Long-Term Effect of Sublingual and Subcutaneous Immunotherapy in Dust Mite-Allergic Children With Asthma/Rhinitis: A 3-Year Prospective Randomized Controlled Trial

J Investig Allergol Clin Immunol. 2015;25(5):334-42.

Abstract

Background and objective: Specific allergen immunotherapy is the only treatment modality that might change the natural course of allergic diseases in childhood. We sought to prospectively compare the long-term clinical and immunological effects of sublingual (SLIT) and subcutaneous (SCIT) immunotherapy compared with pharmacotherapy alone.

Methods: In this single-center, prospective randomized controlled trial, 48 children with mild persistent asthma with/without rhinitis, monosensitized to house dust mites (HDMs) were followed for 3 years. At baseline and years 1 and 3 of follow-up, patients were evaluated and compared for total rhinitis (TRSS) and asthma (TASS) symptom scores, total symptom scores (TSS), total medication scores (TMS), safety profiles, skin-nasal-bronchial reactivity, and immunological parameters.

Results: A significant reduction was observed in TASS for both HDM-SCIT and HDM-SLIT at year 3 of treatment compared with baseline and controls (P<.05 for both), with significant improvement in rhinitis symptoms for both groups compared with controls (P=.01 for both). TSS decreased significantly in both HDM-SCIT and HDM-SLIT at year 3 compared with baseline (P=.007 and P=.04, respectively) and controls (P<.01 for both). A significant reduction in TMS was observed in HDM-SCIT and HDM-SLIT compared with baseline and controls (P=.01 in all cases), with a reduction in skin reactivity to HDM (P<.05). Finally, a significant increase in allergen specific IgG4 was observed in the SCIT group at year 3 compared with baseline, the SLIT group, and controls (P<.001 in all cases).

Conclusions: HDM-sensitized asthmatic children treated for at least 3 years with either SCIT or SLIT showed sustained clinical improvement.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Asthmatic Agents / therapeutic use*
  • Antigens, Dermatophagoides / immunology
  • Arthropod Proteins / immunology
  • Asthma / complications
  • Asthma / immunology
  • Asthma / therapy*
  • Child
  • Cysteine Endopeptidases / immunology
  • Desensitization, Immunologic / methods
  • Female
  • Forced Expiratory Volume
  • Humans
  • Hypersensitivity / complications
  • Hypersensitivity / immunology
  • Hypersensitivity / therapy
  • Immunoglobulin E / immunology
  • Immunoglobulin G / immunology
  • Injections, Subcutaneous
  • Interferon-gamma / immunology
  • Interleukin-10 / immunology
  • Interleukin-5 / immunology
  • Leukocytes, Mononuclear / immunology
  • Longitudinal Studies
  • Male
  • Pyroglyphidae / immunology*
  • Rhinitis, Allergic / complications
  • Rhinitis, Allergic / immunology
  • Rhinitis, Allergic / therapy*
  • Sublingual Immunotherapy / methods*
  • Treatment Outcome

Substances

  • Anti-Asthmatic Agents
  • Antigens, Dermatophagoides
  • Arthropod Proteins
  • Dermatophagoides pteronyssinus antigen p 2
  • IL10 protein, human
  • IL5 protein, human
  • Immunoglobulin G
  • Interleukin-5
  • Interleukin-10
  • Immunoglobulin E
  • Interferon-gamma
  • Cysteine Endopeptidases
  • Dermatophagoides pteronyssinus antigen p 1