The effect of oral steroids with and without vitamin D3 on early efficacy of immunotherapy in asthmatic children

Clin Exp Allergy. 2009 Dec;39(12):1830-41. doi: 10.1111/j.1365-2222.2009.03357.x. Epub 2009 Oct 7.

Abstract

Background: The possibility of additional strategies to enhance the effectiveness of specific immunotherapy (SIT) is highly attractive.

Aim: The aim of our study was to assess the influence of oral corticosteroids and oral corticosteroids combined with vitamin D(3) on the early clinical and immunological effects of SIT.

Methods: It was a randomized, double-blind, placebo-controlled trial conducted in 54 asthmatic children allergic to house dust mites. Intervention was based on receiving a single dose of oral steroid, with or without vitamin D(3), or placebo only on the day of the build-up phase of SIT.

Results: After 12 months of SIT, the median daily inhaled corticosteroid (ICS) dose, which controls the symptoms of asthma, was reduced by 25% in the steroid group. However, a 50% reduction of the median daily ICS dose was observed in the control group. The clinical effects of SIT were not affected in the steroid+D(3) group. Concomitantly, we found that intervention with prednisone significantly impaired the induction of T regulatory lymphocytes. Importantly, the clinical and immunological effects of SIT were not affected by intervention with steroids administered with vitamin D(3).

Conclusions: Our study failed to show a beneficial effect of oral corticosteroids on allergen-specific immunotherapy. We observed that the combined administration of a corticosteroid drug and allergen extract suppressed the early clinical and immunological effects of SIT and that vitamin D(3) prevented this 'adverse' influence of steroids.

Publication types

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

MeSH terms

  • Adrenal Cortex Hormones / administration & dosage
  • Adrenal Cortex Hormones / therapeutic use
  • Animals
  • Antigens, Dermatophagoides / administration & dosage
  • Antigens, Dermatophagoides / immunology
  • Antigens, Dermatophagoides / therapeutic use*
  • Arthropod Proteins
  • Asthma / diagnosis
  • Asthma / immunology
  • Asthma / physiopathology
  • Asthma / therapy*
  • Calcifediol / blood
  • Child
  • Cholecalciferol / administration & dosage
  • Cholecalciferol / therapeutic use*
  • Combined Modality Therapy / methods
  • Dermatophagoides farinae / immunology
  • Dermatophagoides pteronyssinus / immunology
  • Desensitization, Immunologic / methods*
  • Double-Blind Method
  • Female
  • Forced Expiratory Volume / physiology
  • Forkhead Transcription Factors / genetics
  • Gene Expression / genetics
  • Gene Expression / immunology
  • Humans
  • Interleukin-10 / metabolism
  • Interleukin-13 / metabolism
  • Interleukin-5 / metabolism
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Male
  • Prednisone / administration & dosage
  • Prednisone / therapeutic use
  • Steroids / administration & dosage
  • Steroids / therapeutic use*
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / metabolism
  • Transforming Growth Factor beta / metabolism
  • Treatment Outcome

Substances

  • Adrenal Cortex Hormones
  • Antigens, Dermatophagoides
  • Arthropod Proteins
  • Dermatophagoides pteronyssinus antigen p 2
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • IL10 protein, human
  • IL5 protein, human
  • Interleukin-13
  • Interleukin-5
  • Steroids
  • Transforming Growth Factor beta
  • Interleukin-10
  • Cholecalciferol
  • Calcifediol
  • Prednisone