Inhibition reduces allergic lung disease features in mice, suggesting PAR2 is a therapeutic target for asthma.
Inhibition of canonical PAR2 signaling using SAM-11 attenuates multiple features of MWCNT-enhanced allergic lung disease with broader efficacy than PAR2-deficient models. These findings highlight PAR2 as a viable therapeutic target in allergic lung disease and asthma, suggesting that antibody-based blockade is a promising strategy for mitigating allergen and particle-induced disease.
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Tisch et al. (2025) studied this question.
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