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Characterization of a 7 kDa pollen allergen belonging to the gibberellin‐regulated protein family from three Cupressaceae species

Authors :
Jonas Lidholm
C. Klingebiel
A. Ehrenberg
Joana Vitte
J. Östling
Lars Mattsson
Håkan Larsson
ThermoFisher Scientific
Thermofisher Scientific
Laboratoire Synlab Provence
Microbes évolution phylogénie et infections (MEPHI)
Institut de Recherche pour le Développement (IRD)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)
Institut Hospitalier Universitaire Méditerranée Infection (IHU Marseille)
Source :
Clinical and Experimental Allergy, Clinical and Experimental Allergy, 2020, ⟨10.1111/cea.13675⟩, Clinical and Experimental Allergy, Wiley, 2020, ⟨10.1111/cea.13675⟩
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

Background Severe allergy to fruits mediated by a 7 kDa allergen belonging to the gibberellin-regulated protein (GRP) family is known to be associated with Cupressaceae pollinosis. Objective To identify and characterize Cupressaceae pollen allergens involved in GRP-related fruit allergy. Methods Pru p 7-related proteins from pollen of Cupressus sempervirens, Juniperus ashei and Cryptomeria japonica were identified using a rabbit anti-Pru p 7 antiserum, purified chromatographically and sequenced by mass spectrometry and bioinformatic comparisons. The C sempervirens protein was produced as a recombinant allergen in Pichia pastoris. IgE antibody binding to pollen GRP proteins was analysed in a peach allergic (n = 54) and a cypress pollen allergic (n = 88) patient population from southern France using ImmunoCAP. Results In each of the three Cupressaceae species studied, a 7 kDa pollen protein related to Pru p 7 was identified and found to comprise an amino acid sequence of 63 residues in length, 92%-98% identical to each other and 67%-68% identical to Pru p 7. The C sempervirens, J ashei and C japonica GRP allergens have been officially recognized by the WHO/IUIS Allergen Nomenclature Sub-Committee and named Cup s 7, Jun a 7 and Cry j 7, respectively. Recombinant Cup s 7 showed IgE antibody binding capacity comparable to that of the purified natural allergen. Among 51 peach allergic subjects sensitized to Pru p 7, substantially higher levels of IgE to Cup s 7 than to Pru p 7 were found. Further, the pollen protein was able to completely outcompete IgE binding to Pru p 7, while the reverse competition effect was modest, consistent with primary sensitization by the pollen allergen. Conclusion and clinical relevance Pru p 7-related pollen allergens from three Cupressaceae species have been characterized and may become useful for the identification of pollinosis patients at risk of developing severe fruit allergy.

Details

Language :
English
ISSN :
09547894 and 13652222
Database :
OpenAIRE
Journal :
Clinical and Experimental Allergy, Clinical and Experimental Allergy, 2020, ⟨10.1111/cea.13675⟩, Clinical and Experimental Allergy, Wiley, 2020, ⟨10.1111/cea.13675⟩
Accession number :
edsair.doi.dedup.....4d942201c664d70942d6367d111b0dcf