JOURNAL OF NEUROTRAUMA, 2011 · DOI: 10.1089/neu.2010.1626 · Published: April 1, 2011
This study explores the use of human glial-restricted progenitors (hGRP) and astrocytes derived from hGRP (hGDA) to treat spinal cord injuries in rats. The researchers transplanted these cells into rats with spinal cord contusions to observe how they survive, migrate, differentiate, and affect recovery. The hGRP and hGDA grafts showed excellent survival and migration, with cells differentiating mainly into astrocytes. The grafts also improved the lesion environment and did not increase sensory or tactile sensitivity associated with pain. Despite the improved lesion environment, robust functional recovery was not observed, suggesting that additional interventions or optimized administration parameters are needed to achieve significant functional improvements.
Human GRP and astrocytes remain promising candidates for cell-based therapies in spinal cord injury due to their survival, migration, and improvement of the lesion environment.
The manufacturing process of human GRP is designed for clinical use, making it a feasible option for future clinical trials.
Future studies should focus on optimizing transplantation protocols, including dosage, timing, and differentiation methods, and exploring additional interventions to promote axonal growth and functional recovery.