Exploring the clinical transition of engineered exosomes designed for intracellular delivery of therapeutic proteins

被引:8
|
作者
Kim, Minseong [1 ]
Choi, Hojun [1 ,4 ,5 ]
Jang, Deok-Jin [1 ,2 ]
Kim, Hye-Jung [1 ]
Sub, Yujin [3 ]
Gee, Heon Yung [3 ]
Choi, Chulhee [1 ]
机构
[1] ILIAS Biol Inc, 40-20 Techno 6 Ro, Daejeon 34141, South Korea
[2] Kyungpook Natl Univ, Coll Ecol & Environm Sci, Dept Ecol & Environm Syst, Sangju 37224, South Korea
[3] Yonsei Univ, Coll Med, Grad Sch Med Sci, Dept Pharmacol,Brain Korea 21 Project, Seoul 03722, South Korea
[4] Univ Washington, Dept Biochem, Seattle, WA USA
[5] Univ Washington, Int Prot Design, Seattle, WA USA
关键词
extracellular vesicles; exosomes; protein therapeutics; exosome purification; inflammation; drug delivery system; CENTRAL-NERVOUS-SYSTEM; OPPORTUNITIES; VESICLES; BIOLOGY; BRAIN;
D O I
10.1093/stcltm/szae027
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Extracellular vesicles, particularly exosomes, have emerged as promising drug delivery systems owing to their unique advantages, such as biocompatibility, immune tolerability, and target specificity. Various engineering strategies have been implemented to harness these innate qualities, with a focus on enhancing the pharmacokinetic and pharmacodynamic properties of exosomes via payload loading and surface engineering for active targeting. This concise review outlines the challenges in the development of exosomes as drug carriers and offers insights into strategies for their effective clinical translation. We also highlight preclinical studies that have successfully employed anti-inflammatory exosomes and suggest future directions for exosome therapeutics. These advancements underscore the potential for integrating exosome-based therapies into clinical practice, heralding promise for future medical interventions. Graphical Abstract
引用
收藏
页码:637 / 647
页数:11
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