Elastase inhibitors as a potential treatment for DMD
Duchenne UK is co-funding a study into the use of elastase inhibitors to treat the symptoms of Duchenne Muscular Dystrophy (DMD) in partnership with Joining Jack and Charley's Fund. The research is also being supported by a grant from the Medical Research Council.
Neutrophil elastase is an enzyme created by the body in response to inflammation, but which also contributes to inflammation — causing muscle damage and preventing muscles from regenerating. Neutrophil elastase inhibitors could potentially counteract these effects. It’ll be tested in a mouse model, and if successful could be taken to a clinical trial.
The study will be conducted by a leading scientist in the field, Dr. Dada Pisconti, a lecturer in the Institute of Integrative Biology at the University of Liverpool. Dr. Pisconti is an expert in muscle biology and especially in muscle stem cells, muscle regeneration and muscular dystrophy.
Alex Johnson, co-founder of Duchenne UK said:
“This is a potentially groundbreaking piece of work, which targets a potentially new therapeutic pathway for Duchenne. It’s an important step in our fight to find treatments for DMD”
“We need a cocktail of therapies working in concert to defeat Duchenne,” Tracy Seckler from Charley’s Fund said. “Elastase inhibtors could become an important ingredient of an effective treatment regimen. We are enthusiastic about the potential of this approach.”
Dr. Dada Pisconti said:
“I’m very excited to be taking part in this work. Understanding how our muscles work is vital in finding therapies for DMD.”
Charley's Fund, Duchenne UK, and Joining Jack recently announced a collaborative grant to Dr. Dada Pisconti of the University of Liverpool in England. With this grant and additional funding from the Medical Research Council (MRC), Dr. Pisconti is exploring whether a type of therapeutic known as “neutrophil elastase inhibitors” may help slow or stop the progression of Duchenne muscular dystrophy (DMD). We sat down with her for a quick Q+A on what has her excited about this line of research and what she hopes to achieve with this grant.
Q: So let’s cut right to the chase: What has you excited about this particular research project?
A: I think the most exciting thing about the potential use of neutrophil elastase inhibitors for the treatment of DMD is that these drugs have been already in the clinic for other diseases (usually cystic fibrosis and COPD), and this means a potentially faster timeline to delivering them to boys with Duchenne. We know they are safe and have very few side effects. Therefore, if they show promising results in the preclinical studies that we are about to start in dystrophic mice, the repurposing of these drugs for DMD could be relatively quick compared to drugs that start from scratch and have never been in humans before. Moreover, these drugs are expected to be effective in all patients with DMD, irrespective of the specific underlying mutation.
Q: Tell us more about how neutrophil elastase inhibitors work. What does neutrophil elastase do? How could inhibiting it help change DMD progression?
A: Neutrophil elastase (NE) is a “protease” – a protein that cleaves other proteins. NE in particular is a very potent protease released by neutrophils, a subset of white blood cells, in damaged tissues or at the site of an infection. It targets several proteins that play important roles in the muscle regeneration process, such as cytokines, which are mediators of inflammation, and extracellular matrix proteins, which are the “glue” that keeps cells together. In a normal response to injury, NE is present in the muscle tissue only transiently and helps by triggering a healthy regenerative response. We found, however, that muscles of dystrophic mice show constantly high levels of NE. The elevated NE levels in dystrophic muscle damage the muscle cells, promote chronic inflammation and fibrosis, and prevent muscle stem cells from regenerating the damaged muscle. By inhibiting NE, we hope to mitigate those negative effects.
Q: I know we all wish it were as simple as “Eureka! Great idea. Now let’s get it into the clinic!” What needs to happen now before we can test this approach in people with Duchenne?
A: In real life, scientists almost never have a Eureka moment. Discoveries like this come from relentless, meticulous work, usually carried out by a team of people who learn something new every day. And after the discovery, there’s much more work like that still yet to be done. It’s pretty much like building a house with many small bricks, step by step, day by day.
So far, we have learned that NE is constantly increased in dystrophic muscles. We have also learned that it negatively affects muscle cell integrity and muscle stem cell function when the cells are studied outside the body, in a Petri dish. And, we know that we can block NE with specific drugs called NE inhibitors, which prevent NE-induced damage to muscle cells and muscle stem cells. Now we need to see what happens if we block NE in a fully formed organism that has muscular dystrophy, such as a mouse.
With this project, we’re doing a few things. To begin with, we have three different NE inhibitors that could be advanced toward the clinic. We have to start by running tests that will help us identify which one should have the best shot of working. Once we know this, we begin a series of tests in mice to see what impact it has on several biological and functional measures. We will give that NE inhibitor to mice that have muscular dystrophy for 12 weeks. During these 12 weeks, we will check whether grip strength of the mice treated with the NE inhibitor has improved compared to the grip strength of mice treated with a placebo. We will also record how much mice exercise when we put a guinea pig wheel in their cage. At the end of the 12 weeks, we will measure tissue integrity via MRI, we’ll measure the force produced by single muscles, CK levels and many other parameters. In parallel, we will also treat mice with prednisolone so that we can compare whether the NE inhibitor is better than the current standard of care at ameliorating signs and symptoms of muscular dystrophy.
Q: That makes a lot of sense. So then if the results of these experiments are positive, what happens next?
A: This study aims to provide what we call a “proof-of-concept” – in other words, proof that NE inhibitors have some efficacy in a living organism with muscular dystrophy. If the results of this initial proof-of-concept study are positive, it means we can build on that knowledge to continue laying more bricks, so to speak. What exactly comes next will depend on what we learn from this research program. If the results are positive, we may want to validate the test in another animal model. We may also find there’s reason to test more doses to be sure that we give this treatment approach the best possible chance of success when it’s time to conduct a human clinical trial. Looking out even further, we can start thinking about things like whether the NE inhibitor might have heightened efficacy in combination with other therapies. But first and foremost, we want to see if we get the proof-of-concept we hope for. If we do, next steps will be designed to get a NE into a human clinical trial swiftly, safely, and smartly.
NOTES FOR EDITORS
For more information please visit our website at www.duchenneuk.org, for interview requests please contact Molly at [email protected]
What is Duchenne Muscular Dystrophy?
Duchenne Muscular Dystrophy is the most common fatal genetic disease diagnosed in childhood. Children born with DMD cannot produce the protein dystrophin which is vital for muscle strength and function. Muscle weakness starts in early childhood. Many use a wheelchair by around the age of 12. As deterioration continues it leads to paralysis and early death, often in their 20s. It almost exclusively affects boys. There is no treatment or cure. In the UK there are around 2,500 boys affected and around 300, 000 worldwide. It is classified as a rare disease.
Who are Duchenne UK?
Duchenne UK is a lean, ambitious, and highly focused charity with a clear vision: to fund and accelerate treatments and a cure for Duchenne muscular dystrophy. The charity has been formed by the coming together of Joining Jack and Duchenne Children's Trust, the two biggest funders of research in the UK in the last three years. Its president is HRH The Duchess of Cornwall. Its patrons include the broadcasters Krishnan Guru-Murthy and Mary Nightingale, and the sports stars Owen Farrell, Kris Radlinski and Andy Farrell.
Published on 28 April 2017Share this articleCategories DMD research