Dual therapy with corticosteroid ablates the beneficial effect of DP2 antagonism in chronic experimental asthma

Nat Commun. 2024 Nov 26;15(1):10253. doi: 10.1038/s41467-024-54670-8.

Abstract

Prostaglandin D2 (PGD2) signals via the DP1 and DP2 receptors. In Phase II trials, DP2 antagonism decreased airway inflammation and airway smooth muscle (ASM) area in moderate-to-severe asthma patients. However, in Phase III, DP2 antagonism failed to lower the rate of exacerbations, and DP2 as a target was shelved. Here, using a preclinical model of chronic experimental asthma, we demonstrate that rhinovirus-induced exacerbations increase PGD2 release, mucus production, transforming growth factor (TGF)-β1 and type-2 inflammation. DP2 antagonism or DP1 agonism ablates these phenotypes, increases epithelial EGF expression and decreases ASM area via increased IFN-γ. In contrast, dual DP1-DP2 antagonism or dual corticosteroid/DP2 antagonism, which attenuates endogenous PGD2, prevented ASM resolution. We demonstrate that DP2 antagonism resolves ASM remodelling via PGD2/DP1-mediated upregulation of IFN-γ expression, and that dual DP2 antagonism/corticosteroid therapy, as often occurred in the human trials, impairs the efficacy of DP2 antagonism by suppressing endogenous PGD2 and IFN-γ production.

MeSH terms

  • Adrenal Cortex Hormones* / pharmacology
  • Adrenal Cortex Hormones* / therapeutic use
  • Airway Remodeling / drug effects
  • Animals
  • Asthma* / drug therapy
  • Asthma* / metabolism
  • Disease Models, Animal
  • Drug Therapy, Combination
  • Female
  • Humans
  • Inflammation / drug therapy
  • Interferon-gamma* / metabolism
  • Male
  • Mice
  • Muscle, Smooth / drug effects
  • Muscle, Smooth / metabolism
  • Picornaviridae Infections / drug therapy
  • Picornaviridae Infections / virology
  • Prostaglandin D2* / metabolism
  • Receptors, Immunologic* / antagonists & inhibitors
  • Receptors, Immunologic* / metabolism
  • Receptors, Prostaglandin* / antagonists & inhibitors
  • Receptors, Prostaglandin* / metabolism
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Prostaglandin D2
  • Receptors, Prostaglandin
  • prostaglandin D2 receptor
  • Adrenal Cortex Hormones
  • Receptors, Immunologic
  • Interferon-gamma
  • Transforming Growth Factor beta1
  • prostanoid D receptor 1, mouse