期刊
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
卷 322, 期 2, 页码 E109-E117出版社
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00310.2021
关键词
diabetes; immunosuppression; in fl ammation; islet transplantation
资金
- 4-yr BHF PhD studentship [FS/19/55/34890]
- Medical Research Council [MR/S03692X/1]
Islet transplantation is a treatment for severe hypoglycemia in adults with type 1 diabetes, but it is not a complete cure. Transplanting more islets and using specific drugs can improve outcomes, but concerns remain regarding the toxicity of immunosuppression. New strategies and therapies, such as using stem cells and regulatory T cells, are being researched to reduce the need for immunosuppression.
Islet transplantation is a treatment for selected adults with type 1 diabetes and severe hypoglycemia. Islets from two or more donor pancreases, a scarce resource, are usually required to impact glycemic control, but the treatment falls short of a cure. Islets are avascular when transplanted into the hypoxic liver environment and subjected to inflammatory insults, immune attack, and toxicity from systemic immunosuppression. The Collaborative Islet Transplant Registry, with outcome data on over 1,000 islet transplant recipients, has demonstrated that larger islet numbers transplanted and older age of recipients are associated with better outcomes. Induction with T-cell depleting agents and the TNF-a inhibitor etanercept and maintenance systemic immunosuppression with mTOR inhibitors in combination with calcineurin inhibitors also appear advantageous, but concerns remain over immunosuppressive toxicity. We discuss strategies and therapeutics that address specific challenges of islet transplantation, many of which are at the preclinical stage of development. On the horizon are adjuvant cell therapies with mesenchymal stromal cells and regulatory T cells that have been used in preclinical models and in humans in other contexts; such a strategy may enable reductions in immunosuppression in the early peri-transplant period when the islets are vulnerable to apoptosis. Human embryonic stem cell-derived islets are in early-phase clinical trials and hold the promise of an inexhaustible supply of insulinproducing cells; effective encapsulation of such cells or, silencing of the human leukocyte antigen (HLA) complex would eliminate the need for immunosuppression, enabling this therapy to be used in all those with type 1 diabetes.
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