High frequency of intestinal T _H17 cells correlates with microbiota alterations and disease activity in multiple sclerosis

Abstract

The headquarter of our immune system resides in the gut and modulates autoimmune disease activation in multiple sclerosis.

Abstract

T helper 17 (T _H17) cells are key players in multiple sclerosis (MS), and studies in animal models demonstrated that effector T _H17 cells that trigger brain autoimmunity originate in the intestine. We validate in humans the crucial role of the intestinal environment in promoting T _H17 cell expansion in MS patients. We found that increased frequency of T _H17 cells correlates with high disease activity and with specific alterations of the gut mucosa-associated microbiota in MS patients. By using 16 S ribosomal RNA sequencing, we analyzed the microbiota isolated from small intestinal tissues and found that MS patients with high disease activity and increased intestinal T _H17 cell frequency showed a higher Firmicutes/Bacteroidetes ratio, increased relative abundance of Streptococcus, and decreased Prevotella strains compared to healthy controls and MS patients with no disease activity. We demonstrated that the intestinal T _H17 cell frequency is inversely related to the relative abundance of Prevotella strains in the human small intestine. Our data demonstrate that brain autoimmunity is associated with specific microbiota modifications and excessive T _H17 cell expansion in the human intestine.