A study about immunomodulatory effect and efficacy and prognosis of human umbilical cord mesenchymal stem cells in patients with chronic hepatitis B‐induced decompensated liver cirrhosis

医学 胃肠病学 肝硬化 内科学 凝血酶原时间 胆红素 白蛋白 乙型肝炎 脐带 肝病 间充质干细胞 肝移植 B组 移植 干细胞 免疫学 病理 生物 遗传学
作者
Xueqing Fang,Liwei Liu,Jing Dong,Junfei Zhang,Haiyan Song,Youliang Song,Yizhe Huang,Xiaoling Cui,Jian Lin,Cong‐Xin Chen,Bo Liu,Zhaolin Chen,Jingjing Pan,Xi Chen
出处
期刊:Journal of Gastroenterology and Hepatology [Wiley]
卷期号:33 (4): 774-780 被引量:43
标识
DOI:10.1111/jgh.14081
摘要

Abstract Background and Aim The aim of our study was to investigate the immunomodulatory effect and short‐term efficacy and long‐term prognosis of decompensated liver cirrhosis patients caused by hepatitis B after a double transplantation with human umbilical cord mesenchymal stem cells (hUCMSCs). Methods Fifty inpatients were recruited and given the same medical treatments, receiving hUCMSCs injection intravenously. Fifty‐three patients (Group B) matched for age, sex, and baseline alanine aminotransferase, aspartate aminotransferase, albumin, total bilirubin, prothrombin time, and model for end‐stage liver disease score and Child–Pugh classification, acted as the control group. Results Interleukin‐6 and tumor necrosis factor alpha levels markedly decreased, and interleukin‐10 level apparently increased in Group A at 2 and 4 weeks after treatment. Transforming growth factor beta in Group A increased more remarkably at 2 weeks after treatment. T4 cells and Treg cells in Group A were apparently higher than those in Group B at 2 and 4 weeks after treatment, and T8 cells and B cells were significantly lower than those in Group B. Aspartate aminotransferase levels in Group A were dramatically declining at 8 and 12 weeks after treatment. Levels of albumin, total bilirubin, and prothrombin time in Group A were apparently improved from 4 to 12 weeks after treatment. The improvements in model for end‐stage liver disease and Child–Pugh scores in Group A were notably superior to those in Group B from 4 to 36 weeks after treatment. There were no remarkable differences in the incidence of developing liver failure throughout the follow‐up period, but the mortality rate of Group A was lower than that of Group B. Conclusion This therapeutic method may be an appropriate choice for patients with decompensated liver cirrhosis.
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