Author: Su, Yue; Guo, Haiyan; Liu, Qinghua
Title: Effects of mesenchymal stromal cellâ€derived extracellular vesicles in acute respiratory distress syndrome (ARDS): Current understanding and future perspectives Cord-id: 2ewmhwu9 Document date: 2021_5_6
ID: 2ewmhwu9
Snippet: Acute respiratory distress syndrome (ARDS) is a devastating and lifeâ€threatening syndrome that results in high morbidity and mortality. Current pharmacologic treatments and mechanical ventilation have limited value in targeting the underlying pathophysiology of ARDS. Mesenchymal stromal cells (MSCs) have shown potent therapeutic advantages in experimental and clinical trials through direct cellâ€toâ€cell interaction and paracrine signaling. However, safety concerns and the indeterminate effe
Document: Acute respiratory distress syndrome (ARDS) is a devastating and lifeâ€threatening syndrome that results in high morbidity and mortality. Current pharmacologic treatments and mechanical ventilation have limited value in targeting the underlying pathophysiology of ARDS. Mesenchymal stromal cells (MSCs) have shown potent therapeutic advantages in experimental and clinical trials through direct cellâ€toâ€cell interaction and paracrine signaling. However, safety concerns and the indeterminate effects of MSCs have resulted in the investigation of MSCâ€derived extracellular vesicles (MSCâ€EVs) due to their low immunogenicity and tumorigenicity. Over the past decades, soluble proteins, microRNAs, and organelles packaged in EVs have been identified as efficacious molecules to orchestrate nearby immune responses, which attenuate acute lung injury by facilitating pulmonary epithelium repair, reducing acute inflammation, and restoring pulmonary vascular leakage. Even though MSCâ€EVs possess similar bioâ€functional effects to their parental cells, there remains existing barriers to employing this alternative from bench to bedside. Here, we summarize the current established research in respect of molecular mechanisms of MSCâ€EV effects in ARDS and highlight the future challenges of MSCâ€EVs for clinical application.
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