Prolonged Immune System Signaling Linked to ADHD
New research has linked a key infection-fighting function to hyperactive behavior in mice.
Complete the form below to unlock access to ALL audio articles.
Building on research that has linked immune responses with certain neurobehavioral conditions, researchers at Duke Health have identified how a key infection-fighting function is involved in triggering hyperactive behaviors in mice.
The finding, appearing this month in the journal Brain, Behavior, and Immunity, adds insight to an on-off switch for genes called STAT1. This gene regulator plays a pivotal role in the immune system’s response to infections and has also been implicated in various neurodevelopmental disorders such as autism and ADHD.
“A lot of these pathways that have been discovered in the immune system also play important roles in the brain,” said senior author Anthony Filiano, Ph.D., assistant professor in the departments of Neurosurgery and Pathology at Duke University School of Medicine and a faculty member in the Marcus Center for Cellular Cures. “There is a very robust communication between the two systems. This is intriguing because the immune system is very targetable from a therapy perspective.”
Filiano and colleagues at Duke worked with a team at Columbia University that bred mice with a STAT1 mutation. Using these mice, they were able to over-activate the immune pathway in different cell types of the brain, including dopamine neurons, which help modulate reward, motivation, and motor control.
Want more breaking news?
Subscribe to Technology Networks’ daily newsletter, delivering breaking science news straight to your inbox every day.
Subscribe for FREEFiliano said further studies will explore whether it’s possible to target the STAT1 pathway with therapies: “We need to understand its function and target it more specifically before we move forward,” he said.
Reference: Clark DN, Brown SV, Xu L, et al. Prolonged STAT1 signaling in neurons causes hyperactive behavior. Brain, Behav Immun. 2025;124:1-8. doi: 10.1016/j.bbi.2024.11.018
This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release publishing policy can be accessed here.