Cargando…
A pooled analysis of mesenchymal stem cell-based therapy for liver disease
BACKGROUND: Liver disease is a major cause of death and disability. Mesenchymal stem cells (MSCs) show promise for the treatment of liver disease. However, whether MSC-based therapy is more effective than conventional treatment is unclear, as are the optimal MSC source, the administration frequency,...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863358/ https://www.ncbi.nlm.nih.gov/pubmed/29562935 http://dx.doi.org/10.1186/s13287-018-0816-2 |
_version_ | 1783308371027296256 |
---|---|
author | Zhao, Lu Chen, Shanquan Shi, Xiaowei Cao, Hongcui Li, Lanjuan |
author_facet | Zhao, Lu Chen, Shanquan Shi, Xiaowei Cao, Hongcui Li, Lanjuan |
author_sort | Zhao, Lu |
collection | PubMed |
description | BACKGROUND: Liver disease is a major cause of death and disability. Mesenchymal stem cells (MSCs) show promise for the treatment of liver disease. However, whether MSC-based therapy is more effective than conventional treatment is unclear, as are the optimal MSC source, the administration frequency, and the most effective MSC delivery route. We therefore undertook a systematic review and meta-analysis of the therapeutic efficacy of MSCs against liver disease and the related factors. METHODS: We systematically searched Medline (PubMed), Cochrane Library, EMBASE, ClinicalTrials.gov, and SinoMed CBM to identify studies published up to June 2017 involving liver disease patients receiving MSC-based therapy and which reported estimates of liver function during the follow-up period. RESULTS: Thirty-nine studies were selected from 672 publications. According to a meta-analysis of 23 controlled studies, compared with conventional treatment MSC therapy significantly improves liver function in patients with liver disease in terms of the model of end-stage liver disease score, albumin, alanine aminotransferase, and total bilirubin levels, and prothrombin time, up to 6 months after administration. However, it has no beneficial effects in terms of prothrombin activity, international normalized ratio, or cholinesterase level. Considerable heterogeneity was identified at most time points. Subgroup analyses showed that a single MSC injection was more effective than multiple injections, MSC administration was more effective via the hepatic artery than the peripheral vein, and MSCs derived from bone marrow were more effective than those derived from the umbilical cord. CONCLUSIONS: MSC-based therapy is relatively safe and improves liver function during the first 6 months after administration. A single injection administration via the hepatic artery and MSCs derived from bone marrow are optimal in terms of improving liver function. However the significant heterogeneity among studies and discontinuous results of the subgroup meta-analysis should be addressed; moreover the long-term efficacy of MSC therapy warrants further investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0816-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5863358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58633582018-03-27 A pooled analysis of mesenchymal stem cell-based therapy for liver disease Zhao, Lu Chen, Shanquan Shi, Xiaowei Cao, Hongcui Li, Lanjuan Stem Cell Res Ther Review BACKGROUND: Liver disease is a major cause of death and disability. Mesenchymal stem cells (MSCs) show promise for the treatment of liver disease. However, whether MSC-based therapy is more effective than conventional treatment is unclear, as are the optimal MSC source, the administration frequency, and the most effective MSC delivery route. We therefore undertook a systematic review and meta-analysis of the therapeutic efficacy of MSCs against liver disease and the related factors. METHODS: We systematically searched Medline (PubMed), Cochrane Library, EMBASE, ClinicalTrials.gov, and SinoMed CBM to identify studies published up to June 2017 involving liver disease patients receiving MSC-based therapy and which reported estimates of liver function during the follow-up period. RESULTS: Thirty-nine studies were selected from 672 publications. According to a meta-analysis of 23 controlled studies, compared with conventional treatment MSC therapy significantly improves liver function in patients with liver disease in terms of the model of end-stage liver disease score, albumin, alanine aminotransferase, and total bilirubin levels, and prothrombin time, up to 6 months after administration. However, it has no beneficial effects in terms of prothrombin activity, international normalized ratio, or cholinesterase level. Considerable heterogeneity was identified at most time points. Subgroup analyses showed that a single MSC injection was more effective than multiple injections, MSC administration was more effective via the hepatic artery than the peripheral vein, and MSCs derived from bone marrow were more effective than those derived from the umbilical cord. CONCLUSIONS: MSC-based therapy is relatively safe and improves liver function during the first 6 months after administration. A single injection administration via the hepatic artery and MSCs derived from bone marrow are optimal in terms of improving liver function. However the significant heterogeneity among studies and discontinuous results of the subgroup meta-analysis should be addressed; moreover the long-term efficacy of MSC therapy warrants further investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0816-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-21 /pmc/articles/PMC5863358/ /pubmed/29562935 http://dx.doi.org/10.1186/s13287-018-0816-2 Text en © The Author(s). 2018 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 | Review Zhao, Lu Chen, Shanquan Shi, Xiaowei Cao, Hongcui Li, Lanjuan A pooled analysis of mesenchymal stem cell-based therapy for liver disease |
title | A pooled analysis of mesenchymal stem cell-based therapy for liver disease |
title_full | A pooled analysis of mesenchymal stem cell-based therapy for liver disease |
title_fullStr | A pooled analysis of mesenchymal stem cell-based therapy for liver disease |
title_full_unstemmed | A pooled analysis of mesenchymal stem cell-based therapy for liver disease |
title_short | A pooled analysis of mesenchymal stem cell-based therapy for liver disease |
title_sort | pooled analysis of mesenchymal stem cell-based therapy for liver disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863358/ https://www.ncbi.nlm.nih.gov/pubmed/29562935 http://dx.doi.org/10.1186/s13287-018-0816-2 |
work_keys_str_mv | AT zhaolu apooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT chenshanquan apooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT shixiaowei apooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT caohongcui apooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT lilanjuan apooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT zhaolu pooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT chenshanquan pooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT shixiaowei pooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT caohongcui pooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease AT lilanjuan pooledanalysisofmesenchymalstemcellbasedtherapyforliverdisease |