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Expression of Toll-like receptors 2 and 4 is downregulated after operation
Authors:Ikushima Hirofumi  Nishida Toshirou  Takeda Kiyoshi  Ito Toshinori  Yasuda Takushi  Yano Masahiko  Akira Shizuo  Matsuda Hikaru
Institution:From the Department of Surgery, Graduate School of Medicine, and the Department of Host Defense, Research Institute for Microbial Disease, Osaka University, Osaka, Japan
Abstract:

Background

Toll-like receptors (TLR) that recognize microbial pathogens play a critical role in innate immunity; however, their expression and function after surgery remain unknown. The aim of this study was to examine TLR2 and TLR4 expression on monocytes and their responses to each agonist after surgical insults.

Methods

Blood samples were obtained from 83 patients who underwent gastrointestinal surgery. TLR2, TLR4, and inducible nitric oxide synthase expressions on peripheral blood mononuclear cells (PBMCs) were analyzed by flow cytometry. Macrophage-activating lipopeptide-2 or lipopolysaccharide-induced tumor necrosis factor-α and interleukin-6 production was measured by enzyme-linked immunosorbent assay.

Results

TLR2 and TLR4 decreased and showed the lowest values on the postoperative days 3 and 1, respectively. Macrophage-activating lipopeptide-2-stimulated tumor necrosis factor-α and interleukin-6 production was decreased immediately after the operation (P<.05), increased to a maximum value on postoperative day 1, and then decreased gradually. Lipopolysaccharide-stimulated tumor necrosis factor-α production was also suppressed immediately (P<.05) after operation then showed a gradual increase to maximum values on postoperative day 3. Inducible nitric oxide synthase in cultured PBMC that was obtained immediately after operation was upregulated (P<.05).

Conclusion

Expressions of TLR2 and TLR4 were downregulated by operation, and agonist-induced cytokine production was suppressed transiently and soon increased through the activation of PBMC. The present study may offer new insights for postoperative modulation of innate immunity under surgical stress.
Keywords:
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