Local allergic rhinitis in children: Novel diagnostic features and potential biomarkers

Am J Rhinol Allergy. 2016 Sep;30(5):329-34. doi: 10.2500/ajra.2016.30.4352.

Abstract

Background: Local allergic rhinitis (LAR) is a phenotype of rhinitis that has been poorly studied in children. It is characterized by the same symptoms of allergic rhinitis but with the absence of markers of systemic atopy.

Objective: To identify children affected by LAR and to analyze the pathogenesis of this disease. We chose to focus our attention on interleukin (IL) and thymic stromal lymphopoietin (TSLP).

Methods: We enrolled 20 children affected by nonallergic rhinitis (negative skin-prick test results and serum specific immunoglobulin E [sIgE] values). Each patient underwent a nasal allergen provocation test (NAPT) with dust mite and grass pollen. Before and after NAPT, nasal lavage was performed to detect sIgE, IL-5, and TSLP; anterior active rhinomanometry was used to evaluate changes in nasal obstruction.

Results: Two patients were positive to a nonspecific NAPT and, thus, were excluded from the study. Of the remaining 18 children, 12 (66.7%) had positive results to at least one NAPT. Among these 12 patients, nasal sIgE levels for Dermatophagoides pteronyssinus, Dermatophagoides farinae, and Lolium perenne increased significantly after NAPT (D. pteronyssinus, p < 0.005; D. farinae, p < 0.05; L. perenne, p < 0.05). Nasal IL-5 levels showed a significant increase after NAPT (p ≤ 0.006), and this increase was significantly higher in children who had positive NAPT results than in those patients with negative NAPT results (p ≤ 0.03). Among the 12 children who had a positive NAPT result, nasal TSLP was detected in 4 patients (33.3%) and its levels showed a relevant increase after NAPT, even though the difference did not reach statistical significance (p ≤ 0.061).

Conclusion: Observed results raise the importance of better refining the diagnostic protocol for LAR in children. Nasal TSLP and IL-5 levels offer new insights concerning localized allergic inflammation, although the role of nasal sIgE has still to be clarified.

MeSH terms

  • Animals
  • Antigens, Dermatophagoides / immunology
  • Biomarkers / metabolism*
  • Child
  • Cytokines / metabolism*
  • Female
  • Humans
  • Immunoglobulin E / metabolism
  • Interleukin-5 / metabolism*
  • Lolium
  • Male
  • Nasal Mucosa / immunology*
  • Nasal Provocation Tests
  • Pollen / immunology
  • Pyroglyphidae
  • Rhinitis, Allergic / diagnosis*
  • Skin Tests
  • Thymic Stromal Lymphopoietin

Substances

  • Antigens, Dermatophagoides
  • Biomarkers
  • Cytokines
  • Interleukin-5
  • Immunoglobulin E
  • Thymic Stromal Lymphopoietin