Increased expression of IL‐19 in the epithelium of patients with chronic rhinosinusitis and nasal polyps

Abstract Background Chronic rhinosinusitis ( CRS ) is an inflammation of the nose and of the paranasal sinuses. The involvement of the respiratory epithelium in the mechanisms of CRS is poorly understood. Aims Among proteins expressed by nasal epithelial cells in CRS , IL ‐19 may have key functions. We here aimed to determine the expression and regulation of IL ‐19. Methods Nasal biopsies from normal subjects ( n = 12), subjects with CRS but without nasal polyps ( NP ) ( CRS s NP , n = 12) and with CRS with NP ( CRS w NP , n = 15) were collected. Human A sthma G ene A rray and real‐time PCR were used to evaluate gene expression, western blot analysis and immunohistochemistry for protein expression. Results for IL ‐19 were confirmed by real‐time PCR . The constitutive and stimulated ( LPS , TGF β) expression of IL ‐19 and cell proliferation were evaluated in a nasal epithelial cell line ( RPMI 2650). Results Human A sthma G ene A rray showed an increased IL ‐19 gene expression in NP from patients with CRS in comparison with normal subjects. Real‐time PCR confirmed the IL ‐19 m RNA up‐regulation in patients with CRS w NP and showed an up‐regulation of IL ‐19, at lower extent, in patients with chronic rhinosinusitis without nasal polyps ( CRS s NP ) in comparison with normal subjects. Western blot analysis confirmed that IL ‐19 is increased also at protein level in patients with CRS w NP in comparison with normal subjects. In NP , IL ‐19 is highly expressed in the metaplastic nasal epithelium when compared to normal or hyperplastic epithelium. LPS stimulation increased IL ‐19 expression, and recombinant IL ‐19 increased cell proliferation in nasal epithelial cells. Conclusions IL ‐19 is overexpressed in the epithelium in CRS w NP and increases epithelial cell proliferation.