Beijing Institute of Microbiology and Epidemiology, Beijing, 100850, P. R. China.
Beijing Youcare Kechuang Pharmaceutical Technology Co., Ltd, Beijing, 100176, P. R. China.
Adv Healthc Mater. 2023 May;12(13):e2202590. doi: 10.1002/adhm.202202590. Epub 2023 Feb 17.
mRNA-based therapy has emerged as the most promising nucleic acid therapy in the fight against COVID-19. However, a safe and efficacious systemic delivery remains a challenge for mRNA therapy. Lipid nanoparticles (LNPs) are currently widely used in mRNA delivery vehicles. Here, a series of ionizable LNPs is rationally designed. YK009-LNP is an optimal delivery platform to carry mRNA. YK009-LNP exhibits higher mRNA delivery efficiency, a more favorable biodistribution pattern, and better safety than the approved MC3-LNP. In addition, mRNA encoding severe acute respiratory syndrome coronavirus 2 Omicron receptor binding domain protein is synthesized and intramuscular administration of mice with YK009-LNP-Omicron mRNA induces a robust immune response and immune protective effect. A novel mRNA delivery vehicle with more powerful delivery efficiency and better safety than the approved LNPs is provided here.
mRNA 疗法已成为抗击 COVID-19 最有前途的核酸疗法。然而,安全有效的全身递送仍然是 mRNA 疗法面临的挑战。脂质纳米粒(LNPs)目前广泛用于 mRNA 递送载体。在这里,合理设计了一系列可离子化的 LNPs。YK009-LNP 是一种携带 mRNA 的最佳递送平台。与已批准的 MC3-LNP 相比,YK009-LNP 表现出更高的 mRNA 递送效率、更有利的生物分布模式和更好的安全性。此外,合成编码严重急性呼吸综合征冠状病毒 2 奥密克戎受体结合域蛋白的 mRNA,并通过 YK009-LNP-Omicron mRNA 肌内给药诱导小鼠产生强烈的免疫反应和免疫保护作用。与已批准的 LNPs 相比,这里提供了一种新型 mRNA 递送载体,具有更强的递送效率和更好的安全性。