98 Specific IGE and IGG Binding to Allergoids of Phleum pratense
Autor: | Silvia Sanchez-Garcia, Eva Abel Fernandez, Barbara Cases, Jose Ignacio Tudela, Miguel Casanovas, M. Dolores Ibáñez, Enrique Fernández-Caldas, C. Escudero |
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Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
Pulmonary and Respiratory Medicine
biology business.industry Oral Abstract Session Immunology biology.organism_classification Immunoglobulin E medicine.disease_cause Abstracts of the XXII World Allergy Congress Phleum chemistry.chemical_compound Allergen chemistry IgG binding biology.protein medicine Immunology and Allergy Effective treatment Glutaraldehyde business |
Zdroj: | The World Allergy Organization Journal |
ISSN: | 1939-4551 |
Popis: | Background Allergoids were first used in the decades of the 60s and 70s of the last century as an effective treatment of allergic respiratory diseases. Allergoids can be modified with formaldehyde or glutaraldehyde. Modified allergens, or allergoids, decrease the risk of adverse reactions while administering higher allergen doses. The objective of this study was to analyse specific IgE and IgG binding to glutaraldehyde modified and non-modified allergen extracts of Phleum pratense. Methods The sera of 69 patients sensitized to P. pratense were tested. All these patients had signs and symptoms of rhinoconjunctivitis with, or without, asthma in May and June of 2011. All these patients had positive skin prick tests to a standardized extract of P. pratense, and other grass species. Most patients were also sensitized to olive pollen. Specific IgE and IgG binding were analysed by direct ELISA against P. pratense native (non-modified) and allergoid extracts. Relative potencies were evaluated through ELISA inhibition assays, and the protein composition of non-modified and allergoid samples was determined by Mass Spectrometry (MS/MS). Results Mean Specific IgE levels against the native extract was 16.68 ± 11.65 Units (U) and against the allergoid: 7.26 ± 8.24 U (P < 0.0001; Mann-Whitney). On the other hand, mean specific IgG binding against the non-modified extract was 90.34 ± 75.57 U versus 76.19 ± 70.31 U against the allergoid (P = 0.16; Mann-Whitney). Linear regression coefficients obtained between immunoglobulin reactivity against both extracts were: r2 = 0.51 for specific IgE and r2 = 0.83 for specific IgG. An important decrease in the allergenic activity, measured by inhibition ELISA, was clearly observed. The MS/MS assay revealed the presence of the mayor allergen, and some isoforms, in non-modified and allergoid extracts. Conclusions Results obtained demonstrate that the glutaraldehyde polymerization process induces an important decrease in specific IgE binding to allergoids of P. pratense while there are no significant differences in specific IgG binding. The allergenic composition of the P. pratense allergoid was equivalent to the non-modified pollen extract. |
Databáze: | OpenAIRE |
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