Review of Clinical Trials of COVID-19 Vaccination Booster in SARS-CoV-2 Variants Era: To Take It or Not To Take It

M. Yan, Ming Yang, Ching‐lung Lai
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引用次数: 1

Abstract

Since the COVID-19 outbreak in China in 2019, the pandemic has spread globally. There is no definitive cure, but vaccines have greatly protected humans from symptomatic infections and severe complications. However, vaccine efficacy has been greatly reduced by the advent of SARS-CoV-2 variants worldwide. The World Health Organization has classified the variants into two groups: variants of concern (Alpha, Beta, Gamma, Delta, Omicron) and variants of interest (Lambda, Mu). Clinical trials and modifications of vaccines are currently undertaken to improve their clinical efficacies. This is particularly worrying in immunocompromised patients since breakthrough infections with multiple lineages of variants can pose a continuous threat of severe diseases in these vulnerable subjects, though there is no evidence showing immunocompromised patients are at a higher risk of vaccine-associated adverse events. However, there is no consensus on the schedule, benefits, and risks as well as contraindications (both absolute and relative) of receiving booster vaccinations. This review looks into the efficacy and safety of COVID-19 vaccination booster to guide clinical decisions on when and who to receive booster vaccination.
COVID-19疫苗增强剂在SARS-CoV-2变异体时代的临床试验综述:服用还是不服用
2019年中国新冠肺炎疫情暴发以来,疫情已向全球蔓延。没有确切的治愈方法,但疫苗极大地保护了人类免受有症状的感染和严重的并发症。然而,由于全球范围内SARS-CoV-2变体的出现,疫苗的效力大大降低。世界卫生组织将这些变异分为两组:令人关注的变异(Alpha、Beta、Gamma、Delta、Omicron)和令人感兴趣的变异(Lambda、Mu)。目前正在对疫苗进行临床试验和修改,以提高其临床疗效。这在免疫功能低下患者中尤其令人担忧,因为具有多种变异谱系的突破性感染可在这些易感人群中持续构成严重疾病的威胁,尽管没有证据表明免疫功能低下患者发生疫苗相关不良事件的风险更高。然而,关于接种加强疫苗的时间表、益处、风险以及禁忌症(绝对和相对)尚无共识。本综述探讨了COVID-19疫苗增强剂的有效性和安全性,以指导临床决策何时和谁接受加强疫苗接种。
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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