» Articles » PMID: 39681477

Efficacy of Mesenchymal Stem Cells in the Treatment of Peritoneal Fibrosis in Animal Models: a Systematic Review and Meta-analysis

Overview
Journal Ren Fail
Publisher Informa Healthcare
Date 2024 Dec 16
PMID 39681477
Authors
Affiliations
Soon will be listed here.
Abstract

Background: 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.

Methods: 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.

Result: 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.

Conclusion: 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.

References
1.
Margetts P, Bonniaud P . Basic mechanisms and clinical implications of peritoneal fibrosis. Perit Dial Int. 2004; 23(6):530-41. View

2.
Costalonga E, Fanelli C, Garnica M, Noronha I . Adipose-Derived Mesenchymal Stem Cells Modulate Fibrosis and Inflammation in the Peritoneal Fibrosis Model Developed in Uremic Rats. Stem Cells Int. 2020; 2020:3768718. PMC: 7256710. DOI: 10.1155/2020/3768718. View

3.
Li D, Lu Z, Li X, Xu Z, Jiang J, Zheng Z . Human umbilical cord mesenchymal stem cells facilitate the up-regulation of miR-153-3p, whereby attenuating MGO-induced peritoneal fibrosis in rats. J Cell Mol Med. 2018; 22(7):3452-3463. PMC: 6010808. DOI: 10.1111/jcmm.13622. View

4.
Zhao J, Zhao L, Zhan Q, Liu M, Zhang T, Chu W . BMSC-derived Exosomes Ameliorate Peritoneal Dialysis-associated Peritoneal Fibrosis via the Mir-27a-3p/TP53 Pathway. Curr Med Sci. 2024; 44(2):333-345. DOI: 10.1007/s11596-024-2853-7. View

5.
Jiao T, Huang Y, Sun H, Yang L . Exosomal lnc-CDHR derived from human umbilical cord mesenchymal stem cells attenuates peritoneal epithelial-mesenchymal transition through AKT/FOXO pathway. Aging (Albany NY). 2023; 15(14):6921-6932. PMC: 10415546. DOI: 10.18632/aging.204883. View