Daily Nation Newspaper

Gene therapy first to 'halt' most common cause of blindness

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A WOMAN from Oxford has become the first person in the world to have gene therapy to try to halt the most common form of blindness in the Western world.

Surgeons injected a synthetic gene into the back of Janet Osborne’s eye in a bid to prevent more cells from dying.

It is the first treatment to target the underlying genetic cause of age-related macular degenerati­on (AMD).

About 600,000 people in the UK are affected by AMD, most of whom are severely sight impaired.

Janet Osborne told BBC News: “I find it difficult to recognise faces with my left eye because my central vision is blurred - and if this treatment could stop that getting worse, it would be amazing.”

The treatment was carried out under local anaestheti­c last month at Oxford Eye Hospital by Robert MacLaren, professor of ophthalmol­ogy at the University of Oxford.

He told BBC News: “A genetic treatment administer­ed early on to preserve vision in patients who would otherwise lose their sight would be a tremendous breakthrou­gh in ophthalmol­ogy and certainly something I hope to see in the near future.”

Mrs Osborne, 80, is the first of 10 patients with AMD taking part in a trial of the gene therapy treatment, manufactur­ed by Gyroscope Therapeuti­cs, funded by Syncona, the Wellcome Trust founded investment firm. he macula is part of the retina and responsibl­e for central vision and fine detail.

In age-related macular degenerati­on, the retinal cells die and are not renewed.

The risk of getting AMD increases with age.

Most of those affected, including all those on this trial, have what is known as dry AMD, where the decline in sight is gradual and can take many years.

Wet AMD can develop suddenly and lead to rapid vision loss but can be treated if caught quickly. As some people age, genes responsibl­e for the eye’s natural defences start to malfunctio­n and begin destroying cells in the macula, leading to vision loss.

An injection is made at the back of the eye, which delivers a harmless virus containing a synthetic gene.

The virus infects the retinal cells and releases the gene. This enables the eye to make a protein designed to stop cells from dying and so keep the macula healthy.

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