Breakthrough Researchers Cure Type I Diabetes With No Side Effects
The discovery, made at The University of Texas Health Science Center, increases the types
of pancreatic cells that secrete insulin.
In Type 1 diabetes, people must theoretically take daily insulin shots because their bodies
don't produce any insulin, and is most commonly diagnosed in children and young adults. This
makes up less than 10 per cent of all diabetic cases.
A study published in Diabetologia found a correlation between serum levels of vitamin
D3 and subsequent incidence of Type 1 diabetes.
They found that deficiency in vitamin D may be associated with an increased risk of developing
type 1 diabetes.
The risk of insulin-requiring diabetes was 3.5 times higher in individuals with the lowest
Vitamin D concentrations compared with those with the highest.
The scientists received a U.S. patent in January, and UT Health San Antonio is spinning out
a company to begin commercialization.
The strategy has cured diabetes in mice. "It worked perfectly," Dr. Doiron, assistant
professor of medicine at UT Health, said. "We cured mice for one year without any side
effects. That�s never been seen. But it�s a mouse model, so caution is needed. We want
to bring this to large animals that are closer to humans in physiology of the endocrine system."
Ralph DeFronzo, M.D., professor of medicine and chief of the Division of Diabetes at UT
Health, is co-inventor on the patent. He described the therapy:
"The pancreas has many other cell types besides beta cells, and our approach is to alter these
cells so that they start to secrete insulin, but only in response to glucose [sugar],"
he said. "This is basically just like beta cells."
Insulin, which lowers blood sugar, is only made by beta cells. In Type 1 diabetes, beta
cells are destroyed by the immune system and the person has no insulin.
In Type 2 diabetes, beta cells fail and insulin decreases. At the same time in Type 2, the
body doesn�t use insulin efficiently.
Incorporating genes into the pancreas
The therapy is accomplished by a technique called gene transfer. A virus is used as a
vector, or carrier, to introduce selected genes into the pancreas. These genes become
incorporated and cause digestive enzymes and other cell types to make insulin.
Gene transfer using a viral vector has been approved nearly 50 times by the U.S. Food
& Drug Administration to treat various diseases, Dr. DeFronzo said. It is proven in treating
rare childhood diseases, and Good Manufacturing Processes ensure safety.
Unlike beta cells, which the body rejects in Type 1 diabetes, the other cell populations
of the pancreas co-exist with the body�s immune defenses.
"If a Type 1 diabetic has been living with these cells for 30, 40 or 50 years, and all
we�re getting them to do is secrete insulin, we expect there to be no adverse immune response,"
Dr. DeFronzo said. Second-by-second sugar control
The therapy precisely regulates blood sugar in mice. This could be a major advance over
traditional insulin therapy and some diabetes medications that drop blood sugar too low
if not closely monitored. "A major problem we have in the field of Type
1 diabetes is hypoglycemia (low blood sugar)," Dr. Doiron said. "The gene transfer we propose
is remarkable because the altered cells match the characteristics of beta cells. Insulin
is only released in response to glucose." People don�t have symptoms of diabetes until
they have lost at least 80 percent of their beta cells, Dr. Doiron said.
"We don�t need to replicate all of the insulin-making function of beta cells," he said. "Only 20
percent restoration of this capacity is sufficient
for a cure of Type 1."
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