Nasal fluid release of eotaxin-3 and eotaxin-2 in persistent sinonasal eosinophilic inflammation

Int Forum Allergy Rhinol. 2014 Aug;4(8):617-24. doi: 10.1002/alr.21348. Epub 2014 Jul 2.

Abstract

Background: The aim of the present study was to measure eotaxin-3 (CCL26) and eotaxin-2 (CCL24) in nasal lavage fluid of patients with different forms of chronic sinonasal eosinophilic inflammation to evaluate their role in the pathophysiology of nasal hypereosinophilia.

Methods: The study was an analytic cross-section study, level of evidence 3b. Patients (n = 80) with nasal hypereosinophilia were randomly recruited and grouped in the following categories: persistent allergic rhinitis (AR) (n = 25), nonallergic rhinitis with eosinophilia syndrome (NARES) (n = 30), and chronic rhinosinusitis with polyps (CRSwNP) (n = 25). Non-rhinitic volunteers (n = 20) were recruited as controls. CCL24 and CCL26 concentrations were measured by enzyme-linked immunosorbent assay (ELISA) Quantikine Human Immunoassays (R&D Systems, Minneapolis, MN) in nasal lavage fluids. Differential cell counts were performed by microscopic cytological examination of nasal tissue scraped from the inferior turbinate.

Results: Mean CCL26 levels were significantly higher (p < 0.05) in AR and in NARES (132.0 pg/mL and 187.63 pg/mL, respectively) than in the control group (13.5 pg/mL); in patients with CRSwNP, CCL26 values were increased compared to controls even though the difference was not statistically significant (58.9 pg/mL vs 16.5 pg/mL). Mean CCL24 levels measured in AR, NARES, and CRSwNP were significantly increased (p < 0.05) compared to controls (96.7 pg/mL, 135.4 pg/mL, and 107.0 pg/mL, respectively, vs 32.2 pg/mL). Moreover, we observed a significant correlation between CCL24 and CCL26 levels, evaluating them intraindividually by Spearman's rank correlation test. Finally, a significant correlation was found between CCL24 and CCL26 levels and the percentage of eosinophilic infiltration of nasal mucosa.

Conclusion: Our data suggest that CCL26 and CCL24 are likely involved in the pathogenesis of chronic nasal hypereosinophilia, with a complex cooperation and different involvement of the various members of eotaxin family. Further studies are necessary to better understand the actual physiopathologic mechanism, possible clinical relevance, and therapeutic implications.

Keywords: NARES; eotaxin-2; eotaxin-3; nasal polyps; persistent allergic rhinitis.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Chemokine CCL24 / analysis*
  • Chemokine CCL24 / immunology
  • Chemokine CCL26
  • Chemokines, CC / analysis*
  • Chemokines, CC / immunology
  • Chronic Disease
  • Cross-Sectional Studies
  • Eosinophils / immunology*
  • Female
  • Humans
  • Hypereosinophilic Syndrome / immunology*
  • Male
  • Middle Aged
  • Nasal Lavage Fluid / chemistry*
  • Nasal Lavage Fluid / immunology
  • Nasal Mucosa / immunology
  • Nasal Polyps / immunology*
  • Rhinitis, Allergic / immunology*
  • Sinusitis / immunology*
  • Young Adult

Substances

  • CCL26 protein, human
  • Chemokine CCL24
  • Chemokine CCL26
  • Chemokines, CC