信使核糖核酸
2019年冠状病毒病(COVID-19)
大流行
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
生物
软件部署
专家意见
临床试验
计算生物学
计算机科学
疾病
生物信息学
医学
遗传学
基因
传染病(医学专业)
重症监护医学
操作系统
病理
作者
Andrew J. Geall,Zoltán Kis,Jeffrey B. Ulmer
标识
DOI:10.1080/17460441.2022.2147501
摘要
Introduction:Prior to the emergence of SARS-CoV-2, the potential use of mRNA vaccines for a rapid pandemic response had been well described in the scientific literature, however during the SARS-CoV-2 outbreak we witnessed the large-scale deployment of the platform in a real pandemic setting. Of the three RNA platforms evaluated in clinical trials, including 1) conventional, non-amplifying mRNA (mRNA), 2) base-modified, non-amplifying mRNA (bmRNA), which incorporate chemically modified nucleotides, and 3) self-amplifying RNA (saRNA), the bmRNA technology emerged with superior clinical efficacy.Areas covered:This review describes the current state of these mRNA vaccine technologies, evaluates their strengths and limitations, and argues that saRNA may have significant advantages if the limitations of stability and complexities of manufacturing can be overcome.Expert opinion:The success of the SARS-CoV-2 mRNA vaccines has been remarkable. However, several challenges remain to be addressed before this technology can successfully be applied broadly to other disease targets. Innovation in the areas of mRNA engineering, novel delivery systems, antigen design, and high-quality manufacturing will be required to achieve the full potential of this disruptive technology.
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