Yale Researchers Find New Trigger For Autoimmune Diseases

Main Category: Multiple Sclerosis
Also Included In: Immune System / Vaccines;  Lupus
Article Date: 29 Jul 2008 - 2:00 PDT

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Yale University researchers have discovered a new way that autoimmune diseases like multiple sclerosis (MS) can be triggered, they reported Monday in the journal Proceedings of the National Academy of Sciences.

Scientists have long known the molecule TGF-Beta (transforming growth factor Beta) plays a pivotal role in preventing T cells from launching an attack on the body's own tissues.

A team led by Richard Flavell, professor and chairman of Immunobiology at the Yale School of Medicine, investigated whether TGF-Beta might also influence activity of other immune system cells as well.

Flavell, an investigator for the Howard Hughes Medical Institute, and his colleagues engineered mice in which TGF-Beta was blocked at different places in the immune system. They found that when they blocked TGF-Beta in dendritic cells (DC's) the mice developed lesions on myelin sheathing of central nervous system cells, the hallmark of MS.

"Previous work suggested that the immune dysfunction seen when TGF-Beta is removed could all be explained by T cells," said Flavell. "Now we know that TGF-Beta control of DC's is important to prevent autoimmunity."

The PNAS study may explain why efforts to spur TGF-Beta activity only in T cells have had limited effects in treating autoimmune diseases, Flavell said.

The authors also speculated that bolstering TGF-Beta activity on dendritic cells might have a potentially therapeutic effect on patients with MS and other autoimmune diseases.

Authors on the study include Yasmina Laouar, Terrence Town, David Jeng, Elise Tran, Yisong Wan, and Vijay K. Kuchroo

The research was supported by National Institutes of Health.
Citation: PNAS July 28, 2008

Yale University

Article adapted by Medical News Today from original press release.
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