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新型可离子化脂质纳米颗粒用于 SARS-CoV-2 奥密克戎 mRNA 递送。

Novel Ionizable Lipid Nanoparticles for SARS-CoV-2 Omicron mRNA Delivery.

机构信息

Beijing Institute of Microbiology and Epidemiology, Beijing, 100850, P. R. China.

Beijing Youcare Kechuang Pharmaceutical Technology Co., Ltd, Beijing, 100176, P. R. China.

出版信息

Adv Healthc Mater. 2023 May;12(13):e2202590. doi: 10.1002/adhm.202202590. Epub 2023 Feb 17.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ab/11468017/4b343bcd41aa/ADHM-12-2202590-g005.jpg

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