PHOTO: Mykenzie Johnson/Unsplash
PHOTO: Mykenzie Johnson/Unsplash

Animal trials show promise for new diabetes treatment

Embargoed until: Publicly released:
Peer-reviewed: This work was reviewed and scrutinised by relevant independent experts.

Experimental study: At least one thing in the experiment was changed to see if it had an impact on the subjects (often people or animals) – eg: changing the amount of time mice spend on an exercise wheel to find out what impact it has on weight loss.

Animals: This is a study based on research on whole animals.

Some patients with type 1 diabetes receive a transplant of cells from the pancreas into the liver as a way to control blood sugar, but the treatment can result in complications. US researchers have tested a new way to transplant these cells under the skin on rodents, and found that the animals were able to maintain normal insulin and hormone production. Although more research is needed, the authors conclude that this method could provide a new treatment option for people with type 1 diabetes.

Journal/conference: Nature Metabolism

Link to research (DOI): 10.1038/s42255-020-0269-7

Organisation/s: University of Pennsylvania, USA

Funder: D.A. thanks the Blavatnik Family Foundation for the Graduate Student Fellowship he received during his MD/PhD training. We also thank the National Institutes of Health for award nos. NIH/ NIDDK DK070430, NIH/NIAID AI-102430 and NIH/NIDDK UC4–112217 (HPAP), and the NIDDK IIDP for the grant (Beckman Research Center, no. 10028044) awarded to A.N.

Media release

From: Springer Nature

A new subcutaneous transplantation method for pancreatic islet cells can stabilize blood sugar levels in animal models of type 1 diabetes, reports a study in Nature Metabolism. These findings may have implications for improved treatments for this autoimmune disease.

Some patients with type 1 diabetes receive transplantation of pancreatic islet cells into the liver, but the treatment can result in complications including haemorrhage, thrombosis and graft rejection. Subcutaneous transplantation sites are of interest because they are easy to access and monitor, but the grafts often fail because the cells do not receive enough nutrients and oxygen.

Ali Naji, Divyansh Agarwal and colleagues circumvent this problem by encapsulating the islet cells in a novel collagen-based matrix. The matrix helps the cells survive after subcutaneous transplantation. When the procedure was tested in rodent models and a small number of non-human primates, it enabled the animals to maintain normal insulin and glucagon production.

Transplantable pancreatic islet cells are in short supply because the cells come from donor cadavers; therefore, the authors suggest that their method could be used to improve the viability of other transplant cell types. If, for example, stem-cell-derived beta cells could be treated in this way, they could provide a renewable source of insulin-secreting cells to replace those that are lost in people with type I diabetes.

The authors conclude that, although further research is needed, subcutaneous islet transplantation could provide a new treatment option for patients with type 1 diabetes.

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