Autoimmune Disease Initiated by Abnormal Regulation of Viral Sensors

by Kathy Jones on  January 30, 2012 at 7:00 PM Research News
RSS Email Print This Page Comment
Font : A-A+

The way in which abnormal regulation of the intracellular sensors that detect invading viruses can lead to autoimmune pathology has been elaborated in a new mouse model study.
 Autoimmune Disease Initiated by Abnormal Regulation of Viral Sensors
Autoimmune Disease Initiated by Abnormal Regulation of Viral Sensors

The research, published online on January 26th in the journal Immunity by Cell Press, provides key insight into mechanisms that underlie the development of autoimmune disease and may lead to more effective strategies for therapeutic intervention.

There are multiple intracellular sensors that detect viral infection by binding to viral nucleic acids (RNA and DNA). The majority of these receptors activate type I interferon (IFN) cytokines, which prevent viruses from copying themselves and facilitate appropriate antiviral immune responses. "The interferon response triggered by these sensors is important for protection against infection, but it must be carefully regulated to prevent inappropriate activation by the cells' own DNA and RNA," explains senior study author, Dr. Daniel B. Stetson from the Department of Immunology at the University of Washington School of Medicine.

In an earlier study, Dr. Stetson and colleagues identified an enzyme called Trex1 as an essential negative regulator of the antiviral response. Mutations that inactivate the gene for Trex1 have been linked with multiple IFN-associated human autoimmune diseases, including Aicardi-Goutieres syndrome (AGS). In the current study, the researchers used a Trex1-deficient mouse model of AGS to present a detailed step-wise characterization of the development of autoimmune disease. They identified the specific pathway linking DNA detection with IFN production and described how IFNs drive different aspects of the immune response.

"Together, our results provide an integrated picture of the development of autoimmune disease caused by Trex1 deficiency and a framework for understanding its progression," concludes Dr. Stetson. "Our findings have important implications for the development of therapies for IFN-associated human autoimmune diseases, such as systemic lupus erythematosus and AGS, a rare and severe disease that is currently untreatable and incurable."



Source: Eurekalert

Post your Comments

Comments should be on the topic and should not be abusive. The editorial team reserves the right to review and moderate the comments posted on the site.
* Your comment can be maximum of 2500 characters
Notify me when reply is posted
I agree to the terms and conditions

Related Links

More News on:

Systemic Lupus Erythematosus Chemotherapy Multiple Sclerosis Myasthenia Gravis Multiple Sclerosis Treatment and Modify Vitiligo Autoimmune Disorders Wegener’s Granulomatosis Microscopic Polyangiitis Goodpasture Syndrome 

News A - Z

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

News Search

Medindia Newsletters

Subscribe to our Free Newsletters!

Terms & Conditions and Privacy Policy.

Stay Connected

  • Available on the Android Market
  • Available on the App Store

Facebook

News Category

News Archive