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On-going Mechanical Damage from Mastication Drives Homeostatic Th17 Cell Responses at the Oral Barrier

  • Nicolas Dutzan
  • , Loreto Abusleme
  • , Hayley Bridgeman
  • , Teresa Greenwell-Wild
  • , Tamsin Zangerle-Murray
  • , Mark E. Fife
  • , Nicolas Bouladoux
  • , Holly Linley
  • , Laurie Brenchley
  • , Kelly Wemyss
  • , Gloria Calderon
  • , Bo Young Hong
  • , Timothy J. Break
  • , Dawn M.E. Bowdish
  • , Michail S. Lionakis
  • , Simon A. Jones
  • , Giorgio Trinchieri
  • , Patricia I. Diaz
  • , Yasmine Belkaid
  • , Joanne E. Konkel
  • Niki M. Moutsopoulos
  • National Institutes of Health
  • University of Manchester
  • University of Connecticut
  • McMaster University
  • Cardiff University

Research output: Contribution to journalArticlepeer-review

233 Scopus citations

Abstract

Immuno-surveillance networks operating at barrier sites are tuned by local tissue cues to ensure effective immunity. Site-specific commensal bacteria provide key signals ensuring host defense in the skin and gut. However, how the oral microbiome and tissue-specific signals balance immunity and regulation at the gingiva, a key oral barrier, remains minimally explored. In contrast to the skin and gut, we demonstrate that gingiva-resident T helper 17 (Th17) cells developed via a commensal colonization-independent mechanism. Accumulation of Th17 cells at the gingiva was driven in response to the physiological barrier damage that occurs during mastication. Physiological mechanical damage, via induction of interleukin 6 (IL-6) from epithelial cells, tailored effector T cell function, promoting increases in gingival Th17 cell numbers. These data highlight that diverse tissue-specific mechanisms govern education of Th17 cell responses and demonstrate that mechanical damage helps define the immune tone of this important oral barrier.

Original languageEnglish
Pages (from-to)133-147
Number of pages15
JournalImmunity
Volume46
Issue number1
DOIs
StatePublished - Jan 17 2017

Keywords

  • barrier immunity
  • IL-17
  • mucosal immunology
  • oral immunity
  • periodontitis
  • T cells
  • Th17 cells

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