4.8 Article

An Ocular Commensal Protects against Corneal Infection by Driving an Interleukin-17 Response from Mucosal γδ T Cells

Journal

IMMUNITY
Volume 47, Issue 1, Pages 148-+

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2017.06.014

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Funding

  1. NIH [NEI EY000184, K99EY025761, R01EY022054]
  2. NIAID [AI001175]
  3. Prevention of Blindness Society of Metropolitan Washington
  4. American Association of Immunology Fellowship Award
  5. Grants-in-Aid for Scientific Research [15H05787] Funding Source: KAKEN

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Mucosal sites such as the intestine, oral cavity, nasopharynx, and vagina all have associated commensal flora. The surface of the eye is also a mucosal site, but proof of a living, resident ocular microbiome remains elusive. Here, we used a mouse model of ocular surface disease to reveal that commensals were present in the ocular mucosa and had functional immunological consequences. We isolated one such candidate commensal, Corynebacterium mastitidis, and showed that this organism elicited a commensal-specific interleukin-17 response from gamma delta T cells in the ocular mucosa that was central to local immunity. The commensal-specific response drove neutrophil recruitment and the release of antimicrobials into the tears and protected the eye from pathogenic Candida albicans or Pseudomonas aeruginosa infection. Our findings provide direct evidence that a resident commensal microbiome exists on the ocular surface and identify the cellular mechanisms underlying its effects on ocular immune homeostasis and host defense.

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