donate
WHAT WE FUND

Cystic Fibrosis

Respiratory diseases

At a glance

Role of glucose in Cystic Fibrosis lung: friend or foe in respiratory infections?

Lead researcher

Dr James Garnett

Institution

University of Newcastle

Status

Completed

Amount awarded

£231,930.00

Last updated

08/01/24

Share

A fellowship to understand how glucose levels are controlled in the airways to provide the correct balance in cystic fibrosis (CF) patients – enough to allow the white blood cells to fight infection, but not so much that it creates a favourable environment for bacteria. This is crucial in determining the role glucose plays during lung infections in people with CF. Modulating glucose levels may be a new therapeutic approach.

Glucose is a critical energy source for bacteria and is associated with an increased risk of infection in CF patients

It is known that people with Cystic Fibrosis (CF) have higher levels of glucose in their lungs than those unaffected and CF-related diabetes develops in 50% of adults with CF. Glucose is a vital energy source for humans and bacteria alike. Glucose is important for the bacteria that cause lung infections and for the white blood cells (phagocytes) that try to kill them. Glucose is a critical energy source for bacteria and is associated with an increased risk of infection in CF patients. In contrast, glucose is also an important energy source for white blood cells which protect the body from infection.

Dr James Garnett from Newcastle University was awarded a fellowship to understand how glucose levels are controlled in the airways to provide the correct balance – enough to allow white blood cells to fight infection, but not so much that it creates a favourable environment for bacterial survival and growth. This research is crucial in determining the role glucose plays during lung infections in people with CF and modulating glucose levels may prove to be a novel therapeutic approach to CF.

Get in touch

To find out more about the research we fund and the difference it makes.

Contact us

Respiratory Diseases - Cystic Fibrosis

  • Why there is a need to fund new research

    Cystic Fibrosis (CF) is a rare lung disease with a poor prognosis. Its incidence varies across the globe and in the European Union 1 in 2,000-3,000 new-borns are affected. CF is a genetic disorder caused by mutations in a gene that leads to the build-up of abnormally thick mucus in the bodies’ passageways, in particular in the lining of the lungs. The mucus provides a favourable environment for bacteria to grow and increases the susceptibility of CF patients to fatal lung infections.

Support us

Help change lives

We fund and support the most promising health research wherever we discover great opportunities that are not being pursued. We use our donations responsibly and ensure we make the greatest impact where it is most needed.

Support the power of science
Couple Laughing Outdoors