IL-17+ γδ T cells as kick-starters of inflammation

Pedro H Papotto, Julie C Ribot, Bruno Silva-Santos

Research output: Contribution to journalReview articlepeer-review

Abstract

Shortly after the discovery of interleukin 17 (IL-17)-producing CD4+ helper T cells (TH17 cells), it was found that γδ T cells can also secrete large amounts of this pro-inflammatory cytokine. A decade later, it is now known that IL-17+ γδ T cells (γδ17 T cells) are often the main providers of IL-17A in various models of inflammatory diseases, while they also contribute to protective immune responses to infectious organisms. Due to an intricate thymic program of differentiation, γδ17 T cells are able to respond faster than TH17 cells do and thus predominate in the early stages of inflammatory responses. Here we review the current knowledge of the development, activation and pathophysiological functions of γδ17 T cells, aiming to increase the awareness in the community of the therapeutic potential of this 'other side' of IL-17-mediated immune responses.

Original languageEnglish
Pages (from-to)604-611
Number of pages8
JournalNature Immunology
Volume18
Issue number6
DOIs
Publication statusPublished - 18 May 2017

Keywords

  • Animals
  • Cell Differentiation/immunology
  • Humans
  • Immunity, Innate/immunology
  • Inflammation/immunology
  • Interleukin-17/immunology
  • Mice
  • Receptors, Antigen, T-Cell, gamma-delta/immunology
  • T-Lymphocyte Subsets/immunology
  • Th17 Cells/immunology
  • Thymus Gland
  • V(D)J Recombination

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