IgE cross-inhibition between Ara h 1 and Ara h 2 is explained by complex formation of both major peanut allergens

被引:5
|
作者
Warmenhoven, Hans J. M. [1 ,2 ]
Hulsbos, Luuk [1 ]
Dreskin, Stephen C. [3 ]
Akkerdaas, Jaap H. [2 ]
Versteeg, Serge A. [2 ]
van Ree, Ronald [2 ,4 ,5 ]
机构
[1] HAL Allergy, JH Oortweg, Leiden, Netherlands
[2] Amsterdam Univ Med Ctr, Dept Expt Imnol, Amsterdam, Netherlands
[3] Univ Colorado Denver, Dept Med, Div Allergy & Clin Immunol, Aurora, CO USA
[4] Amsterdam Univ Med Ctr, Dept Otorhinolaryngol, Amsterdam, Netherlands
[5] Amsterdam Univ Med Ctr, Dept Expt Immunol, Locat AMC, Meibergdreef 9, Amsterdam, Netherlands
关键词
Peanut allergens; Ara h 1; Ara h 2; cross-reactivity; impurities; GEOGRAPHICAL LOCATION; MUTATIONAL ANALYSIS; CRYSTAL-STRUCTURE; BINDING EPITOPES; FOOD ALLERGY; TIME TRENDS; PREVALENCE; REACTIVITY; CHILDREN; IDENTIFICATION;
D O I
10.1016/j.jaci.2023.03.025
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Surprisingly, IgE cross-reactivity between the major peanut allergens Ara h 1, 2, and 3 has been reported despite very low sequence identities.Objective: We investigated the unexpected cross-reactivity between peanut major allergens.Methods: Cross-contamination of purified natural Ara h 1, 2, 3, and 6 was assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), Western blot test, liquid chromatography-tandem mass spectrometry (LC-MS/MS), and sandwich enzyme-linked immunosorbent assay (ELISA). IgE cross reactivity was studied with sera of peanut-allergic patients (n 543) by ELISA and ImmunoCAP inhibition using both intact natural and recombinant allergens and synthetic peptides representing postulated Ara h 1 and Ara h 2 cross-reactive epitopes.Results: Both purified nAra h 1 and nAra h 3 were demonstrated to contain small but significant amounts of Ara h 2 and Ara h 6 (<1%) by sandwich ELISA, SDS-PAGE/Western blot analysis, and LC-MS/MS. IgE cross-inhibition between both 2S albumins and Ara h 1 and Ara h 3 was only observed when using natural purified allergens, not recombinant allergens or synthetic peptides. Apparent cross-reactivity was lost when purified nAra h 1 was pretreated under reducing conditions, suggesting that Ara h 2 and Ara h 6 contaminations may be covalently bound to Ara h 1 via disulfide interactions.Conclusion: True cross-reactivity of both peanut 2S albumins with Ara h 1 and Ara h 3 could not be demonstrated. Instead, cross-contamination with small quantities was shown to be sufficient to cause significant cross-inhibition that can be misinterpreted as molecular cross-reactivity. Diagnostic tests using purified nAra h 1 and nAra h 3 can overestimate their importance as major allergens as a result of the presence of contaminating 2S albumins, making recombinant Ara h 1 and Ara h 3 a preferred alternative. (J Allergy Clin Immunol 2023;152:436-44.)
引用
收藏
页码:436 / 444.e6
页数:15
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