Hirsch Tobias, Rothoeft Tobias, Teig Norbert, Bauer Johann W, Pellegrini Graziella, De Rosa Laura, Scaglione Davide, Reichelt Julia, Klausegger Alfred, Kneisz Daniela, Romano Oriana, Secone Seconetti Alessia, Contin Roberta, Enzo Elena, Jurman Irena, Carulli Sonia, Jacobsen Frank, Luecke Thomas, Lehnhardt Marcus, Fischer Meike, Kueckelhaus Maximilian, Quaglino Daniela, Morgante Michele, Bicciato Silvio, Bondanza Sergio, De Luca Michele
Department of Plastic Surgery, Burn Centre, BG University Hospital Bergmannsheil, Ruhr University Bochum, 44789 Bochum, Germany.
Department of Neonatology and Pediatric Intensive Care, University Children's Hospital, Ruhr University Bochum, 44791 Bochum, Germany.
Nature. 2017 Nov 16;551(7680):327-332. doi: 10.1038/nature24487. Epub 2017 Nov 8.
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.
交界性大疱性表皮松解症(JEB)是一种严重且通常致命的遗传性疾病,由编码基底膜成分层粘连蛋白-332的基因突变引起。存活的JEB患者会出现皮肤和黏膜慢性伤口,这会损害他们的生活质量并导致皮肤癌。在此,我们展示了自体转基因角质形成细胞培养物在一名患有严重、危及生命的JEB的7岁儿童身上再生出了完整、功能完全的表皮。前病毒整合模式在体内得以维持,并且表皮更新未引起任何克隆选择。克隆追踪表明,人类表皮并非由等效祖细胞维持,而是由有限数量的长寿命干细胞维持,这些干细胞被检测为全克隆,能够在体外和体内广泛自我更新,并产生补充终末分化角质形成细胞的祖细胞。本研究提供了一个可应用于其他干细胞介导的联合体外细胞和基因治疗的蓝图。