Exp Dermatol. 2012 May;21(5):395-8. doi: 10.1111/j.1600-0625.2012.01474.x.
Antibodies, specific to murine DEC205, can be used to target antigens to dendritic cells. The immunodominant domain of human type XVII collagen, hNC16A, was fused to this antibody (DEC-hNC16A) and was administered as expression plasmid by gene gun transfection with the aim of inducing tolerance to human type XVII collagen in a skin transplantation model. Mice transfected with DEC-hNC16A were challenged with skin grafts from transgenic mice engineered to express human type XVII collagen. Graft survival was either prolonged or grafts were accepted infinitely (33% and 16%, respectively) upon treatment with DEC-hNC16A while 100% of grafts were rejected in untreated controls. Graft acceptance was associated with the absence of a CD4+ infiltrate and a dense CD8+ T-cell infiltrate and was not strictly dependent on antibody production. Our results show that DEC-hNC16A targets dendritic cells in vivo leading to prolonged survival of transgenic skin grafts. This indicates that DEC205-targeting may be used for the induction of tolerance to skin antigens, which would increase the chances of successful skin gene therapy of epidermolysis bullosa patients.
针对 DEC205 的抗体可用于将抗原靶向树突状细胞。人 XVII 型胶原的免疫优势域 hNC16A 与该抗体(DEC-hNC16A)融合,并通过基因枪转染表达质粒进行给药,目的是在皮肤移植模型中诱导对人 XVII 型胶原的耐受。用 DEC-hNC16A 转染的小鼠接受来自表达人 XVII 型胶原的转基因小鼠的皮肤移植物的挑战。用 DEC-hNC16A 处理后,移植物的存活时间延长或无限期接受(分别为 33%和 16%),而未经处理的对照组中 100%的移植物被排斥。移植物接受与不存在 CD4+浸润和密集的 CD8+T 细胞浸润有关,而并不严格依赖于抗体产生。我们的结果表明,DEC-hNC16A 在体内靶向树突状细胞,导致转基因皮肤移植物的存活时间延长。这表明 DEC205 靶向可能用于诱导对皮肤抗原的耐受,从而增加成功治疗大疱性表皮松解症患者皮肤基因治疗的机会。