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Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases
In the inflammatory microenvironment, there are numerous exosomes secreted by immune cells (Macrophages, neutrophils, dendritic cells), mesenchymal stem cells (MSCs) and platelets as intercellular communicators, which participate in the regulation of inflammation by modulating gene expression and re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shenyang Pharmaceutical University
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989662/ https://www.ncbi.nlm.nih.gov/pubmed/36896446 http://dx.doi.org/10.1016/j.ajps.2022.100772 |
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author | Wang, Chenglong Xu, Maochang Fan, Qingze Li, Chunhong Zhou, Xiangyu |
author_facet | Wang, Chenglong Xu, Maochang Fan, Qingze Li, Chunhong Zhou, Xiangyu |
author_sort | Wang, Chenglong |
collection | PubMed |
description | In the inflammatory microenvironment, there are numerous exosomes secreted by immune cells (Macrophages, neutrophils, dendritic cells), mesenchymal stem cells (MSCs) and platelets as intercellular communicators, which participate in the regulation of inflammation by modulating gene expression and releasing anti-inflammatory factors. Due to their good biocompatibility, accurate targeting, low toxicity and immunogenicity, these exosomes are able to selectively deliver therapeutic drugs to the site of inflammation through interactions between their surface-antibody or modified ligand with cell surface receptors. Therefore, the role of exosome-based biomimetic delivery strategies in inflammatory diseases has attracted increasing attention. Here we review current knowledge and techniques for exosome identification, isolation, modification and drug loading. More importantly, we highlight progress in using exosomes to treat chronic inflammatory diseases such as rheumatoid arthritis (RA), osteoarthritis (OA), atherosclerosis (AS), and inflammatory bowel disease (IBD). Finally, we also discuss their potential and challenges as anti-inflammatory drug carriers. |
format | Online Article Text |
id | pubmed-9989662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Shenyang Pharmaceutical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-99896622023-03-08 Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases Wang, Chenglong Xu, Maochang Fan, Qingze Li, Chunhong Zhou, Xiangyu Asian J Pharm Sci Review In the inflammatory microenvironment, there are numerous exosomes secreted by immune cells (Macrophages, neutrophils, dendritic cells), mesenchymal stem cells (MSCs) and platelets as intercellular communicators, which participate in the regulation of inflammation by modulating gene expression and releasing anti-inflammatory factors. Due to their good biocompatibility, accurate targeting, low toxicity and immunogenicity, these exosomes are able to selectively deliver therapeutic drugs to the site of inflammation through interactions between their surface-antibody or modified ligand with cell surface receptors. Therefore, the role of exosome-based biomimetic delivery strategies in inflammatory diseases has attracted increasing attention. Here we review current knowledge and techniques for exosome identification, isolation, modification and drug loading. More importantly, we highlight progress in using exosomes to treat chronic inflammatory diseases such as rheumatoid arthritis (RA), osteoarthritis (OA), atherosclerosis (AS), and inflammatory bowel disease (IBD). Finally, we also discuss their potential and challenges as anti-inflammatory drug carriers. Shenyang Pharmaceutical University 2023-01 2022-12-31 /pmc/articles/PMC9989662/ /pubmed/36896446 http://dx.doi.org/10.1016/j.ajps.2022.100772 Text en © 2022 Shenyang Pharmaceutical University. Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Wang, Chenglong Xu, Maochang Fan, Qingze Li, Chunhong Zhou, Xiangyu Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases |
title | Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases |
title_full | Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases |
title_fullStr | Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases |
title_full_unstemmed | Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases |
title_short | Therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases |
title_sort | therapeutic potential of exosome‐based personalized delivery platform in chronic inflammatory diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989662/ https://www.ncbi.nlm.nih.gov/pubmed/36896446 http://dx.doi.org/10.1016/j.ajps.2022.100772 |
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