Preclinical evaluation of RQ3013, a broad-spectrum mRNA vaccine against SARS-CoV-2 variants

免疫原 免疫原性 中和抗体 广谱 免疫系统 病毒学 生物 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 2019年冠状病毒病(COVID-19) 免疫学 抗体 医学 疾病 化学 传染病(医学专业) 单克隆抗体 病理 组合化学
作者
Shudan Tan,Jinghua Zhao,Xue Hu,Yufeng Li,Zihan Wu,Guoliang Lu,Zhaoli Yu,Binhe Du,Yan Liu,Li Li,Yuchen Chen,Ye Li,Yanfeng Yao,Xiaoyu Zhang,Juhong Rao,Ge Gao,Yun Peng,Hang Liu,Zhiming Yuan,Jia Liu
出处
期刊:Science Bulletin [Elsevier BV]
卷期号:68 (24): 3192-3206 被引量:14
标识
DOI:10.1016/j.scib.2023.11.024
摘要

The global emergence of SARS-CoV-2 variants has led to increasing breakthrough infections in vaccinated populations, calling for an urgent need to develop more effective and broad-spectrum vaccines to combat COVID-19. Here we report the preclinical development of RQ3013, an mRNA vaccine candidate intended to bring broad protection against SARS-CoV-2 variants of concern (VOCs). RQ3013, which contains pseudouridine-modified mRNAs formulated in lipid nanoparticles, encodes the spike (S) protein harboring a combination of mutations responsible for immune evasion of VOCs. Here we characterized the expressed S immunogen and evaluated the immunogenicity, efficacy, and safety of RQ3013 in various animal models. RQ3013 elicited robust immune responses in mice, hamsters, and nonhuman primates (NHP). It can induce high titers of antibodies with broad cross-neutralizing ability against the wild-type, B.1.1.7, B.1.351, B.1.617.2, and the newly emerging Omicron variants. In mice and NHP, two doses of RQ3013 protected the upper and lower respiratory tract against infection by SARS-CoV-2 and its variants. Furthermore, our safety assessment of RQ3013 in NHP showed no observable adverse effects. These results provide strong support for the evaluation of RQ3013 in clinical trials and suggest that it may be a promising candidate for broad protection against COVID-19 and its variants.
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