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Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment

Title
Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment
Author(s)
Lee, Eun SookKo, HyewonKim, Chan HoKim, Hyun-ChulChoi, Seong-KyoonJeong, Sang WonLee, Se-GuenLee, Sung-JunNa, Hee-KyungPark, Jae HyungShin, Jung Min
Issued Date
2023-08
Citation
Biomaterials Research, v.27, no.1, pp.1963 - 1998
Type
Article
Author Keywords
ExosomeRheumatoid arthritisDisease microenvironmentEngineered exosome
Keywords
REGULATORY T-CELLSFIBROBLAST-LIKE SYNOVIOCYTESCOLLAGEN-INDUCED ARTHRITISMESENCHYMAL STEM-CELLSEXTRACELLULAR VESICLESDENDRITIC CELLSB-CELLSSYNOVIAL-FLUIDTNF-ALPHAINFLAMMATION
ISSN
1226-4601
Abstract
Background: Exosomes are extracellular vesicles secreted by eukaryotic cells and have been extensively studied for their surface markers and internal cargo with unique functions. A deeper understanding of exosomes has allowed their application in various research areas, particularly in diagnostics and therapy. Main body: Exosomes have great potential as biomarkers and delivery vehicles for encapsulating therapeutic cargo. However, the limitations of bare exosomes, such as rapid phagocytic clearance and non-specific biodistribution after injection, pose significant challenges to their application as drug delivery systems. This review focuses on exosome-based drug delivery for treating rheumatoid arthritis, emphasizing pre/post-engineering approaches to overcome these challenges. Conclusion: This review will serve as an essential resource for future studies to develop novel exosome-based therapeutic approaches for rheumatoid arthritis. Overall, the review highlights the potential of exosomes as a promising therapeutic approach for rheumatoid arthritis treatment. Graphical Abstract: [Figure not available: see fulltext.] © 2023, The Korean Society for Biomaterials.
URI
http://hdl.handle.net/20.500.11750/46697
DOI
10.1186/s40824-023-00418-2
Publisher
BioMed Central Ltd
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Appears in Collections:
Division of Biotechnology 1. Journal Articles

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