Skip to content

Because of a lapse in government funding, the information on this website may not be up to date, transactions submitted via the website may not be processed, and the agency may not be able to respond to inquiries until appropriations are enacted.
The NIH Clinical Center (the research hospital of NIH) is open. For more details about its operating status, please visit cc.nih.gov.
Updates regarding government operating status and resumption of normal operations can be found at OPM.gov.

Medical College of Georgia scientists searching for new treatment target for diabetic retinopathy

September 12, 2024
Diabetic Eye Disease Immunology
Translational Research
Grantee
Shruti Sharma in the laboratory.

Shruti Sharma, Ph.D. Image credit: Michael Holahan, Augusta University

Scientists at the Medical College of Georgia at Augusta University are searching for a new treatment target for a common complication of diabetes that can cause retinal blood vessels to break down, leak or become blocked.

The current treatment standard is anti-VEGF, which targets and blocks the activity of vascular endothelial growth factor, a protein that promotes the growth of blood vessels and causes them to leak. But that treatment doesn’t work for everyone.

With a new $1.5 million grant from the National Eye Institute, vascular and endothelial biologist Shruti Sharma, PhD, and a team from the MCG Center for Biotechnology and Genomic Medicine, hope to zero in on a new treatment pathway. They suspect the key to that may be a protein called Interleukin-6 (IL-6), a versatile protein involved in both immunity and inflammation throughout the body.

She and her research team think the answer lies in how IL-6 signals or initiates physiological changes in the body.

In preliminary studies, she and her research team found that specifically blocking pro-inflammatory IL-6 signaling, with a drug called sgp130Fc, helped balance levels of two important proteins in the retina. They believe that disruption to that balance is what ultimately leads to the development of diabetic retinopathy.