[PDF][PDF] Insulin expression and C-peptide in type 1 diabetes subjects implanted with stem cell-derived pancreatic endoderm cells in an encapsulation device

AMJ Shapiro, D Thompson, TW Donner, MD Bellin… - Cell Reports …, 2021 - cell.com
AMJ Shapiro, D Thompson, TW Donner, MD Bellin, W Hsueh, J Pettus, J Wilensky…
Cell Reports Medicine, 2021cell.com
These preliminary data from an ongoing first-in-human phase 1/2, open-label study provide
proof-of-concept that pluripotent stem cell-derived pancreatic endoderm cells (PEC-01)
engrafted in type 1 diabetes patients become islet cells releasing insulin in a physiologically
regulated fashion. In this study of 17 subjects aged 22-57 with type 1 diabetes, PEC-01 cells
were implanted subcutaneously in VC-02 macroencapsulation devices, allowing for direct
vascularization of the cells. Engraftment and insulin expression were observed in 63% of VC …
Summary
These preliminary data from an ongoing first-in-human phase 1/2, open-label study provide proof-of-concept that pluripotent stem cell-derived pancreatic endoderm cells (PEC-01) engrafted in type 1 diabetes patients become islet cells releasing insulin in a physiologically regulated fashion. In this study of 17 subjects aged 22-57 with type 1 diabetes, PEC-01 cells were implanted subcutaneously in VC-02 macroencapsulation devices, allowing for direct vascularization of the cells. Engraftment and insulin expression were observed in 63% of VC-02 units explanted from subjects at 3–12 months post-implant. Six of 17 subjects (35.3%) demonstrated positive C-peptide as early as 6 months post-implant. Most reported adverse events were related to surgical implant or explant procedures (27.9%) or to side-effects of immunosuppression (33.7%). Initial data suggest that pluripotent stem cells, which can be propagated to the desired biomass and differentiated into pancreatic islet-like tissue, may offer a scalable, renewable alternative to pancreatic islet transplants.
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