2S protein Ara h 7.0201 has unique epitopes compared to other Ara h 7 isoforms and is comparable to 2S proteins Ara h 2 and 6 in basophil degranulation capacity

S.M. Hayen, A.M. Ehlers, C.F. den Hartog Jager, J. Garssen, E.F. Knol, A.C. Knulst, W. Suer, L.E.M. Willemsen, H.G. Otten

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: Screening for specific IgE against 2S albumin proteins Ara h 2 and 6 has good positive predictive value in diagnosing peanut allergy. From the third 2S member Ara h 7, 3 isoforms have been identified. Their allergenicity has not been elucidated. Objective: This study investigated the allergenicity of Ara h 7 isoforms compared to Ara h 2 and 6. Methods: Sensitization of 15 DBPCFC-confirmed peanut-allergic patients to recombinant Ara h 2.0201, Ara h 6.01 and isoforms of recombinant Ara h 7 was determined by IgE immunoblotting strips. A basophil activation test (BAT) was performed in 9 patients to determine IgE-cross-linking capacities of the allergens. Sensitivity to the allergens was tested in 5 patients who were sensitized to at least 1 Ara h 7 isoform, by a concentration range in the BAT. 3D prediction models and sequence alignments were used to visualize differences between isoforms and to predict allergenic epitope regions. Results: Sensitization to Ara h 7.0201 was most frequent (80%) and showed to be equally potent as Ara h 2.0201 and 6.01 in inducing basophil degranulation. Sensitization to Ara h 7.0201 together with Ara h 2.0201 and/or 6.01 was observed, indicating the presence of unique epitopes compared to the other 2 isoforms. Differences between the 3 Ara h 7 isoforms were observed in C-terminal cysteine residues, pepsin and trypsin cleavage sites and 3 single amino acid substitutions. Conclusion & clinical relevance: The majority of peanut-allergic patients are sensitized to isoform Ara h 7.0201, which is functionally as active as Ara h 2.0201 and 6.01. Unique epitopes are most likely located in the C-terminus or an allergenic loop region which is a known allergenic epitope region for Ara h 2.0201 and 6.01. Due to its unique epitopes and allergenicity, it is an interesting candidate to improve the diagnostic accuracy for peanut allergy.
Original languageEnglish
Pages (from-to)890-897
Number of pages8
JournalClinical and Experimental Allergy
Volume48
Issue number7
DOIs
Publication statusPublished - 1 Jul 2018

Keywords

  • allergens and epitopes
  • basophil
  • food allergy
  • IgE
  • albumin
  • ara h 6 isoform
  • ara h 7 isoform
  • CD123 antigen
  • epitope
  • fibrinogen receptor
  • HLA DR antigen
  • immunoglobulin E
  • isoprotein
  • peanut extract
  • pepsin A
  • receptor type tyrosine protein phosphatase C
  • trypsin
  • unclassified drug
  • adult
  • allergenicity
  • amino acid substitution
  • article
  • basophil activation test
  • basophil degranulation
  • blood sampling
  • carboxy terminal sequence
  • clinical article
  • comparative study
  • controlled study
  • cross linking
  • diagnostic accuracy
  • double blind procedure
  • female
  • human
  • human cell
  • hydrophobicity
  • immunoblotting
  • male
  • nonhuman
  • peanut allergy
  • prediction
  • predictive value
  • priority journal
  • sequence alignment
  • sequence homology

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