Phillyrin significantly attenuated LCWE-induced lung inflammation and suppressed megakaryocyte-derived platelet production by inhibiting the NLRP3/IL-1β axis, thereby impeding IL-1β-mediated NF-E2 expression and subsequent thrombopoiesis. These findings identify Phillyrin as a promising therapeutic candidate for Kawasaki disease by targeting the NLRP3/IL-1β/NF-E2 pathway to ameliorate pathological platelet overproduction and pulmonary complications.
Mai et al. (Sat,) studied this question.