Epidermal CCR6+ γδ T cells are major producers of IL-22 and IL-17 in a murine model of psoriasiform dermatitis

J Immunol. 2011 Nov 15;187(10):5026-31. doi: 10.4049/jimmunol.1101817. Epub 2011 Oct 7.

Abstract

Cytokine components of Th17 pathway play vital roles in human psoriasis. Although much is known about TCR αβ T cells in psoriasis, the role of unconventional T cells, including γδ T cells, is unclear. In this study, using an IL-23 skin injection model of psoriasiform dermatitis in mice, we demonstrate that IL-22, IL-17A, and the IL-23R were highly enriched in a population of CCR6(+), TCR γδ-low expressing (GDL) T cells that accumulated in the epidermis after IL-23 injections. GDL cells were distinct from resident TCR γδ-high, Vγ3(+),CCR6(-) T cells in the epidermis that did not change appreciably in numbers following IL-23 injection. Large numbers of CCR6(+) cells were detected at or above the level of the epidermal basement membrane by confocal microscopy 5 d after repeated IL-23 injections at the same time GDL cells increased in numbers in the epidermis. TCR δ-deficient mice (lacking γδ T cells) exhibited decreased ear swelling and downregulated expression of IL-22 and IL-17A in the epidermis following IL-23 injection. Our data suggest that a subset of γδ T cells play a critical role in IL-23-mediated psoriasiform dermatitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dermatitis / immunology*
  • Dermatitis / metabolism
  • Dermatitis / pathology
  • Disease Models, Animal
  • Epidermis / immunology*
  • Epidermis / metabolism
  • Epidermis / pathology
  • Interleukin-17 / biosynthesis*
  • Interleukin-17 / genetics
  • Interleukin-22
  • Interleukin-23 / administration & dosage
  • Interleukins / biosynthesis*
  • Interleukins / genetics
  • Keratinocytes / immunology
  • Keratinocytes / metabolism
  • Keratinocytes / pathology
  • Mice
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Psoriasis / immunology*
  • Psoriasis / metabolism
  • Psoriasis / pathology
  • RNA, Messenger / biosynthesis
  • Receptors, CCR6 / biosynthesis*
  • Receptors, CCR6 / genetics
  • Receptors, Interleukin / biosynthesis
  • Receptors, Interleukin / genetics
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / pathology
  • Th17 Cells / immunology
  • Th17 Cells / metabolism
  • Th17 Cells / pathology

Substances

  • CCR6 protein, human
  • CCR6 protein, mouse
  • IL23R protein, human
  • Interleukin-17
  • Interleukin-23
  • Interleukins
  • RNA, Messenger
  • Receptors, CCR6
  • Receptors, Interleukin
  • interleukin-23 receptor, mouse