Transplant International (Oct 2024)

Activation of the Innate Immune System in Brain-Dead Donors Can Be Reduced by Luminal Intestinal Preservation During Organ Procurement Surgery - A Porcine Model

  • Marc Gjern Weiss,
  • Marc Gjern Weiss,
  • Anne Marye de Jong,
  • Helene Seegert,
  • Niels Moeslund,
  • Niels Moeslund,
  • Hanno Maassen,
  • Camilla Schjalm,
  • Camilla Schjalm,
  • Eline de Boer,
  • Eline de Boer,
  • Henri Leuvenink,
  • Tom Eirik Mollnes,
  • Tom Eirik Mollnes,
  • Tom Eirik Mollnes,
  • Marco Eijken,
  • Marco Eijken,
  • Marco Eijken,
  • Anna Krarup Keller,
  • Anna Krarup Keller,
  • Gerard Dijkstra,
  • Bente Jespersen,
  • Bente Jespersen,
  • Søren Erik Pischke,
  • Søren Erik Pischke,
  • Søren Erik Pischke

DOI
https://doi.org/10.3389/ti.2024.13569
Journal volume & issue
Vol. 37

Abstract

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Organs obtained from brain dead donors can have suboptimal outcomes. Activation of the innate immune system and translocation of intestinal bacteria could be causative. Thirty two pigs were assigned to control, brain death (BD), BD + luminal intestinal polyethylene glycol (PEG), and BD + luminal intestinal University of Wisconsin solution (UW) groups. Animals were observed for 360 min after BD before organ retrieval. 2,000 mL luminal intestinal preservation solution was instilled into the duodenum at the start of organ procurement. Repeated measurements of plasma C3a, Terminal Complement Complex (TCC), IL-8, TNF, and lipopolysaccharide binding protein were analysed by immunoassays. C3a was significantly higher in the BD groups compared to controls at 480 min after brain death. TCC was significantly higher in BD and BD + UW, but not BD + PEG, compared to controls at 480 min. TNF was significantly higher in the BD group compared to all other groups at 480 min. LPS binding protein increased following BD in all groups except BD + PEG, which at 480 min was significantly lower compared with all other groups. Brain death induced innate immune system activation was decreased by luminal preservation using PEG during organ procurement, possibly due to reduced bacterial translocation.

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