Cylindromatosis (CYLD) protein, which is a de-ubiquitinase that acts as a negative regulator of NF-κB signaling, plays a prominent role in IBD.1 This manuscript also provided good evidence that genetic polymorphisms in CYLD are significantly associated with human CD.1 Moreover, the authors showed that pathogenic bacteria (E. Coli strain LF82) decrease the expression of CYLD, thereby resulting in enhanced NF-kB activation in intestinal epithelial cells.1 This transcription factor has frequently been cited as a central mediator of inflammation in IBD.2 Other manuscripts published over the last 10years have also implicated various components of the UPS as being important in the pathogenesis of IBD.