Injection of genetically engineered fibroblasts corrects regenerated human epidermolysis bullosa skin tissue.
basic_science · Level V
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- Record sourced from PubMed, PMID 12531881.
- Also identified by PMC identifier 151880.
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Abstract
Current therapeutic strategies for genetic skin disorders rely on the complex process of grafting genetically engineered tissue to recipient wound beds. Because fibroblasts synthesize and secrete extracellular matrix, we explored their utility in recessive dystrophic epidermolysis bullosa (RDEB), a blistering disease due to defective extracellular type VII collagen. Intradermal injection of RDEB fibroblasts overexpressing type VII collagen into intact RDEB skin stably restored correctly localized type VII collagen expression in vivo and normalized hallmark RDEB disease features, including subepidermal blistering and anchoring fibril defects. This article was published online in advance of the print edition. The date of publication is available from the JCI website, http://www.jci.org.
Medical subject headings
- Collagen Type VII
- Epidermolysis Bullosa Dystrophica
- Fibroblasts
- Genetic Engineering
- Genetic Therapy