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Updated: Sep 20, 2026

Isolation, Characterization, and Therapeutic Application of Extracellular Vesicles from Cultured Human Mesenchymal Stem Cells
Published on: September 23, 2022
Therapeutic potential of mesenchymal stem cell-derived extracellular vesicles as a cell-free approach in autism
Tayebeh Mohtashami1, Amir Hossein Aghayan2, Alireza Masoudi3
1Student Research Committee, School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.
Background:
Autism Spectrum Disorder (ASD) is an intricate neurodevelopmental condition distinguished by challenges in social interaction, repetitive behavioral patterns, and neuroinflammation, with limited effective treatments. Mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) offer a promising cell-free therapy due to their immunomodulatory and regenerative properties. This study evaluates their therapeutic efficacy in preclinical ASD models.
Methods:
Following PRISMA guidelines, we conducted a systematic review and meta-analysis, searching PubMed, Embase, Scopus, and Web of Science. The SYRCLE tool assessed risk of bias. Standardized mean difference (SMD) was calculated using a random-effects model to evaluate MSC-EV effects on sociability, repetitive behaviors, and inflammatory cytokines. Subgroup analysis, sensitivity analysis, and publication bias assessment addressed heterogeneity.
Results:
Five studies (2018-2024) were included. MSC-EV-treated mice showed significant improvements in sociability (SMD =1.34, 95% CI:0.68-2.76), reduced repetitive behaviors (SMD =-1.12, 95% CI:-0.65 to -1.59), and modulated neuroinflammation, with decreased pro-inflammatory cytokines (IL-1, SMD = -2.28, 95% CI:-0.33 to -4.24 and TNF-a, SMD = -1.22, 95% CI:-0.47 to -1.97 and IL-6, SMD = -1.03, 95% CI:-0.38 to -1.68) and increased IL-10 (SMD =0.58, 95% CI:0.03-1.13). Subgroup analysis indicated umbilical cord- and adipose-derived MSC-EVs had superior efficacy.
Conclusion:
MSC-EVs demonstrate significant therapeutic potential in preclinical ASD models by improving core symptoms and modulating inflammation. However, limited studies and heterogeneity highlight the need for standardized protocols and further preclinical research to facilitate clinical translation.
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