Absence of systemic immunologic changes during dose build-up phase and early maintenance period in effective specific sublingual immunotherapy in children

被引:49
作者
Dehlink, E
Eiwegger, T
Gerstmayr, M
Kampl, E
Bohle, B
Chen, KW
Vrtala, S
Urbanek, R
Szépfalusi, Z
机构
[1] Med Univ Vienna, Ctr Physiol & Pathophysiol, Dept Pediat & Juvenile Med, A-1090 Vienna, Austria
[2] Med Univ Vienna, Ctr Physiol & Pathophysiol, Dept Pathophysiol, A-1090 Vienna, Austria
关键词
children; cytokines; ELISA; flow cytometry; Igs; lymphocyte proliferation assay; sublingual immunotherapy;
D O I
10.1111/j.1365-2222.2006.02400.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background Sublingual immunotherapy (SLIT) has been reported to be a safe treatment for inhalant allergies in children. Yet the immunologic mechanisms resulting in clinical improvement are poorly understood. Objective To identify early systemic immunologic changes during the first 8 weeks of clinically effective SLIT to grass pollen, tree pollen or house dust mite in paediatric patients with allergic rhinoconjunctivitis and/or asthma. Methods Peripheral blood mononuclear cells and plasma samples of 13 children with reduced symptoms after 1 year of SLIT were obtained before therapy and at 2 and 8 weeks after the initiation of SLIT. Allergen-specific lymphocyte proliferation assays were performed, and allergen-induced cytokine production (IL-2, IL-4, IL-10, IFN-gamma, and TGF-beta(1)) was measured by ELISA and flow cytometry. Allergen-specific IgE, IgG1, IgG4, and IgA levels in plasma samples were determined in ELISA. Results During the first 8 weeks of successful SLIT, allergen-specific lymphoproliferation (n=13) as well as levels of allergen-specific intracellular (n=8) and secreted cytokines (n=9) did not change significantly. In addition, no alterations in levels of allergen-specific Igs (n=7) were observed. Conclusion We could not find any early systemic immunologic changes during the first 8 weeks of clinically effective SLIT to inhalant allergens in paediatric patients with allergic rhinoconjunctivitis and/or asthma.
引用
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页码:32 / 39
页数:8
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