Encapsulated islets for diabetes therapy: History, current progress, and critical issues requiring solution
Abstract
Insulin therapy became a reality in 1921 dramatically saving lives of people with diabetes, but not protecting them from long-term complications. Clinically successful free islet implants began in 1989 but require life long immunosuppression. Several encapsulated islet approaches have been ongoing for over 30 years without defining a clinically relevant product. Macro-devices encapsulating islet mass in a single device have shown long-term success in large animals but human trials have been limited by critical challenges. Micro-capsules using alginate or similar hydrogels encapsulate individual islets with many hundreds of promising rodent results published, but a low incidence of successful translation to large animal and human results. Reduction of encapsulated islet mass for clinical transplantation is in progress. This review covers the status of both early and current studies including the presentation of corporate efforts involved. It concludes by defining the critical items requiring solution to enable a successful clinical diabetes therapy.
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In humans, host recognition and fibrosis of alginate capsules, regardless of donor tissue, is the main obstacle to using encapsulated donor islets to treat type-1 diabetes.
“Host recognition and fibrosis of alginate capsules in humans, independent of donor tissue, is the key barrier to the clinical translation of encapsulated donor islets for treatment of type-1 diabetes26, 27, 28.”
From Size- and shape-dependent foreign body immune response to materials implanted in rodents and non-human primates (2015) · cites this paper as [27]
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References 360 · Cited by 314
- Authors
- Scharp, D. W., & Marchetti, P.
- Affiliations
- Scharp-Lacy Research Institute (US)
- University of Pisa (IT)
- Corresponding author
- Scharp, David W.
- ORCID
- Marchetti, Piero
- Venue
- Advanced Drug Delivery Reviews
- Publisher
- Elsevier BV
- Published
- 2014-04
- Volume
- 67-68
- Pages
- 35-73
- ISSN
- 0169-409X (ISSN-L)
- OpenAlex
- W2029940162
- Cited by
- 314
- References
- 360
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 18 · 2023: 18 · 2022: 17 · 2021: 38 · 2020: 30 · 2019: 37 · 2018: 27 · 2017: 36 · 2016: 39 · 2015: 23 · 2014: 11 · 2013: 1
- FWCI
- 4.36
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Advanced Drug Delivery Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Juvenile Diabetes Research Foundation International
- Juvenile Diabetes Research Foundation United States of America
- Topics
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Keywords
- encapsulated islets, islet transplantation, diabetes treatment, alginate hydrogel, immunosuppression, clinical translation, insulin therapy
- MeSH terms
- Insulin Secretion, Animals, Diabetes Mellitus, Humans, Insulin, Transplantation, Heterologous, Pancreas Transplantation, Islets of Langerhans Transplantation
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