Perioperative alterations in the intestinal microbiota and functional changes mediate innate immune activation after small bowel transplantation

Life Sci. 2021 Jul 15:277:119468. doi: 10.1016/j.lfs.2021.119468. Epub 2021 Mar 31.

Abstract

Aim: Small bowel transplantation (SBT) is the only therapy for end-stage short bowel syndrome. However, complicated pathological changes and an increased risk of postoperative infections in the perioperative period are major obstacles to patient survival, but the associated mechanisms remain unclear.

Methods: To explore perioperative alterations in the intestinal microbiota and their functional changes after SBT, 16S rRNA sequencing of ileostomy effluents and plasma analysis were performed pre-SBT and periodically post-SBT.

Results: The results suggested that the presence of Proteobacteria accelerated bacterial motility and chemotaxis during the first week in post-SBT recipients. Altered gut microbiota impaired intestinal barrier integrity and upregulated 16S rDNA, pathogen-associated molecular pattern (PAMP) and pattern-recognition molecule (PRM) levels in peripheral circulation. Importantly, the levels of neutrophils, monocytes, cytotoxic T lymphocytes, and natural killer cells and the expression of proinflammatory cytokines were increased in the peripheral blood and had potential roles in activating innate immune-mediated inflammatory injury after SBT.

Conclusion: Together, our results suggest that altered microbiota and functional changes are probably related to innate immune-mediated inflammatory injury and graft survival after SBT, suggesting that the monitoring and regulation of intestinal microbiota are necessary for SBT patients.

Keywords: Innate immune-mediated inflammatory injury; Microbiota; Small bowel transplantation.

MeSH terms

  • China
  • Cytokines / immunology
  • Gastrointestinal Microbiome / genetics
  • Gastrointestinal Microbiome / immunology*
  • Gastrointestinal Microbiome / physiology
  • Graft Survival / immunology
  • Humans
  • Immunity, Innate / immunology
  • Inflammation / immunology
  • Intestine, Small / microbiology*
  • Intestine, Small / transplantation*
  • RNA, Ribosomal, 16S / genetics

Substances

  • Cytokines
  • RNA, Ribosomal, 16S