Recessive Dystrophic Epidermolysis Bullosa Clinical Trial
Official title:
Study of Immune Tolerance and Capacity for Wound Healing of Patients With Recessive Dystrophic Epidermolysis Bullosa (RDEB)
Recessive Dystrophic Epidermolysis Bullosa (RDEB) is one of the most severe rare inherited
skin disorders affecting children and adults. Current medical care protocols for RDEB
patients are limited to palliative procedures to treat blistering and erosive lesions,
wounds, and severe local and systemic complications such as fusion and contracture of the
digits, skin cancer, esophageal stricture, severe anemia, infections, malnutrition and
growth retardation. However, current medical treatments still cannot prevent the recurrence
of the lesions arising from defective expression of type VII collagen (COL7A1), the main
constituent of anchoring fibrils which form essential structures for dermal-epidermal
adherence.
The purpose of this study is to investigate the capacity of keratinocytes and fibroblasts to
repair skin wounds in patients suffering from Recessive Dystrophic Epidermolysis Bullosa
(RDEB).
In the perspective of future therapeutic interventions, which could involve protein, cellular and/or gene therapy, it is essential to investigate RDEB patients with regards to their immune tolerance to type VII collagen and their capacity of their cells for tissue reconstruction. ;
Observational Model: Cohort
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