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常见新冠疫苗的安全性和有效性

Safety and Efficacy of the Common Vaccines against COVID-19.

作者信息

Liu Ying, Ye Qing

机构信息

Department of Clinical Laboratory, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310057, China.

出版信息

Vaccines (Basel). 2022 Mar 25;10(4):513. doi: 10.3390/vaccines10040513.

Abstract

The worldwide pandemic of coronavirus disease 2019 (COVID-19) has imposed a challenge on human health worldwide, and vaccination represents a vital strategy to control the pandemic. To date, multiple COVID-19 vaccines have been granted emergency use authorization, including inactivated vaccines, adenovirus-vectored vaccines, and nucleic acid vaccines. These vaccines have different technical principles, which will necessarily lead to differences in safety and efficacy. Therefore, we aim to implement a systematic review by synthesizing clinical experimental data combined with mass vaccination data and conducting a synthesis to evaluate the safety and efficacy of COVID-19 vaccines. Compared with other vaccines, adverse reactions after vaccination with inactivated vaccines are relatively low. The efficacy of inactivated vaccines is approximately 60%, adenovirus-vectored vaccines are 65%, and mRNA vaccines are 90%, which are always efficient against asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, symptomatic COVID-19, COVID-19 hospitalization, severe or critical hospitalization, and death. RNA-based vaccines have a number of advantages and are one of the most promising vaccines identified to date and are particularly important during a pandemic. However, further improvements are required. In time, all the antibody levels weaken gradually, so a booster dose is needed to maintain immunity. Compared with homologous prime-boost immunization, heterologous prime-boost immunization prompts more robust humoral and cellular immune responses.

摘要

2019年冠状病毒病(COVID-19)全球大流行给全球人类健康带来了挑战,而疫苗接种是控制该大流行的一项关键策略。迄今为止,多种COVID-19疫苗已获得紧急使用授权,包括灭活疫苗、腺病毒载体疫苗和核酸疫苗。这些疫苗有不同的技术原理,这必然会导致安全性和有效性方面的差异。因此,我们旨在通过综合临床试验数据与大规模疫苗接种数据并进行汇总分析,来评估COVID-19疫苗的安全性和有效性,从而开展一项系统评价。与其他疫苗相比,接种灭活疫苗后的不良反应相对较少。灭活疫苗的有效性约为60%,腺病毒载体疫苗为65%,信使核糖核酸(mRNA)疫苗为90%,这些疫苗在预防无症状严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染、有症状的COVID-19、COVID-19住院、重症或危重症住院以及死亡方面始终有效。基于RNA的疫苗有诸多优势,是迄今为止已确定的最有前景的疫苗之一,在大流行期间尤为重要。然而,仍需进一步改进。随着时间推移,所有抗体水平会逐渐减弱,因此需要接种加强针来维持免疫力。与同源初免-加强免疫相比,异源初免-加强免疫能激发更强的体液免疫和细胞免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d06/9027683/c64e62d9cf8e/vaccines-10-00513-g001.jpg

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