Researchers at Case Western Reserve University School of Medicine have discovered why a gene that, when mutated, is a common cause of two debilitating brain diseases: amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD).
A brain 3D model – illustrative photo. Image credit: Lisa Yount via Unsplash, free license
The study found that the protein generated by this mutant gene, C9ORF72, influences the immune system by regulating the production of Interleukin 17A (IL-17A), a potent inflammatory molecule.
ALS is a neurodegenerative disease that results in progressive paralysis due to the loss of neurons in the central nervous system. ALS patients often have pre-existing autoimmune disease and inflammation of the brain that worsens as muscle function declines.
Aaron Burberry, an assistant professor of pathology at the School of Medicine and the study’s principal investigator, discovered in mouse models with the C9ORF72 mutation—which affects roughly 10% of ALS patients—brain inflammation decreased and mobility improved when the IL-17A gene was blocked.
Burberry and his research team also discovered that another molecule found in the gut (CD80) contributes to inflammation in response to elevations of IL-17A in the brain. Their research was recently published in the peer-reviewed journal Science Translational Medicine.
“Our research indicates that IL-17A blockade may be quickly repurposed to treat ALS patients to slow down the progression of their disease or possibly stop ALS from ever occurring,” Burberry said.
The U.S. Food and Drug Administration has already approved treatments that block IL-17A to treat autoimmune diseases, such as psoriasis and rheumatoid arthritis. These comparable therapies may help ALS patients stop or perhaps reverse the disease’s progression.
“For people living with a neurodegenerative disease,” Burberry said, “our work offers hope for a future where quality-of-life and cognition can be maintained long after their diagnosis.”
Burberry will next investigate the mechanisms by which C9ORF72 inhibits IL-17A in lymphoid cells and identify the gut microbiome elements causing inflammation in the brain.
Source: Case Western Reserve University