Liu Ying, Ye Qing
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 310052, China.
Vaccines (Basel). 2022 Oct 31;10(11):1849. doi: 10.3390/vaccines10111849.
The coronavirus disease 2019 (COVID-19) has spread worldwide and imposed a substantial burden on human health, the environment, and socioeconomic development, which has also accelerated the process of nucleic acid vaccine development and licensure. Nucleic acid vaccines are viral genetic sequence-based vaccines and third-generation vaccines after whole virus vaccines and recombinant subunit vaccines, including DNA vaccines and RNA vaccines. They have many unique advantages, but there are many aspects that require optimization. Therefore, the purpose of this review is to discuss the research and development processes of nucleic acid vaccines, summarize the advantages and shortcomings, and propose further optimization strategies by taking COVID-19 vaccines as an example. Hopefully, this work can make a modest contribution in promoting the construction of emergency nucleic acid vaccine platforms and in avoiding the reemergence of similar public health emergencies.
2019年冠状病毒病(COVID-19)已在全球范围内传播,给人类健康、环境和社会经济发展带来了沉重负担,这也加速了核酸疫苗的研发和获批进程。核酸疫苗是以病毒基因序列为基础的疫苗,是继全病毒疫苗和重组亚单位疫苗之后的第三代疫苗,包括DNA疫苗和RNA疫苗。它们有许多独特的优势,但也有许多方面需要优化。因此,本综述的目的是以COVID-19疫苗为例,探讨核酸疫苗的研发过程,总结其优缺点,并提出进一步的优化策略。希望这项工作能为推动应急核酸疫苗平台的建设以及避免类似公共卫生事件的再次出现做出微薄贡献。