» Articles » PMID: 22320928

Human Umbilical Cord Mesenchymal Stem Cells Improve Liver Function and Ascites in Decompensated Liver Cirrhosis Patients

Overview
Specialty Gastroenterology
Date 2012 Feb 11
PMID 22320928
Citations 156
Authors
Affiliations
Soon will be listed here.
Abstract

Decompensated liver cirrhosis (LC), a life-threatening complication of chronic liver disease, is one of the major indications for liver transplantation. Recently, mesenchymal stem cell (MSC) transfusion has been shown to lead to the regression of liver fibrosis in mice and humans. This study examined the safety and efficacy of umbilical cord-derived MSC (UC-MSC) in patients with decompensated LC. A total of 45 chronic hepatitis B patients with decompensated LC, including 30 patients receiving UC-MSC transfusion, and 15 patients receiving saline as the control, were recruited; clinical parameters were detected during a 1-year follow-up period. No significant side-effects and complications were observed in either group. There was a significant reduction in the volume of ascites in patients treated with UC-MSC transfusion compared with controls (P < 0.05). UC-MSC therapy also significantly improved liver function, as indicated by the increase of serum albumin levels, decrease in total serum bilirubin levels, and decrease in the sodium model for end-stage liver disease scores. UC-MSC transfusion is clinically safe and could improve liver function and reduce ascites in patients with decompensated LC. UC-MSC transfusion, therefore, might present a novel therapeutic approach for patients with decompensated LC.

Citing Articles

Exosomes containing miR-148a-3p derived from mesenchymal stem cells suppress epithelial-mesenchymal transition in lens epithelial cells.

Ma J, Sun Q, Chen Y, Li J, Chen S, Luo L Stem Cells Transl Med. 2025; 14(2).

PMID: 40036306 PMC: 11878568. DOI: 10.1093/stcltm/szae091.


Characterization and Proteomic Profiling of Hepatocyte-like Cells Derived from Human Wharton's Jelly Mesenchymal Stromal Cells: De Novo Expression of Liver-Specific Enzymes.

Lo Iacono M, Corrao S, Alberti G, Amico G, Timoneri F, Russo E Biology (Basel). 2025; 14(2).

PMID: 40001892 PMC: 11851833. DOI: 10.3390/biology14020124.


Hotspots and trends in stem cell therapy for liver fibrosis and cirrhosis: A bibliometric analysis.

Zhu W, Li X, Xie J, Lu Q, Ma Y, Zhu Z World J Hepatol. 2025; 17(1):96105.

PMID: 39871895 PMC: 11736489. DOI: 10.4254/wjh.v17.i1.96105.


Human Liver MSCs Retain Their Basic Cellular Properties in Chronically Inflamed Liver Tissue.

Kim Y, Lupatov A, Burunova V, Bagmet N, Chardarov N, Malov S Int J Mol Sci. 2025; 25(24.

PMID: 39769138 PMC: 11676302. DOI: 10.3390/ijms252413374.


A comprehensive evaluation system for ultrasound-guided infusion of human umbilical cord-derived MSCs in liver cirrhosis patients.

Zhou G, You Y, Wang B, Wang S, Feng T, Lai C Stem Cells Transl Med. 2024; 14(1).

PMID: 39520328 PMC: 11821905. DOI: 10.1093/stcltm/szae081.