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.

Life Sciences
|March 2, 2021
PubMed

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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