Exogenous IL-6 inhibits acute inflammatory responses and prevents ischemia/reperfusion injury after intestinal transplantation

Am J Transplant. 2004 Apr;4(4):482-94. doi: 10.1111/j.1600-6143.2004.00368.x.

Abstract

Interleukin-6 (IL-6) is a pleiotropic acute reactant cytokine involved in inflammatory responses. To explore the role of IL-6 in inflammation, this study examined the efficacy of exogenous IL-6 in preventing intestinal ischemia/reperfusion (I/R) injury associated with small bowel transplantation (SBTx). Syngenic orthotopic SBTx was performed in Lewis rats after 6-h graft preservation in University of Wisconsin (UW) at 4 degrees C. IL-6 mutein (IL-6m, 500 microg/kg), a recombinant molecular variant of human IL-6, was subcutaneously given to donors 2 h before harvesting (IL-6mD) or to excised grafts by luminal infusion (IL-6mG). Animal survival was 100% and 75% in IL-6mD (p<0.05 vs. control) and IL-6mG groups, respectively, compared with 64.3% in untreated controls. The severity of I/R injury (e.g. epithelial denudation, villous congestion) was reduced with IL-6m, in addition to a striking increase in re-epithelization. With IL-6m, neutrophil extravasation was markedly reduced in intestinal grafts and in remote organs (e.g. lung). IL-6m mediated anti-inflammatory effects through the inhibition of I/R-induced up-regulation of intragraft and circulating IL-1-beta, tumor necrosis factor-alpha (TNF-alpha) and IL-6. IL-6m also increased intestinal graft tissue blood flow. These results show that IL-6 is effective in protecting the intestine from cold I/R injury by maintaining graft blood flow and reducing pro-inflammatory cytokine up-regulation and neutrophil infiltration.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acute Disease
  • Animals
  • Benzothiazoles
  • Blotting, Western
  • Cytokines / biosynthesis
  • Cytokines / metabolism
  • Diamines
  • Immunohistochemistry
  • Inflammation / drug therapy*
  • Interleukin-1 / biosynthesis
  • Interleukin-6 / metabolism
  • Interleukin-6 / physiology*
  • Intestinal Mucosa / metabolism
  • Intestines / blood supply
  • Intestines / pathology*
  • Lung / metabolism
  • Lung / pathology
  • Male
  • Mutation
  • Neutrophils / metabolism
  • Organ Transplantation / methods*
  • Organic Chemicals / pharmacology
  • Peroxidase / metabolism
  • Quinolines
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred Lew
  • Reperfusion Injury / prevention & control*
  • Repressor Proteins / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Time Factors
  • Transcription Factors / biosynthesis
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Up-Regulation

Substances

  • Benzothiazoles
  • Cytokines
  • Diamines
  • Interleukin-1
  • Interleukin-6
  • Organic Chemicals
  • Quinolines
  • RNA, Messenger
  • Repressor Proteins
  • SOCS3 protein, human
  • Socs3 protein, rat
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • SYBR Green I
  • Peroxidase