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. 2023 Jan 24;14:1120175. doi: 10.3389/fimmu.2023.1120175

Table 5.

Examples of EV use in preclinical studies related to the treatment of the respiratory system diseases.

Source of EVs Model Major outcomes References
Human UC-MSCs In vivo murine model
of asthma
Reduced inflammatory response and airway remodelling
Prevented lung remodelling
Reduced inflammatory cell infiltration
Decreased level of pro-inflammatory cytokines
Inhibited TGF-β1-Smad2/3 signaling pathway
(200)
In vivo murine model of lung ischemia-reperfusion injury Attenuated inflammation and edema
Attenuated activation of iNKT cells and macrophages
Decreased level of pro-inflammatory cytokines
Inhibition of macrophage and iNKT cells activation
(201)
Porcine BM-MSCs In vitro Inhibition of virus replication in lung epithelial cells
Inhibition of virus-induced apoptosis replication in lymphatic endothelial cells
(202)
In vivo porcine model
of influenza-induced ALI
Inhibition of virus replication in lung epithelial cells
Reduced lung injury
Attenuated level of pro-inflammatory cytokines
Human BM-MSCs In vivo murine model of lung injury Decreased lung vascular endothelial permeability (203)
Ex vivo human model of pneumonia Improved alveolar fluid clearance in lungs
Reduced level of bacteria
(204)
Human Amnion Epithelial Cells In vivo murine model of idiopathic pulmonary fibrosis Prevention against lung injury (205)
Human iPSC-MSCs In vivo murine model of asthma Ameliorated allergic airway inflammation
Alleviation of airway hyperresponsiveness
Decrease of inflammatory cell infiltration
(206)

ALI, acute lung injury; BM-MSCs, bone marrow MSCs; iNKT, invariant natural killer T cells; iPSCs, induced pluripotent stem cells; MSCs, mesenchymal stem/stromal cells; UC-MSCs, umbilical cord Wharton’s jelly MSCs.