| Literature DB >> 29144448 |
Tobias Hirsch1, Tobias Rothoeft2, Norbert Teig2, Johann W Bauer3, Graziella Pellegrini4,5, Laura De Rosa5, Davide Scaglione6, Julia Reichelt3, Alfred Klausegger3, Daniela Kneisz3, Oriana Romano7, Alessia Secone Seconetti5, Roberta Contin5, Elena Enzo5, Irena Jurman8, Sonia Carulli9, Frank Jacobsen1, Thomas Luecke10, Marcus Lehnhardt1, Meike Fischer2, Maximilian Kueckelhaus1, Daniela Quaglino7, Michele Morgante8, Silvio Bicciato7, Sergio Bondanza9, Michele De Luca5.
Abstract
Junctional epidermolysis bullosa (JEB) is a severe and often lethal genetic disease caused by mutations in genes encoding the basement membrane component laminin-332. Surviving patients with JEB develop chronic wounds to the skin and mucosa, which impair their quality of life and lead to skin cancer. Here we show that autologous transgenic keratinocyte cultures regenerated an entire, fully functional epidermis on a seven-year-old child suffering from a devastating, life-threatening form of JEB. The proviral integration pattern was maintained in vivo and epidermal renewal did not cause any clonal selection. Clonal tracing showed that the human epidermis is sustained not by equipotent progenitors, but by a limited number of long-lived stem cells, detected as holoclones, that can extensively self-renew in vitro and in vivo and produce progenitors that replenish terminally differentiated keratinocytes. This study provides a blueprint that can be applied to other stem cell-mediated combined ex vivo cell and gene therapies.Entities:
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Year: 2017 PMID: 29144448 PMCID: PMC6283270 DOI: 10.1038/nature24487
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962