Reduced serum interleukin-2 associates with higher motor severity and along with CD4 T cell alterations may be an early event in isolated REM Sleep Behaviour Disorder

Brain, Behavior, & Immunity - Health · Published 2026-05-14 · DOI 10.1016/j.bbih.2026.101257

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Authors (9)

Fatima Afaar, Priscilla Youssef, Laura Hughes, Michelle Chua, Elie Matar, Woojin S. Kim, Glenda M. Halliday, Simon J.G. Lewis, Nicolas Dzamko

Abstract

Background: Emerging evidence indicates that peripheral immune changes occur in patients with isolated REM sleep behaviour disorder (iRBD) and may contribute to the conversion of this dream enactment disorder to a neurodegenerative synucleinopathy such as Parkinson's disease, dementia with Lewy bodies or multiple system atrophy. However, with only a limited number of studies conducted, the extent to which immune changes occur across diverse iRBD cohorts remains to be determined. Objectives: We therefore aimed to assess peripheral immune changes in an Australian cohort of iRBD patients (n = 65) compared to controls (n = 35). Methods: A 9-plex cytokine assay was used to measure serum levels of IFNγ, IL-10, IL-12, IL-17A, IL-1β, IL-2, IL-4, IL-6 and TFNα. Flow cytometry was used to assess T cell populations in the same participants. Results: Exploratory analyses revealed lower levels of the T cell regulating cytokine interleukin 2 (IL-2) in participants with iRBD, along with lower frequencies of CD4 T cells positive for IL-2, IL-4 and IL-10. Conclusions: These results add to evidence of immune alterations in iRBD and suggest that dysregulation of cytokines with anti-inflammatory properties may be an early event that could associate with subsequent development of a neurodegenerative synucleinopathy.

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Publication details

Year
2026

Citation

Afaar, F., Youssef, P., Hughes, L., et al. (2026). Reduced serum interleukin-2 associates with higher motor severity and along with CD4 T cell alterations may be an early event in isolated REM Sleep Behaviour Disorder. Brain, Behavior, & Immunity - Health. https://doi.org/10.1016/j.bbih.2026.101257

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