诊断聚乙二醇和聚山梨醇酯80过敏的挑战:对COVID-19 mRNA疫苗接种计划过敏反应的影响:来自卡塔尔的经验

IF 3.3 Q2 ALLERGY
Frontiers in allergy Pub Date : 2025-01-07 eCollection Date: 2024-01-01 DOI:10.3389/falgy.2024.1502285
Sami Aqel, Sherin Thalappil, Asaad Imameldin, Dalal Mudawi, Muna Al Maslamani, Abdullatif Al-Khal, Hassan Mobayed, Maryam Ali Al-Nesf, Tayseer Ibrahim
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引用次数: 0

摘要

导论:COVID-19疫苗接种一直是减轻症状严重程度的关键干预措施;然而,对疫苗安全性的担忧,特别是对过敏反应的担忧,很早就出现了。卫生保健工作者面临着解决这些问题以确保安全接种疫苗的挑战。本研究旨在回顾在mRNA - COVID-19疫苗接种后出现过敏反应史的患者中对COVID-19疫苗辅料进行过敏皮肤试验的实际方面。方法:回顾性分析卡塔尔多哈哈马德医疗公司成人过敏和免疫服务部COVID-19疫苗接种后报告过敏反应并接受COVID-19疫苗辅料过敏皮肤试验的患者的图表。测试方案是根据大流行期间公布的数据制定的,包括使用含有聚山梨酸酯80和聚乙二醇(PEG)的药物进行皮肤点刺(SPT)和皮内(ID)测试,这两种药物是疑似引发过敏反应的COVID-19疫苗的主要辅料。结果:在88例患者中,38例报告了mRNA - COVID-19疫苗接种后不同类型的过敏反应,其中大多数为女性。21.1%的患者出现过敏反应,其余患者出现较轻的过敏反应。所有患者均采用聚乙二醇和聚山梨酯80进行SPT和ID检测。经SPT检测,两例患者PEG阳性,聚山梨酯80阴性。经鉴定,7人聚山梨酯80阳性,1人聚乙二醇阳性。在发生过敏反应的患者中,50%的过敏试验结果呈阳性。23%检测结果为阴性的患者可以接受额外的疫苗剂量,而不会出现不良反应。结论:对有COVID-19疫苗过敏反应史的患者进行管理具有挑战性,因为其确切机制和准确有效的过敏测试尚未确定。在我们的队列中,大多数患者在接种疫苗后出现轻度过敏反应。赋形剂过敏皮肤试验有助于减少疫苗犹豫,尽管其在临床实践中的效用值得怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Challenges in diagnosing polyethylene glycol and polysorbate 80 allergies: implications for allergic reactions in COVID-19 mRNA vaccination program: experience from Qatar.

Introduction: COVID-19 vaccination has been a key intervention in reducing the severity of symptoms; however, concerns about vaccine safety, particularly regarding allergic reactions, arose early on. Healthcare workers faced the challenge of addressing these concerns to ensure safe vaccine administration. This study aimed to review the practical aspects of using allergy skin testing for COVID-19 vaccine excipients in patients with a history of allergic reactions developed following mRNA COVID-19 vaccination.

Methods: A retrospective chart review was conducted for patients who reported allergic reactions after the COVID-19 vaccine and underwent allergy skin testing for COVID-19 vaccine excipients in the Adult Allergy and Immunology Service at Hamad Medical Corporation, Doha, Qatar. The testing protocol, developed based on published data during the pandemic, included skin prick (SPT) and intradermal (ID) testing using medications containing polysorbate 80 and polyethylene glycol (PEG), the primary excipients in the COVID-19 vaccines suspected of triggering allergic responses.

Results: Of the 88 patients reviewed, 38 reported different types of allergic reactions following mRNA COVID-19 vaccination, with the majority being female. Anaphylaxis was reported in 21.1% of the patients, while the remaining experienced less severe allergic reactions. All patients underwent SPT and ID testing with PEG and polysorbate 80. By SPT, two patients tested positive for PEG and none for polysorbate 80. By ID, seven tested positive for polysorbate 80 and one for PEG. Among patients who experienced anaphylaxis, 50% had positive allergy test results. Twenty-three percent of patients with negative test results could receive additional vaccine doses without adverse reactions.

Conclusion: Managing patients with a history of allergic reactions to the COVID-19 vaccine is challenging, as the exact mechanisms and accurate and valid allergy testing are yet to be determined. In our cohort, most patients had mild allergic reactions following vaccination. Excipients' allergy skin testing has helped to reduce vaccine hesitancy despite its questionable utility in clinical practice.

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