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Gene gun immunization with clinically relevant allergens aggravates allergen induced pathology and is contraindicated for allergen immunotherapy

Authors :
Scheiblhofer, Sandra
Stoecklinger, Angelika
Gruber, Christina
Hauser-Kronberger, Cornelia
Alinger, Beate
Hammerl, Peter
Thalhamer, Josef
Weiss, Richard
Source :
Molecular Immunology. Mar2007, Vol. 44 Issue 8, p1889-1897. 9p.
Publication Year :
2007

Abstract

Abstract: Gene gun immunization has been associated with the induction of a heterologous type of immune response characterized by a TH1-like immune reaction on the cellular level, i.e. generation of IFN-γ secreting CD8+ T-cells, yet a TH2 biased serology as indicated by high IgG1:IgG2a ratios and induction of IgE. Nevertheless, gene gun immunization using the model molecule β-galactosidase has been argued to prevent IgE induction and to promote TH1 cells with respect to allergy DNA immunization. In our current study, we evaluated the potential of gene gun immunization to prevent type I allergic reactions comparing β-galactosidase with two clinically relevant allergens, and further investigated the effect of gene gun immunization on relevant lung parameters. BALB/c mice were immunized with plasmids encoding the birch pollen allergen Bet v 1, the grass pollen allergen Phl p 5, or the model molecule β-galactosidase, either by gene gun or intradermal injection followed by sensitization and intranasal provocation with the respective allergen. IgG1 and IgG2a antibody titers were determined by ELISA. IgE levels were evaluated in a rat basophil release assay. The severity of eosinophilia was determined in bronchoalveolar lavages, and the overall infiltrate was analyzed by histology on lung paraffin sections. Gene gun immunization induced a TH2-biased immune reaction, which did not prevent from production of IgE after subsequent sensitization. This TH2 effect was influenced by the nature of the antigen, with a more pronounced TH2-bias for the allergens Bet v 1 and Phl p 5 compared to β-galactosidase. Gene gun immunization with all three antigens promoted eosinophil influx into the lung and did not alleviate lung pathology after intranasal provocation. In contrast to needle injection of plasmid DNA, which triggers a clearly TH1-biased and allergy-preventing immune response, gene gun application fails to induce anti-allergic reactions with all tested antigens and is therefore contraindicated for allergen-specific immunotherapy. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01615890
Volume :
44
Issue :
8
Database :
Academic Search Index
Journal :
Molecular Immunology
Publication Type :
Academic Journal
Accession number :
23298822
Full Text :
https://doi.org/10.1016/j.molimm.2006.09.023