Current understanding of the therapeutic benefits of mesenchymal stem cells in acute respiratory distress syndrome

Cell Biol Toxicol. 2020 Feb;36(1):83-102. doi: 10.1007/s10565-019-09493-5. Epub 2019 Sep 4.

Abstract

The acute respiratory distress syndrome (ARDS) is a multifaceted lung disorder in which no specific therapeutic intervention is able to effectively improve clinical outcomes. Despite an improved understanding of molecular mechanisms and advances in supportive care strategies, ARDS remains associated with high mortality, and survivors usually face long-term morbidity. In recent years, preclinical studies have provided mounting evidence of the potential of mesenchymal stem cell (MSC)-based therapies in lung diseases and critical illnesses. In several models of ARDS, MSCs have been demonstrated to induce anti-inflammatory and anti-apoptotic effects, improve epithelial and endothelial cell recovery, and enhance microbial and alveolar fluid clearance, thus resulting in improved lung and distal organ function and survival. Early-stage clinical trials have also demonstrated the safety of MSC administration in patients with ARDS, but further, large-scale investigations are required to assess the safety and efficacy profile of these therapies. In this review, we summarize the main mechanisms whereby MSCs have been shown to exert therapeutic effects in experimental ARDS. We also highlight questions that need to be further elucidated and barriers that must be overcome in order to efficiently translate MSC research into clinical practice.

Keywords: Acute respiratory distress syndrome; Biomarkers; Cell therapy; Clinical trials; Lung; Mesenchymal stem cells; Paracrine effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / metabolism
  • Animals
  • Disease Models, Animal
  • Endothelial Cells / metabolism
  • Humans
  • Lung / cytology
  • Mesenchymal Stem Cell Transplantation / trends
  • Mesenchymal Stem Cells / metabolism
  • Mesenchymal Stem Cells / physiology*
  • Respiratory Distress Syndrome / metabolism*
  • Respiratory Distress Syndrome / physiopathology*