Abstract
© AlphaMed Press.Mesenchymal stem cells and multipotent adult progenitor cells (MAPCs) have been proposed as novel therapeutics for solid organ transplant recipients with the aim of reducing exposure to pharmacological immunosuppression and its side effects. In the present study,wedescribe the clinical course of the first patient of the phase I, dose-escalation safety and feasibility study, MiSOT-I (Mesenchymal Stem Cells in Solid Organ Transplantation Phase I). After receiving a living-related liver graft, the patient was given one intraportal injection and one intravenous infusion of third-party MAPC in a low-dose pharmacological immunosuppressive background. Cell administration was found to be technically feasible; importantly,wefound no evidence of acute toxicity associated withMAPCinfusions.
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CITATION STYLE
Soeder, Y., Loss, M., Johnson, C. L., Hutchinson, J. A., Haarer, J., Ahrens, N., … Dahlke, M. H. (2015). First-in-Human Case Study: Multipotent Adult Progenitor Cells for Immunomodulation After Liver Transplantation. Stem Cells Translational Medicine, 4(8), 899–904. https://doi.org/10.5966/sctm.2015-0002
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