A systematic review of cellular transplantation therapies for spinal cord injury

Wolfram Tetzlaff1, Elena B Okon, Soheila Karimi-Abdolrezaee

  • 1University of British Columbia, ICORD, Vancouver, British Columbia, Canada. tetzlaff@icord.org

Journal of Neurotrauma
|February 12, 2010
PubMed

Insights

This review of cell transplantation for spinal cord injury (SCI) found that rodent cells and models dominate research. Human cell studies are limited, and chronic intervention timing often yields poor functional benefits.

Area of Science:

  • Neuroscience
  • Regenerative Medicine
  • Cell Biology

Background:

  • Cell transplantation is a key pre-clinical strategy for spinal cord injury (SCI) treatment.
  • Numerous cell types are being investigated for their therapeutic potential in SCI.
  • Translational success requires a thorough understanding of pre-clinical evidence.

Purpose of the Study:

  • To systematically review pre-clinical literature on cell transplantation for SCI.
  • To assess the evidence supporting the translation of various cell types to human SCI patients.
  • To identify research gaps and trends in cell-based SCI therapies.

Main Methods:

  • Systematic review of 162 in-vivo studies involving cell transplantation into traumatic SCI models.
  • Inclusion criteria focused on traumatic SCI models and cell transplantation.
  • Emphasis on behavioral effects, but scope included other outcomes.

Main Results:

  • Rodent-derived cells and rodent SCI models are most extensively studied.
  • Only 19 studies used human cells, primarily bone-marrow stromal cells.
  • Most studies used acute or subacute transplantation; chronic interventions were rare and often ineffective.
  • Significant variability exists within cell types based on donor species, age, culture, and delivery.

Conclusions:

  • The current pre-clinical evidence for cell transplantation in SCI is heavily biased towards rodent models and cells.
  • Further research is needed using human cells and larger animal models to facilitate clinical translation.
  • Optimizing the timing of cell delivery, particularly exploring chronic interventions, is crucial for improving functional recovery in SCI.