• J Trauma · Aug 2006

    Increased Toll-like receptor 4 expression on T cells may be a mechanism for enhanced T cell response late after burn injury.

    • Bruce Cairns, Robert Maile, Carie M Barnes, Jeffrey A Frelinger, and Anthony A Meyer.
    • Department of Surgery, Division of Trauma, Critical Care, and Burns, North Carolina Jaycee Burn Center University of North Carolina, Chapel Hill, North Carolina 27599-7228, USA. bruce.cairns@med.unc.edu
    • J Trauma. 2006 Aug 1; 61 (2): 293-8; discussion 298-9.

    BackgroundBurn injury is associated with a dynamic T cell response. We have previously reported an enhanced functional T cell response 14 days after burn injury. Toll-like receptors (TLR), primarily expressed on innate immune cells, have recently been identified on certain T cell subsets, including activated and memory T cells. Our hypothesis is that increased TLR4 expression on memory T cells may be a mechanism for enhanced T cell response 14 days after burn injury.MethodsSplenocytes from wild-type C57Bl/6 mice were harvested 14 days after a 20% total body surface area (TBSA) scald burn or sham injury. Splenocytes ex vivo were surface stained either with monoclonal anti-CD3, anti-CD4, anti-CD8, or anti-CD44 antibodies or a two-step biotin-TLR4 monoclonal antibody-streptavidin-FITC surface stain and results analyzed by flow cytometry.ResultsTLR4 expression is successfully detected on CD4 and CD8 T cells. TLR4 expression is significantly (p < 0.05) increased on CD4 T cells and CD8 T cells 14 days after burn injury. There is a significant (p < 0.05) increase in CD44 (memory) CD4 and CD44 (memory) CD8 T cells 14 days after burn injury and this is associated with a significant (p < 0.05) increase of TLR4 expression in both T cell populations.ConclusionsThis study demonstrates for the first time the potential role of TLR4 expression on memory T cells generated late after burn injury. Although further analysis is required, these data reiterate the importance of adaptive immunity and the complexity of the immune response to burn injury.

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