Liu Cong, Rcheulishvili Nino, Shen Zhigao, Papukashvili Dimitri, Xie Fengfei, Wang Ziqian, Wang Xingyun, He Yunjiao, Wang Peng George
School of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Pharmaceutics. 2022 May 20;14(5):1101. doi: 10.3390/pharmaceutics14051101.
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is undoubtedly the most challenging pandemic in the current century and remains a global health emergency. As the number of COVID-19 cases in the world is on the rise and variants continue to emerge, there is an urgent need for vaccines. Among all immunization approaches, mRNA vaccines have demonstrated more promising results in response to this challenge. Herein, we designed an mRNA-based vaccine encoding the receptor-binding domain (RBD) of SARS-CoV-2 encapsulated in lipid nanoparticles (LNPs). Intramuscular (i.m.) administration of the mRNA-RBD vaccine elicited broad-spectrum neutralizing antibodies and cellular responses against not only the wild-type SARS-CoV-2 virus but also Delta and Omicron variants. These results indicated that two doses of mRNA-RBD immunization conferred a strong immune response in mice against the wild-type SARS-CoV-2, while the booster dose provided a sufficient immunity against SARS-CoV-2 and its variants. Taken together, the three-dose regimen strategy of the mRNA-RBD vaccine proposed in the present study appears to be a promising reference for the development of mRNA vaccines targeting SARS-CoV-2 variants.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)无疑是本世纪最具挑战性的大流行病,目前仍然是全球卫生紧急事件。随着全球COVID-19病例数量不断增加,病毒变体持续出现,对疫苗的需求极为迫切。在所有免疫方法中,mRNA疫苗在应对这一挑战方面已展现出更具前景的效果。在此,我们设计了一种基于mRNA的疫苗,其编码封装于脂质纳米颗粒(LNP)中的SARS-CoV-2受体结合域(RBD)。肌肉注射该mRNA-RBD疫苗可引发广谱中和抗体以及针对野生型SARS-CoV-2病毒、Delta和Omicron变体的细胞免疫反应。这些结果表明,两剂mRNA-RBD免疫接种可使小鼠对野生型SARS-CoV-2产生强烈免疫反应,而加强剂量则可为抵抗SARS-CoV-2及其变体提供足够免疫力。综上所述,本研究提出的mRNA-RBD疫苗三剂接种方案策略似乎可为开发针对SARS-CoV-2变体的mRNA疫苗提供有前景的参考。