The MR1/MAIT cell axis in CNS diseases

Brain Behav Immun. 2024 Feb:116:321-328. doi: 10.1016/j.bbi.2023.12.029. Epub 2023 Dec 27.

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.

Keywords: Alzheimer’s disease; Cerebral palsy; Glioblastoma; Ischemia; Multiple sclerosis; Neuroinflammation.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Central Nervous System Diseases* / metabolism
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Minor Histocompatibility Antigens / metabolism
  • Mucosal-Associated Invariant T Cells*
  • Riboflavin / metabolism

Substances

  • Minor Histocompatibility Antigens
  • Histocompatibility Antigens Class I
  • Riboflavin
  • MR1 protein, human