Taxanes hypersensitivity is not a risk factor for severe reactions to SARS-CoV-2 vaccines.

IF 2.6 Q2 ALLERGY
G Cortellini, A Raiteri, B Biagioni, S Liberati, D Lippolis, G Cortellini, F Piscaglia
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Abstract

Summary: Background. Hypersensitivity reactions (HSR) to taxanes have been related to a complement activation by their excipients, polyoxyethylated castor oil and Polysorbate 80, structurally related to those of SARS-CoV-2 vaccines. The aim of this study was to verify the presence of a higher risk of HSR to SARS-CoV-2 vaccines in patients with history of HSR to taxanes. Methods. Patients with history of HSR to taxanes were evaluated before the vaccination in our center and underwent skin tests for PEG and Polysorbate 80 (PandP). Some patients completed the vaccination course in other centers without prior PandP skin tests because they had not manifested taxanes hypersensitivity before vaccination, or because those tests were not available. Results. 50 patients were evaluated. 100% of patients with history of hypersensitivity to taxanes completed the vaccine course with no cases of anaphylaxis. 33 underwent skin tests for PandP before the vaccination and no correlation was found between the positivity of PandP and taxanes skin tests (p = 0.538). 7 patients developed mild symptoms during skin tests and vaccination, similar but weaker than those suffered at the time of the taxane infusion, independently from the results of skin tests. Conclusions. In our cohort patients with history of reaction to taxanes were not at higher risk to develop anaphylaxis to SARS-CoV-2 vaccines. However, a common non-IgE mediated mechanism behind those HSRs cannot be completely excluded. This can only account for mild and harmless symptoms in case of SARS-CoV-2 vaccines. However, prudence is still recommended in these patients.

紫杉烷超敏反应不是严重急性呼吸系统综合征冠状病毒2型疫苗严重反应的风险因素。
摘要:背景。对紫杉烷的超敏反应(HSR)与其赋形剂聚氧乙烯蓖麻油和聚山梨醇酯80的补体激活有关,在结构上与严重急性呼吸系统综合征冠状病毒2型疫苗有关。本研究的目的是验证有紫杉烷HSR病史的患者是否存在更高的严重急性呼吸系统综合征冠状病毒2型疫苗HSR风险。方法。在我们中心接种疫苗之前,对有紫杉烷HSR病史的患者进行了评估,并接受了PEG和聚山梨酯80(PandP)的皮肤测试。一些患者在其他中心完成了疫苗接种过程,之前没有进行PandP皮肤测试,因为他们在接种疫苗前没有表现出紫杉烷超敏反应,或者因为这些测试不可用。后果对50例患者进行了评估。100%有紫杉烷超敏反应史的患者完成了疫苗疗程,没有出现过敏反应。33名患者在接种疫苗前接受了PandP皮肤测试,PandP阳性与紫杉烷皮肤测试之间没有相关性(p=0.538)。7名患者在皮肤测试和接种疫苗期间出现了轻微症状,与紫杉烷输注时的症状相似但较弱,与皮肤测试结果无关。结论。在我们的队列中,有紫杉烷反应史的患者对严重急性呼吸系统综合征冠状病毒2型疫苗发生过敏反应的风险并不高。然而,不能完全排除这些HSV背后常见的非IgE介导的机制。这只能解释严重急性呼吸系统综合征冠状病毒2型疫苗的轻微无害症状。然而,仍建议这些患者谨慎治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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