Publication | Open Access
Tissue Engineering Strategies for Improving Beta Cell Transplantation Outcome
22
Citations
139
References
2021
Year
Tissue EngineeringCell TherapyEngineeringTissue TransplantationBiomedical EngineeringPancreas TransplantationIslet Donor PancreasRegenerative MedicineType 1Translational Tissue EngineeringInsulin DeliveryCell TransplantationCell-based Drug DeliveryRegenerative EngineeringPancreatic Islet BiologyFunctional Tissue EngineeringCell EngineeringCell BiologyTissue Engineering StrategiesIslet TransplantationStem Cell EngineeringMedicine
Abstract Purpose of Review Beta cell replacement therapy as a form of islet transplantation is a promising alternative therapy with the possibility to make selected patients with type 1 diabetes (T1D) insulin independent. However, this technique faces challenges such as extensive activation of the host immune system post-transplantation, lifelong need for immunosuppression, and the scarcity of islet donor pancreas. Advancement in tissue engineering strategies can improve these challenges and allow for a more widespread application of this therapy. This review will discuss the recent development and clinical translation of tissue engineering strategies in beta cell replacement therapy. Recent Findings Tissue engineering offers innovative solutions for producing unlimited glucose responsive cells and fabrication of appropriate devices/scaffolds for transplantation applications. Generation of pancreatic organoids with supporting cells in biocompatible biomaterials is a powerful technique to improve the function of insulin-producing cell clusters. Fabrication of physical barriers such as encapsulation strategies can protect the cells from the host immune system and allow for graft retrieval, although this strategy still faces major challenges to fully restore physiological glucose regulation. Summary The three main components of tissue engineering strategies including the generation of stem cell-derived insulin-producing cells and organoids and the possibilities for therapeutic delivery of cell-seeded devices to extra-hepatic sites need to come together in order to provide safe and functional insulin-producing devices for clinical beta cell replacement therapy.
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