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Cell therapy for the degenerating intervertebral disc.

Wei Tong1, Zhouyu Lu2, Ling Qin3

  • 1Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pa; Department of Orthopaedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, P.R.China.

Translational Research : the Journal of Laboratory and Clinical Medicine
|December 18, 2016
PubMed
Summary
This summary is machine-generated.

Developing new treatments for intervertebral disc (IVD) degeneration is crucial. Cell therapy shows promise for moderate degeneration, with hydrogel scaffolds potentially preventing cell leakage and reducing inflammation.

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Area of Science:

  • Regenerative Medicine
  • Spinal Surgery
  • Biomaterials

Background:

  • Intervertebral disc (IVD) degeneration is a prevalent condition causing significant healthcare costs.
  • Current treatments lack the ability to restore physiological IVD function.
  • Cell therapy is a potential strategy for moderate IVD degeneration, particularly in patients with severe pain or instability.

Purpose of the Study:

  • To review current strategies for repairing degenerating intervertebral discs (IVDs).
  • To evaluate the efficacy and challenges of cell therapy and cell-based gene therapy for IVD repair.
  • To assess the suitability of various animal models and scaffold materials in preclinical research.

Main Methods:

  • Systematic review of 50 studies focusing on cell therapy for IVD degeneration.
  • Analysis of cell survival, scaffold use, cell leakage, and animal model relevance.
  • Evaluation of reported improvements in disc structure, inflammation, and clinical outcomes.

Main Results:

  • Transplanted cells demonstrated good survival in the IVD, indicating its immunologically privileged nature.
  • Scaffolds, particularly hydrogels, were used in half of the studies to mitigate cell leakage and provide support.
  • Animal studies showed some disc structure improvement and inflammation reduction, but no complete restoration.

Conclusions:

  • Cell therapy offers a promising avenue for treating moderate IVD degeneration.
  • Optimizing scaffolds to prevent cell leakage and enhance integration remains a key challenge.
  • Attenuating inflammation and developing minimally invasive therapies are priorities for successful clinical translation.