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Updated: Nov 15, 2025

Isolation, Characterization, and Therapeutic Application of Extracellular Vesicles from Cultured Human Mesenchymal Stem Cells
Published on: September 23, 2022
Therapeutic role of extracellular vesicles derived from stem cells in cutaneous wound models: A systematic review
Razieh Dalirfardouei1, Aida Gholoobi2, Mehrangiz Vahabian3
1Research center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Abstract:
A growing body of evidence has shown that extracellular vesicles can be efficient as experimental therapeutics in pre-clinical models of skin wounds, but there is a significant unmet need to translate this to clinical utilization. The objectives of the current systematic review were to identify the strength of the therapeutic effects of EVs derived from stem cells in cutaneous wounds and to assess which EV-mediated mechanisms could be involved in the therapeutic response. PubMed, ISI Web of Science, and Scopus databases were systematically searched. We retrieved English-language articles published through June 2020. In vivo studies which applied stem cell-derived EVs were included for further analysis. The Risk of bias was assessed by the SYRCLE tool. We identified thirty-nine pre-clinical studies that evaluated the effects of EVs on the wound healing process. The included studies varied greatly in EVs isolation techniques, route of administration, EVs producing cells, and follow-up time. In vivo application revealed beneficial effects of EVs on accelerating wound closure and re-epithelialization in a dose-dependent manner. Elevated angiogenesis was reported in twelve eligible studies through multiple signaling pathways such as PI3K/Akt, MAPK/ERK, and JAK/STAT. The well-known signaling pathway to inhibit scar formation was TGF-β2/SMAD2. However, all included studies were not blinded enough which may have introduced bias. Therefore, the transition of EV's efficacy into the clinics is deeply rooted in the following important factors: 1) pre-clinical studies with a lower risk of bias and longer follow-up time, and 2) consistent, reproducible, and feasible manufacturing of EVs production in a large-scale commercial program.
Insights
Extracellular vesicles (EVs) show promise for skin wound healing in preclinical studies, accelerating closure and improving re-epithelialization. Further research with reduced bias and standardized manufacturing is needed for clinical translation.
Area of Science:
- Regenerative Medicine
- Wound Healing Research
- Biotechnology
Background:
- Extracellular vesicles (EVs) derived from stem cells demonstrate therapeutic potential in preclinical skin wound models.
- A significant gap exists in translating these promising preclinical findings to clinical applications for wound management.
Purpose of the Study:
- To systematically review the therapeutic efficacy of stem cell-derived EVs in cutaneous wound healing.
- To identify the underlying EV-mediated mechanisms contributing to wound repair.
- To assess the quality and potential biases in existing preclinical studies.
Main Methods:
- A systematic literature search was conducted across PubMed, ISI Web of Science, and Scopus databases for English-language articles published up to June 2020.
- Inclusion criteria focused on in vivo studies utilizing stem cell-derived EVs for cutaneous wound treatment.
- Risk of bias was evaluated using the SYRCLE tool.
Main Results:
- Thirty-nine preclinical studies indicated that EVs accelerate wound closure and re-epithelialization in a dose-dependent manner.
- EVs promoted angiogenesis via pathways including PI3K/Akt, MAPK/ERK, and JAK/STAT.
- Scar formation inhibition was linked to the TGF-β2/SMAD2 pathway, though study blinding was often insufficient, suggesting potential bias.
Conclusions:
- Stem cell-derived EVs exhibit significant therapeutic effects on preclinical wound healing, notably enhancing closure and angiogenesis.
- Key mechanisms involve modulation of signaling pathways critical for tissue regeneration and scar reduction.
- Clinical translation requires higher-quality preclinical studies with rigorous bias assessment, longer follow-up, and scalable, reproducible EV manufacturing.
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