New insights into lipopolysaccharide inactivation mechanisms in sepsis

Biomed Pharmacother. 2021 Sep:141:111890. doi: 10.1016/j.biopha.2021.111890. Epub 2021 Jul 3.

Abstract

The complex pathophysiology of sepsis makes it a syndrome with limited therapeutic options and a high mortality rate. Gram-negative bacteria containing lipopolysaccharides (LPS) in their outer membrane correspond to the most common cause of sepsis. Since the gut is considered an important source of LPS, intestinal damage has been considered a cause and a consequence of sepsis. Although important in the maintenance of the intestinal epithelial cell homeostasis, the microbiota has been considered a source of LPS. Recent studies have started to shed light on how sepsis is triggered by dysbiosis, and an increased inflammatory state of the intestinal epithelial cells, expanding the understanding of the gut-liver axis in sepsis. Here, we review the gut-liver interaction in Gram-negative sepsis, exploring the mechanisms of LPS inactivation, including the recently described contribution of an isoform of the cholesteryl-ester transfer protein (CETPI). Although several key questions remain to be answered when the pathophysiology of sepsis is reviewed, new contributions coming to light exploring the way LPS might be inactivated in vivo, suggest that new applications might soon reach the clinical setting.

Keywords: CETPI; Dysbiosis; Gut-liver axis; Lipopolysaccharide; Sepsis.

Publication types

  • Review

MeSH terms

  • Animals
  • Cholesterol Ester Transfer Proteins / genetics
  • Gastrointestinal Microbiome
  • Humans
  • Lipopolysaccharides / antagonists & inhibitors*
  • Sepsis / drug therapy*
  • Sepsis / microbiology
  • Sepsis / physiopathology

Substances

  • CETP protein, human
  • Cholesterol Ester Transfer Proteins
  • Lipopolysaccharides