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Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review

BACKGROUND: Mesenchymal stem cells (MSCs) have been reported to possess immune regulatory effects in innate and adaptive immune reactions. MSCs can mediate intercellular communications by releasing extracellular vesicles (EVs), which deliver functional molecules to targeted cells. MSC derived EVs (M...

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Autores principales: Wang, Jing-Hua, Liu, Xiao-Ling, Sun, Jian-Mei, Yang, Jing-Han, Xu, Dong-Hua, Yan, Shu-Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477661/
https://www.ncbi.nlm.nih.gov/pubmed/32952864
http://dx.doi.org/10.4252/wjsc.v12.i8.879
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author Wang, Jing-Hua
Liu, Xiao-Ling
Sun, Jian-Mei
Yang, Jing-Han
Xu, Dong-Hua
Yan, Shu-Shan
author_facet Wang, Jing-Hua
Liu, Xiao-Ling
Sun, Jian-Mei
Yang, Jing-Han
Xu, Dong-Hua
Yan, Shu-Shan
author_sort Wang, Jing-Hua
collection PubMed
description BACKGROUND: Mesenchymal stem cells (MSCs) have been reported to possess immune regulatory effects in innate and adaptive immune reactions. MSCs can mediate intercellular communications by releasing extracellular vesicles (EVs), which deliver functional molecules to targeted cells. MSC derived EVs (MSC-EVs) confer altering effects on many immune cells, including T lymphocytes, B lymphocytes, natural killer cells, dendritic cells, and macrophages. A large number of studies have suggested that MSC-EVs participate in regulating autoimmunity related diseases. This characteristic of MSC-EVs makes them be potential biomarkers for the diagnosis and treatment of autoimmunity related diseases. AIM: To verify the potential of MSC-EVs for molecular targeted therapy of autoimmunity related diseases. METHODS: Literature search was conducted in PubMed to retrieve the articles published between 2010 and 2020 in the English language. The keywords, such as “MSCs,” “EVs,” “exosome,” “autoimmunity,” “tumor immunity,” and “transplantation immunity,” and Boolean operator “AND” and “NOT” coalesced admirably to be used for searching studies on the specific molecular mechanisms of MSC-EVs in many immune cell types and many autoimmunity related diseases. Studies that did not investigate the molecular mechanisms of MSC-EVs in the occurrence and development of autoimmune diseases were excluded. RESULTS: A total of 96 articles were chosen for final reference lists. After analyzing those publications, we found that it had been well documented that MSC-EVs have the ability to induce multiple immune cells, like T lymphocytes, B lymphocytes, natural killer cells, dendritic cells, and macrophages, to regulate immune responses in innate immunity and adaptive immunity. Many validated EVs-delivered molecules have been identified as key biomarkers, such as proteins, lipids, and nucleotides. Some EVs-encapsulated functional molecules can serve as promising therapeutic targets particularly for autoimmune disease. CONCLUSION: MSC-EVs play an equally important part in the differentiation, activation, and proliferation of immune cells, and they may become potential biomarkers for diagnosis and treatment of autoimmunity related diseases.
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spelling pubmed-74776612020-09-18 Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review Wang, Jing-Hua Liu, Xiao-Ling Sun, Jian-Mei Yang, Jing-Han Xu, Dong-Hua Yan, Shu-Shan World J Stem Cells Systematic Reviews BACKGROUND: Mesenchymal stem cells (MSCs) have been reported to possess immune regulatory effects in innate and adaptive immune reactions. MSCs can mediate intercellular communications by releasing extracellular vesicles (EVs), which deliver functional molecules to targeted cells. MSC derived EVs (MSC-EVs) confer altering effects on many immune cells, including T lymphocytes, B lymphocytes, natural killer cells, dendritic cells, and macrophages. A large number of studies have suggested that MSC-EVs participate in regulating autoimmunity related diseases. This characteristic of MSC-EVs makes them be potential biomarkers for the diagnosis and treatment of autoimmunity related diseases. AIM: To verify the potential of MSC-EVs for molecular targeted therapy of autoimmunity related diseases. METHODS: Literature search was conducted in PubMed to retrieve the articles published between 2010 and 2020 in the English language. The keywords, such as “MSCs,” “EVs,” “exosome,” “autoimmunity,” “tumor immunity,” and “transplantation immunity,” and Boolean operator “AND” and “NOT” coalesced admirably to be used for searching studies on the specific molecular mechanisms of MSC-EVs in many immune cell types and many autoimmunity related diseases. Studies that did not investigate the molecular mechanisms of MSC-EVs in the occurrence and development of autoimmune diseases were excluded. RESULTS: A total of 96 articles were chosen for final reference lists. After analyzing those publications, we found that it had been well documented that MSC-EVs have the ability to induce multiple immune cells, like T lymphocytes, B lymphocytes, natural killer cells, dendritic cells, and macrophages, to regulate immune responses in innate immunity and adaptive immunity. Many validated EVs-delivered molecules have been identified as key biomarkers, such as proteins, lipids, and nucleotides. Some EVs-encapsulated functional molecules can serve as promising therapeutic targets particularly for autoimmune disease. CONCLUSION: MSC-EVs play an equally important part in the differentiation, activation, and proliferation of immune cells, and they may become potential biomarkers for diagnosis and treatment of autoimmunity related diseases. Baishideng Publishing Group Inc 2020-08-26 2020-08-26 /pmc/articles/PMC7477661/ /pubmed/32952864 http://dx.doi.org/10.4252/wjsc.v12.i8.879 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Systematic Reviews
Wang, Jing-Hua
Liu, Xiao-Ling
Sun, Jian-Mei
Yang, Jing-Han
Xu, Dong-Hua
Yan, Shu-Shan
Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review
title Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review
title_full Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review
title_fullStr Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review
title_full_unstemmed Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review
title_short Role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: A systematic review
title_sort role of mesenchymal stem cell derived extracellular vesicles in autoimmunity: a systematic review
topic Systematic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477661/
https://www.ncbi.nlm.nih.gov/pubmed/32952864
http://dx.doi.org/10.4252/wjsc.v12.i8.879
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