Genetically Altered Skin Saves A Boy Dying Of A Rare Disease : Shots - Health News An inherited disease called epidermolysis bullosa destroyed the 7-year-old's skin. Scientists grew new skin in the lab without the genetic flaw, and replaced 80 percent of his skin. He is thriving.
NPR logo

Genetically Altered Skin Saves A Boy Dying Of A Rare Disease

  • Download
  • <iframe src="https://www.npr.org/player/embed/562647401/562903280" width="100%" height="290" frameborder="0" scrolling="no" title="NPR embedded audio player">
  • Transcript
Genetically Altered Skin Saves A Boy Dying Of A Rare Disease

Genetically Altered Skin Saves A Boy Dying Of A Rare Disease

  • Download
  • <iframe src="https://www.npr.org/player/embed/562647401/562903280" width="100%" height="290" frameborder="0" scrolling="no" title="NPR embedded audio player">
  • Transcript

ROBERT SIEGEL, HOST:

We're going to hear now how doctors in Europe used genetically engineered skin cells to treat a child who was on the verge of death from a rare inherited disease. The treatment represents a notable success for the field of gene therapy, which has suffered many setbacks. And it's potentially good news for children with this painful and often deadly skin condition. NPR's Richard Harris has the story.

RICHARD HARRIS, BYLINE: The boy was born with a genetic flaw that left him with a condition called junctional epidermolysis bullosa. The outer layer of his skin didn't bind well to the inner layer, and as a result, excruciating blisters appeared all over his body. In 2015, the 7-year-old boy ended up in a hospital after 60 percent of the outer layer of his skin, his epidermis, had sloughed off. Tobias Rothoeft, a surgeon at a burn unit in Bochum, Germany, says doctors tried everything, including a skin transplant from the boy's father. But nothing helped.

TOBIAS ROTHOEFT: After nearly two months, we were absolutely sure that we could do nothing for this kid and that he would die.

HARRIS: Rothoeft and his colleagues took one last look around the medical literature and learned of an Italian team that was experimenting with a new treatment for this disease. Michele De Luca at the University of Modena was genetically engineering skin cells to repair the inborn flaw.

ROTHOEFT: And he promised us he could give us enough skin to heal this kid.

HARRIS: In a phone press conference hosted by the journal Nature, De Luca explained that he used a virus to insert a healthy gene into cells taken from the boy's skin. Some of those cells - stem cells - multiply indefinitely. So De Luca was able to grow entire sheets of engineered epidermis.

(SOUNDBITE OF PRESS CONFERENCE)

MICHELE DE LUCA: They are then packaged and transferred to the hospital where they are applied.

HARRIS: De Luca used this procedure successfully 12 years ago to replace a relatively small patch of skin. But this boy needed to have 80 percent of his skin replaced with grafts of this genetically modified material. It took two operations both in the fall of 2015, starting with his arms and legs.

(SOUNDBITE OF PRESS CONFERENCE)

DE LUCA: In the first one, we grafted all four limbs. In the second operation, we grafted the remaining part of the body, mainly the back.

HARRIS: After eight months in the intensive care unit, the boy was well enough to go home. And two years later, the grafts are still going strong. Tobias Rothoeft says the boy is in school, even playing soccer.

ROTHOEFT: The kid is doing quite well. The skin is of good quality. It doesn't need any ointments or stuff like that. It's perfectly smooth, and it's quite stable. If he gets any bruises like small kids have, they just heal like bruises in every other kid do.

HARRIS: One lingering question is the concern that gene therapies like this involving viruses can increase the risk of cancer.

(SOUNDBITE OF PRESS CONFERENCE)

DE LUCA: Certainly it is a potential problem.

HARRIS: But Dr. de Luca says the risk is small compared with the life-saving benefit of this treatment. News of this is just starting to trickle out to advocates who have children with epidermolysis bullosa.

BRETT KOPELAN: I think it's groundbreaking. You know, I think it's incredibly exciting.

HARRIS: Brett Kopelan heads a U.S. organization focused on this disease known by its acronym DEBRA. His 10-year-old daughter, Rafi, has a severe case of the disease requiring frequent throat surgeries and the use of a wheelchair. The skin therapy described in the Nature paper wouldn't cure her, but it could reduce the agony of daily living. And Kopelan says medical interest in this disease is now growing rapidly.

KOPELAN: We've gone from zero biotechnology and pharmaceutical to 12 companies. So we're really at an inflection point right now.

HARRIS: Experimental treatments are getting underway in the United States and Asia as well as in Europe. Richard Harris, NPR News.

Copyright © 2017 NPR. All rights reserved. Visit our website terms of use and permissions pages at www.npr.org for further information.

NPR transcripts are created on a rush deadline by Verb8tm, Inc., an NPR contractor, and produced using a proprietary transcription process developed with NPR. This text may not be in its final form and may be updated or revised in the future. Accuracy and availability may vary. The authoritative record of NPR’s programming is the audio record.