Discovery could open door to new COPD treatment

Publicly released:
Australia; NSW

Research led by the Centenary Institute, the University of Technology Sydney and Ghent University Hospital, Belgium has identified a new therapeutic approach for chronic obstructive pulmonary disease (COPD) – the targeting and inhibition of a protein called RIPK1.

Media release

From: Centenary Institute

Research led by the Centenary Institute, the University of Technology Sydney and Ghent University Hospital, Belgium has identified a new therapeutic approach for chronic obstructive pulmonary disease (COPD) – the targeting and inhibition of a protein called RIPK1.

The third leading cause of death worldwide and with no effective treatments, COPD is a chronic lung disease also known as emphysema. It is characterised by a mix of airway inflammation and blockage, and lung damage which makes it difficult to breathe.

Reported in the prestigious European Respiratory Journal, the researchers found increased levels of the protein RIPK1 in the lungs of people suffering from COPD as well as in experimental COPD mouse models. Inhibiting RIPK1 helped protect against COPD and may represent a new approach for treatment.

Co-senior study author Professor Phil Hansbro, Director of the Centenary UTS Centre for Inflammation said that the primary risk factor for COPD is smoking tobacco but that the disease can also be caused by breathing in dust, fumes, chemicals and air pollution.

“Cigarette smoke or exposure to other irritants triggers inflammation and can induce cell death in the lungs and airways, which directly contributes to the development of COPD,” Professor Hansbro said.

“We investigated RIPK1 as it plays a key role in cell survival and death as well as inflammation. We found that there were far higher levels of RIPK1 in patients suffering from COPD as well as in our COPD mouse models.”

Subsequent study by the researchers, with COPD mouse models, found that inhibiting RIPK1 provided a significant protective effect against COPD.

“We saw reduced structural changes to the airways and decreased damage to the air sacs of the lungs. Our data indicates that inhibiting RIPK1 lessened both inflammation and the death of healthy lung and airway cells meaning less tissue damage overall,” said Professor Hansbro.

The research team say that their findings provide an exciting new avenue of study for treating COPD, an incurable and often fatal lung disease.

[ENDS]

Publication:

RIPK1 kinase-dependent inflammation and cell death contribute to the pathogenesis of COPD. https://erj.ersjournals.com/content/early/2022/12/01/13993003.01506-2022

Images:

Professor Phil Hansbro:

https://drive.google.com/file/d/1NhZCKLlllOPvdple9SWwmfDi6NOKRRIu/view?usp=sharing

About the Centenary Institute

The Centenary Institute is a world-leading independent medical research institute, closely affiliated to the University of Sydney and the Royal Prince Alfred Hospital. Our research focuses on three key areas: cancer, inflammation and cardiovascular disease. Our strength lies in uncovering disease mechanisms and applying this knowledge to improve diagnostics and treatments for patients.

For more information about the Centenary Institute, visit centenary.org.au

Journal/
conference:
European Respiratory Journal
Organisation/s: Centenary Institute, University of Technology Sydney (UTS)
Funder: The research described in this article was supported by the Concerted Research Action of the Ghent University (BOF/GOA 01G00819) and by the Fund for Scientific Research in Flanders (FWO Vlaanderen, G052518N and FWO041819N and EOS‐contract G0H1222N). KR Bracke holds an AstraZeneca Chair on Translational Research into the Pathogenesis of COPD. Research in the Vandenabeele group is supported by EOS MODEL-IDI (30826052), EOS-CD-INFLADIS (40007512), FWO research grants (G.0E04.16N, G.0C76.18N, G.0B71.18N, G.0B96.20N, G.0A93.22N), Methusalem (BOF16/MET_V/007), iBOF20/IBF/039 ATLANTIS, Foundation against Cancer (FAF-F/2016/865, F/2020/1505), CRIG and GIGG consortia, and VIB. P.M.H., N.G.H., S.I. and A.F. are funded by a Fellowship and grants from the National Health and Medical Research Council (NHMRC) of Australia (1175134, 2008937, 2010287, 2011467) and by UTS. Research in the Bertrand group is supported by EOS‐contract G0G6618N and G0I5722N.
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