Ghazizadeh S, Taichman L B
Department of Oral Biology and Pathology, SUNY at Stony Brook, Stony Brook, NY 11794, USA.
Hum Gene Ther. 2000 Nov 1;11(16):2247-51. doi: 10.1089/104303400750035771.
Cutaneous gene therapy offers unique opportunities and limitations in the use of viral vectors for corrective gene transfer. Skin presents a formidable barrier to microbial invasion and is nourished by small blood vessels, thus ruling out the possibility of directed virus delivery through cannulated blood vessels. However, skin is physically accessible and its resident keratinocyte stem cell population is susceptible to direct in vivo transduction with retroviral vectors. Furthermore, keratinocyte stem cells transduced in culture have been shown to persist and to express the encoded transgene when grafted to immunocompromised mice. Cutaneous gene therapy trials are likely to involve virus-mediated transduction as a principal means of gene transfer.
皮肤基因治疗在使用病毒载体进行矫正基因转移方面具有独特的机遇和局限性。皮肤对微生物入侵构成了巨大障碍,且由小血管供血,因此排除了通过插管血管进行定向病毒递送的可能性。然而,皮肤在物理上易于接触,其驻留的角质形成干细胞群体易受逆转录病毒载体的直接体内转导。此外,在培养中经转导的角质形成干细胞移植到免疫受损小鼠后,已显示出能够持续存在并表达编码的转基因。皮肤基因治疗试验可能会将病毒介导的转导作为基因转移的主要手段。