Perdoni Christopher, Osborn Mark J, Tolar Jakub
Stem Cell Institute, University of Minnesota, Minneapolis, Minn; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, Minn.
Stem Cell Institute, University of Minnesota, Minneapolis, Minn; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, Minn.
Transl Res. 2016 Feb;168:50-58. doi: 10.1016/j.trsl.2015.05.008. Epub 2015 May 27.
Recessive dystrophic epidermolysis bullosa (RDEB) is a disease caused by mutations in the COL7A1 gene that result in absent or dysfunctional type VII collagen protein production. Clinically, RDEB manifests as early and severe chronic cutaneous blistering, damage to internal epithelium, an increased risk for squamous cell carcinoma, and an overall reduced life expectancy. Recent localized and systemic treatments have shown promise for lessening the disease severity in RDEB, but the concept of ex vivo therapy would allow a patient's own cells to be engineered to express functional type VII collagen. Here, we review gene delivery and editing platforms and their application toward the development of next-generation treatments designed to correct the causative genetic defects of RDEB.
隐性营养不良型大疱性表皮松解症(RDEB)是一种由COL7A1基因突变引起的疾病,该突变导致VII型胶原蛋白的产生缺失或功能失调。临床上,RDEB表现为早期严重的慢性皮肤水疱形成、内部上皮损伤、鳞状细胞癌风险增加以及总体预期寿命缩短。最近的局部和全身治疗已显示出减轻RDEB疾病严重程度的前景,但体外治疗的概念将使患者自身的细胞经过改造后表达功能性VII型胶原蛋白。在此,我们综述了基因递送和编辑平台及其在开发旨在纠正RDEB致病基因缺陷的下一代治疗方法中的应用。