Strategies for durable β cell replacement in type 1 diabetes

Author:

Brusko Todd M.12ORCID,Russ Holger A.3ORCID,Stabler Cherie L.4ORCID

Affiliation:

1. Department of Pathology, Immunology and Laboratory Medicine, and Department of Pediatrics, College of Medicine, University of Florida, Gainesville, FL 32610, USA.

2. University of Florida Diabetes Institute, University of Florida, Gainesville, FL 32610, USA.

3. Barbara Davis Center for Diabetes, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA.

4. Department of Biomedical Engineering, College of Engineering, University of Florida, Gainesville, FL 32610, USA.

Abstract

Technological advancements in blood glucose monitoring and therapeutic insulin administration have improved the quality of life for people with type 1 diabetes. However, these efforts fall short of replicating the exquisite metabolic control provided by native islets. We examine the integrated advancements in islet cell replacement and immunomodulatory therapies that are coalescing to enable the restoration of endogenous glucose regulation. We highlight advances in stem cell biology and graft site design, which offer innovative sources of cellular material and improved engraftment. We also cover cutting-edge approaches for preventing allograft rejection and recurrent autoimmunity. These insights reflect a growing understanding of type 1 diabetes etiology, β cell biology, and biomaterial design, together highlighting therapeutic opportunities to durably replace the β cells destroyed in type 1 diabetes.

Funder

National Institute of Allergy and Infectious Diseases

National Institute of Diabetes and Digestive and Kidney Diseases

Leona M. and Harry B. Helmsley Charitable Trust

JDRF

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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