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  4. Human Schwann Cell Transplantation for Spinal Cord Injury: Prospects and Challenges in Translational Medicine

Human Schwann Cell Transplantation for Spinal Cord Injury: Prospects and Challenges in Translational Medicine

Frontiers in Cellular Neuroscience, 2021 · DOI: 10.3389/fncel.2021.690894 · Published: June 18, 2021

Spinal Cord InjuryRegenerative MedicineNeurology

Simple Explanation

Schwann cells (SCs) are a type of cell that supports nerve regeneration and myelin formation in the peripheral nervous system. Transplanting these cells into the injured spinal cord can help to fill cystic cavities, reduce scarring, and support axon regrowth. Human Schwann cells (hSCs) are advantageous for autotransplantation because they can be isolated from a patient’s own nerve and expanded in vitro prior to implantation, alleviating the need for chronic immunosuppression. While clinical trials have established the safety of hSC transplantation for SCI, several knowledge gaps and manufacturing challenges need to be addressed to enable accessible and effective treatments for SCI patients.

Study Duration
Not specified
Participants
Human SCI patients in clinical trials
Evidence Level
Review

Key Findings

  • 1
    hSC transplants are relatively understudied compared to rodent SCs, possibly due to the sophisticated resources and expertise needed for hSC culture from human nerves.
  • 2
    Clinical trials have demonstrated the safety of hSC transplantation in SCI patients, but questions remain about their effectiveness in promoting significant functional recovery.
  • 3
    The myelin-forming capability of SCs has been essential to the formulation of a therapeutic hypothesis supportive of progression to clinical trials for SCI.

Research Summary

This review discusses the progress and challenges of using human Schwann cell (hSC) transplantation for spinal cord injury (SCI) treatment, highlighting the potential benefits and limitations of hSC-based therapies. The review emphasizes the need for further research to understand the therapeutic value of hSC transplants, improve manufacturing methods, and address the knowledge gap between rodent and human SC studies. The review concludes that simplifying the current transplantation strategy and exploring alternative hSC-based products may facilitate the development of effective biotherapeutics for SCI.

Practical Implications

Enhance hSC Manufacturing

Develop more efficient and cost-effective methods for isolating, expanding, and purifying hSCs to increase their availability for research and clinical applications.

Investigate hSC Mechanisms

Conduct more comprehensive studies to elucidate the mechanisms by which hSCs promote spinal cord repair, including their effects on axon regeneration, myelination, and immune modulation.

Optimize Clinical Trial Design

Design clinical trials with more rigorous controls and outcome measures to assess the efficacy of hSC transplantation in SCI patients, and explore combination therapies to enhance hSC-mediated repair.

Study Limitations

  • 1
    Limited number of studies on hSC transplantation compared to rodent SCs.
  • 2
    Incomplete data on particular outcome measures for SCI
  • 3
    High variability in hSC batches and their effects on spinal cord repair.

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