Du Shuang, Yang Liu, Chen Xingguang, Chen Yonghao, Weng Liang, Huang Hui, Pang Silin
Shenzhen Shenxin Biotechnology Co., Ltd., 518052, China.
Nanjing Shenxin Biotechnology Co., Ltd., 211800, China.
Biochem Biophys Res Commun. 2025 Feb;746:151224. doi: 10.1016/j.bbrc.2024.151224. Epub 2024 Dec 25.
Herd immunity through mass vaccination is an effective method for preventing infectious diseases. However, the emerging SARS-CoV-2 variants, with their frequent mutations, largely evade the immune response and protection induced by COVID-19 vaccines. Here, we designed messenger RNAs encoding mutant epitopes of the spike protein shared among various COVID-19 variants. These mRNAs were encapsulated in lipid nanoparticles to formulate a vaccine named 'mPANVAX@COVID'. Post-vaccination, this approach elicited effective immunity against multiple SARS-CoV-2 variants, including Delta and Omicron, and demonstrated good safety. This study suggests a novel direction for the design of broadly protective vaccines.
通过大规模疫苗接种实现群体免疫是预防传染病的有效方法。然而,新出现的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体频繁突变,在很大程度上逃避了由2019冠状病毒病(COVID-19)疫苗诱导的免疫反应和保护作用。在此,我们设计了编码多种COVID-19变体共有的刺突蛋白突变表位的信使核糖核酸(mRNA)。这些mRNA被包裹在脂质纳米颗粒中,制成一种名为“mPANVAX@COVID”的疫苗。接种疫苗后,这种方法引发了针对包括德尔塔和奥密克戎在内的多种SARS-CoV-2变体的有效免疫反应,并显示出良好的安全性。这项研究为广泛保护性疫苗的设计提出了一个新方向。