Local Immunomodulation with Anti-inflammatory Cytokine-Encoding Lentivirus Enhances Functional Recovery after Spinal Cord Injury.

Mol Ther

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48105, USA; Department of Chemical Engineering, University of Michigan, Ann Arbor, MI 48105, USA. Electronic address:

Published: July 2018

AI Article Synopsis

  • Trauma to the spinal cord can lead to permanent loss of movement and sensation, creating an environment that impedes healing.
  • This study evaluates the use of anti-inflammatory cytokines IL-10 and IL-4 delivered via lentiviral techniques in porous multichannel bridges to promote nerve regeneration.
  • Results show that these cytokines reduced inflammation, increased axon and myelin production, and improved movement recovery, suggesting a new approach to spinal cord injury treatment.

Article Abstract

Trauma to the spinal cord and associated secondary inflammation can lead to permanent loss of sensory and motor function below the injury level, with the resulting environment serving as a barrier that limits regeneration. In this study, we investigate the localized expression of anti-inflammatory cytokines IL-10 and IL-4 via lentiviral transduction in multichannel bridges. Porous multichannel bridges provide physical guidance for axonal outgrowth with the cytokines hypothesized to modulate the neuroinflammatory microenvironment and enhance axonal regeneration. Gene expression analyses indicated that induced IL-10 and IL-4 expression decreased expression of pro-inflammatory genes and increased pro-regenerative genes relative to control. Moreover, these factors led to increased numbers of axons and myelination, with approximately 45% of axons myelinated and the number of oligodendrocyte myelinated axons significantly increased by 3- to 4-fold. Furthermore, the combination of a bridge with IL-10 and IL-4 expression improved locomotor function after injury to an average score of 6 relative to an average score of 3 for injury alone. Collectively, these studies highlight the potential for localized immunomodulation to decrease secondary inflammation and enhance regeneration that may have numerous applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037204PMC
http://dx.doi.org/10.1016/j.ymthe.2018.04.022DOI Listing

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