Blog – Page 14

In a breakthrough that reimagines the way the gut and brain communicate, researchers have uncovered what they call a “neurobiotic sense,” a newly identified system that lets the brain respond in real time to signals from microbes living in our gut.

The new research, led by Duke University School of Medicine neuroscientists Diego Bohórquez, Ph.D., and M. Maya Kaelberer, Ph.D., published in Nature, centers on neuropods, tiny sensor cells lining the colon’s epithelium. These cells detect a common microbial protein and send rapid messages to the brain that help curb appetite.

But this is just the beginning. The team believes this neurobiotic sense may be a broader platform for understanding how the gut detects microbes, influencing everything from eating habits to mood—and even how the brain might shape the microbiome in return.

The existing treatment options include biological and targeted synthetic disease-modifying anti-rheumatic drugs, which some patients find hard to tolerate, and around 50 percent of patients discontinue their therapies within two years. SetPoint’s goal is to provide an alternative that can effectively manage autoimmune conditions without suppressing the immune system.

Its FDA approval follows a randomized, double-blind, sham-controlled study that followed 242 patients. It showed that the therapy was well-tolerated with a low level of serious adverse events related to it (1.7 percent). It also provides a long-term solution for patients living with this chronic disease.

“The approval of the SetPoint System highlights the potential of neuroimmune modulation as a novel approach for autoimmune disease, by harnessing the body’s neural pathways to combat inflammation,” said the study’s principal investigator, Dr Mark Richardson, Director of Functional Neurosurgery at Massachusetts General Hospital and Professor of Neurosciences at Harvard Medical School, in a statement. “After implantation during a minimally invasive outpatient procedure, the SetPoint device is programmed to automatically administer therapy on a predetermined schedule for up to 10 years, simplifying care for people living with RA.”

After transplantation into the brain of patients with Parkinson’s disease, allogeneic dopaminergic progenitors derived from induced pluripotent stem cells survived, produced dopamine and did not form tumours, therefore suggesting safety and potential clinical benefits for Parkinson’s disease.