Up-regulation of tim-3 expression contributes to development of burn-induced T cell immune suppression in mice

Zhaohui Tang , Yan Yu , Wenhong Qiu , Jian Zhang , Xiangping Yang

Current Medical Science ›› 2011, Vol. 31 ›› Issue (5) : 642 -651.

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Current Medical Science ›› 2011, Vol. 31 ›› Issue (5) : 642 -651. DOI: 10.1007/s11596-011-0575-0
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Up-regulation of tim-3 expression contributes to development of burn-induced T cell immune suppression in mice

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Abstract

T cell immunoglobulin and mucin domain 3 (Tim-3) is well known to negatively regulate T cells responses, but its role in burn-induced T cells immune suppression remains unclear. In the present study, in order to identify the relationship between Tim-3 expression and post-burn T cells immune suppression, C57BL/6 mice were subjected to burn injury or sham injury, and the liver and spleen were harvested at the day 1 after operation. The expression level of Tim-3 on hepatic or splenic T cells and the functional properties of Tim-3+ T cells were evaluated. It was found burn injury induced dramatically elevated Tim-3 expression on both hepatic and splenic CD4+ and CD8+ T cells in contrast with the post-burn depletion of T cells. Furthermore, Tim-3 expression was correlated with the suppressive phenotype of T cells following burn injury, including increased expression of anti-inflammatory cytokine IL-10, decreased expression of pro-inflammatory cytokines IFN-γ and TNF-α, reduced T cell proliferation and elevated co-expression of Tim-3 and PD-1. Moreover, Tim-3+ T cells subsets were more prone to spontaneous apoptosis than Tim-3 T cells subsets. Our findings reinforce the idea that the up-regulated expression of Tim-3 on T cells after burn injury plays an important role in the development and maintenance of burn-induced T cell immune suppression.

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T cell immunoglobulin and mucin domain 3 / T cells / burn injury / immune suppression

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Zhaohui Tang, Yan Yu, Wenhong Qiu, Jian Zhang, Xiangping Yang. Up-regulation of tim-3 expression contributes to development of burn-induced T cell immune suppression in mice. Current Medical Science, 2011, 31(5): 642-651 DOI:10.1007/s11596-011-0575-0

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