[PDF][PDF] On-going mechanical damage from mastication drives homeostatic Th17 cell responses at the oral barrier

N Dutzan, L Abusleme, H Bridgeman, T Greenwell-Wild… - Immunity, 2017 - cell.com
N Dutzan, L Abusleme, H Bridgeman, T Greenwell-Wild, T Zangerle-Murray, ME Fife…
Immunity, 2017cell.com
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 …
Summary
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.
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