
Vol. 136, No. 2, 2005
Free Abstract
Article (Fulltext)
Article (PDF 191 KB)
Original Paper
Lack of Detectable Alterations in Immune Responses during Sublingual Immunotherapy in Children with Seasonal Allergic Rhinoconjunctivitis to Grass Pollen
C. Rolinck-Werninghausa, M. Koppb, C. Liebkea, J. Langeb, U. Wahna, B. Niggemanna
aDepartment of Pediatric Pneumology and Immunology, Charité, Berlin, and bDepartment of Pediatric and Adolescent Medicine, University of Freiburg, Freiburg, Germany
Address of Corresponding Author
Int Arch Allergy Immunol 2005;136:134-141 (DOI: 10.1159/000083320)
Key Words
- Allergy
- Children
- Cytokines
- Grass pollen
- Sublingual immunotherapy
- T cells
Abstract
Background: Recent work indicates that subcutaneous specific immunotherapy induces specific T-cell anergy, a shift in the TH1/TH2 ratio, and antibody production in favor of IgG4. There are few data on sublingual immunotherapy (SLIT), especially in children. Methods: We assessed the proliferation of peripheral blood mononuclear cells (3H-thymidine incorporation) and secretion of interleukin (IL)-4, interferon (IFN) and IL-5 (ELISA) after in vitro stimulation with allergen or phytohemagglutinin (PHA) in 29 children with allergic rhinoconjunctivitis receiving SLIT with grass pollen before, and after 1 and 2 years of treatment in a multicenter placebo-controlled study on the efficacy of the treatment. Further, non-specific intracellular production of IL-4, IL-13, IFN , IL-2, IL-10 and IL-5 (FACS) and serum total and specific IgE and IgG4 (ELISA) were analyzed. Results: Proliferation and IL-4 and IL-5 secretion after stimulation with allergen or PHA did not differ between the groups. In addition, we observed no effect of SLIT on intracellular cytokine production. IFN secretion after allergen coculture was comparable between the groups. Following PHA stimulation, IFN secretion was significantly higher in the SLIT group after 1 year, and a trend was observable already before and after 2 years of treatment, probably due to the inhomogeneity in the groups despite randomization (for age and asthma). No significant changes were observed for sIgE/sIgG4 ratios over time either in or between the groups. Conclusion: During 2 years of SLIT in children with a positive effect on rescue medication use, we observed no significant effects on in vitro T-cell immune responses or immunoglobulins. So far, pediatric studies demonstrating stable effects of SLIT on such reactions are missing, probably due to limited effects of SLIT on systemic immunologic reactions. Copyright © 2005 S. Karger AG, Basel
Author Contacts
Correspondence to: Dr. Bodo Niggemann Department of Pediatric Pneumology and Immunology Charité, Humboldt University, Augustenburger Platz 1 DE-13353 Berlin (Germany) Tel. +49 30 450 566643, Fax +49 30 450 566931, E-Mail bodo.niggemann@charite.de
Article Information
Received: May 19, 2004
Accepted after revision: September 22, 2004
Published online: January 12, 2005
Number of Print Pages : 8
Number of Figures : 1, Number of Tables : 3, Number of References : 39 |
|

|

For non-native English speakers and international authors who would like assistance with their writing before submission, we suggest American Journal Experts for their scientific editing service. |
|
|