Yale Researchers Pave Way To Target Autoimmune Disease-associated Gene Variant

In a new study, Yale researchers identified a molecule that binds to a disease-associated macrophage migration inhibitory factor (MIF) gene variant. The discovery, they say, could lead to the development of a new generation of precision medicine-based therapies that address diverse autoimmune and inflammatory conditions.

The findings were published in the Journal of Biological Chemistry.

Many autoimmune and inflammatory diseases develop because of susceptibilities encoded by genetic variants in our DNA. MIF gene variants are common in people and confer risk for multiple autoimmune, infectious, and oncologic diseases, explains corresponding author Richard Bucala, MD, PhD, Waldemar Von Zedtwitz Professor of Medicine (Rheumatology) and professor of pathology and of epidemiology at Yale School of Medicine (YSM). MIF, an inflammatory mediator, plays a significant role in the body’s immune response.

“These natural gene variants produce different levels of the MIF protein that influence the risk of developing a particular disease or of having an especially severe form of it,” Bucala said.

Researchers in the Bucala lab developed a highly sensitive, high-throughput assay to identify molecules that could bind to the variant DNA sequence in the MIF gene and prevent its interaction with the transcription factor, or protein that controls the transcription of genetic information. The assay was used to screen tens of thousands of molecules to identify ones that might reduce MIF production in the high MIF gene-variant cells.

From a library of almost 30,000 compounds available at the Yale Center for Molecular Discovery, the researchers found that the druglike molecule 1-carbomethoxy-5-formyl-4,6,8-trihydroxyphenazin (CMFT) selectively binds to a disease-associated MIF gene variant and inhibits the transcription factor ICBP90, which activates the MIF gene.

“The ability to inhibit MIF in a way that is selective for a disease-associated gene variant is the most precise means to interfere with MIF’s disease-causing action and would likely be far less toxic than less selective treatments,” Bucala said.

Co-author Elias Lolis, PhD, professor of pharmacology at YSM, considers the study a major advancement toward a therapeutic strategy in cases where greater protein expression is associated with disease pathology.

“It shows what is essential for the growing field of precision medicine using pharmacogenomics, or how our genes affect our response to medications,” he said.

The DNA-based assay and prototype molecule demonstrate the feasibility of advancing the development of precision-based MIF inhibitors for many autoimmune and inflammatory diseases, Bucala added.

“It provides a way to pharmacologically re-set one’s genetic susceptibility toward a healthy state,” he said.

Other authors of the study include Jia Li, Lin Leng, Georgios Pantouris, Manjula Ramu, Marta Piecychna, Laura Abriola, Buqu Hu, Michelle Armstrong, and Seamas Donnelly.

The study was supported by the National Institutes of Health, the Rheumatology Research Fund, the Mathers Foundation, and the Program in Innovative Therapeutics for Connecticut’s Health.

Yale School of Medicine’s Department of Internal Medicine Section of Rheumatology, Allergy and Immunology is dedicated to providing care for patients with rheumatic, allergic and immunologic disorders; educating future generations of thought leaders in the field; and conducting research into fundamental questions of autoimmunity and immunology. To learn more about their work, visit Rheumatology, Allergy & Immunology.