Antibodies Reverse Type 1 Diabetes in New Immunotherapy StudyTuesday, July 10, 2012
Scientists at the University of North Carolina School of Medicine have used injections of antibodies to rapidly reverse the onset of type 1 diabetes in mice genetically bred to develop the disease. Moreover, just two injections maintained disease remission indefinitely without harming the immune system.
The findings, published online in the journal Diabetes, suggest for the first time that using a short course of immunotherapy may someday be of value for reversing the onset of Type I diabetes in recently diagnosed people. This form of diabetes, formerly known as insulin-dependent diabetes mellitus, is an autoimmune disease in which the body’s own immune T cells target and destroy insulin-producing beta cells in the pancreas.
The immune system consists of T cells that are required for maintaining immunity against different bacterial and viral pathogens. In people who develop Type 1 diabetes, “autoreactive” T cells that actively destroy beta cells are not kept in check as they are in healthy people.
Senior study author Roland Tisch, PhD, professor of microbiology and immunology at UNC, said a need for effective immunotherapies also exists to treat Type 1 diabetes in people already living with the disease.
“Clinically, there have been some promising results using so-called depleting antibodies in recently diagnosed Type 1 diabetic patients, but the disease process is blocked for only a short period of time,” says Tisch. “These antibodies don’t discriminate between T cells normally required for maintaining immunity to disease-causing pathogens and the autoreactive T cells. Therefore T cells involved in maintaining normal immune function are also going to be depleted. You’re getting some efficacy from immunotherapy but its only transient, it doesn’t reverse the disease, and there are various complications associated with the use of these depleting antibodies.”
Tisch said his UNC lab has been studying the use of certain “non-depleting antibodies.” These bind to particular proteins known as CD4 and CD8 expressed by all T cells. Just as the name implies, when these non-depleting antibodies selectively bind to CD4 and CD8 they don’t destroy the T cells; the overall numbers of T cells are unaffected.
With this in mind Tisch wanted to determine whether these non-depleting antibodies could have a therapeutic effect in the non-obese diabetic, or NOD mouse, an excellent model for human Type 1 diabetes.
The answer is yes. In some of the recently diagnosed NOD mice, blood sugar levels returned to normal within 48 hours of treatment. Within five days, about 80 percent of the animals had undergone diabetes remission, reversal of clinical diabetes.
“The protective effect is very rapid, and once established, is long-term,” he says. “We followed the animals in excess of 400 days after the two antibody treatments, and the majority remained free of diabetes. And although the antibodies are cleared from within the animals in 2-3 weeks after treatment, the protective effect persists.”
The study showed that beta cells in the NOD mice had been rescued from ongoing autoimmune destruction.
In looking for the mechanism to explain how the therapy worked, the researchers found that the antibodies had a very selective effect on T cells that mediated beta cell destruction. After treatment, “all the T cells that we would normally see in the pancreas or in tissues associated with the pancreas had been purged,” says Tisch. This despite the fact that the numbers of T cells found in other tissues and blood were unaffected.
The researchers also found an increase in the numbers of “immune regulatory” T cells. In the healthy individual, these regulatory T cells block autoimmunity, explains Tisch. “They protect us from the autoreactive cells that all of us have. And that’s why most of us don’t develop autoimmune diseases such as Type 1 diabetes. We’ve demonstrated that the use of non-depleting antibodies is very robust. We’re now generating and plan to test antibodies that are specific for the human version of the CD4 and CD8 molecules.”