Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 33376202.
- Also identified by DOI 10.1073/pnas.2018457118 and PMC identifier 7817192.
- Licence recorded as CC BY-NC-ND.
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Abstract
Multiple sclerosis (MS) disease risk is associated with reduced sun-exposure. This study assessed the relationship between measures of sun exposure (vitamin D [vitD], latitude) and MS severity in the setting of two multicenter cohort studies (<i>n</i><sub>NationMS</sub> = 946, <i>n</i><sub>BIONAT</sub> = 990). Additionally, effect-modification by medication and photosensitivity-associated <i>MC1R</i> variants was assessed. High serum vitD was associated with a reduced MS severity score (MSSS), reduced risk for relapses, and lower disability accumulation over time. Low latitude was associated with higher vitD, lower MSSS, fewer gadolinium-enhancing lesions, and lower disability accumulation. The association of latitude with disability was lacking in IFN-β-treated patients. In carriers of <i>MC1R</i>:rs1805008(T), who reported increased sensitivity toward sunlight, lower latitude was associated with higher MRI activity, whereas for noncarriers there was less MRI activity at lower latitudes. In a further exploratory approach, the effect of ultraviolet (UV)-phototherapy on the transcriptome of immune cells of MS patients was assessed using samples from an earlier study. Phototherapy induced a vitD and type I IFN signature that was most apparent in monocytes but that could also be detected in B and T cells. In summary, our study suggests beneficial effects of sun exposure on established MS, as demonstrated by a correlative network between the three factors: Latitude, vitD, and disease severity. However, sun exposure might be detrimental for photosensitive patients. Furthermore, a direct induction of type I IFNs through sun exposure could be another mechanism of UV-mediated immune-modulation in MS.
Medical subject headings
- Monocytes
- Multiple Sclerosis
- Receptor, Melanocortin, Type 1
- Transcriptome
- Vitamin D