UK scientists license treatment for Sanfilippo syndrome


UK scientists from The University of Manchester believe children suffering from Sanfilippo — a rare terminal disorder that affects children’s brains — could be treated successfully for the first time.

There are currently four types of Sanfilippo syndrome — Type A, B, C and D — which are caused by a lack of enzymes, which helps to break down and recycle long chain sugars and results in a build-up of sugars in the body and particularly the brain.

Sanfilippo Type B affects around one in 200,000 births, whereas the most common of the four types, Sanfilippo Type A, affects around 100 children in the UK. Affected children suffer from hyperactivity, speech loss, profound mental disability and eventually lose the ability to walk, talk or eat.

Prof Brian Bigger, Professor of Cell and Gene Therapy at The University of Manchester, said a stem cell gene therapy technology developed in his laboratory and recently published in the journal Brain will be used by Orchard Therapeutics to treat Sanfilippo syndrome Type B after the company recently acquired an exclusive licence.

Prof Bigger said:

UK-based clinical-stage biotechnology company Orchard Therapeutics is already a trusted collaborative partner and the acquisition of the licence for Sanfilippo Type B complements the existing collaboration program already in place for Sanfilippo Type A.

We are very hopeful that this will be transformative for patients, and that this technology will change the lives of children with Sanfilippo Type A and Type B. As it stands the disease is incurable and people with Sanfilippo syndrome normally live until adolescence or early adulthood after suffering for many years.

Children with Sanfilippo begin showing symptoms of hyperactivity, severe behavioural problems and miss development milestones as toddlers. Later they show symptoms similar to dementia with most never achieving a developmental age beyond two years.

Dr Jesus Garcia-Segovia, Orchard’s VP Clinical Development, CNS and Metabolic Disorders commented:

The incorporation of Sanfilippo syndrome Type B into our development pipeline is a significant milestone in the consolidation of our neurometabolic franchise, which is currently focused on the development of autologous ex-vivo haematopoietic stem-cell gene therapy for children suffering from Sanfilippo syndrome Type A. We are very excited at the possibility of bringing effective treatments capable of addressing the high unmet medical need in children suffering from these devastating conditions.

However, Prof Bigger said the stem cell gene therapy, if successful, could also lead to major breakthroughs in treatment of more common diseases.

If this is successful we could be in line for treating more common diseases such as Parkinson and Alzheimer diseases. If we can show that it is possible to treat single gene brain diseases such as Sanfilippo with stem cell gene therapy, it will pave the way for other treatments.

We are also grateful to The University of Manchester’s technology transfer company, UMI3 Ltd, for their role in negotiating the terms of this major deal with Orchard Therapeutics.

A number of biotechnology companies and their research partners are exploring the use of stem cell gene therapy to treat rare disorders like Sanflippo syndrome. In October Abeona Therapeutics Inc. announced a collaborative agreement between nine Sanfilippo foundations to provide approximately $13.85 million of grants in instalments to Abeona for the advancement of its clinical stage gene therapies for Sanfilippo syndrome Type A and Type B.

The foundations involved include Team Sanfilippo Foundation, Stop Sanfilippo Fundación, Fundación Sanfilippo B, Sanfilippo Children’s Foundation, the National MPS Society, the Red Sanfilippo Foundation, the Children’s Medical Research Foundation, Abby Grace Foundation, and Fondation Sanfilippo Suisse.


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Special World, from Inclusive Technology, is a free website linking 125,000 special education teachers, speech therapists and occupational therapists in 150 countries. Special World readers and contributors work with children who have additional needs or special educational needs including those with severe, profound and multiple learning difficulties and disabilities.

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