Type-2 dominant cytokine gene expression following hepatic surgery

J Hepatobiliary Pancreat Surg. 2006;13(5):442-9. doi: 10.1007/s00534-006-1103-7.

Abstract

Background/purpose: Hemorrhage and ischemic liver injuries associated with hepatic resection are thought to play a role in postoperative complications, possibly through altered cytokine production. The current study was performed to investigate the effects of hepatectomy on cytokine gene expression.

Methods: We collected blood preoperatively, at completion of operation, and on postoperative days 1 and 5 from ten patients undergoing hepatic resection. The peripheral blood mononuclear cells were evaluated with real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR) for gene expression of interleukin-10 (IL-10), proinflammatory cytokines (interferon-gamma [IFNgamma], IL-15, tumor necrosis factor alpha [TNFalpha], and chemokines regulated on activation, normal T expressed and secreted [RANTES], macrophage inflammatory protein 1 alpha [MIP-1alpha], [MIP-1beta]). Wilcoxon Rank and paired t-tests were used for statistical analysis.

Results: Immediately following hepatectomy there was a significant (31.4 +/- 60.5-fold; P < 0.05) increase in IL-10 gene expression that was sustained until the first postoperative day. In contrast, there was a significant downregulation (38 +/- 71 eight fold lower than preoperative; P < 0.05) of IFNgamma gene expression on day 1. By postoperative day 5, the changes in gene transcript levels of both IL-10 and IFNgamma had returned to the preoperative baselines. This contrasting change in IL-10 and IFNgamma gene expression in response to hepatic resection was statistically significant (P = 0.02).

Conclusions: Hepatectomy elicits an imbalance towards the immunosuppressive type-2 cytokine profile in the early postoperative period. Measurement of cytokine gene transcripts following hepatic resection may have predictive value for clinical outcome, and deserves further study.

Publication types

  • Comparative Study

MeSH terms

  • Chemokines / genetics
  • Colorectal Neoplasms / blood
  • Female
  • Gene Expression
  • Hepatectomy*
  • Humans
  • Interferon-gamma / genetics*
  • Interleukin-10 / genetics*
  • Interleukin-15 / genetics
  • Leukocytes, Mononuclear / chemistry
  • Male
  • Middle Aged
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription, Genetic
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Chemokines
  • Interleukin-15
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Interferon-gamma