The role of invariant T cells in inflammation of the skin and airways

Semin Immunopathol. 2019 May;41(3):401-410. doi: 10.1007/s00281-019-00740-9. Epub 2019 Apr 15.

Abstract

Invariant and semi-invariant T cells are emerging as important regulators of host environment interactions at barrier tissues such as the airway and skin. In contrast to conventional T cells, invariant natural killer T (iNKT) cells and mucosal associated invariant T (MAIT) cells express T cell receptors of very limited diversity. iNKT and MAIT cells recognise antigens presented by the MHC class 1-like monomorphic molecules CD1d and MR1, respectively. Both iNKT cells and MAIT cells have been identified in the skin and airways and can rapidly produce cytokines after activation. Numerous studies have implicated iNKT cells in the pathology of both skin and airway disease, but conflicting evidence in human disease means that more studies are necessary to resolve the exact roles of iNKT in inflammation. The functions of MAIT cells in skin and lung inflammation are even less well defined. We herein describe the current literature on iNKT and MAIT cells in allergic and non-allergic skin diseases (dermatitis and psoriasis) and airway diseases (asthma, chronic obstructive pulmonary disease, rhinitis, and chronic rhinosinusitis).

Keywords: Asthma; Chronic obstructive pulmonary disease; Chronic rhinosinusitis; Dermatitis; Invariant natural killer T; MAIT; Mucosal associated invariant T; Psoriasis; Rhinitis; iNKT.

Publication types

  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Dermatitis / etiology
  • Dermatitis / metabolism
  • Dermatitis / pathology
  • Disease Susceptibility*
  • Gene Expression Regulation
  • HLA Antigens / immunology
  • Humans
  • Inflammation / diagnosis
  • Inflammation / etiology*
  • Inflammation / metabolism*
  • Lymphocyte Activation / immunology
  • Mucosal-Associated Invariant T Cells / immunology*
  • Mucosal-Associated Invariant T Cells / metabolism*
  • Respiratory Tract Diseases / etiology
  • Respiratory Tract Diseases / metabolism
  • Respiratory Tract Diseases / pathology
  • Signal Transduction
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism*

Substances

  • Biomarkers
  • HLA Antigens