Cited by 12T-cell and B-cell ImmunologyNeuroinflammation and Neurodegeneration MechanismsMultiple Sclerosis Research Studies

The MR1/MAIT cell axis in CNS diseases

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Shrinivasan, Rashmi, Wyatt-Johnson, Season K., Brutkiewicz, Randy R.·2024·Brain, Behavior, and Immunity

Abstract

Mucosal-associated invariant T (MAIT) cells are a subpopulation of innate-like T cells that can be found throughout the body, predominantly in mucosal sites, the lungs and in the peripheral blood. MAIT cells recognize microbial-derived vitamin B (e.g., riboflavin) metabolite antigens that are presented by the major histocompatibility complex class I-like protein, MR1, found on a variety of cell types in the periphery and the CNS. Since their original discovery, MAIT cells have been studied predominantly in their roles in diseases in the periphery; however, it was not until the early 2000s that these cells were first examined for their contributions to disorders of the CNS, with the bulk of the work being done within the past few years. Currently, the MR1/MAIT cell axis has been investigated in only a few neurological diseases including, multiple sclerosis and experimental autoimmune encephalomyelitis, brain cancer/tumors, ischemia, cerebral palsy, general aging and, most recently, Alzheimer's disease. Each of these diseases demonstrates a role for this under-studied innate immune axis in its neuropathology. Together, they highlight the importance of studying the MR1/MAIT cell axis in CNS disorders. Here, we review the contributions of the MR1/MAIT cell axis in the progression or remission of these neurological diseases. This work has shed some light in terms of potentially exploiting the MR1/MAIT cell axis in novel therapeutic applications.

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  1. Aiello A, Farzaneh F, Candore G, Caruso C, Davinelli S, Gambino CM, Ligotti ME, Zareian N, Accardi G, 2019. Immunosenescence and Its Hallmarks: How to Oppose Aging Strategically? A Review of Potential Options for Therapeutic Intervention. Front Immunol 10, 2247. [PubMed: 31608061]

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Authors
Shrinivasan, R., Wyatt-Johnson, S. K., & Brutkiewicz, R. R.
Affiliations
  • Indiana University School of Medicine (US)
  • Indiana University Indianapolis (US)
Corresponding author
Brutkiewicz, Randy R.
Venue
Brain, Behavior, and Immunity
Publisher
Elsevier BV
Published
2024-02
Volume
116
Pages
321-328
ISSN
0889-1591 (ISSN-L)
OpenAlex
W4390278076
Cited by
12
References
4
Citations by year
2026: 3 · 2025: 5 · 2024: 4
FWCI
0.33
Type
journal article
Language
en
Open access
Locations
  • Brain Behavior and Immunity (acceptedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion)
Funders
  • Alzheimer's Association (AARGD-NTF-22\u2013928436, TL1TR002531)
  • National Center for Advancing Translational Sciences
  • National Institutes of Health (R21 AG071269-01, TL1TR002531)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
Keywords
mucosal-associated invariant T cells, MR1, innate-like T cells, central nervous system disorders, neurological disorders, multiple sclerosis, experimental autoimmune encephalomyelitis, brain tumors, cerebral ischemia, cerebral palsy, aging, Alzheimer's disease, neuroinflammation, therapeutic target
MeSH terms
Mucosal-Associated Invariant T Cells, Central Nervous System Diseases, Humans, Riboflavin, Histocompatibility Antigens Class I, Minor Histocompatibility Antigens

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