Myopericarditis following both BNT162b2 and NVX-CoV2373.

Saima Ahmad, Chino Yuson, Adrianna Le, Pravin Hissaria
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引用次数: 4

Abstract

Background: Myopericarditis is a well reported complication associated with SARS-Cov-2 (COVID-19) infection and vaccinations; particularly with mRNA vaccines (BNT162b2 and mRNA-1273), and in the young male population. The risk-to-benefit ratio in sequential vaccination dosing in young males is further clouded in the era of the omicron variant with its reported enhanced immune escape.

Study design: A case series of two cases of post vaccination myopericarditis following the NVX-CoV2373 after also developing myopericarditis with BNT162b2.

Conclusion: To our knowledge, we are the first to describe post vaccination myopericarditis following NVX-CoV2373 after also developing myopericarditis with BNT162b2. The similarities in presentation between the reactions of both platforms would suggest a similar pathogenesis, although the exact mechanism remains unknown. Further studies are necessary to identify these mechanisms, as well as to identify biomarkers that may identify vulnerable populations. On-going vigilance is necessary to identify those who may be at an increased risk of post-COVID vaccine myopericarditis.

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BNT162b2和NVX-CoV2373引起心包炎。
背景:心包炎是一种与SARS-Cov-2 (COVID-19)感染和疫苗接种相关的并发症;尤其是mRNA疫苗(BNT162b2和mRNA-1273),以及年轻男性人群。年轻男性连续接种疫苗剂量的风险-收益比在组粒变异时代因其增强免疫逃逸而进一步模糊不清。研究设计:两例接种NVX-CoV2373疫苗后并发心包炎的病例,同时接种BNT162b2疫苗后也发生心包炎。结论:据我们所知,我们是第一个在接种NVX-CoV2373疫苗后,在接种BNT162b2后也发生心包炎的病例。两种平台的反应表现的相似性表明了相似的发病机制,尽管确切的机制尚不清楚。需要进一步的研究来确定这些机制,以及确定可能识别弱势群体的生物标志物。有必要持续保持警惕,以确定那些可能在covid疫苗后罹患心包炎风险增加的人。
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