Woodley David T, Keene Douglas R, Atha Tom, Huang Yi, Lipman Kathi, Li Wei, Chen Mei
Department of Medicine, Division of Dermatology, University of Southern California, CRL 204, 1303 Mission Road, Los Angeles, California 90033, USA.
Nat Med. 2004 Jul;10(7):693-5. doi: 10.1038/nm1063. Epub 2004 Jun 13.
Dystrophic epidermolysis bullosa (DEB) is a family of inherited mechano-bullous disorders that are caused by mutations in the type VII collagen gene and for which ex vivo gene therapy has been considered. To develop a simpler approach for treating DEB, we evaluated the feasibility of protein-based therapy by intradermally injecting human recombinant type VII collagen into mouse skin and a DEB human skin equivalent transplanted onto mice. The injected collagen localized to the basement membrane zone of both types of tissues, was organized into human anchoring fibril structures and reversed the features of DEB disease in the DEB skin equivalent.
营养不良性大疱性表皮松解症(DEB)是一类遗传性机械性大疱性疾病,由VII型胶原蛋白基因突变引起,人们已考虑对其进行离体基因治疗。为开发一种更简单的DEB治疗方法,我们通过将人重组VII型胶原蛋白皮内注射到小鼠皮肤以及移植到小鼠身上的DEB人皮肤等效物中,评估了基于蛋白质疗法的可行性。注射的胶原蛋白定位于两种组织的基底膜区,组织形成人锚定原纤维结构,并逆转了DEB皮肤等效物中的DEB疾病特征。