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新型冠状病毒肺炎疫苗过敏:最新进展

Allergy to COVID-19 vaccines: A current update.

作者信息

Cabanillas Beatriz, Novak Natalija

机构信息

Department of Allergy, Research Institute Hospital 12 de Octubre, Madrid, Spain.

Department of Dermatology and Allergy, University Hospital Bonn, Bonn, Germany.

出版信息

Allergol Int. 2021 Jul;70(3):313-318. doi: 10.1016/j.alit.2021.04.003. Epub 2021 Apr 23.

DOI:10.1016/j.alit.2021.04.003
PMID:33962863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8062405/
Abstract

Adverse allergic reactions due to the administration of the vaccines developed for the protection of coronavirus disease 2019 (COVID-19) have been reported since the initiation of the vaccination campaigns. Current analyses provided by the Center for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA) in the United States have estimated the rates of anaphylactic reactions in 2.5 and 11.1 per million of mRNA-1273 and BNT162b2 vaccines administered, respectively. Although rather low, such rates could have importance due to the uncommon fact that a large majority of the world population will be subjected to vaccination with the aforementioned vaccines in the following months and vaccination will most likely be necessary every season as for influenza vaccines. Health regulators have advised that any subject with a previous history of allergy to drugs or any component of the vaccines should not be vaccinated, however, certain misunderstanding exists since allergy to specific excipients in drugs and vaccines are in occasions misdiagnosed due to an absence of suspicion to specific excipients as allergenic triggers or due to inaccurate labeling or nomenclature. In this review, we provide an updated revision of the most current data regarding the anaphylactic reactions described for BNT162b2 vaccine, mRNA-1273 vaccine, and AZD1222 vaccine. We extensively describe the different excipients in the vaccines with the potential to elicit systemic allergic reactions such as polyethylene glycol (PEG), polysorbates, tromethamine/trometamol, and others and the possible immunological mechanisms involved.

摘要

自开展新冠疫苗接种运动以来,已有因接种用于预防2019冠状病毒病(COVID-19)的疫苗而出现不良过敏反应的报告。美国疾病控制与预防中心(CDC)和食品药品监督管理局(FDA)目前提供的分析估计,每百万剂接种的mRNA-1273疫苗和BNT162b2疫苗中,过敏反应发生率分别为2.5例和11.1例。尽管发生率相当低,但鉴于在接下来的几个月里世界上绝大多数人口都将接种上述疫苗这一不寻常情况,且接种疫苗很可能像流感疫苗那样每个季节都有必要进行,所以这样的发生率可能具有重要意义。卫生监管机构建议,任何有药物或疫苗任何成分过敏史的受试者都不应接种疫苗,然而,由于对药物和疫苗中特定辅料作为致敏触发因素缺乏怀疑,或者由于标签或命名不准确,药物和疫苗中特定辅料过敏有时会被误诊,因此存在一定的误解。在本综述中,我们提供了关于BNT162b2疫苗、mRNA-1273疫苗和AZD1222疫苗所描述的过敏反应的最新数据修订。我们广泛描述了疫苗中可能引发全身过敏反应的不同辅料,如聚乙二醇(PEG)、聚山梨酯、 tromethamine/trometamol等,以及可能涉及的免疫机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad6/8062405/311a9622ddc7/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad6/8062405/7fecb49ccaed/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad6/8062405/3805aa7010e5/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad6/8062405/311a9622ddc7/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad6/8062405/7fecb49ccaed/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad6/8062405/3805aa7010e5/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aad6/8062405/311a9622ddc7/gr3_lrg.jpg

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