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新型冠状病毒肺炎大流行:病毒变异株与疫苗效力。

The COVID-19 pandemic: viral variants and vaccine efficacy.

机构信息

Virology Unit, Polyclinic Tor Vergata Foundation, Rome, Italy.

Unit of Medical Statistics and Molecular Epidemiology, Campus Bio-Medico of Rome, Rome, Italy.

出版信息

Crit Rev Clin Lab Sci. 2022 Jan;59(1):66-75. doi: 10.1080/10408363.2021.1979462. Epub 2021 Oct 1.

DOI:10.1080/10408363.2021.1979462
PMID:34598660
Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has prompted the scientific community and the pharmaceutical companies to put maximum efforts into developing vaccines to contain the spread of this disease. Presently, many vaccines have been developed and authorized for use in human beings in different countries. In particular, in Europe to date, the Pfizer-BioNTech, Moderna, AstraZeneca and Janssen COVID-19 vaccines have been authorized. All of them are based on a version of the spike (S) glycoprotein characterized at the beginning of the pandemic. However, they differ by their level of efficacy against COVID-19. SARS-COV-2, like other RNA viruses, mutates continually. Genome sequencing analysis shows a nucleotide substitution rate of about 1 × 10 substitutions per year that leads to the emergence of variants through point mutations, insertions, deletions and recombination. There is concern about the ability of the current vaccines to protect against emerging viral variants. Mutations in the S-glycoprotein may affect transmission dynamics and the risk of immune escape. In this review, we address the different technological platforms in use for developing COVID-19 vaccines, the impact of emerging viral variants on virus transmission, hospitalization, and response to current vaccines, as well as rare but important adverse reactions to them. Finally, different methods for measuring antibody response to the vaccines, including the importance of using the WHO International Standard to calibrate immunoassays accurately to an arbitrary unit, to reduce interlaboratory variation and to create a common language for reporting results, are reported.

摘要

严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 大流行促使科学界和制药公司全力以赴开发疫苗以遏制这种疾病的传播。目前,许多疫苗已在不同国家开发并获准用于人类。特别是在欧洲,迄今为止,辉瑞-生物技术公司、莫德纳、阿斯利康和杨森 COVID-19 疫苗已获准使用。所有这些疫苗都是基于大流行初期的刺突 (S) 糖蛋白的一种版本开发的。然而,它们在预防 COVID-19 的功效方面有所不同。SARS-CoV-2 像其他 RNA 病毒一样,不断发生突变。基因组测序分析显示,每年约有 1×10 个核苷酸的替代率,导致通过点突变、插入、缺失和重组产生变体。人们担心当前的疫苗是否能够预防新出现的病毒变体。S-糖蛋白中的突变可能会影响传播动态和免疫逃逸的风险。在这篇综述中,我们讨论了用于开发 COVID-19 疫苗的不同技术平台,新出现的病毒变体对病毒传播、住院和对当前疫苗的反应的影响,以及它们的罕见但重要的不良反应。最后,报告了不同的方法来测量对疫苗的抗体反应,包括使用世界卫生组织国际标准准确校准免疫测定到任意单位的重要性,以减少实验室间的差异并为报告结果创建通用语言。

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