Current and Future Perspectives on Alginate Encapsulated Pancreatic Islet

Berit L. Strand, Abba E. Coron, Gudmund Skjåk‐Bræk

Stem Cells Translational Medicine · 2017 · 119 citations · 57 references

DOIFull text

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Concepts

TL;DR

Transplantation of pancreatic islets in immune‑protective capsules offers a potential cure for type 1 diabetes, with semipermeable designs allowing oxygen and nutrients while blocking immune access, though host reactions to biomaterials may limit long‑term graft function, and recent advances in capsule development and stem‑cell‑derived insulin‑producing cells provide promising prospects. The article aims to review capsule properties—stability, permeability, biocompatibility—and strategies to overcome current challenges. It discusses these properties and strategies by evaluating capsule design and material characteristics. Four small clinical trials have shown encapsulated human islets to be safe, yet they have not demonstrated long‑term efficacy.

Abstract

Abstract Transplantation of pancreatic islets in immune protective capsules holds the promise as a functional cure for type 1 diabetes, also about 40 years after the first proof of principal study. The concept is simple in using semipermeable capsules that allow the ingress of oxygen and nutrients, but limit the access of the immune system. Encapsulated human islets have been evaluated in four small clinical trials where the procedure has been evaluated as safe, but lacking long-term efficacy. Host reactions toward the biomaterials used in the capsules may be one parameter limiting the long-term function of the graft in humans. The present article briefly discusses important capsule properties such as stability, permeability and biocompatibility, as well as possible strategies to overcome current challenges. Also, recent progress in capsule development as well as the production of insulin-producing cells from human stem cells that gives promising perspectives for the transplantation of encapsulated insulin-producing tissue is briefly discussed.

References

57