鲑鱼籽过敏患者鲑鱼籽与鳕鱼籽临床交叉反应的血清学检查。

Kaoru Okamoto, Yoichi Nakajima, Tetsushi Yoshikawa, Yasuto Kondo
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引用次数: 0

摘要

目的:鱼籽在日本是一种常见的过敏原。我们之前报道过,虽然来自鲑鱼籽(SR)或鳕鱼籽(PR)过敏患者的免疫球蛋白(IgE)交叉反应,但70%的SR过敏患者可以食用PR而不会出现任何症状。然而,临床交叉反应性和血清学交叉反应性之间的相关性仍有待证实。方法:对15例曾食用过熟PR的SR过敏患者进行血清采集。在这些志愿者中,有四人在食用煮熟的PR后立即出现症状,而其他人没有表现出PR过敏症状。采用竞争性酶联免疫吸附试验(ELISA)分析SR和PR的血清学交叉反应性。使用SR或PR提取物预孵育的血清样品进行免疫印迹抑制试验。结果:在elisa中,SR和PR两种过敏症患者的血清样品与PR提取物预孵育后,与SR的结合抑制率>50% (p=0.0256)。在免疫blots中,用PR提取物预先培养血清样品抑制了16-kDa蛋白的检测,该蛋白可能与SR过敏原的主要成分β′相对应,在SR和PR过敏患者的样品中(100%)明显高于仅SR过敏患者的样品(18.2%)(p=0.011)。结论:SR和PR过敏患者血清对PR的竞争结合优于对SR的竞争结合,可能导致SR和PR的临床交叉反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Serological examination for clinical cross-reactivity between salmon roe and pollock roe in patients with a salmon roe allergy.

Serological examination for clinical cross-reactivity between salmon roe and pollock roe in patients with a salmon roe allergy.

Serological examination for clinical cross-reactivity between salmon roe and pollock roe in patients with a salmon roe allergy.

Objectives: Fish roe is a common allergen in Japan. We have previously reported that although immunoglobulin (IgE) from patients with salmon roe (SR) or pollock roe (PR) allergies cross-react, 70% of patients with SR allergy can consume PR without developing any symptoms. However, a correlation between clinical cross-reactivity and serological cross-reactivity remains to be demonstrated.

Methods: Serum samples were collected from 15 patients with SR allergy who had consumed cooked PR previously. Among these volunteers, four had experienced immediate symptoms after consuming cooked PR, while the others had exhibited no symptoms of PR allergy. A competitive enzyme-linked immunosorbent assay (ELISA) was performed to analyze the serological cross-reactivity with SR and PR. Immunoblotting inhibition assays were performed using serum samples that had been pre-incubated with SR or PR extracts.

Results: In ELISAs, binding to SR was inhibited by >50% when the serum samples from patients with both SR and PR allergies were pre-incubated with PR extract (p=0.0256). In immunoblots, pre-incubation of serum samples with PR extract inhibited detection of the 16-kDa protein, which likely corresponds to the major SR allergen beta' component, significantly more for samples from patients with both SR and PR allergies (100%) than for samples from those with only an SR allergy (18.2%) (p=0.011).

Conclusions: The superior competitive binding of the sera from patients with both SR and PR allergies to PR compared with that to SR may induce clinical cross-reactivity between SR and PR.

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