使用基于腺病毒载体的 SARS-CoV-2 疫苗免疫后,疫苗诱发免疫性血栓性血小板减少症的临床相关性。

IF 4.1 Q2 IMMUNOLOGY
Immunotherapy advances Pub Date : 2021-08-17 eCollection Date: 2021-01-01 DOI:10.1093/immadv/ltab019
Eleanor R Gaunt, Neil A Mabbott
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引用次数: 0

摘要

我们正处于 COVID-19 大流行的关键阶段,疫苗接种工作正在全球范围内展开,争分夺秒地赶在 SARS-CoV-2 冠状病毒和传染性更强的变种出现之前。一系列疫苗已经问世,并获得了紧急批准或正式许可。为了抢占先机,必须尽快最大限度地合成、部署和吸收疫苗。然而,疫苗的接种率,尤其是年轻成年人的接种率正在下降,至少部分原因是与特定疫苗相关的罕见并发症的报道推波助澜。本综述探讨了接种以腺病毒载体为基础的 SARS-CoV-2 冠状病毒疫苗如何可能导致一些受种者出现血栓和血小板减少的罕见病例。透彻了解介导这种综合症的潜在细胞和分子机制可能有助于确定预防这些非常罕见但严重的副作用的方法。这也将有助于确定出现这些后果的最高风险人群,以便我们能够采用分层方法部署疫苗,降低这些风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The clinical correlates of vaccine-induced immune thrombotic thrombocytopenia after immunisation with adenovirus vector-based SARS-CoV-2 vaccines.

The clinical correlates of vaccine-induced immune thrombotic thrombocytopenia after immunisation with adenovirus vector-based SARS-CoV-2 vaccines.

The clinical correlates of vaccine-induced immune thrombotic thrombocytopenia after immunisation with adenovirus vector-based SARS-CoV-2 vaccines.

The clinical correlates of vaccine-induced immune thrombotic thrombocytopenia after immunisation with adenovirus vector-based SARS-CoV-2 vaccines.

We are at a critical stage in the COVID-19 pandemic where vaccinations are being rolled out globally, in a race against time to get ahead of the SARS-CoV-2 coronavirus and the emergence of more highly transmissible variants. A range of vaccines have been created and received either emergency approval or full licensure. To attain the upper hand, maximum vaccine synthesis, deployment, and uptake as rapidly as possible is essential. However, vaccine uptake, particularly in younger adults is dropping, at least in part fuelled by reports of rare complications associated with specific vaccines. This review considers how vaccination with adenovirus vector-based vaccines against the SARS-CoV-2 coronavirus might cause rare cases of thrombosis and thrombocytopenia in some recipients. A thorough understanding of the underlying cellular and molecular mechanisms that mediate this syndrome may help to identify methods to prevent these very rare, but serious side effects. This will also help facilitate the identification of those at highest risk from these outcomes, so that we can work towards a stratified approach to vaccine deployment to mitigate these risks.

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