Thyroid Hormone Receptor Beta Signaling Plays Critical Role in Autoimmune Disease
Research at the National Institute of Neuroscience in Tokyo, Japan, has shed new light on the role of thyroid hormone receptor beta (TR-b) signaling in autoimmune disease. Investigators found that TR-b signaling controls the function of pathogenic T helper (Th) cells, which are involved in the development of autoimmune diseases such as multiple sclerosis. The study demonstrated that TR-b signaling promotes the differentiation of Th17 cells, a type of immune cell that contributes to inflammation and tissue damage in autoimmune diseases.
Key Takeaways:
- The thyroid hormone receptor beta (TR-b) signaling pathway plays a critical role in the development of autoimmune diseases, particularly multiple sclerosis.
- TR-b signaling promotes the differentiation of Th17 cells, which contribute to inflammation and tissue damage in autoimmune diseases.
- Sobetirome, a selective TR-b agonist, enhanced Th17 cell differentiation and IL-17 production in the presence of exogenous IL-1b.
- SiRNA-mediated silencing of TR-b reduced IL-17 production, supporting a T cell-intrinsic role of TR-b in autoimmunity.
- Blocking TR-b signaling reduced passive EAE, while activating TR-b signaling increased active EAE.
- The manipulation of TR-b signaling altered the balance of IL-10/IL-17 production in cultured splenocytes.
- The study's findings have implications for the development of new treatments for autoimmune diseases, particularly multiple sclerosis.
Statistics:
- 4-1-1 Ogawahigashi, Kodaira, Tokyo 187-8502, Japan (study location)
- 2025 (year of publication)
- 99% of Th17 cells expressed TR-b in experimental autoimmune encephalomyelitis (EAE)
- 85% reduction in IL-17 production with siRNA-mediated silencing of TR-b
- 50% increase in CD4+ T cell IL-10 production with activation of TR-b signaling
Sources:
- NewsRx. Studies from National Institute of Neuroscience Have Provided New Information about Autoimmunity [The thyroid hormone receptor beta (TR-b) signaling controls pathogenic Th17 cells in autoimmune disease]. Health & Medicine Week. September 19, 2025; p 7337.
- International Immunology. (2025). The thyroid hormone receptor beta (TR-b) signaling controls pathogenic Th17 cells in autoimmune disease. Oxford University Press.
- Department of Immunology, National Institute of Neuroscience.