Volume 1, Issue S1 O49
Oral Presentation
Open Access

Nitration of ovalbumin decreases the risk for sensitization via the oral route in a mouse food allergy model

Susanne C Diesner

Susanne C Diesner

Department of Pathophysiology and Allergy Research and Department of Pediatrics, Medical University of Vienna, Vienna, Austria

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Eva Untersmayr

Eva Untersmayr

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria

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Gertie J Oostingh

Gertie J Oostingh

Department of Molecular Biology, University of Salzburg, Salzburg, Austria

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Kathrin Selzle

Kathrin Selzle

Max Planck Institute for Chemistry, Biogeochemistry Department, Mainz, Germany

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Tobias Pfaller

Tobias Pfaller

Department of Molecular Biology, University of Salzburg, Salzburg, Austria

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Cornelia Schultz

Cornelia Schultz

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria

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Yingyi Zhang

Yingyi Zhang

Max Planck Institute for Chemistry, Biogeochemistry Department, Mainz, Germany

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Durga Krishnamurthy

Durga Krishnamurthy

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria

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Philipp Starkl

Philipp Starkl

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria

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Regina Knittelfelder

Regina Knittelfelder

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria

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Elisabeth Förster-Waldl

Elisabeth Förster-Waldl

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria

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Arnold Pollak

Arnold Pollak

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria

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Otto Scheiner

Otto Scheiner

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria

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Ulrich Pöschl

Ulrich Pöschl

Max Planck Institute for Chemistry, Biogeochemistry Department, Mainz, Germany

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Erika Jensen-Jarolim

Erika Jensen-Jarolim

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria

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Albert Duschl

Albert Duschl

Department of Molecular Biology, University of Salzburg, Salzburg, Austria

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First published: 12 August 2011

Food Allergy and Anaphylaxis Meeting 2011, Venice, Italy. 17-19 February 2011

Background

Previously, nitration e.g. by ambient pollutants was demonstrated to increase the allergenicity of the major birch pollen allergen Bet v1. As also endogenous nitration during inflammation could influence food protein immunogenicity and contribute to food allergic reactions, we aimed to analyze the impact of protein nitration on sensitization in a murine food allergy model.

Methods and results

BALB/c mice were fed untreated (OVA), sham-nitrated (snOVA) or nitrated ovalbumin (nOVA) with or without concomitant acid-suppression. To analyze systemic effects, mice were injected the allergens intraperitoneally (i.p.). Animals being fed OVA or snOVA with antiacids developed elevated IgE, IgG1 and IgG2a titers. Oral immunizations of nOVA under acid-suppression did not result in IgG and IgE formation. However, all i.p. immunized mice revealed high levels of IgE, which were significantly increased in the group being injected nOVA. In RBL-assays, all groups with OVA-specific IgE showed a significant increased mediator release with nOVA as trigger compared to OVA. To analyze the immune response in the involved organ, gastric tissues were screened for cytokine expression by real-time-PCR. Only the acid-suppressed groups being fed OVA or snOVA revealed a higher expression of Th2 and inflammatory markers. In gastric digestion experiments, nOVA was degraded within minutes, whereas OVA and snOVA remained stable up to 120min. Additionally, HPLC-chip-MS/MS analysis revealed the most efficiently nitrated tyrosine residue within an ovalbumin epitope recognized exclusively after oral immunization.

Conclusion

Despite its enhanced allergenicity nOVA has a reduced oral sensitization potential due to enhanced protein digestibility and/or changes in antibody epitopes.

Acknowledgements

This work was supported by P21577-B11 of the Austrian Science funds FWF.

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