Intestinal immune dysregulation driven by dysbiosis promotes barrier disruption and bacterial translocation in rats with cirrhosis.

In cirrhosis, intestinal dysbiosis, intestinal barrier impairment and systemic immune system abnormalities lead to gut bacterial translocation (GBT) and bacterial infection. However, intestinal immune system dysfunction and its contribution to barrier damage are poorly understood. This study correlates immune system dysregulation in the intestines of rats at different stages of CCl4 -induced cirrhosis with barrier function and pathogenic microbiota. The following variables were addressed in the small intestine: intraepithelial and lamina propria lymphocyte (IEL, LPL) activation status and cytokine production (flow cytometry), cytokine mRNA and protein expression (real-time quantitative PCR (qPCR) and immunofluorescence), microbiota composition of ileum content (16SrDNA massive sequencing), permeability (fecal albumin loss) and epithelial junctions (immunohistochemistry and immunofluorescence). The intestinal mucosa in cirrhotic rats showed a proinflammatory pattern of immune dysregulation in IEL and LPL, which featured the expansion of activated lymphocytes, switch to a Th1 regulatory pattern and Th17 reduction. In cirrhotic rats with ascites, this state was associated with epithelial junction protein disruption, fecal albumin loss, and GBT. Direct correlations (p<0.01) were observed between elevated IFNγ-expressing T cytotoxic LPL and fecal albumin, and between inflammatory taxa abundance and IFNγ-producing immune cells in the ileum. Bowel decontamination led to redistributed microbiota composition, reduced proinflammatory activation of mucosal immune cells, normalized fecal albumin levels and diminished GBT, but there were no modifications in Th17 depletion. Conclusion: The intestinal mucosa of rats with cirrhosis acquires a proinflammatory profile of immune dysregulation that parallels the severity of cirrhosis. This impaired intestinal immune response is driven by gut dysbiosis and leads to disrupted barrier function, promoting GBT. This article is protected by copyright. All rights reserved.