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  • Gonzalez, et al. (2003). Reducing inflammation decreases secondary degeneration and functional ...

    • Gonzalez R, Glaser J, Liu MT, Lane TE and Keirstead HS (2003). Reducing inflammation decreases secondary degeneration and functional deficit after spinal cord injury. Exp Neurol. 184: 456-63. Reeve-Irvine Research Center, Department of Anatomy and Neurobiology, University of California at Irvine,2111 Gillespie Neuroscience Research Facility, Irvine, CA 92697-4292, USA. Injury to the spinal cord is followed by degeneration, which leads to progressive tissue loss and usually cystic cavitation. Cellular and humoral immune responses have been implicated as mediators of secondary degeneration, and the expression of leukocyte chemoattractants has been shown to precede immune cell influx. However, the relationship between the increased expression of chemoattractants, the invasion of lymphocytes, and overall lesion evolution is poorly understood. Here, we show that the T-lymphocyte chemoattractant CXCL10 is upregulated after dorsal hemisection injury to the adult mammalian spinal cord of C57/BL6 mice, and that antibody neutralization of CXCL10 beginning 1 day prior to injury dramatically reduces the T-lymphocyte invasion that normally occurs after trauma. Notably, this treatment resulted in a significant reduction of secondary tissue loss and functional deficit. We conclude that CXCL10 plays a critical role in recruitment of T lymphocytes to sites of spinal cord injury, and that a reduction of T-lymphocyte recruitment significantly enhances tissue preservation and functional outcome.

  • #2
    Dr. Wise,

    What effects does methylpredisolone have in
    regards to t-lymphocyte regulation?

    Are the antibodies used to control CXCL 10 compatible to use with methylpredisolone?



    [This message was edited by Lindox on 12-15-03 at 04:49 PM.]
    Life isn't about getting thru the storm but learning to dance in the rain.


    • #3
      Lindox, I don't know the answer to this question. I don't think that the authors of this study have looked at interactions with methylprednisolone. Wise.