Stem cell transplantation cures boy's skin disease!

Stem cell transplantation cures boy's skin disease!


A group of medical doctors were the first ever to successfully treat a child suffering from extensive skin damage using transplants derived from genetically modified stem cells. The boy is a so-called butterfly child: he suffers from epidermolysis bullosa, a genetic skin disease that had destroyed approximately 80 percent of his epidermis. After all established therapies had failed, the medical team decided to try an experimental approach: they transplanted skin derived from genetically modified stem cells onto the wound surfaces. Thanks to the successful therapy, the boy is now - two years after the treatment - able to participate in his family's life and social life. The scientists published their report in Nature.'

Epidermolysis bullosa is the scientific name of a congenital skin disease that is currently considered to be incurable. Its underlying mechanism is a defect in protein-forming genes that are essential for skin regeneration. Even minor stress can result in blisters, wounds, and skin loss with scar formation. Depending on disease severity, internal organs may likewise be affected, leading to critical dysfunctions.

The disease significantly reduces the patients' quality of life; often it is also life-threatening, as in the case of Hassan, the seven years old: by the time he was admitted to the paediatric intensive care unit in June 2015, 60 percent of his epidermis was lost. "He suffered from severe sepsis with high fever, and his body weight had dropped to a mere 17 kilogrammes - a life-threatening condition," Consultant at the University Children's Hospital at Katholisches Klinikum Bochum, points out. All conservative and surgical therapy approaches failed.

Due to the poor prognosis, the team of paediatricians and plastic surgeons, opted for an experimental therapy: the transplantation of genetically modified epidermal stem cells. Obtained from the patient via skin biopsy, these stem cells were introduced intact gene. During this process, so-called retroviral vectors were deployed, i.e. virus particles that had been specifically modified for gene transfer.

The genetically modified stem cells had been cultivated in a clean room laboratory and subsequently turned into transgenic transplants. After obtaining the parents' permission, authorities' approvals and certification of the operating rooms, the transplantation went ahead.

The transplants were applied to the boy's arms and legs, entire back, flanks, and partially to the stomach, neck and face as well. "Overall, 0.94 square meters of transgenic epidermis were transplanted onto the young patient in order to cover all defects, accounting for 80 percent of his entire body surface," says another author.

Following the first transplantation in October 2015, the patient's condition began to improve. The transgenic stem cells formed a new epidermis with intact binding proteins in all transplanted areas. The integration of the intact gene through retroviral gene transfer into the genome of the epidermal stem cells had been successful and was proven to be stable.

In February 2016, the patient was discharged. Today, almost two years after the experimental therapy was initiated, high-quality, stress-resistant skin with intact hydrolipid film, as well as early formation of hair. No scar contractures have appeared in transplanted areas. Hassan is attending school again and is actively taking part in his family's social life.

According to the international medical team, Hassan is the first patient worldwide who has been treated with skin transplants from transgenic epidermal stem cells on a large body surface area. "This approach has enormous potential for research into and development of new therapies for the treatment of epidermolysis bullosa as well as other diseases and trauma causing large skin defects" says the author.

http://news.rub.de/presseinformationen/wissenschaft/2017-11-08-weltweit-einzigartig-junge-erhaelt-dank-gen-therapie-neue-haut

https://www.nature.com/nature/journal/vaop/ncurrent/full/nature24487.html

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