Efficacy and safety of mesenchymal stem cell therapy in acute on chronic liver failure: a systematic review and meta-analysis of randomized controlled clinical trials
Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, wh...
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Published in | Stem cell research & therapy Vol. 16; no. 1; pp. 197 - 14 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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BioMed Central Ltd
20.04.2025
BioMed Central BMC |
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Abstract | Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, which is related to intense systemic inflammation and subsequently causes the inflammatory cytokine storm, resulting in portal hypertension, organ dysfunction, and organ failure. Mesenchymal stem cells can function as seed cells to remodel and repair damaged liver tissues, thus showing potential therapeutic alternatives for patients with chronic liver disease. However, standard treatment protocols for mesenchymal stem cells in acute-on-chronic liver failure patients have not been established.
We conducted a detailed search from PubMed/Medline, Web of Science, EMBASE, and Cochrane Library to find randomized controlled trials published before October 23, 2021. We formulated criteria for the literature screening according to the PICOS principle (Population, Intervention, Comparison, Outcome, Study design). Subsequently, the bias risk assessment tool was used to assess the quality of all enrolled studies. Finally, outcome measurements including the model of end-stage liver disease score, albumin, total bilirubin, coagulation function, and aminotransferase were extracted for statistical analysis.
A total of 7 clinical trials were included. The results of enrolled studies indicated that patients with acute-on-chronic liver failure who received mesenchymal stem cells inoculation showed a decreased MELD score in 4 weeks and 24 weeks, compared with counterparts who received conventional treatment. Reciprocally, mesenchymal stem cells inoculation improved the ALB levels in 4 weeks and 24 weeks. For secondary indicators, mesenchymal stem cells treatment significantly reduced INR levels and ALT levels, compared with the control group. Our results showed no significant differences in the incidence of adverse reactions or serious adverse events monitored in patients after mesenchymal stem cells inoculation.
This meta-analysis indicated that mesenchymal stem cell infusion is effective and safe in the treatment of patients with acute-on-chronic liver failure. Without increasing the incidence of adverse events or serious adverse events, MSC treatment improved liver function including a decrease in MELD score and an increase in ALB levels in patients with acute-on-chronic liver failure. However, large-cohort randomized controlled trials with longer follow-up periods are required to further confirm our conclusions. |
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AbstractList | Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, which is related to intense systemic inflammation and subsequently causes the inflammatory cytokine storm, resulting in portal hypertension, organ dysfunction, and organ failure. Mesenchymal stem cells can function as seed cells to remodel and repair damaged liver tissues, thus showing potential therapeutic alternatives for patients with chronic liver disease. However, standard treatment protocols for mesenchymal stem cells in acute-on-chronic liver failure patients have not been established. We conducted a detailed search from PubMed/Medline, Web of Science, EMBASE, and Cochrane Library to find randomized controlled trials published before October 23, 2021. We formulated criteria for the literature screening according to the PICOS principle (Population, Intervention, Comparison, Outcome, Study design). Subsequently, the bias risk assessment tool was used to assess the quality of all enrolled studies. Finally, outcome measurements including the model of end-stage liver disease score, albumin, total bilirubin, coagulation function, and aminotransferase were extracted for statistical analysis. A total of 7 clinical trials were included. The results of enrolled studies indicated that patients with acute-on-chronic liver failure who received mesenchymal stem cells inoculation showed a decreased MELD score in 4 weeks and 24 weeks, compared with counterparts who received conventional treatment. Reciprocally, mesenchymal stem cells inoculation improved the ALB levels in 4 weeks and 24 weeks. For secondary indicators, mesenchymal stem cells treatment significantly reduced INR levels and ALT levels, compared with the control group. Our results showed no significant differences in the incidence of adverse reactions or serious adverse events monitored in patients after mesenchymal stem cells inoculation. This meta-analysis indicated that mesenchymal stem cell infusion is effective and safe in the treatment of patients with acute-on-chronic liver failure. Without increasing the incidence of adverse events or serious adverse events, MSC treatment improved liver function including a decrease in MELD score and an increase in ALB levels in patients with acute-on-chronic liver failure. However, large-cohort randomized controlled trials with longer follow-up periods are required to further confirm our conclusions. Background Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, which is related to intense systemic inflammation and subsequently causes the inflammatory cytokine storm, resulting in portal hypertension, organ dysfunction, and organ failure. Mesenchymal stem cells can function as seed cells to remodel and repair damaged liver tissues, thus showing potential therapeutic alternatives for patients with chronic liver disease. However, standard treatment protocols for mesenchymal stem cells in acute-on-chronic liver failure patients have not been established. Methods We conducted a detailed search from PubMed/Medline, Web of Science, EMBASE, and Cochrane Library to find randomized controlled trials published before October 23, 2021. We formulated criteria for the literature screening according to the PICOS principle (Population, Intervention, Comparison, Outcome, Study design). Subsequently, the bias risk assessment tool was used to assess the quality of all enrolled studies. Finally, outcome measurements including the model of end-stage liver disease score, albumin, total bilirubin, coagulation function, and aminotransferase were extracted for statistical analysis. Results A total of 7 clinical trials were included. The results of enrolled studies indicated that patients with acute-on-chronic liver failure who received mesenchymal stem cells inoculation showed a decreased MELD score in 4 weeks and 24 weeks, compared with counterparts who received conventional treatment. Reciprocally, mesenchymal stem cells inoculation improved the ALB levels in 4 weeks and 24 weeks. For secondary indicators, mesenchymal stem cells treatment significantly reduced INR levels and ALT levels, compared with the control group. Our results showed no significant differences in the incidence of adverse reactions or serious adverse events monitored in patients after mesenchymal stem cells inoculation. Conclusion This meta-analysis indicated that mesenchymal stem cell infusion is effective and safe in the treatment of patients with acute-on-chronic liver failure. Without increasing the incidence of adverse events or serious adverse events, MSC treatment improved liver function including a decrease in MELD score and an increase in ALB levels in patients with acute-on-chronic liver failure. However, large-cohort randomized controlled trials with longer follow-up periods are required to further confirm our conclusions. Keywords: Mesenchymal stem cells, Acute-on-chronic liver failure, Efficacy, Safety, Meta-analysis Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, which is related to intense systemic inflammation and subsequently causes the inflammatory cytokine storm, resulting in portal hypertension, organ dysfunction, and organ failure. Mesenchymal stem cells can function as seed cells to remodel and repair damaged liver tissues, thus showing potential therapeutic alternatives for patients with chronic liver disease. However, standard treatment protocols for mesenchymal stem cells in acute-on-chronic liver failure patients have not been established.BACKGROUNDAcute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, which is related to intense systemic inflammation and subsequently causes the inflammatory cytokine storm, resulting in portal hypertension, organ dysfunction, and organ failure. Mesenchymal stem cells can function as seed cells to remodel and repair damaged liver tissues, thus showing potential therapeutic alternatives for patients with chronic liver disease. However, standard treatment protocols for mesenchymal stem cells in acute-on-chronic liver failure patients have not been established.We conducted a detailed search from PubMed/Medline, Web of Science, EMBASE, and Cochrane Library to find randomized controlled trials published before October 23, 2021. We formulated criteria for the literature screening according to the PICOS principle (Population, Intervention, Comparison, Outcome, Study design). Subsequently, the bias risk assessment tool was used to assess the quality of all enrolled studies. Finally, outcome measurements including the model of end-stage liver disease score, albumin, total bilirubin, coagulation function, and aminotransferase were extracted for statistical analysis.METHODSWe conducted a detailed search from PubMed/Medline, Web of Science, EMBASE, and Cochrane Library to find randomized controlled trials published before October 23, 2021. We formulated criteria for the literature screening according to the PICOS principle (Population, Intervention, Comparison, Outcome, Study design). Subsequently, the bias risk assessment tool was used to assess the quality of all enrolled studies. Finally, outcome measurements including the model of end-stage liver disease score, albumin, total bilirubin, coagulation function, and aminotransferase were extracted for statistical analysis.A total of 7 clinical trials were included. The results of enrolled studies indicated that patients with acute-on-chronic liver failure who received mesenchymal stem cells inoculation showed a decreased MELD score in 4 weeks and 24 weeks, compared with counterparts who received conventional treatment. Reciprocally, mesenchymal stem cells inoculation improved the ALB levels in 4 weeks and 24 weeks. For secondary indicators, mesenchymal stem cells treatment significantly reduced INR levels and ALT levels, compared with the control group. Our results showed no significant differences in the incidence of adverse reactions or serious adverse events monitored in patients after mesenchymal stem cells inoculation.RESULTSA total of 7 clinical trials were included. The results of enrolled studies indicated that patients with acute-on-chronic liver failure who received mesenchymal stem cells inoculation showed a decreased MELD score in 4 weeks and 24 weeks, compared with counterparts who received conventional treatment. Reciprocally, mesenchymal stem cells inoculation improved the ALB levels in 4 weeks and 24 weeks. For secondary indicators, mesenchymal stem cells treatment significantly reduced INR levels and ALT levels, compared with the control group. Our results showed no significant differences in the incidence of adverse reactions or serious adverse events monitored in patients after mesenchymal stem cells inoculation.This meta-analysis indicated that mesenchymal stem cell infusion is effective and safe in the treatment of patients with acute-on-chronic liver failure. Without increasing the incidence of adverse events or serious adverse events, MSC treatment improved liver function including a decrease in MELD score and an increase in ALB levels in patients with acute-on-chronic liver failure. However, large-cohort randomized controlled trials with longer follow-up periods are required to further confirm our conclusions.CONCLUSIONThis meta-analysis indicated that mesenchymal stem cell infusion is effective and safe in the treatment of patients with acute-on-chronic liver failure. Without increasing the incidence of adverse events or serious adverse events, MSC treatment improved liver function including a decrease in MELD score and an increase in ALB levels in patients with acute-on-chronic liver failure. However, large-cohort randomized controlled trials with longer follow-up periods are required to further confirm our conclusions. Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, which is related to intense systemic inflammation and subsequently causes the inflammatory cytokine storm, resulting in portal hypertension, organ dysfunction, and organ failure. Mesenchymal stem cells can function as seed cells to remodel and repair damaged liver tissues, thus showing potential therapeutic alternatives for patients with chronic liver disease. However, standard treatment protocols for mesenchymal stem cells in acute-on-chronic liver failure patients have not been established. We conducted a detailed search from PubMed/Medline, Web of Science, EMBASE, and Cochrane Library to find randomized controlled trials published before October 23, 2021. We formulated criteria for the literature screening according to the PICOS principle (Population, Intervention, Comparison, Outcome, Study design). Subsequently, the bias risk assessment tool was used to assess the quality of all enrolled studies. Finally, outcome measurements including the model of end-stage liver disease score, albumin, total bilirubin, coagulation function, and aminotransferase were extracted for statistical analysis. A total of 7 clinical trials were included. The results of enrolled studies indicated that patients with acute-on-chronic liver failure who received mesenchymal stem cells inoculation showed a decreased MELD score in 4 weeks and 24 weeks, compared with counterparts who received conventional treatment. Reciprocally, mesenchymal stem cells inoculation improved the ALB levels in 4 weeks and 24 weeks. For secondary indicators, mesenchymal stem cells treatment significantly reduced INR levels and ALT levels, compared with the control group. Our results showed no significant differences in the incidence of adverse reactions or serious adverse events monitored in patients after mesenchymal stem cells inoculation. This meta-analysis indicated that mesenchymal stem cell infusion is effective and safe in the treatment of patients with acute-on-chronic liver failure. Without increasing the incidence of adverse events or serious adverse events, MSC treatment improved liver function including a decrease in MELD score and an increase in ALB levels in patients with acute-on-chronic liver failure. However, large-cohort randomized controlled trials with longer follow-up periods are required to further confirm our conclusions. Abstract Background Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving organ failure, and high short-term mortality in patients with chronic liver disease. The pathogenesis includes extensive hepatic necrosis, which is related to intense systemic inflammation and subsequently causes the inflammatory cytokine storm, resulting in portal hypertension, organ dysfunction, and organ failure. Mesenchymal stem cells can function as seed cells to remodel and repair damaged liver tissues, thus showing potential therapeutic alternatives for patients with chronic liver disease. However, standard treatment protocols for mesenchymal stem cells in acute-on-chronic liver failure patients have not been established. Methods We conducted a detailed search from PubMed/Medline, Web of Science, EMBASE, and Cochrane Library to find randomized controlled trials published before October 23, 2021. We formulated criteria for the literature screening according to the PICOS principle (Population, Intervention, Comparison, Outcome, Study design). Subsequently, the bias risk assessment tool was used to assess the quality of all enrolled studies. Finally, outcome measurements including the model of end-stage liver disease score, albumin, total bilirubin, coagulation function, and aminotransferase were extracted for statistical analysis. Results A total of 7 clinical trials were included. The results of enrolled studies indicated that patients with acute-on-chronic liver failure who received mesenchymal stem cells inoculation showed a decreased MELD score in 4 weeks and 24 weeks, compared with counterparts who received conventional treatment. Reciprocally, mesenchymal stem cells inoculation improved the ALB levels in 4 weeks and 24 weeks. For secondary indicators, mesenchymal stem cells treatment significantly reduced INR levels and ALT levels, compared with the control group. Our results showed no significant differences in the incidence of adverse reactions or serious adverse events monitored in patients after mesenchymal stem cells inoculation. Conclusion This meta-analysis indicated that mesenchymal stem cell infusion is effective and safe in the treatment of patients with acute-on-chronic liver failure. Without increasing the incidence of adverse events or serious adverse events, MSC treatment improved liver function including a decrease in MELD score and an increase in ALB levels in patients with acute-on-chronic liver failure. However, large-cohort randomized controlled trials with longer follow-up periods are required to further confirm our conclusions. |
ArticleNumber | 197 |
Audience | Academic |
Author | Yan, Longxiang Ye, Junsong Peng, Lulu Zhou, Lin Wang, Xuesong Tang, Xingkun Lin, Jing Du, Jing Zou, Zhengwei Li, Lincai Lu, Wenming |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40254564$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1111/1756-185X.13015 10.1016/j.jhep.2016.12.003 10.1007/s00018-022-04207-3 10.1186/s13287-020-01787-4 10.3389/fmed.2021.752875 10.1186/s13287-023-03494-2 10.1111/j.1365-2249.2011.04327.x 10.1242/jcs.076935 10.1016/j.bbmt.2010.01.011 10.1080/17474124.2022.2097070 10.1359/jbmr.1999.14.7.1115 10.1002/jcla.24353 10.1186/s13287-024-03722-3 10.2174/1574888X18666221214123844 10.1002/wsbm.26 10.1016/j.ajt.2024.02.001 10.1002/hep.24434 10.1371/journal.pone.0006657 10.1186/s13287-021-02468-6 10.1016/S2468-1253(23)00363-1 10.1016/j.heliyon.2024.e25791 10.3389/ti.2022.10108 10.1016/j.bbrc.2007.01.045 10.1007/s12015-016-9683-3 10.1186/s13287-022-03054-0 10.1111/j.1440-1746.2011.07024.x 10.3350/cmh.2022.0103 10.1186/s13287-022-03001-z 10.1186/s13287-023-03518-x 10.3389/fbioe.2022.1006845 10.3390/ijms25042073 10.1038/emm.2017.63 10.1007/s00441-012-1524-3 10.1186/s13287-019-1310-1 10.1097/MEG.0000000000001156 10.3390/ijms140917986 10.3389/fimmu.2021.728190 10.1002/hep.29189 10.1161/01.CIR.0000167553.49133.81 10.1186/s12967-014-0246-6 10.1038/s41598-024-55103-8 10.1007/s10350-005-0052-6 10.1136/gutjnl-2020-322161 10.1136/gutjnl-2016-312670 10.1155/2019/4130757 10.14309/ajg.0000000000000388 10.3389/fimmu.2022.935160 10.1097/SLA.0000000000001155 10.1136/gut.2006.111617 10.1089/scd.2012.0395 10.1136/ard.2009.123463 10.1002/hep.30056 10.1089/scd.2013.0142 10.1016/j.jneuroim.2010.07.013 10.3389/fphar.2016.00231 10.1038/s41598-018-23396-1 10.3748/wjg.v21.i42.12125 10.3748/wjg.v20.i38.14051 10.3727/096368911X566208 10.1186/s13287-018-0814-4 10.1186/s13287-019-1287-9 10.1038/bmt.2008.348 10.3748/wjg.v26.i2.219 10.1053/j.gastro.2013.02.042 10.3727/096368909X484707a 10.1136/gut.2005.090050 10.1155/2018/6079642 10.1111/j.1478-3231.2009.02031.x 10.1089/scd.2013.0477 10.1186/s13287-021-02138-7 10.1016/S1499-3872(16)60141-8 10.3390/ijms25042285 10.1073/pnas.0608249103 10.1002/ueg2.12482 10.1186/s13287-022-02858-4 10.3350/cmh.2024.0758 10.1002/lt.21715 10.1016/j.jcyt.2015.10.008 10.1186/s13613-017-0249-6 10.1186/s13287-022-02882-4 10.1002/lt.25678 10.1155/2021/3662776 10.1038/s41423-023-00983-5 10.21037/atm.2020.02.119 10.3389/fped.2022.897398 10.5966/sctm.2012-0034 10.3748/wjg.v29.i2.232 10.1016/S0140-6736(19)31894-X |
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Keywords | Acute-on-chronic liver failure Efficacy Safety Mesenchymal stem cells Meta-analysis |
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References | BL Lin (4303_CR45) 2017; 66 R Moreau (4303_CR4) 2013; 144 Y Zhang (4303_CR84) 2014; 6 NS Hwang (4303_CR80) 2009; 1 J Veevers-Lowe (4303_CR36) 2011; 124 D García-Olmo (4303_CR31) 2005; 48 F Cheng (4303_CR48) 2023; 18 M Shi (4303_CR87) 2011; 164 F Artru (4303_CR5) 2024; 24 CZ Bai (4303_CR6) 2024; 10 G D’Ippolito (4303_CR62) 1999; 14 TS Li (4303_CR32) 2005; 111 M Wu (4303_CR61) 2018; 8 A Marote (4303_CR69) 2016; 7 C Hu (4303_CR63) 2019; 10 J Liang (4303_CR82) 2017; 20 L Yao (4303_CR68) 2022; 13 S Gawrieh (4303_CR85) 2019; 114 4303_CR27 HJ Jin (4303_CR59) 2013; 14 S Diederichs (4303_CR60) 2014; 23 B Yamout (4303_CR29) 2010; 227 X Liu (4303_CR64) 2022; 36 J Qu (4303_CR79) 2022; 10 G Maged (4303_CR24) 2024; 15 4303_CR73 M Morrison (4303_CR3) 2023; 11 J Wendon (4303_CR11) 2017; 66 VB Konala (4303_CR70) 2016; 18 T Li (4303_CR71) 2013; 22 R Qiang (4303_CR8) 2022; 13 MS Schulz (4303_CR7) 2022; 35 A Li (4303_CR23) 2021; 12 W Lu (4303_CR26) 2023; 14 L Wei (4303_CR83) 2014; 12 AA Khan (4303_CR77) 2010; 19 L Zhao (4303_CR25) 2019; 10 F Artru (4303_CR16) 2024; 9 G Lou (4303_CR72) 2017; 49 I Aurich (4303_CR88) 2007; 56 XN Pan (4303_CR19) 2014; 20 ML Macmillan (4303_CR38) 2009; 43 JS Bajaj (4303_CR12) 2022; 117 R Hernaez (4303_CR1) 2017; 66 NLY Ngu (4303_CR2) 2023; 29 F Baron (4303_CR37) 2010; 16 J Qu (4303_CR35) 2022; 10 EX Tan (4303_CR53) 2020; 26 4303_CR44 J Puppi (4303_CR76) 2012; 21 D Weil (4303_CR14) 2017; 7 N Abbas (4303_CR15) 2022; 16 H Guo (4303_CR28) 2024; 14 4303_CR41 KH Jung (4303_CR66) 2009; 29 X Yang (4303_CR81) 2023; 20 X Zhu (4303_CR86) 2013; 351 Y He (4303_CR55) 2021; 12 Y Iso (4303_CR33) 2007; 354 RH Lee (4303_CR34) 2006; 103 Y Tang (4303_CR20) 2021; 12 B Chen (4303_CR47) 2018; 30 H Wang (4303_CR49) 2023; 14 Y Zhang (4303_CR18) 2018; 9 Y Cao (4303_CR58) 2020; 8 Y Liu (4303_CR46) 2022; 13 G Mezzano (4303_CR52) 2022; 71 G Cullaro (4303_CR10) 2020; 26 4303_CR13 A Khanam (4303_CR51) 2021; 8 4303_CR54 R Margiana (4303_CR21) 2022; 13 YH Li (4303_CR40) 2016; 12 L Peng (4303_CR42) 2011; 54 VK Br (4303_CR9) 2023; 29 J Liang (4303_CR30) 2010; 69 M Shi (4303_CR43) 2012; 1 RM Baertschiger (4303_CR90) 2009; 4 F Velarde (4303_CR22) 2022; 79 LV di Bonzo (4303_CR89) 2008; 57 Y Jia (4303_CR50) 2020; 11 JS Bajaj (4303_CR57) 2018; 68 PC Tsai (4303_CR67) 2009; 15 Z Zhang (4303_CR65) 2012; 27 HM Tautenhahn (4303_CR39) 2016; 263 S Blasco-Algora (4303_CR17) 2015; 21 JF Sang (4303_CR78) 2016; 15 L Zhang (4303_CR75) 2013; 22 RT Stravitz (4303_CR56) 2019; 394 M Yuan (4303_CR74) 2022; 13 |
References_xml | – volume: 20 start-page: 1219 issue: 9 year: 2017 ident: 4303_CR82 publication-title: Int J Rheum Dis doi: 10.1111/1756-185X.13015 – volume: 66 start-page: 1047 issue: 5 year: 2017 ident: 4303_CR11 publication-title: J Hepatol doi: 10.1016/j.jhep.2016.12.003 – volume: 79 start-page: 177 issue: 3 year: 2022 ident: 4303_CR22 publication-title: Cell Mol Life Sci doi: 10.1007/s00018-022-04207-3 – volume: 11 start-page: 277 issue: 1 year: 2020 ident: 4303_CR50 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-020-01787-4 – volume: 8 start-page: 752875 year: 2021 ident: 4303_CR51 publication-title: Front Med (Lausanne) doi: 10.3389/fmed.2021.752875 – volume: 14 start-page: 267 issue: 1 year: 2023 ident: 4303_CR49 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-023-03494-2 – volume: 164 start-page: 1 issue: 1 year: 2011 ident: 4303_CR87 publication-title: Clin Exp Immunol doi: 10.1111/j.1365-2249.2011.04327.x – volume: 124 start-page: 1288 issue: Pt 8 year: 2011 ident: 4303_CR36 publication-title: J Cell Sci doi: 10.1242/jcs.076935 – volume: 16 start-page: 838 issue: 6 year: 2010 ident: 4303_CR37 publication-title: Biol Blood Marrow Transpl doi: 10.1016/j.bbmt.2010.01.011 – volume: 16 start-page: 639 issue: 7 year: 2022 ident: 4303_CR15 publication-title: Expert Rev Gastroenterol Hepatol doi: 10.1080/17474124.2022.2097070 – volume: 14 start-page: 1115 issue: 7 year: 1999 ident: 4303_CR62 publication-title: J Bone Min Res doi: 10.1359/jbmr.1999.14.7.1115 – volume: 36 start-page: e24353 issue: 5 year: 2022 ident: 4303_CR64 publication-title: J Clin Lab Anal doi: 10.1002/jcla.24353 – volume: 15 start-page: 112 issue: 1 year: 2024 ident: 4303_CR24 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-024-03722-3 – volume: 18 start-page: 834 issue: 6 year: 2023 ident: 4303_CR48 publication-title: Curr Stem Cell Res Ther doi: 10.2174/1574888X18666221214123844 – volume: 1 start-page: 97 issue: 1 year: 2009 ident: 4303_CR80 publication-title: Wiley Interdiscip Rev Syst Biol Med doi: 10.1002/wsbm.26 – volume: 24 start-page: 724 issue: 5 year: 2024 ident: 4303_CR5 publication-title: Am J Transpl doi: 10.1016/j.ajt.2024.02.001 – volume: 54 start-page: 820 issue: 3 year: 2011 ident: 4303_CR42 publication-title: Hepatology doi: 10.1002/hep.24434 – volume: 4 start-page: e6657 issue: 8 year: 2009 ident: 4303_CR90 publication-title: PLoS ONE doi: 10.1371/journal.pone.0006657 – volume: 12 start-page: 396 issue: 1 year: 2021 ident: 4303_CR55 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-021-02468-6 – volume: 9 start-page: 564 issue: 6 year: 2024 ident: 4303_CR16 publication-title: Lancet Gastroenterol Hepatol doi: 10.1016/S2468-1253(23)00363-1 – volume: 10 start-page: e25791 issue: 3 year: 2024 ident: 4303_CR6 publication-title: Heliyon doi: 10.1016/j.heliyon.2024.e25791 – volume: 35 start-page: 10108 year: 2022 ident: 4303_CR7 publication-title: Transpl Int doi: 10.3389/ti.2022.10108 – volume: 354 start-page: 700 issue: 3 year: 2007 ident: 4303_CR33 publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2007.01.045 – volume: 12 start-page: 645 issue: 6 year: 2016 ident: 4303_CR40 publication-title: Stem Cell Rev Rep doi: 10.1007/s12015-016-9683-3 – volume: 13 start-page: 366 issue: 1 year: 2022 ident: 4303_CR21 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-022-03054-0 – volume: 27 start-page: 112 issue: Suppl 2 year: 2012 ident: 4303_CR65 publication-title: J Gastroenterol Hepatol doi: 10.1111/j.1440-1746.2011.07024.x – volume: 29 start-page: 670 issue: 3 year: 2023 ident: 4303_CR9 publication-title: Clin Mol Hepatol doi: 10.3350/cmh.2022.0103 – volume: 13 start-page: 308 issue: 1 year: 2022 ident: 4303_CR68 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-022-03001-z – volume: 14 start-page: 301 issue: 1 year: 2023 ident: 4303_CR26 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-023-03518-x – volume: 10 start-page: 1006845 year: 2022 ident: 4303_CR79 publication-title: Front Bioeng Biotechnol doi: 10.3389/fbioe.2022.1006845 – ident: 4303_CR54 doi: 10.3390/ijms25042073 – volume: 49 start-page: e346 issue: 6 year: 2017 ident: 4303_CR72 publication-title: Exp Mol Med doi: 10.1038/emm.2017.63 – volume: 351 start-page: 477 issue: 3 year: 2013 ident: 4303_CR86 publication-title: Cell Tissue Res doi: 10.1007/s00441-012-1524-3 – volume: 10 start-page: 199 issue: 1 year: 2019 ident: 4303_CR63 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-019-1310-1 – volume: 30 start-page: 1224 issue: 10 year: 2018 ident: 4303_CR47 publication-title: Eur J Gastroenterol Hepatol doi: 10.1097/MEG.0000000000001156 – volume: 14 start-page: 17986 issue: 9 year: 2013 ident: 4303_CR59 publication-title: Int J Mol Sci doi: 10.3390/ijms140917986 – volume: 12 start-page: 728190 year: 2021 ident: 4303_CR23 publication-title: Front Immunol doi: 10.3389/fimmu.2021.728190 – volume: 66 start-page: 209 issue: 1 year: 2017 ident: 4303_CR45 publication-title: Hepatology doi: 10.1002/hep.29189 – volume: 111 start-page: 2438 issue: 19 year: 2005 ident: 4303_CR32 publication-title: Circulation doi: 10.1161/01.CIR.0000167553.49133.81 – volume: 12 start-page: 246 year: 2014 ident: 4303_CR83 publication-title: J Transl Med doi: 10.1186/s12967-014-0246-6 – volume: 14 start-page: 5838 issue: 1 year: 2024 ident: 4303_CR28 publication-title: Sci Rep doi: 10.1038/s41598-024-55103-8 – volume: 48 start-page: 1416 issue: 7 year: 2005 ident: 4303_CR31 publication-title: Dis Colon Rectum doi: 10.1007/s10350-005-0052-6 – volume: 71 start-page: 148 issue: 1 year: 2022 ident: 4303_CR52 publication-title: Gut doi: 10.1136/gutjnl-2020-322161 – volume: 66 start-page: 541 issue: 3 year: 2017 ident: 4303_CR1 publication-title: Gut doi: 10.1136/gutjnl-2016-312670 – ident: 4303_CR44 doi: 10.1155/2019/4130757 – volume: 114 start-page: 1626 issue: 10 year: 2019 ident: 4303_CR85 publication-title: Am J Gastroenterol doi: 10.14309/ajg.0000000000000388 – volume: 13 start-page: 935160 year: 2022 ident: 4303_CR8 publication-title: Front Immunol doi: 10.3389/fimmu.2022.935160 – volume: 263 start-page: 546 issue: 3 year: 2016 ident: 4303_CR39 publication-title: Ann Surg doi: 10.1097/SLA.0000000000001155 – volume: 57 start-page: 223 issue: 2 year: 2008 ident: 4303_CR89 publication-title: Gut doi: 10.1136/gut.2006.111617 – volume: 22 start-page: 845 issue: 6 year: 2013 ident: 4303_CR71 publication-title: Stem Cells Dev doi: 10.1089/scd.2012.0395 – volume: 69 start-page: 1423 issue: 8 year: 2010 ident: 4303_CR30 publication-title: Ann Rheum Dis doi: 10.1136/ard.2009.123463 – volume: 68 start-page: 1621 issue: 4 year: 2018 ident: 4303_CR57 publication-title: Hepatology doi: 10.1002/hep.30056 – volume: 22 start-page: 3074 issue: 23 year: 2013 ident: 4303_CR75 publication-title: Stem Cells Dev doi: 10.1089/scd.2013.0142 – volume: 227 start-page: 185 issue: 1–2 year: 2010 ident: 4303_CR29 publication-title: J Neuroimmunol doi: 10.1016/j.jneuroim.2010.07.013 – volume: 7 start-page: 231 year: 2016 ident: 4303_CR69 publication-title: Front Pharmacol doi: 10.3389/fphar.2016.00231 – volume: 6 start-page: 109 issue: 2 year: 2014 ident: 4303_CR84 publication-title: J Thorac Dis – volume: 8 start-page: 5014 issue: 1 year: 2018 ident: 4303_CR61 publication-title: Sci Rep doi: 10.1038/s41598-018-23396-1 – volume: 21 start-page: 12125 issue: 42 year: 2015 ident: 4303_CR17 publication-title: World J Gastroenterol doi: 10.3748/wjg.v21.i42.12125 – volume: 20 start-page: 14051 issue: 38 year: 2014 ident: 4303_CR19 publication-title: World J Gastroenterol doi: 10.3748/wjg.v20.i38.14051 – volume: 21 start-page: 1 issue: 1 year: 2012 ident: 4303_CR76 publication-title: Cell Transpl doi: 10.3727/096368911X566208 – volume: 9 start-page: 59 issue: 1 year: 2018 ident: 4303_CR18 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-018-0814-4 – volume: 10 start-page: 182 issue: 1 year: 2019 ident: 4303_CR25 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-019-1287-9 – volume: 43 start-page: 447 issue: 6 year: 2009 ident: 4303_CR38 publication-title: Bone Marrow Transpl doi: 10.1038/bmt.2008.348 – volume: 26 start-page: 219 issue: 2 year: 2020 ident: 4303_CR53 publication-title: World J Gastroenterol doi: 10.3748/wjg.v26.i2.219 – volume: 144 start-page: 1426 issue: 7 year: 2013 ident: 4303_CR4 publication-title: Gastroenterology doi: 10.1053/j.gastro.2013.02.042 – volume: 19 start-page: 409 issue: 4 year: 2010 ident: 4303_CR77 publication-title: Cell Transpl doi: 10.3727/096368909X484707a – volume: 56 start-page: 405 issue: 3 year: 2007 ident: 4303_CR88 publication-title: Gut doi: 10.1136/gut.2005.090050 – ident: 4303_CR73 doi: 10.1155/2018/6079642 – volume: 29 start-page: 898 issue: 6 year: 2009 ident: 4303_CR66 publication-title: Liver Int doi: 10.1111/j.1478-3231.2009.02031.x – volume: 23 start-page: 1594 issue: 14 year: 2014 ident: 4303_CR60 publication-title: Stem Cells Dev doi: 10.1089/scd.2013.0477 – volume: 12 start-page: 71 issue: 1 year: 2021 ident: 4303_CR20 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-021-02138-7 – volume: 15 start-page: 602 issue: 6 year: 2016 ident: 4303_CR78 publication-title: Hepatobiliary Pancreat Dis Int doi: 10.1016/S1499-3872(16)60141-8 – ident: 4303_CR27 doi: 10.3390/ijms25042285 – volume: 103 start-page: 17438 issue: 46 year: 2006 ident: 4303_CR34 publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0608249103 – volume: 11 start-page: 813 issue: 9 year: 2023 ident: 4303_CR3 publication-title: United Eur Gastroenterol J doi: 10.1002/ueg2.12482 – volume: 13 start-page: 179 issue: 1 year: 2022 ident: 4303_CR74 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-022-02858-4 – ident: 4303_CR13 doi: 10.3350/cmh.2024.0758 – volume: 15 start-page: 484 issue: 5 year: 2009 ident: 4303_CR67 publication-title: Liver Transpl doi: 10.1002/lt.21715 – volume: 18 start-page: 13 issue: 1 year: 2016 ident: 4303_CR70 publication-title: Cytotherapy doi: 10.1016/j.jcyt.2015.10.008 – volume: 7 start-page: 33 issue: 1 year: 2017 ident: 4303_CR14 publication-title: Ann Intensive Care doi: 10.1186/s13613-017-0249-6 – volume: 13 start-page: 204 issue: 1 year: 2022 ident: 4303_CR46 publication-title: Stem Cell Res Ther doi: 10.1186/s13287-022-02882-4 – volume: 26 start-page: 283 issue: 2 year: 2020 ident: 4303_CR10 publication-title: Liver Transpl doi: 10.1002/lt.25678 – volume: 117 start-page: 225 issue: 2 year: 2022 ident: 4303_CR12 publication-title: Am J Gastroenterol – ident: 4303_CR41 doi: 10.1155/2021/3662776 – volume: 20 start-page: 583 issue: 6 year: 2023 ident: 4303_CR81 publication-title: Cell Mol Immunol doi: 10.1038/s41423-023-00983-5 – volume: 8 start-page: 562 issue: 8 year: 2020 ident: 4303_CR58 publication-title: Ann Transl Med doi: 10.21037/atm.2020.02.119 – volume: 10 start-page: 897398 year: 2022 ident: 4303_CR35 publication-title: Front Pediatr doi: 10.3389/fped.2022.897398 – volume: 1 start-page: 725 issue: 10 year: 2012 ident: 4303_CR43 publication-title: Stem Cells Transl Med doi: 10.5966/sctm.2012-0034 – volume: 29 start-page: 232 issue: 2 year: 2023 ident: 4303_CR2 publication-title: World J Gastroenterol doi: 10.3748/wjg.v29.i2.232 – volume: 394 start-page: 869 issue: 10201 year: 2019 ident: 4303_CR56 publication-title: Lancet doi: 10.1016/S0140-6736(19)31894-X |
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Snippet | Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function, rapidly evolving... Background Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver function,... Abstract Background Acute-on-chronic liver failure has become a serious global health burden, which is characterized by an acute deterioration of liver... |
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SubjectTerms | Acute-on-chronic liver failure Acute-On-Chronic Liver Failure - therapy Bilirubin Cytokines Efficacy Health aspects Humans Inflammation Liver failure Medical research Medicine, Experimental Mesenchymal Stem Cell Transplantation - adverse effects Mesenchymal Stem Cell Transplantation - methods Mesenchymal stem cells Mesenchymal Stem Cells - cytology Meta-analysis Randomized Controlled Trials as Topic Review Safety Stem cells Transplantation |
Title | Efficacy and safety of mesenchymal stem cell therapy in acute on chronic liver failure: a systematic review and meta-analysis of randomized controlled clinical trials |
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