Systematic review and meta-analysis of mesenchymal stem/stromal cells therapy for impaired renal function in small

Yan Wang1, Juan He, Xiaohua Pei

  • 1Department of Geriatrics, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Nephrology (Carlton, Vic.)
|December 11, 2012
PubMed
Abstract

Insights

Mesenchymal stem/stromal cell (MSC) therapy shows promise in improving kidney function in animal models. Early arterial delivery of MSCs appears most effective for reducing serum creatinine in renal failure.

Area of Science:

  • Regenerative Medicine
  • Nephrology
  • Stem Cell Biology

Background:

  • Mesenchymal stem/stromal cells (MSCs) are being investigated for their therapeutic potential in kidney diseases.
  • Previous small animal studies suggest MSC therapy may improve renal function.
  • A comprehensive analysis is needed to guide future large animal and human clinical trials.

Purpose of the Study:

  • To meta-analyze recent small animal experiments on MSC therapy for impaired kidney function.
  • To identify factors influencing the efficacy of MSC therapy in renal failure models.
  • To provide evidence-based insights for designing future preclinical and clinical studies.

Main Methods:

  • Systematic review and meta-analysis of 21 studies from PubMed and Embase.
  • Data analyzed using RevMan 5.1 and SPSS 17.0 with random effects models.
  • Exploratory multivariable meta-regression, heterogeneity, and publication bias were assessed.

Main Results:

  • Pooled analysis demonstrated a reduction in serum creatinine (Scr) following MSC therapy in renal failure models.
  • Early Scr measurement (P=0.005) and arterial MSC delivery (P=0.040) were associated with greater Scr reduction.
  • Higher MSC numbers (>10^6), renal ischemia-reperfusion injury (IRI) models, and late administration (>1 day) showed trends towards improved outcomes.

Conclusions:

  • MSC therapy is confirmed to improve impaired renal function in animal models.
  • Optimal therapeutic effects may be achieved with early administration via arterial delivery.
  • Findings offer critical guidance for the design of future MSC-based animal experiments and human clinical trials.