Zheng Lingqian, Chen Wenmin, Yao Kaijin, Xie Yina, Liao Chunling, Lin Yongda, Zhou Tianbiao
Department of Nephrology, the Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Ren Fail. 2024 Dec;46(2):2438863. doi: 10.1080/0886022X.2024.2438863. Epub 2024 Dec 16.
Peritoneal fibrosis is a serious complication of long-term peritoneal dialysis, often resulting in functional deterioration and withdrawal from therapy. Mesenchymal stem cells (MSCs) have demonstrated immunomodulatory and antifibrotic effects in various models. This meta-analysis evaluated the efficacy of MSCs therapy in animal models of peritoneal fibrosis.
A comprehensive search of PubMed, the Cochrane Library, Web of Science, and EMBASE was conducted for studies published up to April 27, 2024. Two independent reviewers (LQZ and WMC) screened studies for inclusion, extracted data, and analyzed outcomes using RevMan 5.3 and STATA 17.0.
Fifteen studies met the inclusion criteria. MSC therapy significantly reduced inflammatory cytokines, including IL-6, TGF-β (SMD = -1.79, 95% CI: -2.32, -1.25, < 0.00001), and TNF-α (SMD = -1.57, 95% CI: -2.71, -0.44, = 0.006) levels. Additionally, MSCs reduced submesothelial thickness (MD = -63.14, 95% CI: -78.52, -47.76, < 0.00001), Collagen I and Collagen III levels. MSCs treatment also improved ultrafiltration capacity (MD = 1.21, 95% CI: 0.64, 1.77, < 0.0001), D/D0 of glucose and E-cadherin levels. However, no significant differences were observed in VEGF, D/P of Na, D/P of BUN, D/P of protein, or glucose mass transfer between the MSCs treatment group and the control group.
MSC therapy significantly improves peritoneal function and attenuates fibrotic and inflammatory responses in animal models. These findings highlight the potential of MSCs as a promising therapeutic strategy for managing peritoneal fibrosis in clinical settings.
腹膜纤维化是长期腹膜透析的严重并发症,常导致功能恶化并退出治疗。间充质干细胞(MSCs)在各种模型中已显示出免疫调节和抗纤维化作用。本荟萃分析评估了间充质干细胞治疗在腹膜纤维化动物模型中的疗效。
全面检索了截至2024年4月27日发表的PubMed、Cochrane图书馆、Web of Science和EMBASE上的研究。两名独立审阅者(LQZ和WMC)筛选纳入研究,提取数据,并使用RevMan 5.3和STATA 17.0分析结果。
15项研究符合纳入标准。间充质干细胞治疗显著降低了炎症细胞因子水平,包括IL-6、转化生长因子-β(标准化均数差[SMD]=-1.79,95%置信区间[CI]:-2.32,-1.25,P<0.00001)和肿瘤坏死因子-α(SMD=-1.57,95%CI:-2.71,-0.44,P=0.006)。此外,间充质干细胞减少了间皮下厚度(均差[MD]=-63.14,95%CI:-78.52,-47.76,P<0.00001)、I型胶原蛋白和III型胶原蛋白水平。间充质干细胞治疗还改善了超滤能力(MD = 1.21,95%CI:0.64,1.77,P<0.0001)、葡萄糖的D/D0和E-钙黏蛋白水平。然而,在间充质干细胞治疗组和对照组之间,血管内皮生长因子、钠的D/P、尿素氮的D/P、蛋白质的D/P或葡萄糖质量转运方面未观察到显著差异。
间充质干细胞治疗显著改善了动物模型中的腹膜功能,并减轻了纤维化和炎症反应。这些发现突出了间充质干细胞作为临床治疗腹膜纤维化的一种有前景的治疗策略的潜力。