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Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis

INTRODUCTION: Extracellular vesicles (EVs), especially stem cell-derived EVs, have emerged as a potential novel therapy for acute kidney injury (AKI). However, their effects remain incompletely understood. Therefore, we performed this meta-analysis to systematically review the efficacy of EVs on AKI...

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Autores principales: Liu, Chao, Wang, Jin, Hu, Jie, Fu, Bo, Mao, Zhi, Zhang, Hengda, Cai, Guangyan, Chen, Xiangmei, Sun, Xuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942291/
https://www.ncbi.nlm.nih.gov/pubmed/31900218
http://dx.doi.org/10.1186/s13287-019-1530-4
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author Liu, Chao
Wang, Jin
Hu, Jie
Fu, Bo
Mao, Zhi
Zhang, Hengda
Cai, Guangyan
Chen, Xiangmei
Sun, Xuefeng
author_facet Liu, Chao
Wang, Jin
Hu, Jie
Fu, Bo
Mao, Zhi
Zhang, Hengda
Cai, Guangyan
Chen, Xiangmei
Sun, Xuefeng
author_sort Liu, Chao
collection PubMed
description INTRODUCTION: Extracellular vesicles (EVs), especially stem cell-derived EVs, have emerged as a potential novel therapy for acute kidney injury (AKI). However, their effects remain incompletely understood. Therefore, we performed this meta-analysis to systematically review the efficacy of EVs on AKI in preclinical rodent models. METHODS: We searched PubMed, EMBASE, and the Web of Science up to March 2019 to identify studies that reported the treatment effects of EVs in a rodent AKI model. The primary outcome was serum creatinine (Scr) levels. The secondary outcomes were the blood urea nitrogen (BUN) levels, renal injury score, percentage of apoptotic cells, and interleukin (IL)-10 and tumour necrosis factor (TNF)-α levels. Two authors independently screened articles based on the inclusion and exclusion criteria. The meta-analysis was conducted using RevMan 5.3 and R software. RESULTS: Thirty-one studies (n = 552) satisfied the inclusion criteria. Pooled analyses demonstrated that the levels of Scr (SMD = − 3.71; 95% CI = − 4.32, − 3.10; P < 0.01), BUN (SMD = − 3.68; 95% CI = − 4.42, − 2.94; P < 0.01), and TNF-α (SMD = − 2.65; 95% CI = − 4.98, − 0.32; P < 0.01); the percentage of apoptotic cells (SMD = − 6.25; 95% CI = − 8.10, − 4.39; P < 0.01); and the injury score (SMD = − 3.90; 95% CI = − 5.26, − 2.53; P < 0.01) were significantly decreased in the EV group, and the level of IL-10 (SMD = 2.10; 95% CI = 1.18, 3.02; P < 0.01) was significantly increased. Meanwhile, no significant difference was found between stem cell-derived EVs and stem cells. CONCLUSION: The present meta-analysis confirmed that EV therapy could improve renal function and the inflammatory response status and reduce cell apoptosis in a preclinical rodent AKI model. This provides important clues for human clinical trials on EVs.
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spelling pubmed-69422912020-01-07 Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis Liu, Chao Wang, Jin Hu, Jie Fu, Bo Mao, Zhi Zhang, Hengda Cai, Guangyan Chen, Xiangmei Sun, Xuefeng Stem Cell Res Ther Research INTRODUCTION: Extracellular vesicles (EVs), especially stem cell-derived EVs, have emerged as a potential novel therapy for acute kidney injury (AKI). However, their effects remain incompletely understood. Therefore, we performed this meta-analysis to systematically review the efficacy of EVs on AKI in preclinical rodent models. METHODS: We searched PubMed, EMBASE, and the Web of Science up to March 2019 to identify studies that reported the treatment effects of EVs in a rodent AKI model. The primary outcome was serum creatinine (Scr) levels. The secondary outcomes were the blood urea nitrogen (BUN) levels, renal injury score, percentage of apoptotic cells, and interleukin (IL)-10 and tumour necrosis factor (TNF)-α levels. Two authors independently screened articles based on the inclusion and exclusion criteria. The meta-analysis was conducted using RevMan 5.3 and R software. RESULTS: Thirty-one studies (n = 552) satisfied the inclusion criteria. Pooled analyses demonstrated that the levels of Scr (SMD = − 3.71; 95% CI = − 4.32, − 3.10; P < 0.01), BUN (SMD = − 3.68; 95% CI = − 4.42, − 2.94; P < 0.01), and TNF-α (SMD = − 2.65; 95% CI = − 4.98, − 0.32; P < 0.01); the percentage of apoptotic cells (SMD = − 6.25; 95% CI = − 8.10, − 4.39; P < 0.01); and the injury score (SMD = − 3.90; 95% CI = − 5.26, − 2.53; P < 0.01) were significantly decreased in the EV group, and the level of IL-10 (SMD = 2.10; 95% CI = 1.18, 3.02; P < 0.01) was significantly increased. Meanwhile, no significant difference was found between stem cell-derived EVs and stem cells. CONCLUSION: The present meta-analysis confirmed that EV therapy could improve renal function and the inflammatory response status and reduce cell apoptosis in a preclinical rodent AKI model. This provides important clues for human clinical trials on EVs. BioMed Central 2020-01-03 /pmc/articles/PMC6942291/ /pubmed/31900218 http://dx.doi.org/10.1186/s13287-019-1530-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Liu, Chao
Wang, Jin
Hu, Jie
Fu, Bo
Mao, Zhi
Zhang, Hengda
Cai, Guangyan
Chen, Xiangmei
Sun, Xuefeng
Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis
title Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis
title_full Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis
title_fullStr Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis
title_full_unstemmed Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis
title_short Extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis
title_sort extracellular vesicles for acute kidney injury in preclinical rodent models: a meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942291/
https://www.ncbi.nlm.nih.gov/pubmed/31900218
http://dx.doi.org/10.1186/s13287-019-1530-4
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