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Urdu“The discovery of this autoantibody provides a new diagnostic tool for AGL patients and could potentially result in novel therapeutic options,” said Abhimanyu Garg, M.D., Professor of Internal Medicine, Section Chief of Nutrition and Metabolic Diseases in the Division of Endocrinology, and Director of Metabolic Diseases in UT Southwestern’s Center for Human Nutrition. Dr. Garg was one of three senior authors of the study, conducted in collaboration with colleagues at the University of California, San Francisco, and institutions in France, Norway, and Russia.
The underlying cause of AGL, which is most often diagnosed in children but also can appear in adults, has so far remained unclear. Approximately 100 cases have been reported worldwide, making it difficult to study the commonalities among patients. For years, researchers have suspected the disorder is an autoimmune condition, in which a person’s immune system attacks the body. However, they had been unable to pinpoint any unusual or unique autoantibodies in AGL patients.
Dr. Garg and his colleagues utilized their UT Southwestern biorepository containing blood, DNA, and clinical data collected from 46 patients with AGL over the past 30 years.
“We now have the largest collection of data on AGL patients in the world,” Dr. Garg said. “The banked samples from these patients were key to our new discovery.”
The team sought to detect antibodies against nearly 19,500 different human proteins in the blood samples from the patients and healthy controls, homing in on the perilipin-1 autoantibody as the key finding differentiating people with AGL from those without the disease. Perilipin-1 is a protein known to play a role in the storage of fat molecules in fat cells. The autoantibody was found to be present in 17 of the 46 patients but in none of the controls.
The researchers concluded that the perilipin-1 autoantibody – which would direct the immune system to attack the protein and therefore harm fat cells – might play a role in AGL.
More detailed profiling of the patients whose blood contained the perilipin-1 autoantibody showed that those with one subtype of AGL, known as AGL with panniculitis, were even more likely to have them. Panniculitis is a process whereby immune cells infiltrate fat tissue, causing destruction and death of fat cells. The researchers also found that laboratory mice known to develop AGL-like disease also had the autoantibody to perilipin-1.
Further work is needed to understand the prevalence of the perilipin-1 autoantibody among patients with AGL and related disorders, as well as whether an immunotherapy drug or procedure could remove or block the autoantibody to treat those developing AGL.
Other UTSW researchers who contributed to this study include Anil K. Agarwal, Xilong Li, and Chengsong Zhu.
Dr. Garg holds a Distinguished Chair in Human Nutrition Research.
The research was supported by funding from the National Institutes of Health (R01-DK105448) and the Southwestern Medical Foundation.
About UT Southwestern Medical Center
UT Southwestern, one of the nation’s premier academic medical centers, integrates pioneering biomedical research with exceptional clinical care and education. The institution’s faculty has received six Nobel Prizes, and includes 24 members of the National Academy of Sciences, 18 members of the National Academy of Medicine, and 14 Howard Hughes Medical Institute Investigators. The full-time faculty of more than 2,900 is responsible for groundbreaking medical advances and is committed to translating science-driven research quickly to new clinical treatments. UT Southwestern physicians provide care in more than 80 specialties to more than 100,000 hospitalized patients, more than 360,000 emergency room cases, and oversee nearly 4 million outpatient visits a year.
