免疫原性
病毒学
生物
中和抗体
广谱
病毒
2019年冠状病毒病(COVID-19)
免疫系统
免疫学
医学
化学
传染病(医学专业)
疾病
病理
组合化学
作者
Pei Du,Lei Huang,Yi Fang,Fanfan Zhao,Qianyun Li,Xuehui Ma,Rui-Qi Li,Qian Chen,Haifa Shen,Qihui Wang,Hangwen Li,George F. Gao
出处
期刊:PLOS Pathogens
[Public Library of Science]
日期:2024-04-01
卷期号:20 (4): e1012116-e1012116
标识
DOI:10.1371/journal.ppat.1012116
摘要
Since the beginning of the coronavirus disease 2019 (COVID-19) pandemic, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, continues to mutate and generates new variants with increasingly severe immune escape, urging the upgrade of COVID-19 vaccines. Here, based on a similar dimeric RBD design as our previous ZF2001 vaccine, we developed a novel broad-spectrum COVID-19 mRNA vaccine, SWIM516, with chimeric Delta-BA.2 RBD dimer delivered by lipopolyplex (LPP). Unlike the popular lipid nanoparticle (LNP), this LPP-delivered mRNA expresses only in the injection site, which avoids potential toxicity to the liver. We demonstrated the broad-spectrum humoral and cellular immunogenicity of this vaccine to Delta and Omicron sub-variants in naïve mice and as booster shots. When challenged with Delta or Omicron live virus, vaccinated human angiotensin-converting enzyme (hACE2) transgenic mice and rhesus macaques were both protected, displaying significantly reduced viral loads and markedly relieved pathological damages. We believe the SWIM516 vaccine qualifies as a candidate for the next-generation broad-spectrum COVID-19 vaccine.
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