Abstract
Congenital metabolic diseases are a group of hereditary disorders caused by the deficiency of a single specific enzyme activity. Without appropriate therapy, affected patients suffer severe neurologic disability and eventual death. The current mainstays of management attempt to slow disease progression, but are not curative. Several of these diseases have demonstrated significant benefits from liver transplantation; however, this approach is limited by the morbidity associated with this invasive procedure and a shortage of donor organs. Therefore, there is a need to establish a new strategy for improving the quality of a life for these patients. One potential solution is regenerative therapy using hepatocytes generated from stem cells. Herein, we discuss pertinent issues necessary for clinical application of the human amniotic epithelial cell, a type of placental stem cell. Focusing on maple syrup urine disease as an example, where liver replacement is an effective therapy, we explore this approach from a clinician's perspective.
Original language | English |
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Pages (from-to) | 829-835 |
Number of pages | 7 |
Journal | Stem cells translational medicine |
Volume | 10 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jun 2021 |
Keywords
- cell transplantation
- cellular therapy
- liver regeneration
- placenta
- stem cell transplantation