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

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 a...

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Autores principales: Lee, Eun Sook, Ko, Hyewon, Kim, Chan Ho, Kim, Hyun-Chul, Choi, Seong-Kyoon, Jeong, Sang Won, Lee, Se-Guen, Lee, Sung-Jun, Na, Hee-Kyung, Park, Jae Hyung, Shin, Jung Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464174/
https://www.ncbi.nlm.nih.gov/pubmed/37635253
http://dx.doi.org/10.1186/s40824-023-00418-2
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author Lee, Eun Sook
Ko, Hyewon
Kim, Chan Ho
Kim, Hyun-Chul
Choi, Seong-Kyoon
Jeong, Sang Won
Lee, Se-Guen
Lee, Sung-Jun
Na, Hee-Kyung
Park, Jae Hyung
Shin, Jung Min
author_facet Lee, Eun Sook
Ko, Hyewon
Kim, Chan Ho
Kim, Hyun-Chul
Choi, Seong-Kyoon
Jeong, Sang Won
Lee, Se-Guen
Lee, Sung-Jun
Na, Hee-Kyung
Park, Jae Hyung
Shin, Jung Min
author_sort Lee, Eun Sook
collection PubMed
description 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: [Image: see text]
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spelling pubmed-104641742023-08-30 Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment Lee, Eun Sook Ko, Hyewon Kim, Chan Ho Kim, Hyun-Chul Choi, Seong-Kyoon Jeong, Sang Won Lee, Se-Guen Lee, Sung-Jun Na, Hee-Kyung Park, Jae Hyung Shin, Jung Min Biomater Res Review 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: [Image: see text] BioMed Central 2023-08-28 /pmc/articles/PMC10464174/ /pubmed/37635253 http://dx.doi.org/10.1186/s40824-023-00418-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Lee, Eun Sook
Ko, Hyewon
Kim, Chan Ho
Kim, Hyun-Chul
Choi, Seong-Kyoon
Jeong, Sang Won
Lee, Se-Guen
Lee, Sung-Jun
Na, Hee-Kyung
Park, Jae Hyung
Shin, Jung Min
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
title_full Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment
title_fullStr Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment
title_full_unstemmed Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment
title_short Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment
title_sort disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464174/
https://www.ncbi.nlm.nih.gov/pubmed/37635253
http://dx.doi.org/10.1186/s40824-023-00418-2
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