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Preclinical Validation of Multilevel Intraparenchymal Stem Cell Therapy in the Porcine Spinal Cord

  • Juanmarco Gutierrez
  • , Jason J. Lamanna
  • , Natalia Grin
  • , Carl V. Hurtig
  • , Joseph H. Miller
  • , Jonathan Riley
  • , Lindsey Urquia
  • , Pablo Avalos
  • , Clive N. Svendsen
  • , Thais Federici
  • , Nicholas M. Boulis
  • Emory University
  • Wallace H. Coulter Department of Biomedical Engineering
  • University of Alabama at Birmingham
  • Cedars-Sinai Medical Center

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

BACKGROUND: Although multiple clinical trials are currently testing different stem cell therapies as treatment alternatives for many neurodegenerative diseases and spinal cord injury, the optimal injection parameters have not yet been defined. OBJECTIVE: To test the spinal cord's tolerance to increasing volumes and numbers of stem cell injections in the pig. METHODS: Twenty-seven female Göttingen minipigs received human neural progenitor cell injections using a stereotactic platform device. Cell transplantation in groups 1 to 5 (5-7 pigs in each) was undertaken with the intent of assessing the safety of an injection volume escalation (10, 25, and 50 L) and an injection number escalation (20, 30, and 40 injections). Motor function and general morbidity were assessed for 21 days. Full necropsy was performed; spinal cords were analyzed for graft survival and microscopic tissue damage. RESULTS: No mortality or permanent surgical complications were observed during the 21-day study period. All animals returned to preoperative baseline within 14 days, showing complete motor function recovery. The histological analysis showed that there was no significant decrease in neuronal density between groups, and cell engraftment ranged from 12% to 31% depending on the injection paradigm. However, tissue damage was identified when injecting large volumes into the spinal cord (50 L). CONCLUSION: This series supports the functional safety of various injection volumes and numbers in the spinal cord and gives critical insight into important safety thresholds. These results are relevant to all translational programs delivering cell therapeutics to the spinal cord. ABBREVIATIONS: hNPC, human fetal cortex-derived neural progenitor cell IM, intramuscularly IV, intravenously .

Original languageEnglish
Pages (from-to)604-612
Number of pages9
JournalNeurosurgery
Volume77
Issue number4
DOIs
StatePublished - Oct 21 2015

Keywords

  • KEY WORDS: Cell therapy
  • Neurodegenerative
  • Preclinical
  • Safety
  • Spinal cord
  • Tolerance
  • Transplantation

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