The combination of gene therapy and tissue engineering is one of the most promising strategies for the treatment of recessive dystrophic epidermolysis bullosa (RDEB). RDEB is a rare genetic disease characterised by mutations in the COL7A1 gene， encoding type VII collagen (COLVII)， which forms anchoring fibrils at the dermal-epidermal junction of the skin. This disease causes severe blistering and only palliative treatments are offered. In this study， the base of a strategy combining gene therapy and a tissue-engineered skin substitute (TES)， which would be suitable for the permanent closure of skin wounds， was set-up. As a high transduction efficiency into fibroblasts and/or keratinocytes seems to be ... More
The combination of gene therapy and tissue engineering is one of the most promising strategies for the treatment of recessive dystrophic epidermolysis bullosa (RDEB). RDEB is a rare genetic disease characterised by mutations in the COL7A1 gene， encoding type VII collagen (COLVII)， which forms anchoring fibrils at the dermal-epidermal junction of the skin. This disease causes severe blistering and only palliative treatments are offered. In this study， the base of a strategy combining gene therapy and a tissue-engineered skin substitute (TES)， which would be suitable for the permanent closure of skin wounds， was set-up. As a high transduction efficiency into fibroblasts and/or keratinocytes seems to be a prerequisite for a robust and sustained correction of RDEB， different envelope pseudotyped retroviral vectors and the transduction enhancer EF-C were tested. When green fluorescent protein (GFP) was used as a reporter gene to evaluate the retroviral-mediated gene transfer， the fibroblast infection efficiency was 30 % higher with the Ampho pseudotyped vector as compared with the other pseudotypes. At least a 3.1-fold and a 1.3-fold increased transduction were obtained in fibroblasts and keratinocytes， respectively， with EF-C as compared with polybrene. A continuous and intense deposit of haemagglutinin (HA)-COLVII was observed at the dermal-epidermal junction of self-assembled TESs made of cells transduced with a HA-tagged COL7A1 vector. Furthermore， HA-tagged basal epidermal cells expressing keratin 19 were observed in TESs， suggesting stem cell transduction. This approach could be a valuable therapeutic option to further develop， in order to improve the long-term life quality of RDEB patients.
