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在高血清流行的地中海环境中使用综合诊断算法诊断异尖线虫过敏。

Use of a comprehensive diagnostic algorithm for Anisakis allergy in a high seroprevalence Mediterranean setting.

机构信息

Clinical Pathology Buccheri La Ferla Hospital, Palermo, Italy.

National Reference Centre for Anisakiasis, Istituto Zooprofilattico Sperimentale della Sicilia A. Mirri, Palermo, Italy.

出版信息

Eur Ann Allergy Clin Immunol. 2020 May;52(3):131-141. doi: 10.23822/EurAnnACI.1764-1489.118. Epub 2020 May 5.

Abstract

Diagnosis of anisakis allergy (AA) is based on the skin prick test (SPT) and specific IgE (sIgE) determination. Anyway, false positivity cases are due to cross reactivity with numerous allergens. The aim of the study was to evaluate the reliability of a comprehensive diagnostic algorithm for the AA. An observational study was conducted on a sample of consecutive subjects accessing the allergology outpatient ambulatories of two hospitals located in Western Sicily. All the recruited outpatients were tested by Skin Prick Test performed using anisakis extracts by ALK-Abellò (Madrid, Spain). Specific IgE dosage for anisakis extracts was then performed by using ImmunoCAP250 (Immunodiagnostics Uppsala, Sweden). Consequently, outpatients who tested positive to first line tests underwent sIgE testing for ascaris and tropomyosin. Lastly, outpatients positive to the first line were invited to be further tested by basophil activation test (BAT) by using Flow CAST kit and anisakis commercial extract (Bühlmann Laboratories AG, Schönenbuch, Switzerland), as confirmatory analysis. One hundred and eleven outpatients with an anamnesis suggestive of sensitization to anisakis (AS) and 466 subjects with chronic urticaria (CU) were recruited in the study. Of these, 22 with AS and 41 with CU showed a sensitization to anisakis allergens. The diagnostic algorithm revealed that 8.8% of outpatients who tested positive to sIgE determination were affected by CU, while 82.5% of all the sIgE positivity was related to cross-reactivity. Overall, a genuine anisakis seroprevalence of 2.3% was documented. Within a sub-sample of 15 subjects with clinical symptoms related to AA, n. 8 showed a real positivity after BAT. A greater response to A. pegreffii allergens as compared to A. simplex was reported. Our preliminary findings support the high clinical specificity of BAT for AA diagnosis, suggesting implementing this method in a comprehensive diagnostic algorithm.

摘要

嗜酸性粒细胞性食管炎(EoE)的诊断基于皮肤点刺试验(SPT)和特异性 IgE(sIgE)测定。然而,假阳性病例是由于与许多过敏原的交叉反应引起的。本研究旨在评估一种用于嗜酸性粒细胞性食管炎(AA)诊断的综合诊断算法的可靠性。在位于西西里岛西部的两家医院的过敏门诊,对连续就诊的患者进行了一项观察性研究。所有入组的患者均接受了使用来自西班牙马德里的 ALK-Abellò的嗜酸性粒细胞性食管炎提取物进行的皮肤点刺试验。然后使用 ImmunoCAP250(瑞典 Uppsala 的 Immunodiagnostics)对嗜酸性粒细胞性食管炎提取物进行特异性 IgE 定量检测。随后,对一线检测呈阳性的患者进行了蛔虫和肌球蛋白的 sIgE 检测。最后,对一线检测呈阳性的患者,通过使用 Flow CAST 试剂盒和嗜酸性粒细胞性食管炎商业提取物(瑞士 Schönenbuch 的 Bühmann Laboratories AG)进行嗜酸性粒细胞活化试验(BAT)作为确认分析,邀请他们进一步进行检测。本研究共纳入 111 例有嗜酸性粒细胞性食管炎致敏史(AS)和 466 例慢性荨麻疹(CU)的患者。其中,22 例 AS 和 41 例 CU 患者对嗜酸性粒细胞性食管炎过敏原呈过敏反应。该诊断算法显示,8.8%的 sIgE 检测呈阳性的患者患有慢性荨麻疹,而所有 sIgE 阳性的 82.5%与交叉反应有关。总体而言,记录到真正的嗜酸性粒细胞性食管炎血清流行率为 2.3%。在与嗜酸性粒细胞性食管炎相关的临床症状的亚样本中,15 例患者中有 8 例在 BAT 后显示真正的阳性。报告称,与 A. simplex 相比,A. pegreffii 过敏原的反应更大。我们的初步研究结果支持嗜酸性粒细胞活化试验(BAT)对嗜酸性粒细胞性食管炎(AA)诊断的高临床特异性,建议将该方法纳入综合诊断算法中。

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