MSCs exert paracrine effects: anti inflammatory, anti apoptotic, anti oxidant, pro angiogenic, antimicrobial, and antifibrotic actions that improve epithelial/endothelial barrier function and fluid clearance in ARDS and other injuries (Harrell et al., 2019; Fernández-Francos et al., 2021; Qin & Zhao, 2020; Lopes-Pacheco et al., 2019; Behnke et al., 2020). They modulate innate and adaptive immune cells, shift macrophages to a reparative M2 phenotype, and can partly support alveolar epithelial regeneration or transdifferentiate into AT2 like cells in models (Harrell et al., 2019; Yuan et al., 2024; Zhang et al., 2025; Lopes-Pacheco et al., 2019).
| Indication | MSC role (evidence) | Key points | Citations |
|---|---|---|---|
| ARDS / COVID ARDS | Reduce cytokine storm, improve barrier integrity, enhance survival (animals; early trials, H7N9 study) | Safety shown; some signals of lower mortality, but larger RCTs needed | (Fernández-Francos et al., 2021; Qin & Zhao, 2020; Lopes-Pacheco et al., 2019; Chen et al., 2020) |
| COPD & asthma | Decrease inflammation, oxidative stress, remodeling; improve lung function (mostly preclinical; small trials) | Clinical trials show safety; limited efficacy so far | (Cruz & Rocco, 2020; Harrell et al., 2019; Abbaszadeh et al., 2022; Wang et al., 2021; Lai & Guo, 2024; Wecht & Rojas, 2016; Antoniou et al., 2018) |
| Idiopathic pulmonary fibrosis / chronic fibrotic ILD | Antifibrotic, pro-repair in models; phase I/II show safety | Optimal timing likely early disease; long-term effects unknown | (Cruz & Rocco, 2020; Yuan et al., 2024; Chen et al., 2021; Wecht & Rojas, 2016; Antoniou et al., 2018) |
| BPD, PAH, silicosis, pneumonia | Experimental and early clinical use, especially with UC MSCs | Benefit mainly in animal models | (Cruz & Rocco, 2020; Fernández-Francos et al., 2021; Zhang et al., 2025; Chen et al., 2021; Mohammadipoor et al., 2018) |
Figure: Key pulmonary indications explored for MSC therapy.
MSC extracellular vesicles (EVs)/exosomes reproduce many benefits of cells with lower immunogenicity and tumor risk and easier storage, and show efficacy in models of COPD, asthma, fibrosis and ARDS (Abbaszadeh et al., 2022; Zhang et al., 2025; Yiming et al., 2022; Mohammadipoor et al., 2018). Secretome based approaches are emerging as favored “cell free” therapeutics (Fernández-Francos et al., 2021; Yiming et al., 2022; Mohammadipoor et al., 2018).
Across >100 pulmonary clinical trials, IV MSCs (often bone marrow or umbilical cord derived) appear safe, but effects on lung function, symptoms and survival are modest and inconsistent so far (Cruz & Rocco, 2020; Wang et al., 2021; Chen et al., 2021; Antoniou et al., 2018). Critical gaps include best source (UC MSCs may be superior in ARDS), dose, route, timing, and need for repeated dosing or genetic/conditioning strategies to boost potency (Cruz & Rocco, 2020; Fernández-Francos et al., 2021; Wang et al., 2021; Regmi et al., 2024). In pulmonology, MSCs and their EVs are promising tools for inflammatory and fibrotic lung diseases, especially ARDS, COPD, asthma and IPF. For now they remain experimental: safe in early trials, clearly effective in animal models, but with human efficacy still to be proven in large, well designed studies.

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