Volume 125, Issue 3 , Pages 711-718.e2, March 2010
Naturally processed T cell–activating peptides of the major birch pollen allergen
Background
Although antigen processing and presentation of allergens to CD4+T lymphocytes are key events in the pathophysiology of allergic disorders, they still remain poorly understood.
Objective
To investigate allergen processing and presentation by dendritic cells using the major birch pollen allergen Bet v 1 as a model.
Methods
Endolysosomal extracts of dendritic cells derived from patients with birch pollen allergy were used to digest Bet v 1. Dendritic cells were pulsed with Bet v 1, and peptides were eluted from MHC class II molecules. Peptides obtained by either approach were sequenced by tandem mass spectrometry. Bet v 1–specific T-cell cultures were stimulated with HLA-DR–eluted Bet v 1–derived peptides. Bet v 1–specific T-cell lines were generated from each patient and analyzed for epitope recognition.
Results
A high proportion of Bet v 1 remained intact for a long period of endolysosomal degradation. The peptides that appeared early in the degradation process contained frequently recognized T-cell epitopes. Bet v 1–derived peptides eluted from MHC class II molecules corresponded to those generated by endolysosomal degradation, matched known T-cell epitopes, and showed T cell–activating capacity. The Bet v 1–specific T-cell line of each individual harbored T cells reactive with peptides located within the MHC class II–eluted Bet v 1–derived sequences demonstrating their occurrence in vivo.
Conclusion
We report for the first time how epitopes of allergens are generated and selected for presentation to T lymphocytes. The limited susceptibility of Bet v 1 to endolysosomal processing might contribute to its high allergenic potential.
Key words: Birch pollen allergy, Bet v 1, antigen processing, antigen presentation, dendritic cells, T cells, T-cell epitopes
Abbreviations used: aa, Amino acid, APC, Antigen-presenting cell, cpm, Counts per minute, DC, Dendritic cell, SI, Stimulation index, TCC, T-cell clone, TCL, T-cell line
Supported by P10150 of the Österreichische Nationalbank, the Christian Doppler Laboratory for Allergy Diagnosis and Therapy, and the Christian Doppler Laboratory for Immunomodulation, Austria.
Disclosure of potential conflict of interest: F. Ferreira has received research support from Biomay AG, the Austrian Science Fund, the Christian Doppler Research Association, and the Austrian National Bank and has provided legal consultation services or expert witness testimony relevant to Indoor Biotechnologies and AllergenOnline Database. B. Bohle has received research support from the Austrian Science Fund and the Christian Doppler Laboratory. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(09)01629-7
doi:10.1016/j.jaci.2009.10.052
© 2010 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 125, Issue 3 , Pages 711-718.e2, March 2010
