Published online Apr 26, 2025. doi: 10.4252/wjsc.v17.i4.102421
Revised: January 23, 2025
Accepted: March 3, 2025
Published online: April 26, 2025
Processing time: 187 Days and 23.6 Hours
Mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) can traverse the blood-brain barrier due to their small size. This characteristic makes them a research hotspot for the treatment of Parkinson’s disease (PD) and is expected to be a potentially revolutionary strategy for treating PD. Despite this, no summary of clinical trial results has been reported.
To assess the efficacy and durability of MSC-EVs in treating PD.
Systematic searches were conducted in four electronic databases until June 2024 to collect studies on the use of MSC-EVs for this purpose. Thirteen relevant randomized controlled trials, encompassing 16 experiments, were selected for inclusion.
Behavioral assessments, including the rotarod and apomorphine turning behavior tests, indicated improvements in motor coordination (P < 0.00001); the Pole test and the Wire-hang test showed enhanced limb motor agility and synchronization (P = 0.003 and P < 0.00001, respectively). Histopathologically, there was a reduction in inflammatory markers such as tumor necrosis factor-α and interleukin-6 (P = 0.03 and P = 0.01, respectively) and an increase in tyrosine hydroxylase-positive cells in the lesion areas (P < 0.00001).
MSC-EV therapy for PD is a gradual process, with significant improvements observable more than 2 weeks after administration and lasting at least 8 weeks. This study is the first to demonstrate the efficacy and durability of MSC-EV treatment in PD.
Core Tip: Mesenchymal stem cell extracellular vesicles (MSC-EVs) have become a popular direction for tissue engineering research in recent years and have been shown to have many advantages, especially in neurological diseases. Unfortunately, the treatment of Parkinson’s disease (PD) with MSC-EVs is still in the clinical void stage due to insufficient guideline protocols. Our study was the first to validate the efficacy and durability of MSC-EVs in the treatment of PD and to draw a number of valuable guiding conclusions. The results of our analyses are of great reference value for future clinical translation of stem cell exosomes for PD.