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A British toddler has had her hearing restored after becoming the first person in the world to take part in a pioneering gene therapy trial, in a development that doctors say marks a new era in treating deafness.
Opal Sandy was born unable to hear anything due to auditory neuropathy, a condition that disrupts nerve impulses travelling from the inner ear to the brain and can be caused by a faulty gene.
But after receiving an infusion containing a working copy of the gene during groundbreaking surgery that took just 16 minutes, the 18-month-old can hear almost perfectly and enjoys playing with toy drums.
Her parents were left âgobsmackedâ when they realised she could hear for the first time after the treatment. âI couldnât really believe it,â Opalâs mother, Jo Sandy, said. âIt was ⊠bonkers.â
The girl, from Oxfordshire, was treated at Addenbrookeâs hospital, part of Cambridge university hospitals NHS foundation trust, which is running the Chord trial. More deaf children from the UK, Spain and the US are being recruited to the trial and will all be followed up for five years.
Prof Manohar Bance, an ear surgeon at the trust and chief investigator for the trial, said the initial results were âbetter than I hoped or expectedâ and could cure patients with this type of deafness.
âWe have results from [Opal] which are very spectacular â so close to normal hearing restoration. So we do hope it could be a potential cure.â
He added: âThereâs been so much work, decades of work ⊠to finally see something that actually worked in humans âŠ. It was quite spectacular and a bit awe-inspiring really. It felt very special.â
Auditory neuropathy can be caused by a fault in the OTOF gene, which makes a protein called otoferlin. This enables cells in the ear to communicate with the hearing nerve. To overcome the fault, the new therapy from biotech firm Regeneron sends a working copy of the gene to the ear.
A second child has also recently received the gene therapy treatment at Cambridge university hospitals, with positive results.
The overall Chord trial consists of three parts, with three deaf children including Opal receiving a low dose of gene therapy in one ear only.
A different set of three children will get a high dose on one side. Then, if that is shown to be safe, more children will receive a dose in both ears at the same time. In total, 18 children worldwide will be recruited to the trial.
Opal is the first patient globally to receive the therapy and is âthe youngest globally thatâs been done to date as far as we knowâ, Bance said.
The gene therapy â DB-OTO â is specifically for children with OTOF mutations. A harmless virus is used to carry the working gene into the patient.
The trial is âjust the beginning of gene therapiesâ, Bance said. âIt marks a new era in the treatment for deafness.â
Martin McLean, a senior policy adviser at the National Deaf Childrenâs Society, said deafness should never be a barrier to happiness or fulfilment. âMany families will welcome these developments, and we look forward to learning about the long-term outcomes for the children treated.â
With Opalâs hearing restored, her parents now have a fresh problem to contend with: their daughterâs new favourite hobby is slamming cutlery on the table to make as much noise as possible.
Source: theguardian.com