The Inflammasome NLRP3 as a Novel Therapeutic Target for Idiopathic Pulmonary Fibrosis (IPF)

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The authors review evidence of NOD-like receptor (NLR) P3 activation in IPF, of NLRP3 inhibition in different animal models of fibrosis, and highlight the recent advances in direct and indirect NLRP3 inhibitors.
[American Journal of Pathology]
Abstract