Exploring host-commensal-pathogen dynamics in cell line and organotypic human intestinal epithelial models

Highlights

• Our intestinal models are suitable to understand immune processes in the gut

• These models are viable in co-culture with gut bacteria and in anaerobic conditions

• R. torques and/or AIEC induced similar cytokine/chemokine profiles in both models

• Co-culture with immune cells can trigger responses by the epithelium in both models

Summary

Host and microbiome intricately interact in the ecosystem of the human digestive tract, playing a crucial role in our health. These interactions can initiate immune responses in the epithelial cells, which, in turn, activate downstream responses in other immune cells. Here, we used a CaCo-2 and a human intestinal enteroid (HIE) model to explore epithelial responses to both commensal and pathogenic bacteria, individually and combined. CaCo-2 cells were co-cultured with peripheral blood mononuclear cells, revealing downstream activation of immune cells. While both systems showed comparable cytokine profiles, they differed in their responses to the different bacteria, with the organoid system being more representative of responses observed in humans. We provide evidence of the pro-inflammatory responses associated with these bacteria. These models contribute to a deeper understanding of the interactions between the microbiota, intestinal epithelium, and immune cells in the gut, promoting advances in the field of host-microbe interactions.