信使核糖核酸
从长凳到床边
计算生物学
免疫原性
生物
计算机科学
生物信息学
医学
基因
免疫学
免疫系统
医学物理学
遗传学
作者
Yuhua Weng,Chunhui Li,Tongren Yang,Bo Hu,Jun Zhang,Shuai Guo,Haihua Xiao,Xing‐Jie Liang,Yuanyu Huang
标识
DOI:10.1016/j.biotechadv.2020.107534
摘要
Messenger RNA (mRNA)-based therapeutics hold the potential to cause a major revolution in the pharmaceutical industry because they can be used for precise and individualized therapy, and enable patients to produce therapeutic proteins in their own bodies without struggling with the comprehensive manufacturing issues associated with recombinant proteins. Compared with the current therapeutics, the production of mRNA is much cost-effective, faster and more flexible because it can be easily produced by in vitro transcription, and the process is independent of mRNA sequence. Moreover, mRNA vaccines allow people to develop personalized medications based on sequencing results and/or personalized conditions rapidly. Along with the great potential from bench to bedside, technical obstacles facing mRNA pharmaceuticals are also obvious. The stability, immunogenicity, translation efficiency, and delivery are all pivotal issues need to be addressed. In the recently published research results, these issues are gradually being overcome by state-of-the-art development technologies. In this review, we describe the structural properties and modification technologies of mRNA, summarize the latest advances in developing mRNA delivery systems, review the preclinical and clinical applications, and put forward our views on the prospect and challenges of developing mRNA into a new class of drug.
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