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• W2896476173 abstract "Mesenchymal stromal cell (MSC) therapies have demonstrated therapeutic efficacy in a wide-ranging array of tissue injury and disease indications. An important aspect of MSC-mediated therapeutic activities is immune modulation. Consistent with the concentration of MSC therapeutic potency in its secretion, a significant proportion of MSC immune potency resides in the small extracellular vesicles (sEVs) secreted by MSCs. These sEVs, which also include exosomes, carry a large cargo enriched in proteins with potent immunomodulatory activities. They have been reported to exert potent effects on humoral and cellular components of the immune system in vitro and in vivo, and may have the potential to support the diametrically opposite pro- and anti-inflammatory functions necessary for tissue repair and regeneration following injury. Following injury, pro-inflammatory activities are necessary to neutralize injury and remove dead or injured tissue, while anti-inflammatory activities to facilitate migration and proliferation of reparative cell types and to increase vascularization and nutrient supply are necessary to repair and regenerate new tissue. Therefore, a critical immunomodulatory requisite of MSC sEVs in tissue regeneration is the capacity to support the appropriate immune activities at the appropriate time. Here, we review how some of the immune regulatory targets of MSC sEVs could support the dynamic immunomodulatory activities during tissue repair and regeneration." @default.
• W2896476173 created "2018-10-26" @default.
• W2896476173 creator A5026850740 @default.
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• W2896476173 creator A5046881277 @default.
• W2896476173 creator A5068858743 @default.
• W2896476173 date "2018-12-01" @default.
• W2896476173 modified "2023-10-17" @default.
• W2896476173 title "Immune regulatory targets of mesenchymal stromal cell exosomes/small extracellular vesicles in tissue regeneration" @default.
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• W2896476173 doi "https://doi.org/10.1016/j.jcyt.2018.09.008" @default.
• W2896476173 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30352735" @default.
• W2896476173 hasPublicationYear "2018" @default.
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