MAIT Cells and Microbiota in Multiple Sclerosis and Other Autoimmune Diseases
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The functions of mucosal-associated invariant T (MAIT) cells in homeostatic conditions include the interaction with the microbiota and its products, the protection of body barriers, and the mounting of a tissue-repair response to injuries or infections. Dysfunction of MAIT cells and dysbiosis occur in common chronic diseases of inflammatory, metabolic, and tumor nature. This review is aimed at analyzing the changes of MAIT cells, as well as of the microbiota, in multiple sclerosis and other autoimmune disorders. Common features of dysbiosis in these conditions are the reduced richness of microbial species and the unbalance between pro-inflammatory and immune regulatory components of the gut microbiota. The literature concerning MAIT cells in these disorders is rather complex, and sometimes not consistent. In multiple sclerosis and other autoimmune conditions, several studies have been done, or are in progress, to find correlations between intestinal permeability, dysbiosis, MAIT cell responses, and clinical biomarkers in treated and treatment-naïve patients. The final aims are to explain what activates MAIT cells in diseases not primarily infective, which interactions with the microbiota are potentially pathogenic, and their dynamics related to disease course and disease-modifying treatments.
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MR1 presents microbial vitamin B-derived metabolites to an innate T cell subpopulation called mucosal-associated invariant T (MAIT) cells.
“The MHC class I-related molecule MR1 [9], presents microbial vitamin B-derived metabolites to an innate T cell subpopulation called mucosal-associated invariant T (MAIT) cells [10, 11].”
From Control of the temporal development of Alzheimer’s disease pathology by the MR1/MAIT cell axis (2023) · cites this paper as [11]
The MR1/MAIT cell axis has been associated with a number of inflammatory disorders, including those in the CNS.
“The MR1/MAIT cell axis has been associated with a number of inflammatory disorders, including those in the CNS [11, 12].”
From Control of the temporal development of Alzheimer’s disease pathology by the MR1/MAIT cell axis (2023) · cites this paper as [11]
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“Moreover, elevations in MR1 levels have been detected in CNS lesions of MS patients [13].”
BackgroundInfluential
- Authors
- Mechelli, R., Romano, S., Romano, C., Morena, E., Buscarinu, M. C., Bigi, R., Bellucci, G., Reniè, R., Pellicciari, G., Salvetti, M., & Ristori, G.
- Affiliations
- San Raffaele University of Rome (IT)
- Sapienza University of Rome (IT)
- Istituto Neurologico Mediterraneo (IT)
- Fondazione Santa Lucia (IT)
- Corresponding author
- Salvetti, Marco
- ORCID
- Venue
- Microorganisms
- Publisher
- MDPI AG
- Published
- 2021-05-24
- Volume
- 9
- Issue
- 6
- Pages
- 1132
- ISSN
- 2076-2607 (ISSN-L)
- PMC
- PMC8225125
- OpenAlex
- W3164954225
- Cited by
- 24
- References
- 9
- Citations by year
- 2025: 4 · 2024: 3 · 2023: 9 · 2022: 3 · 2021: 5
- FWCI
- 0.52
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Microorganisms (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- mucosal-associated invariant T cells, gut microbiota, dysbiosis, multiple sclerosis, autoimmune disease, intestinal permeability, disease-modifying therapy, biomarkers, tissue repair
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