Sublingual specific immunotherapy reduces PBMC proliferations

Eur Ann Allergy Clin Immunol. 2005 Apr;37(4):147-51.

Abstract

Background: Subcutaneous specific immunotherapy has been demonstrated capable of inducing T regulatory response. There is few evidence concerning immunological changes induced by sublingual immunotherapy.

Objective: The aim of this study was to evaluate T cell proliferation in subjects successfully treated with SLIT for HDM.

Methods: PBMCs were isolated from patients after at least 3 years of successful HDM SLIT and from matched untreated allergic and healthy control subjects. After 3 and 6 days of in vitro stimulation with PHA, Candida albicans, Dermatophagoides farinae, grasses, Parietaria judaica, and cat, proliferation.

Results: Subjects treated with SLIT showed significant reduction of proliferation induced by Candida albicans, Parietaria, and grasses in comparison with untreated atopics (p=0.0002, 0.0033, and 0.009 respectively).

Conclusion: This pilot study confirms reduced T cell proliferation in allergic subjects treated with SLIT.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Sublingual
  • Allergens / administration & dosage
  • Allergens / immunology
  • Allergens / therapeutic use*
  • Animals
  • Antigens, Dermatophagoides / administration & dosage
  • Antigens, Dermatophagoides / immunology
  • Antigens, Dermatophagoides / therapeutic use
  • Candida albicans / immunology
  • Cats / immunology
  • Dermatophagoides farinae / immunology
  • Desensitization, Immunologic*
  • Female
  • Hair / immunology
  • Humans
  • Leukocytes, Mononuclear / immunology*
  • Lymphocyte Activation*
  • Male
  • Parietaria / immunology
  • Poaceae / immunology
  • Pollen / immunology
  • Rhinitis, Allergic, Perennial / blood
  • Rhinitis, Allergic, Perennial / etiology
  • Rhinitis, Allergic, Perennial / immunology
  • Rhinitis, Allergic, Perennial / therapy*
  • Skin Tests
  • T-Lymphocyte Subsets / immunology
  • Th2 Cells / immunology

Substances

  • Allergens
  • Antigens, Dermatophagoides