Lipid nanoparticles for mRNA delivery

被引:1811
|
作者
Hou, Xucheng [1 ]
Zaks, Tal [2 ]
Langer, Robert [3 ,4 ]
Dong, Yizhou [1 ]
机构
[1] Ohio State Univ, Coll Pharm, Div Pharmaceut & Pharmacol, Columbus, OH 43210 USA
[2] Moderna Inc, Cambridge, MA 02139 USA
[3] MIT, David H Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
关键词
MEDIATED SIRNA DELIVERY; EFFICIENT GENE-TRANSFER; IN-VIVO; SYSTEMIC DELIVERY; CATIONIC LIPIDS; IMMUNE-RESPONSES; CO-DELIVERY; INTRACELLULAR DELIVERY; PROTECTIVE EFFICACY; ANTITUMOR IMMUNITY;
D O I
10.1038/s41578-021-00358-0
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Messenger RNA (mRNA) has emerged as a new category of therapeutic agent to prevent and treat various diseases. To function in vivo, mRNA requires safe, effective and stable delivery systems that protect the nucleic acid from degradation and that allow cellular uptake and mRNA release. Lipid nanoparticles have successfully entered the clinic for the delivery of mRNA; in particular, lipid nanoparticle-mRNA vaccines are now in clinical use against coronavirus disease 2019 (COVID-19), which marks a milestone for mRNA therapeutics. In this Review, we discuss the design of lipid nanoparticles for mRNA delivery and examine physiological barriers and possible administration routes for lipid nanoparticle-mRNA systems. We then consider key points for the clinical translation of lipid nanoparticle-mRNA formulations, including good manufacturing practice, stability, storage and safety, and highlight preclinical and clinical studies of lipid nanoparticle-mRNA therapeutics for infectious diseases, cancer and genetic disorders. Finally, we give an outlook to future possibilities and remaining challenges for this promising technology. Lipid nanoparticle-mRNA formulations have entered the clinic as coronavirus disease 2019 (COVID-19) vaccines, marking an important milestone for mRNA therapeutics. This Review discusses lipid nanoparticle design for mRNA delivery, highlighting key points for clinical translation and preclinical studies of lipid nanoparticle-mRNA therapeutics for various diseases.
引用
收藏
页码:1078 / 1094
页数:17
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