Table 1:
Experimental animal studies | Human studies | |
---|---|---|
NLR family proteins | • Attenuation or exacerbation of colitis • Maintenance of epithelial barrier integrity, repair and recovery • Gut homeostasis and mucosal renewal • Maintenance of intestinal mucus layer • Alteration or no effect on microbiota • Induction of T-cell activation |
• Increased severity to intestinal inflammation • Increased activation in CD and UC patients • Increased expression in intestinal epithelial cells, neutrophils and lamina propria cells |
Caspases | • Attenuation of colitis • Maintenance of intestinal epithelial barrier integrity • Release of IL-18 and IL-1β cytokines • Regulation of STAT1 signaling in IECs |
• Increased activation in CD and UC patients |
IL-18 | • Attenuation or exacerbation of colitis • Controlling the outgrowth of colitogenic bacteria and maintenance of intestinal microbiota • Maintenance of intestinal barrier function and mucosal renewal • Induces release of other cytokines |
• Increased severity to intestinal inflammation • Increased activation in CD patients • Maintenance of intestinal barrier integrity • Increased expression in intestinal epithelial cells and lamina propria cells |
IL-1β | • No dominant role in intestinal inflammation • Activation of T-cell immune response |
• Increased activation in CD and UC patients • Increased severity to intestinal inflammation |
UC: Ulcerative colitis, CD: Crohn’s disease, IECs: Intestinal epithelial cells