Relevant mechanisms of MAIT cells involved in the pathogenesis of periodontitis
- PMID: 36896188
- PMCID: PMC9988952
- DOI: 10.3389/fcimb.2023.1104932
Relevant mechanisms of MAIT cells involved in the pathogenesis of periodontitis
Abstract
Mucosal-associated invariant T (MAIT) cells are a group of unconventional T cells that are abundant in the human body, recognize microbial-derived vitamin B metabolites presented by MHC class I-related protein 1 (MR1), and rapidly produce proinflammatory cytokines, which are widely involved in the immune response to various infectious diseases. In the oral mucosa, MAIT cells tend to accumulate near the mucosal basal lamina and are more inclined to secrete IL-17 when activated. Periodontitis is a group of diseases that manifests mainly as inflammation of the gums and resorption of the alveolar bone due to periodontal tissue invasion by plaque bacteria on the dental surface. The course of periodontitis is often accompanied by a T-cell-mediated immune response. This paper discussed the pathogenesis of periodontitis and the potential contribution of MAIT cells to periodontitis.
Keywords: IL-17; alveolar bone resorption; immune reaction; mucosal-associated invariant T cell; periodontitis.
Copyright © 2023 Jiang, Zhao, Huang, Ma, Chen and Li.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
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- Ali Mohammed M. M., Pettersen V. K., Nerland A. H., Wiker H. G., Bakken V. (2021). Label-free quantitative proteomic analysis of the oral bacteria fusobacterium nucleatum and porphyromonas gingivalis to identify protein features relevant in biofilm formation. Anaerobe 72, 102449. doi: 10.1016/j.anaerobe.2021.102449 - DOI - PubMed
-
- Balfour A., Schutz C., Goliath R., Wilkinson K. A., Sayed S., Sossen B., et al. (2021). Functional and activation profiles of mucosal-associated invariant T cells in patients with tuberculosis and HIV in a high endemic setting. Front. Immunol. 12, 648216. doi: 10.3389/fimmu.2021.648216 - DOI - PMC - PubMed
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