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A Phase I/II open-label trial of intravenous allogeneic mesenchymal stromal cell therapy in adults with recessive dystrophic epidermolysis bullosa.

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BACKGROUND Recessive dystrophic epidermolysis bullosa (RDEB) is a hereditary blistering disorder due to lack of type VII collagen (C7). At present, treatment is mainly supportive. OBJECTIVE To determine whether intravenous… Click to show full abstract

BACKGROUND Recessive dystrophic epidermolysis bullosa (RDEB) is a hereditary blistering disorder due to lack of type VII collagen (C7). At present, treatment is mainly supportive. OBJECTIVE To determine whether intravenous allogeneic bone marrow-derived mesenchymal stromal/stem cells (BM-MSC) are safe in RDEB adults and if the cells improve wound healing and quality of life. METHODS We conducted a prospective, phase I/II, open-label study recruiting 10 RDEB adults to receive two intravenous infusions of BM-MSCs (Day 0 and Day 14; each dose 2-4 x 106 cells / kg). RESULTS BM-MSCs were well tolerated with no serious adverse events to 12-months. Regarding efficacy, there was transient reduction in disease activity scores (8 of 10 subjects) and significant reduction in itch. One individual showed a transient increase in C7. LIMITATIONS Open label trial with no placebo. CONCLUSIONS MSC infusion is safe in RDEB adults and can have clinical benefits for at least 2 months.

Keywords: intravenous allogeneic; label; recessive dystrophic; dystrophic epidermolysis; epidermolysis bullosa; open label

Journal Title: Journal of the American Academy of Dermatology
Year Published: 2019

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