Zhou Tianbiao, Liao Chunling, Lin Shujun, Lin Wenshan, Zhong Hongzhen, Huang Shuangyi
Department of Nephrology, The Second Affiliated Hospital, Shantou University Medical College, 515041 Shantou, China.
Stem Cells Int. 2020 Aug 3;2020:1873921. doi: 10.1155/2020/1873921. eCollection 2020.
Mesenchymal stem cells (MSCs), discovered and isolated from the bone marrow in the 1960s and with self-renewal capacity and multilineage differentiation potential, have valuable immunomodulatory abilities. Acute kidney injury (AKI) refers to rapid renal failure, which exhibits as quickly progressive decreasing excretion in few hours or days. This study was performed to assess the efficacy of MSCs in the treatment of AKI induced by ischemia-reperfusion using a meta-analysis method. A literature search using corresponding terms was performed in the following databases: Embase, Cochrane Library, PubMed, and ISI Web of Science databases up to Dec 31, 2019. Data for outcomes were identified, and the efficacy of MSCs for AKI was assessed using Cochrane Review Manager Version 5.3. Nineteen studies were eligible and recruited for this meta-analysis. MSC treatment can reduce the Scr levels at 1 day, 2 days, 3 days, 5 days, and >7 days (1 day: WMD = -0.56, 95% CI: -0.78, -0.34, < 0.00001; 2 days: WMD = -0.58, 95% CI: -0.89, -0.28, = 0.0002; 3 days: WMD = -0.65, 95% CI: -0.84, -0.45, < 0.00001; 5 days: WMD = -0.35, 95% CI: -0.54, -0.16, = 0.0003; and >7 days: WMD = -0.22, 95% CI: -0.36, -0.08, = 0.002) and can reduce the levels of BUN at 1 day, 2 days, 3 days, and 5 days (1 day: WMD = -11.72, 95% CI: -18.80, -4.64, = 0.001; 2 days: WMD = -33.60, 95% CI: -40.15, -27.05, < 0.00001; 3 days: WMD = -21.14, 95% CI: -26.15, -16.14, < 0.00001; and 5 days: WMD = -8.88, 95% CI: -11.06, -6.69, < 0.00001), and it also can reduce the levels of proteinuria at 3 days and >7 days and alleviate the renal damage in animal models of AKI. In conclusion, MSCs might be a promising therapeutic agent for AKI induced by ischemia-reperfusion.
间充质干细胞(MSCs)于20世纪60年代从骨髓中被发现和分离出来,具有自我更新能力和多向分化潜能,还具备有价值的免疫调节能力。急性肾损伤(AKI)指的是快速肾衰竭,表现为在数小时或数天内排泄迅速进行性减少。本研究采用荟萃分析方法评估间充质干细胞治疗缺血再灌注诱导的急性肾损伤的疗效。使用相应术语在以下数据库进行文献检索:截至2019年12月31日的Embase、Cochrane图书馆、PubMed和ISI科学网数据库。确定了结局数据,并使用Cochrane系统评价管理器5.3版评估间充质干细胞治疗急性肾损伤的疗效。19项研究符合条件并被纳入该荟萃分析。间充质干细胞治疗可降低1天、2天、3天、5天和>7天时的血清肌酐(Scr)水平(1天:加权均数差(WMD)=-0.56,95%可信区间(CI):-0.78,-0.34,P<0.00001;2天:WMD=-0.58,95%CI:-0.89,-0.28,P=0.0002;3天:WMD=-0.65,95%CI:-0.84,-0.45,P<0.00001;5天:WMD=-0.35,95%CI:-0.54,-0.16,P=0.0003;>7天:WMD=-0.22,95%CI:-0.36,-0.08,P=0.002),并可降低1天、2天、3天和5天时的血尿素氮(BUN)水平(1天:WMD=-11.72,95%CI:-18.80,-4.64,P=0.001;2天:WMD=-33.60,95%CI:-40.15,-27.05,P<0.00001;3天:WMD=-21.14,95%CI:-26.15,-16.14,P<0.00001;5天:WMD=-8.88,95%CI:-11.06,-6.69,P<0.00001),并且还可降低3天和>7天时的蛋白尿水平,并减轻急性肾损伤动物模型中的肾损伤。总之,间充质干细胞可能是治疗缺血再灌注诱导的急性肾损伤的一种有前景的治疗药物。