
Harnessing the regenerative capacity of keratinocytes and fibroblasts from human skin has created new opportunities to develop cell-based therapies for patients. Cultured cells and bioengineered skin products are being used to treat patients with inherited and acquired skin disorders associated with defective skin, and further clinical trials of new products are in progress. The capacity of extracutaneous sources of cells such as bone marrow is also being investigated for its plasticity in regenerating skin, and new strategies, such as the derivation of inducible pluripotent stem cells, also hold great promise for future cell therapies in dermatology. This article reviews some of the preclinical and clinical studies and future directions relating to cell therapy in dermatology, particularly for inherited skin diseases associated with fragile skin and poor wound healing.
Keratinocytes, VII COLLAGEN, Cell Transplantation, BONE-MARROW, 610, Dermatology, PLACEBO-CONTROLLED TRIAL, Mesenchymal Stem Cell Transplantation, Skin Diseases, MESENCHYMAL STEM-CELLS, Mice, Animals, Humans, INTRACTABLE SKIN ULCERS, Cells, Cultured, Bone Marrow Transplantation, CULTURED DERMAL SUBSTITUTE, MARROW-DERIVED CELLS, Tissue Engineering, Guided Tissue Regeneration, 600, Skin Transplantation, Fibroblasts, SINGLE-CENTER EXPERIENCE, DYSTROPHIC EPIDERMOLYSIS-BULLOSA, PARTIAL-THICKNESS BURNS
Keratinocytes, VII COLLAGEN, Cell Transplantation, BONE-MARROW, 610, Dermatology, PLACEBO-CONTROLLED TRIAL, Mesenchymal Stem Cell Transplantation, Skin Diseases, MESENCHYMAL STEM-CELLS, Mice, Animals, Humans, INTRACTABLE SKIN ULCERS, Cells, Cultured, Bone Marrow Transplantation, CULTURED DERMAL SUBSTITUTE, MARROW-DERIVED CELLS, Tissue Engineering, Guided Tissue Regeneration, 600, Skin Transplantation, Fibroblasts, SINGLE-CENTER EXPERIENCE, DYSTROPHIC EPIDERMOLYSIS-BULLOSA, PARTIAL-THICKNESS BURNS
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