Skin-Derived ABCB5 + Mesenchymal Stem Cells for High-Medical-Need Inflammatory Diseases: From Discovery to Entering Clinical Routine.
Elke Niebergall-RothNatasha Y FrankChristoph GanssMarkus H FrankMark Andreas KluthPublished in: International journal of molecular sciences (2022)
The ATP-binding cassette superfamily member ABCB5 identifies a subset of skin-resident mesenchymal stem cells (MSCs) that exhibit potent immunomodulatory and wound healing-promoting capacities along with superior homing ability. The ABCB5 + MSCs can be easily accessed from discarded skin samples, expanded, and delivered as a highly homogenous medicinal product with standardized potency. A range of preclinical studies has suggested therapeutic efficacy of ABCB5 + MSCs in a variety of currently uncurable skin and non-skin inflammatory diseases, which has been substantiated thus far by distinct clinical trials in chronic skin wounds or recessive dystrophic epidermolysis bullosa. Therefore, skin-derived ABCB5 + MSCs have the potential to provide a breakthrough at the forefront of MSC-based therapies striving to fulfill current unmet medical needs. The most recent milestones in this regard are the approval of a phase III pivotal trial of ABCB5 + MSCs for treatment of recessive dystrophic and junctional epidermolysis bullosa by the US Food and Drug Administration, and national market access of ABCB5 + MSCs (AMESANAR ® ) for therapy-refractory chronic venous ulcers under the national hospital exemption pathway in Germany.
Keyphrases
- mesenchymal stem cells
- wound healing
- umbilical cord
- soft tissue
- phase iii
- clinical trial
- bone marrow
- healthcare
- quality improvement
- open label
- risk assessment
- stem cells
- intellectual disability
- climate change
- high throughput
- clinical practice
- small molecule
- patient safety
- combination therapy
- transcription factor
- dna methylation
- binding protein
- single cell
- autism spectrum disorder