Journal
CELL
Volume 162, Issue 6, Pages 1338-1352Publisher
CELL PRESS
DOI: 10.1016/j.cell.2015.08.025
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Funding
- Allende Foundation
- MSIF Du-Pree grant
- Biogen Idec
- Novartis Argentina
- Merck Serono Argentina
- NIH [AI093903, NS087867]
- National Multiple Sclerosis Society [RG4111A1, JF2161-A-5]
- International Progressive MS Alliance [PA0069]
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Seasonal changes in disease activity have been observed in multiple sclerosis, an autoimmune disorder that affects the CNS. These epidemiological observations suggest that environmental factors influence the disease course. Here, we report that melatonin levels, whose production is modulated by seasonal variations in night length, negatively correlate with multiple sclerosis activity in humans. Treatment with melatonin ameliorates disease in an experimental model of multiple sclerosis and directly interferes with the differentiation of human and mouse T cells. Melatonin induces the expression of the repressor transcription factor Nfil3, blocking the differentiation of pathogenic Th17 cells and boosts the generation of protective Tr1 cells via Erk1/2 and the transactivation of the IL-10 promoter by ROR-alpha. These results suggest that melatonin is another example of how environmental-driven cues can impact T cell differentiation and have implications for autoimmune disorders such as multiple sclerosis.
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