State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China; School of Medicine, Tsinghua University, Beijing 100084, China.
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
Cell. 2020 Sep 3;182(5):1271-1283.e16. doi: 10.1016/j.cell.2020.07.024. Epub 2020 Jul 23.
There is an urgent need for vaccines against coronavirus disease 2019 (COVID-19) because of the ongoing SARS-CoV-2 pandemic. Among all approaches, a messenger RNA (mRNA)-based vaccine has emerged as a rapid and versatile platform to quickly respond to this challenge. Here, we developed a lipid nanoparticle-encapsulated mRNA (mRNA-LNP) encoding the receptor binding domain (RBD) of SARS-CoV-2 as a vaccine candidate (called ARCoV). Intramuscular immunization of ARCoV mRNA-LNP elicited robust neutralizing antibodies against SARS-CoV-2 as well as a Th1-biased cellular response in mice and non-human primates. Two doses of ARCoV immunization in mice conferred complete protection against the challenge of a SARS-CoV-2 mouse-adapted strain. Additionally, ARCoV is manufactured as a liquid formulation and can be stored at room temperature for at least 1 week. ARCoV is currently being evaluated in phase 1 clinical trials.
由于持续的严重急性呼吸系统综合征冠状病毒 2 型(SARS-CoV-2)大流行,目前急需针对 2019 年冠状病毒病(COVID-19)的疫苗。在所有方法中,信使 RNA(mRNA)为基础的疫苗已成为快速应对这一挑战的通用平台。在此,我们开发了一种包裹在脂质纳米颗粒中的编码 SARS-CoV-2 受体结合域(RBD)的 mRNA(mRNA-LNP)作为候选疫苗(称为 ARCoV)。ARCoV mRNA-LNP 的肌内免疫在小鼠和非人类灵长类动物中引发了针对 SARS-CoV-2 的强大中和抗体以及 Th1 偏向的细胞反应。在小鼠中进行两剂 ARCoV 免疫可完全防止 SARS-CoV-2 适应的小鼠株的挑战。此外,ARCoV 可制成液体制剂,并可在室温下至少储存 1 周。ARCoV 目前正在进行 I 期临床试验。