Systematic review and meta-analysis of preclinical studies testing mesenchymal stromal cells for traumatic brain injury.

NPJ Regen Med

Laboratory of Acute Brain Injury and Therapeutic Strategies, Department of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Published: October 2021

AI Article Synopsis

  • Mesenchymal stromal cells (MSCs) show promise in helping animals recover from traumatic brain injury (TBI), especially by improving movement and thinking skills.
  • Researchers reviewed 80 studies to see how well MSCs work, finding that they help reduce brain damage when given soon after an injury.
  • The best results came from using MSCs in special ways, like in a gel or implanting them directly into the injured area.

Article Abstract

Mesenchymal stromal cells (MSCs) are widely used in preclinical models of traumatic brain injury (TBI). Results are promising in terms of neurological improvement but are hampered by wide variability in treatment responses. We made a systematic review and meta-analysis: (1) to assess the quality of evidence for MSC treatment in TBI rodent models; (2) to determine the effect size of MSCs on sensorimotor function, cognitive function, and anatomical damage; (3) to identify MSC-related and protocol-related variables associated with greater efficacy; (4) to understand whether MSC manipulations boost therapeutic efficacy. The meta-analysis included 80 studies. After TBI, MSCs improved sensorimotor and cognitive deficits and reduced anatomical damage. Stratified meta-analysis on sensorimotor outcome showed similar efficacy for different MSC sources and for syngeneic or xenogenic transplants. Efficacy was greater when MSCs were delivered in the first-week post-injury, and when implanted directly into the lesion cavity. The greatest effect size was for cells embedded in matrices or for MSC-derivatives. MSC therapy is effective in preclinical TBI models, improving sensorimotor, cognitive, and anatomical outcomes, with large effect sizes. These findings support clinical studies in TBI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556393PMC
http://dx.doi.org/10.1038/s41536-021-00182-8DOI Listing

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