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A novel approach in allergen-specific immunotherapy: Combination of sublingual and subcutaneous routes - 30/09/11

Doi : 10.1016/j.jaci.2011.04.033 
Sevgi Keles, MD a, , Elif Karakoc-Aydiner, MD a, Ahmet Ozen, MD b, Ayse Gul Izgi, MS a, Ayzer Tevetoglu, MS a, Tunc Akkoc, PhD a, Nerin N. Bahceciler, MD a, Isil Barlan, MD a
a Division of Pediatric Allergy and Immunology, Marmara University, Istanbul, Turkey 
b Division of Pediatric Allergy and Immunology, Yeditepe University, Istanbul, Turkey 

Corresponding author: Sevgi Keles, MD, Marmara University, Division of Pediatric Allergy and Immunology, Tophanelioglu cad No 13-15, Altunizade 34660, Istanbul, Turkey.

Abstract

Background

Subcutaneous allergen-specific immunotherapy (SIT) has an early onset of action, whereas repeated injections and safety concerns have limited its use in the pediatric age group. Meanwhile, the improved safety profile of the sublingual route has been accepted as an alternative despite its relatively late onset of action.

Objective

We sought to improve the efficacy and safety of SIT with a combination of the subcutaneous route in the build-up phase and sublingual maintenance in comparison with the sublingual or subcutaneous routes alone.

Methods

Fifty-one house dust mite–sensitized children with mild-to-moderate asthma were randomized into one of 4 groups to receive either (1) subcutaneous immunotherapy (SCIT), (2) sublingual immunotherapy (SLIT), (3) SCIT plus SLIT, or (4) pharmacotherapy. Clinical parameters were evaluated at baseline and months 1, 4, 12, and 18. Allergen-specific immunoglobulin levels and allergen-induced IL-5, IL-10, IL-13, IL-17, TGF-β, and IFN-γ levels were evaluated as well.

Results

In the SCIT and SCIT plus SLIT groups, the number of asthma attacks and inhaled corticosteroid dosage decreased compared with baseline values at the months 4, 12, and 18 but only at month 12 in the SLIT group. The improvement in visual analog scores for rhinitis was significant only in the SCIT plus SLIT group. Increases in the levels of regulatory and TH1 cytokines were observed both in the SCIT and SLIT groups, with some differences in dynamics. Antigen-specific IgG4 levels increased in the SCIT and SCIT plus SLIT groups but not in the SLIT group. Clinical symptom scores were correlated positively with IL-5 levels and negatively with antigen-specific IgG4, IFN-γ, and TGF-β levels.

Conclusion

Our novel regimen of immunotherapy, SCIT plus SLIT, appeared promising in that it successfully combined the advantages of the 2 alternatives: rapid onset and potency in SCIT and safety and avoidance of injections in SLIT.

El texto completo de este artículo está disponible en PDF.

Key words : Children, cytokine, Der p 1, subcutaneous immunotherapy, sublingual immunotherapy

Abbreviations used : ASNPT, HDM, ICS, MSA, MSR, NSBPT, SCIT, SIT, SLIT, SSA, SSR, TMS, VAS


Esquema


 Supported by the Marmara University Scientific Research Committee (SAG-C-TUP-030408-0072).
 Disclosure of potential conflict of interest: The authors have declared that they have no conflict of interest.


© 2011  American Academy of Allergy, Asthma & Immunology. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
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Vol 128 - N° 4

P. 808 - octobre 2011 Regresar al número
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