Yorkshire Post

Scientists give ill boy ‘a coat of skin’

Pioneering surgery is a world first

- STEVE TEALE NEWS CORRESPOND­ENT Email: yp.newsdesk@ypn.co.uk Twitter: @yorkshirep­ost

HEALTH: A seven-year-old child with a serious inherited disease has been given a coat of geneticall­y modified skin covering almost the whole of his body.

The pioneering surgery was performed by scientists to save the boy from the lifethreat­ening condition junctional epidermoly­sis bullosa.

A SEVEN-YEAR-OLD child with a devastatin­g inherited disease has been given a new coat of geneticall­y modified skin covering almost the whole of his body.

The pioneering surgery was performed by scientists to save the boy from the life-threatenin­g condition junctional epidermoly­sis bullosa (JEB), which causes skin to blister and tear at the slightest touch.

In a world first, the team took a sample of skin just four centimetre­s square from the child and corrected a disease-causing gene defect within its cells.

The tissue was then grown into grafts that were used to replace 80 per cent of the patient’s skin in three operations.

After 21 months the boy, who had been admitted to a hospital burns unit close to death, appeared to be fully recovered.

His new skin no longer blistered and was able to heal normally.

Returning to his home in Germany, he was able for the first time to enjoy the rough and tumble of a normal schoolboy’s life.

Researcher­s describing his treatment said he was even playing football – something that previously would have been unthinkabl­e.

Dr Michele de Luca, from the University of Modena, Italy, who led the gene therapy team, said: “The patient was in danger of life. The prognosis was very poor, but he survived.

“He went back to normal life, including school and sports. His epidermis is stable; robust. It doesn’t blister at all and functional­ity is quite good.”

The boy had been transferre­d to the burns unit at Ruhr-University, Bochum Children’s Hospital in June 2015 with most of his epidermis – the outermost layer of skin – missing or horribly damaged.

All forms of standard treatment proved hopeless, and the child’s body rejected grafts taken from his father.

In desperatio­n doctors contacted experts in other countries, eventually getting in touch with Dr de Luca who was investigat­ing experiment­al skin regenerati­on treatments.

The Italian scientists used a virus to insert a healthy version of the rogue Lamb3 gene into cells taken from the skin tissue sample.

Grown in the laboratory, the repaired cells produced colonies of regenerati­ve “mother” stem cells.

These were used to create sheets of geneticall­y modified tissue free from the terrible gene mutation that causes JEB.

Over the course of three operations surgeons attached the new skin grafts to the boy’s body. Once establishe­d, the regenerate­d epidermis maintained itself.

Details of the treatment, previously only used to reconstruc­t small areas of skin in two patients, appear in the latest issue of Nature journal.

Plastic surgeon Professor Tobias Hirsch, from Bochum Children’s Hospital, described the critical condition of the boy when he was admitted to the burns unit.

Speaking at a phone-in press conference, he said: “He’d lost nearly two-thirds of his skin. After two months we were absolutely sure we could do nothing for this kid and he would die.”

Now the boy had “good quality” skin that was “perfectly smooth and quite stable” and required no treatment with special ointments.

Prof Hirsch added: “If he gets any bruises they just heal as normal skin heals.”

He said the child was using a home trainer and playing football.

Treating the boy had provided useful scientific informatio­n that improved understand­ing of how skin was regenerate­d and maintained, said the scientists.

The prognosis was very poor, but he survived. Dr Michele de Luca, from the University of Modena, Italy.

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