Self-assembled mRNA vaccines

被引:417
作者
Kim, Jeonghwan [1 ]
Eygeris, Yulia [1 ]
Gupta, Mohit [1 ]
Sahay, Gaurav [1 ,2 ,3 ]
机构
[1] Oregon State Univ, Coll Pharm, Dept Pharmaceut Sci, Robertson Life Sci Bldg,2730 South Moody Ave, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Biomed Engn, Robertson Life Sci Bldg,2730 South Moody Ave, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Casey Eye Inst, Dept Ophthalmol, Portland, OR 97239 USA
关键词
mRNA delivery; Gene delivery; Lipid nanoparticles; Self-assembly; Immunization; COVID-19; LIPID NANOPARTICLE FORMULATIONS; ANTIGEN-PRESENTING CELLS; DENDRITIC CELLS; IN-VIVO; INTRACELLULAR DELIVERY; CATIONIC LIPIDS; SIRNA DELIVERY; POLY(ETHYLENE GLYCOL); CLINICAL CHARACTERISTICS; NEUTRALIZING ANTIBODIES;
D O I
10.1016/j.addr.2020.12.014
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
mRNA vaccines have evolved from being a mere curiosity to emerging as COVID-19 vaccine front-runners. Recent advancements in the field of RNA technology, vaccinology, and nanotechnology have generated interest in delivering safe and effective mRNA therapeutics. In this review, we discuss design and self-assembly of mRNA vaccines. Self-assembly, a spontaneous organization of individual molecules, allows for design of nanoparticles with customizable properties. We highlight the materials commonly utilized to deliver mRNA, their physicochemical characteristics, and other relevant considerations, such as mRNA optimization, routes of administration, cellular fate, and immune activation, that are important for successful mRNA vaccination. We also examine the COVID-19 mRNA vaccines currently in clinical trials. mRNA vaccines are ready for the clinic, showing tremendous promise in the COVID-19 vaccine race, and have pushed the boundaries of gene therapy. ? 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 112
页数:30
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