TY - JOUR
T1 - CD8+ T cells express a T-helper 1-like phenotype after burn injury
AU - Cairns, Bruce A.
AU - Maile, Rob
AU - Buchanan, Ian
AU - Pilati, David
AU - DeSerres, Suzan
AU - Collins, Edward J.
AU - Frelinger, Jeffrey A.
AU - Meyer, Anthony A.
PY - 2001
Y1 - 2001
N2 - Background. Previous studies suggest that CD8+ T cells are immunosuppressive after burn injury, but recent reports indicate that CD8+ T cells have several functions similar to CD4+ T cells, including the secretion of cytokines. This study uses HY male antigen in transgenic HY female mice to determine the antigen-specific response of activated CD8+ T cells after burn injury. Methods. HY TCR transgenic female mice underwent burn or sham injury. Seventy-two hours after the burn, splenocytes were stimulated with 20 μmol/L HY peptide for 16, 48, and 64 hours; cellular proliferation, intracellular interferon-γ and interleukin-2, and apoptosis were measured. Results. Burn injury significantly impaired proliferation to HY antigen (P ≤ .05). Activated CD8+ T cells from burned mice showed increased intracellular interferon-γ and interleukin-2 16 hours after stimulation compared with sham (P ≤ .05) and at no time was less than control mice. The percent of CD8+ T cells decreased with the time of stimulation but was not due to apoptosis by Annexin V staining. Conclusions. Activated CD8+ T cells express a TH1-like phenotype after burn injury. This provides evidence that CD8+ T cells are not simply suppressive and that is consistent with data that CD4+ T cells are primed for a TH1 response after burn injury.
AB - Background. Previous studies suggest that CD8+ T cells are immunosuppressive after burn injury, but recent reports indicate that CD8+ T cells have several functions similar to CD4+ T cells, including the secretion of cytokines. This study uses HY male antigen in transgenic HY female mice to determine the antigen-specific response of activated CD8+ T cells after burn injury. Methods. HY TCR transgenic female mice underwent burn or sham injury. Seventy-two hours after the burn, splenocytes were stimulated with 20 μmol/L HY peptide for 16, 48, and 64 hours; cellular proliferation, intracellular interferon-γ and interleukin-2, and apoptosis were measured. Results. Burn injury significantly impaired proliferation to HY antigen (P ≤ .05). Activated CD8+ T cells from burned mice showed increased intracellular interferon-γ and interleukin-2 16 hours after stimulation compared with sham (P ≤ .05) and at no time was less than control mice. The percent of CD8+ T cells decreased with the time of stimulation but was not due to apoptosis by Annexin V staining. Conclusions. Activated CD8+ T cells express a TH1-like phenotype after burn injury. This provides evidence that CD8+ T cells are not simply suppressive and that is consistent with data that CD4+ T cells are primed for a TH1 response after burn injury.
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U2 - 10.1067/msy.2001.115835
DO - 10.1067/msy.2001.115835
M3 - Article
C2 - 11490351
AN - SCOPUS:0034907978
SN - 0039-6060
VL - 130
SP - 210
EP - 216
JO - Surgery
JF - Surgery
IS - 2
ER -