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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

Authors :
Hayen, S.M.
Ehlers, A.M.
den Hartog Jager, C.F.
Garssen, J.
Knol, E.F.
Knulst, A.C.
Suer, W.
Willemsen, L.E.M.
Otten, H.G.
Afd Pharmacology
Pharmacology
Afd Pharmacology
Pharmacology
Source :
Clinical and Experimental Allergy, 48(7), 890. Blackwell Publishing Ltd, Clinical and Experimental Allergy, 48(7), 890. Wiley-Blackwell
Publication Year :
2018

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.

Subjects

Subjects :
Models, Molecular
0301 basic medicine
double blind procedure
Protein Conformation
Fibrinogen receptor
HLA DR antigen
Basophil
Immunoglobulin E
Cell Degranulation
Epitope
law.invention
immunoglobulin E
Epitopes
basophil
0302 clinical medicine
law
Protein Isoforms
Immunology and Allergy
heterocyclic compounds
receptor type tyrosine protein phosphatase C
Allergens and epitopes
Non-U.S. Gov't
comparative study
peanut extract
epitope
clinical article
biology
predictive value
Chemistry
adult
Research Support, Non-U.S. Gov't
article
food and beverages
peanut allergy
Middle Aged
Basophils
unclassified drug
trypsin
medicine.anatomical_structure
CD123 antigen
female
priority journal
allergenicity
ara h 7 isoform
sequence alignment
Recombinant DNA
isoprotein
lipids (amino acids, peptides, and proteins)
blood sampling
diagnostic accuracy
IgE
immunoblotting
2S Albumins, Plant
amino acid substitution
cross linking
Immunology
Research Support
Basophil degranulation
Structure-Activity Relationship
03 medical and health sciences
male
fibrinogen receptor
Food allergy
medicine
Journal Article
Humans
Peanut Hypersensitivity
controlled study
Amino Acid Sequence
human
albumin
hydrophobicity
food allergy
carboxy terminal sequence
nonhuman
basophil degranulation
human cell
pepsin A
prediction
sequence homology
Antigens, Plant
biochemical phenomena, metabolism, and nutrition
Molecular biology
carbohydrates (lipids)
Basophil activation
030104 developmental biology
allergens and epitopes
030228 respiratory system
basophil activation test
biology.protein
ara h 6 isoform
Blood sampling

Details

Language :
English
ISSN :
09547894
Database :
OpenAIRE
Journal :
Clinical and Experimental Allergy, 48(7), 890. Blackwell Publishing Ltd, Clinical and Experimental Allergy, 48(7), 890. Wiley-Blackwell
Accession number :
edsair.doi.dedup.....7db62e7697cbe871aa669483d9380c1d