Developing a new treatment for children with a rare disorder who are vulnerable to life-threatening infections
This research was completed on 1 April 2017
Published on 17 February 2015
Children with a rare disorder called chronic granulomatous disorder, or CGD, may one day benefit from a new treatment that’s being developed by Professor Adrian Thrasher and Dr Giorgia Santilli of University College London. Children with this disorder are vulnerable to infections that can be life threatening. Although bone marrow transplants offer a cure, suitable donors can’t always be found. Without a transplant, children need lifelong medication to protect them from infection. Sadly, some lose their lives early. Professor Thrasher and Dr Santilli are developing a new treatment – a gene therapy – which they hope will one day transform children’s lives by offering them a cure.
How are children’s lives affected now?
“Children with CGD are extraordinarily vulnerable to bacterial and fungal infections,” says Professor Thrasher. “Despite treatment with antibiotics they are still susceptible to severe life-threatening infections such as pneumonia, and liver and skin abscesses.”
Children born with CGD, a genetic disorder, are vulnerable to infection because certain cells in their immune system don’t work properly and can’t kill some bacteria and fungi. Estimates suggest up to one in every 200,000 children has the disorder in the UK.1
“So far, the only way to cure CGD is to give children a bone marrow transplant,” says Professor Thrasher. “Unfortunately, though, it is often very difficult to find a donor who’s a good match.”
Children who can’t have a transplant need lifelong treatment with antibiotics and antifungals, but they remain vulnerable to severe infections and inflammation that can cause permanent organ damage. Sadly, some people with CGD lose their lives early, often because of repeated lung infections.
How could this research help?
“We’re developing a new gene therapy for children with CGD,” says Dr Santilli.
Children with CGD have faults in the gene for a protein that helps immune cells fight infection. The new therapy will work by inserting a corrected copy of that gene into children’s immune cells.
“There are different forms of CGD,” says Dr Santilli. “We’ve already begun clinical trials of a new gene therapy for children with the most common form. In this project, we’re in the laboratory stages of developing a similar therapy for children with the second most common form of CGD, which is called p47 deficiency. Around one in four children with CGD have this form.”1
Dr Santilli hopes the new gene therapy will prove life-changing for children with CGD: “We are optimistic that gene therapy for CGD will not only be a treatment, but a cure. This could free children from the need to take lifelong medication and stop them from experiencing repeated infections.”
1. Holland SM. Chronic Granulomatous Disease. Hematol Oncol Clin North Am 2013; 27: 89-99.
|Project Leader||Professor Adrian J Thrasher PhD MBBS FSB FMedSci FRCP FRCPath FRCPCH|
|Location||Molecular Immunology Unit, Institute of Child Health, University College London|
|Grant awarded||21 November 2014|
|Start date||18 May 2015|
|End date||1 April 2017|
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