Abstract

Eotaxin-2 and regulated on activation normal T cell expressed and secreted (RANTES) are involved in the eosinophil trafficking in patients with persistent allergic rhinitis (PAR). Clara cell protein 16 (CC16) is an anti-inflammatory protein mainly produced by the epithelial non-ciliated Clara cells. The aim of this study was to investigate the production of CC16 and chemokines eotaxin-2 and RANTES in nasal mucosa of patients with PAR. Twenty-one PAR patients and 20 healthy participants were included. CC16, eotaxin-2, and RANTES concentrations were measured in nasal secretions. PAR patients were administered fluticasone furoate nasal spray (220 μg daily for 14 days). We performed nasal cytology, symptom score assessment, and inflammatory mediator detection before and after the therapy. The level of CC16 in patients with PAR was lower than in the healthy subjects (p=0.023). The eosinophil counts and local concentrations of eotaxin-2 and RANTES were higher in patients with PAR in comparison with controls (p=0.008, p=0.001, p=0.031, respectively). We also found a negative correlation between the CC16 and eotaxin-2 levels in nasal secretions of PAR patients (r=-0.492, p=0.023). After corticosteroid therapy, the patients with PAR had lower nasal symptoms, eosinophil counts, eotaxin-2, and RANTES levels and higher levels of CC16 (p<0.001 for all parameters). Our results suggest the presence of a negative correlation in production of CC16 and eotaxin-2 in nasal mucosa of patients with PAR. Intranasal corticosteroids have a suppressive effect on mucosal eosinophilic inflammation and a stimulating effect on local CC16 production.

Highlights

  • Persistent allergic rhinitis (PAR) is a chronic, immunoglobulin E (IgE)-mediated, T helper 2 (Th2)type immune response disease, histologically characterized by intense mucosal infiltration by eosinophils, mucosal hypersecretion, and tissue remodeling [1]

  • The eosinophil counts and local concentrations of eotaxin-2 and RANTES were higher in patients with PAR in comparison with controls (p=0.008, p=0.001, p=0.031, respectively)

  • We found a negative correlation between the Clara cell protein 16 (CC16) and eotaxin-2 levels in nasal secretions of PAR patients (r=−0.492, p=0.023)

Read more

Summary

Introduction

Persistent allergic rhinitis (PAR) is a chronic, immunoglobulin E (IgE)-mediated, T helper 2 (Th2)type immune response disease, histologically characterized by intense mucosal infiltration by eosinophils, mucosal hypersecretion, and tissue remodeling [1]. Eosinophils can directly damage the epithelium of the nasal mucosa by toxic products, such as eosinophil cationic protein (ECP), Perić et al Chemokines and CC16 Production in Nasal Mucosa of PAR Patients 179 mayor basic protein (MBP), and eosinophil peroxidases (EPOs) [2]. These enzymes stimulate the production of epidermal and neural growth factors resulting in hypertrophy and neuronal hyperreactivity of the nasal mucosa [3, 4]. Eotaxin-1, -2, and -3 are strong selective chemokines and they attract only eosinophils via specific CC chemokine receptor 3 (CCR3) [7]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call