Mechanisms and implications of adaptive immune responses after traumatic spinal cord injury

D P Ankeny1, P G Popovich

  • 1Center for Brain and Spinal Cord Repair, Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University Medical Center, Biomedical Research Tower-Room 786, 460 West 12th Avenue, Columbus, OH 43210, USA.

Neuroscience
|August 5, 2008
PubMed

Traumatic spinal cord injury (SCI) in mammals causes widespread glial activation and recruitment to the CNS of innate (e.g. neutrophils, monocytes) and adaptive (e.g. T and B lymphocytes) immune cells. To date, most studies have sought to understand or manipulate the post-traumatic functions of astrocytes, microglia, neutrophils or monocytes. Significantly less is known about the consequences of SCI-induced lymphocyte activation. Yet, emerging data suggest that T and B cells are activated by SCI and play significant roles in shaping post-traumatic inflammation and downstream cascades of neurodegeneration and repair. Here, we provide neurobiologists with a timely review of the mechanisms and implications of SCI-induced lymphocyte activation, including a discussion of different experimental strategies that have been designed to manipulate lymphocyte function for therapeutic gain.

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