News Release

Stop the rogue ADAM gene and you stop asthma

Peer-Reviewed Publication

University of Southampton

Scientists at the University of Southampton have discovered a potential and novel way of preventing asthma at the origin of the disease, a finding that could challenge the current understanding of the condition.

The research, published in The Journal of Clinical Investigation (JCI) Insight, analysed the impact of the gene ADAM33, which is associated with the development of asthma.

ADAM33 makes an enzyme, which is attached to cells in the airway muscles. When the enzyme loses its anchor to the cell surface, it is prone to going rogue around the lung causing poorer lung function in people who have asthma.

The studies in human tissue samples and mice, led by Hans Michel Haitchi, Associate Professor in Respiratory Medicine at the University of Southampton, suggests that if you switch off ADAM33 or prevent it from going rouge, the features of asthma -- airway remodelling (more muscle and blood vessels around the airways), twitchiness and inflammation -- will be reduced.

"This finding radically alters our understanding of the field, to say the least," says Professor Haitchi. "For years we have thought that airway remodelling is the result of the inflammation caused by an allergic reaction, but our research tells us otherwise."

The first study showed that rogue human ADAM33 causes airway remodelling resulting in more muscle and blood vessels around the airways of developing lungs but it did not cause inflammation. When a house dust mite allergen was introduced, which is a common human allergen, both, airway remodelling and allergic airway inflammation were more significantly enhanced.

In another study, remodelling of the airway was shown in mice that had ADAM33 switched on from in utero. The gene was then switched off and the airway remodelling was completely reversed.

Furthermore they studied the impact of house dust mite allergen on asthma features in mice that had the ADAM33 gene removed. Airway remodelling and twitchiness as well as airway inflammation rates were significantly reduced by 50 per cent and respectively 35 per cent in mice that did not have the rogue gene.

These findings identify ADAM33 as a novel target for disease modifying therapy in asthma.

Professor Haitchi, whose research was primarily funded by a Medical Research Council Clinician Scientist Fellowship said: "Our studies have challenged the common paradigm that airway remodelling in asthma is a consequence of inflammation. Instead, we have shown that rogue human ADAM33 initiates airway remodelling that promotes allergic inflammation and twitchiness of the airways in the presence of allergen."

"More importantly, we believe that if you block ADAM33 from going rogue or you stop its activity if it does go rogue, asthma could be prevented. ADAM33 initiated airway remodelling reduces the ability of the lungs to function normally, which is not prevented by current anti-inflammatory steroid therapy. Therefore, stopping this ADAM33 induced process would prevent a harmful effect that promotes the development of allergic asthma for many of the 5.4 million people in the UK with the condition."


Notes to Editors

1. A copy of the paper entitled: Soluble ADAM33 initiates airway remodelling to promote susceptibility for allergic asthma in early life is available from Media Relations upon request.

Other sources of funding for the study came from the Asthma Allergy and Inflammation Research (AAIR) Charity and the Faculty of Medicine, University of Southampton.

2. Through world-leading research and enterprise activities, the University of Southampton connects with businesses to create real-world solutions to global issues. Through its educational offering, it works with partners around the world to offer relevant, flexible education, which trains students for jobs not even thought of. This connectivity is what sets Southampton apart from the rest; we make connections and change the world.


For more information:

Becky Attwood
Media Relations
University of Southampton
Tel 023-8059-3212
twitter beckyattwood07

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