Type 1 diabetes is a form of diabetes mellitus that is caused by the body’s own immune system attacking its pancreatic islet β cells. These cells would normally produce insulin, which regulates glucose metabolism. Therefore, type 1 diabetic patients require life-long daily insulin injections in order to avoid health complications such as atherosclerosis, neuropathy and kidney disease.
Affecting around 10% of all diabetes patients, type 1 diabetes is far less common than type 2 diabetes, but its incidence has doubled in the past 20 years. This, in combination with the current, often inconvenient management of type 1 diabetes, has led researchers to develop alternative treatment strategies.
This resulted in regeneration of islet β cells that were then able to produce insulin again, so that 12 weeks after treatment all the patients who received the therapy had improved β cell function. This continued to improve and was maintained to the end of the study. Interestingly, this also meant that the daily dose of insulin required to maintain patients’ blood glucose levels could be reduced.
These remarkable results may provide a new approach to overcome the autoimmunity underlying type 1 diabetes, and may have important implications for other autoimmune and inflammation-related diseases.
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