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

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dc.contributor.authorE S Lee-
dc.contributor.authorHyewon Ko-
dc.contributor.authorC H Kim-
dc.contributor.authorH C Kim-
dc.contributor.authorS K Choi-
dc.contributor.authorS W Jeong-
dc.contributor.authorS G Lee-
dc.contributor.authorS J Lee-
dc.contributor.authorH K Na-
dc.contributor.authorJ H Park-
dc.contributor.authorJ M Shin-
dc.date.accessioned2023-08-29T16:32:42Z-
dc.date.available2023-08-29T16:32:42Z-
dc.date.issued2023-
dc.identifier.issn1226-1226-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/32572-
dc.description.abstractBackground: 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.-
dc.publisherSpringer-BMC-
dc.titleDisease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment-
dc.title.alternativeDisease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment-
dc.typeArticle-
dc.citation.titleBiomaterials Research-
dc.citation.number0-
dc.citation.endPage81-
dc.citation.startPage81-
dc.citation.volume27-
dc.contributor.affiliatedAuthorHyewon Ko-
dc.contributor.alternativeName이은숙-
dc.contributor.alternativeName고혜원-
dc.contributor.alternativeName김찬호-
dc.contributor.alternativeName김현철-
dc.contributor.alternativeName최성균-
dc.contributor.alternativeName정상원-
dc.contributor.alternativeName이세건-
dc.contributor.alternativeName이성준-
dc.contributor.alternativeName나희경-
dc.contributor.alternativeName박재형-
dc.contributor.alternativeName신정민-
dc.identifier.bibliographicCitationBiomaterials Research, vol. 27, pp. 81-81-
dc.identifier.doi10.1186/s40824-023-00418-2-
dc.subject.keywordExosome-
dc.subject.keywordRheumatoid arthritis-
dc.subject.keywordDisease microenvironment-
dc.subject.keywordEngineered exosome-
dc.subject.localExosome-
dc.subject.localexosome-
dc.subject.localRheumatoid Arthritis-
dc.subject.localRheumatoid arthritis-
dc.subject.localrheumatoid arthritis-
dc.subject.localrheumatoid arthritis (RA)-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
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