2016-986 A NEW MECHANISM FOR HYPERTRIGLYCERIDEMIA IN HUMANS

Summary

UCLA researchers in the Department of Medicine have identified autoantibodies against GPIHBP1, a GPI anchored protein of capillary endothelial cells, which may provide a novel therapeutic strategy for patients with hypertriglyceridemia.

 

Background

Hypertriglyceridemia patients suffer from elevated levels of triglycerides in their blood.  It has been associated with atherosclerosis and predisposition for cardiovascular disease.  In certain circumstances, the underlying cause of hypertriglyceridemia is unknown and traditional treatments, such as lifestyle modulation or pharmacological therapies are ineffective.  There is a need for more detailed understanding of the etiology of the disease and more effective therapies in cases for which traditional therapies are ineffective.

 

Innovation

Researchers at UCLA have identified a novel thereapeutic strategy for patients with hypertriglyceridemia who also have autoantibodies to GPIHBP1.  It has been found that autoantibodies to GPIHBP1 were found present in patients with hypertriglyceridemia and that these autoantibodies blocked the binding of lipoprotein lipase (LPL) to GPIHBP1.  Researchers has shown that patients may be treated for hypertriglyceridemia by administration of an immunosuppressive treatment and/or HPIhBP1 activator.

 

Applications

▶ Diagnosis of the etiology of hypertriglyceridemia

 

Advantages

▶ Can address patients for which traditional therapies are ineffective

▶ Diagnostic kit can be developed to detect autoantibodies in patients

 

State Of Development

Autoantibodies have been documented in four human subjects suffering from hypertriglyceridemia. Development is ongoing.

Patent Information:
For More Information:
Earl Weinstein
Associate Director of Business Development
eweinstein@tdg.ucla.edu
Inventors:
Stephen Young
Anne Beigneux
Loren Fong
Katsuyuki Nakajima
Kazuya Miyashita