Growth Factor Gene-Modified Cells in Spinal Cord Injury Recovery: A Systematic Review

Mahmoud Yousefifard1, Arash Sarveazad2, Asrin Babahajian3

  • 1Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran.

World Neurosurgery
|March 11, 2022
PubMed
Abstract

Insights

Growth factor gene-modified cells significantly improved locomotion in animal models of spinal cord injury (SCI). However, safety concerns regarding overexpression require further investigation before human trials.

Area of Science:

  • Regenerative Medicine
  • Neuroscience
  • Biotechnology

Background:

  • Preclinical studies on growth factor gene-modified cells for spinal cord injury (SCI) have yielded contradictory findings.
  • The therapeutic potential of these modified cells remains uncertain due to inconsistent results.

Purpose of the Study:

  • To systematically review and meta-analyze animal studies on the efficacy of growth factor gene-modified cells for locomotion recovery after SCI.
  • To consolidate evidence and identify factors influencing treatment outcomes.

Main Methods:

  • A comprehensive literature search was conducted across major databases (MEDLINE, Embase, Scopus, Web of Science) up to December 2020.
  • Thirty-three relevant animal studies were included, with independent screening, data extraction, and risk of bias assessment by two researchers.

Main Results:

  • Transplantation of growth factor gene-modified cells significantly improved locomotion in SCI animal models compared to both untreated and non-genetically modified cell-treated groups.
  • Efficacy was not significant for moderate lesions, modified neural stem/progenitor cells, synthetic neurotrophins, or when transplanting fewer than 1.0 × 10^5 cells.

Conclusions:

  • Growth factor gene-modified cell transplantation demonstrates significant potential for improving locomotion in SCI animal models.
  • Safety concerns, particularly regarding growth factor overexpression, necessitate further research before clinical translation.
  • Additional studies are crucial to address safety and optimize treatment parameters for future human trials.