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PRECLINICAL PUBLICATION · 2018

Ozone exposure induces respiratory barrier biphasic injury and inflammation controlled by IL-33.

Mouse / Chemical/toxin

Evidence by therapy association

Study details and outcomes are extracted in the context of a specific intervention. Separate associations are retained rather than silently merged.

PMID 29331644 ↗2018Reported benefit

Ozone exposure induces respiratory barrier biphasic injury and inflammation controlled by IL-33.

MouseChemical/toxinC57BL/6 wild-type, ST2-deficient, Il33-deficient, IL-33 citrine reporterFemale

Model: Single acute ozone exposure (1 ppm for 1 h) causing lung epithelial barrier injury and neutrophilic inflammation

Administration of recombinant mouse IL-33 reduced neutrophil recruitment in Il33-deficient mice, and loss of IL-33 or ST2 worsened epithelial injury and myeloid inflammation, indicating IL-33/ST2 signalling protects the epithelial barrier after ozone exposure.

Extraction: extract · Supplied extraction confidence: 0.55. Machine-extracted fields require source verification.