花生过敏原的特征和整个发育过程中的过敏性。

IF 3.3 Q2 ALLERGY Frontiers in allergy Pub Date : 2024-08-27 eCollection Date: 2024-01-01 DOI:10.3389/falgy.2024.1395834
Casey G Cohen, Yael Levy, Diana Toscano-Rivero, Ekaterina Manasherova, Nancy Agmon-Levin, Ron S Kenett, Bertrand J Jean-Claude, Bruce D Mazer, Ran Hovav, Mona I Kidon
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引用次数: 0

摘要

导言:儿童花生过敏症(PA)是一个备受关注的问题。诊断和口服免疫疗法(OIT)治疗都需要更好的生物材料。种子在早期生殖阶段的独特状态可能会影响贮藏蛋白的过敏性,并对临床诊断和口服免疫疗法方案产生影响。本研究的目的是评估种子连续发育阶段的主要过敏原含量,并通过特异性 IgE 结合定量和皮肤点刺试验监测过敏性:从花生植株中采集种子,并将其分为五个发育阶段:初始种子(S1)、发育中种子(S2)、未着色的饱满种子(S3)、着色的饱满种子(S4)和完全成熟种子(S5)。通过 RNA-Seq、ELISA 和免疫组化对样本进行鉴定。冻干磨碎的制剂用于评估 60 名经挑战证实的 PA 儿童的皮肤测试反应:结果:在整个种子成熟和发育过程中,过敏原蛋白的基因表达、蛋白含量和特异性 IgE 结合率都在增加。在早期阶段,尤其是在 S2 阶段,发现主要过敏原 Ara h 2 的 A 基因组拷贝的表达偏向于过敏性较低的 A 基因组拷贝。免疫组化染色显示,与 S4 阶段相比,Ara h 2 在 S2 阶段更分散于细胞中,在有组织体中的积累较少。在对 PA 患者进行皮肤点刺试验时,发现商品花生提取物(相当于 S5 阶段)与 S1 和 S2 阶段的平均喘息反应有显著差异,但与 S4 阶段没有差异:讨论:所观察到的未成熟花生种子与花生特异性 IgE 结合力下降的现象,可能不仅是过敏性蛋白质数量减少的结果,也是种子成分和构象发生深刻变化的结果。这可能对开发更安全、更有效的花生 OIT 方案具有重要意义。
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Peanut allergen characterization and allergenicity throughout development.

Introduction: Peanut allergy (PA) in children is a major concern. There is a need for better biological material for both diagnosis and oral immunotherapy (OIT) treatments. The unique state of seeds at early reproductive stages may affect the allergenicity of storage proteins, and impact clinical diagnostic and OIT protocols. The objective of this study was to evaluate the major allergen content in sequential seed developmental stages and monitor allergenicity via specific IgE binding quantification and skin prick testing.

Methods: Seeds were collected from peanut plants and sorted into five developmental stages: initial (S1), developing (S2), full-size without coloration (S3), full-size with coloration (S4), and fully mature (S5) seeds. Samples were characterized by RNA-Seq, ELISA, and immunohistochemistry. Lyophilized, ground preparations were used for evaluation of skin test responses in sixty challenge-proven PA children.

Results: Gene expression, protein content, and specific IgE binding of allergenic proteins increased throughout seed maturation and development. An expression bias towards the less allergenic A-genome copy of the major allergen Ara h 2 was found in earlier stages, especially in stage S2. Immunohistochemical staining showed that Ara h 2 is more dispersed in the cell and less accumulated within organized bodies at stage S2 versus stage S4. Significant differences were found in mean wheal responses between the commercial peanut extract (equivalent to stage S5) and stages S1 and S2, but not with stage S4, upon skin prick testing in subjects with PA.

Discussion: The observed decrease in peanut-specific IgE binding of immature peanut seeds may be a result not only of decreased amounts of allergenic proteins, but also of profound changes in seed composition and conformation. This may be significant for developing a safer and more effective peanut OIT protocol.

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CiteScore
2.80
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0.00%
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12 weeks
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