Enhancement of Islet β-cell based therapies for T1D

Description:

Cell Therapy for T1D
While insulin replacement therapy has long been the standard of care for individuals with Type 1 Diabetes (T1D), it represents a lifelong treatment burden, replete with associated complications, such as hypoglycemia from repeated insulin injections, neuropathies, as well as kidney failure, and ongoing financial costs. In contrast, cell replacement therapy utilizing cadaveric human islets offers the promise of attaining enduring insulin independence, heralding a significant enhancement in the quality of life while mitigating the grave complications linked to exogenous insulin. Yet, the shortage of a readily available supply of insulin-producing cells has impeded the widespread adoption of this treatment approach.


ENTPD3+ Stem cell-derived β-like cells
Current direct differentiation protocols result in the generation of heterogneous insulin proiducing cell popualtions with different function. Nucleoside triphosphate diphosphohydrolase-3, ENTPD3, is a surface protein that is a marker for mature, highly fucntional stem cell-derived β-like cells (sBC). ENTPD3 can be used to monitor or enriche for mature sBCs generation in vitro, resulting in imrpoved quantity and quality of insulin-producing cells available for transplantation, thereby reducing also the numbers of sBCs needed (Figure A).
Overall Advantage: Monitor and enrich for most mature sBCs
1. Improved Function = increased insulin content & enhanced insulin secretion from mature population.
2. Homogenous population = mitigates unwanted cell proliferation within graft.
ENTPD3 can serve as a valuable tool for both monitoring and enhancing the generation of mature sBCs in vitro. This contributes to an increased quantity and improved quality of insulin-producing cells suitable for transplantation. Consequently, it also leads to a reduction in the number of sBCs required for transplantation. By enhancing the functionality and characteristics of sBCs (1) and refining the cell population by eliminating unwanted cells (2), this approach optimizes cell therapy for Type 1 Diabetes (T1D), making it more efficient and precisely targeted.

 

Download the Summary Here:

https://cuamc.technologypublisher.com/files/sites/cu5178h_-_entpd3_marks_mature_stem_cell_derived_insulin-producing_cells_ncs_hr_v1.pdf

Category:
Therapeutics
For Information, Contact:
Doreen Molk
University of Colorado
doreen.molk@cuanschutz.edu
Inventors:
Holger Russ
Fiona Docherty
Disease Areas:
Regenerative Medicine
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