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Updated: Jun 17, 2025

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Published on: November 17, 2020
Circulating MAIT cells in multiple sclerosis and amyotrophic lateral sclerosis.
Davide De Federicis1, Claudia Bassani1, Rosaria Rita Chiarelli1
1Institute of Experimental Neurology and Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
Circulating mucosal-associated invariant T (MAIT) cells are specifically lost in primary progressive multiple sclerosis (PP-MS), unlike other MS types or ALS. This blood cell alteration may aid in defining PP-MS disease course.
Area of Science:
- Immunology
- Neuroimmunology
- Cellular Biology
Background:
- Neurological disorders like multiple sclerosis (MS) and amyotrophic lateral sclerosis (ALS) can involve changes in blood cell composition.
- Mucosal-associated invariant T (MAIT) cells are a subset of CD8+ T cells with specific T cell receptor and marker expression.
Purpose of the Study:
- To investigate alterations in circulating MAIT cells in different courses of MS and ALS.
- To determine if MAIT cell changes correlate with specific neurological disease phenotypes.
Main Methods:
- Transcriptomic analysis of peripheral blood mononuclear cells (PBMC) from MS patients and healthy controls.
- Multiparametric flow cytometry to quantify CD8+ MAIT cells in PBMC from patients with relapsing-remitting MS (RR-MS), progressive MS (PP-MS, SP-MS), ALS, and healthy controls.
Main Results:
- Transcriptomics showed downregulation of MAIT cell markers in progressive MS compared to healthy controls.
- Flow cytometry revealed a significant loss of circulating CD8+ MAIT cells specifically in primary progressive MS (PP-MS).
- No significant changes in MAIT cells were observed in RR-MS, SP-MS, or ALS patients compared to controls.
Conclusions:
- A specific reduction in circulating CD8+ MAIT cells is associated with the primary progressive course of multiple sclerosis.
- These immunological findings in blood may contribute to the clinical definition and understanding of PP-MS.
- MAIT cell analysis could serve as a potential biomarker for distinct MS disease trajectories.
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