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Donor islets are placed inside of the device, which has a special exterior that shields the islets from any attacks from the immune system.
March 11, 2019
By: University of Arizona Health Sciences
Children with Type 1 diabetes have only one option to control their blood sugar: insulin treatment. Ravaged by an autoimmune disease that attacks their own pancreas and islets—microscopic clusters of cells that sense blood sugar and produce insulin—patients are forced to rely on insulin from an external source. But for the 200,000 youth living with Type 1 diabetes in the United States, insulin shots, pens, and pumps fail to perfectly manage blood sugar, which may lead to long-term complications. When the body fails to tightly regulate sugar levels, like in diabetes, much can go wrong. “The absence of this natural ability—minute-to-minute regulation of glucose levels—can result in long-term complications, such as blindness, amputation, and kidney failure,” said Klearchos Papas, Ph.D., a professor in the Departments of Surgery and Medical Imaging at the University of Arizona College of Medicine – Tucson. “Even with automated insulin delivery devices and continuous glucose monitoring—the best way possible to control your blood sugar—you still can end up with these consequences.” Dr. Papas adds, “Interestingly, if you administer insulin aggressively to help lower and keep your blood sugar in the normal range, you actually increase your risk of potentially deadly hypoglycemic, or low blood sugar, episodes.” For the last two decades, Dr. Papas has been working on a solution to this problem. In collaboration with other scientists across the nation, the UA researcher has been developing a tiny, implantable device that senses glucose levels and releases insulin when needed. Now, with a two-year, $1.2 million grant from the JDRF, Dr. Papas will continue to perfect and test his device in preparation for clinical trials in humans. The project, which also includes a contribution from Novo Nordisk, is in collaboration with Tom Loudovaris, Ph.D., of St. Vincent’s Institute, and Greg Korbutt, Ph.D., of the University of Alberta. The device operates using a medical innovation known as islet transplantation. In adults with Type 1 diabetes, islets are taken from donor bodies and dripped into the patient’s liver, similar to an intravenous, or IV drip. Eventually, these islets begin producing insulin for the body, but in order for the patient’s body to accept the transplanted cells, the patient must take lifelong immunosuppressive drugs. Because of this need for immunosuppressive drugs, islet transplantation is not recommended in children. “The need for lifelong immunosuppression is a major concern,” said Dr. Papas, who leads the UA Institute for Cellular Transplantation. “Children would be more susceptible to infections and lifelong treatment could cause other serious health conditions.”
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