IL-33 and the intestine: The good, the bad, and the inflammatory

Zerina Hodzic, Ellen Merrick Schill, Alexa M. Bolock, Misty Good

Research output: Contribution to journalReview articlepeer-review

47 Scopus citations

Abstract

Interleukin-33 (IL-33) is a member of the IL-1 cytokine family that has been widely studied since its discovery in 2005 for its dichotomous functions in homeostasis and inflammation. IL-33, along with its receptor suppression of tumorigenicity 2 (ST2), has been shown to modulate both the innate and adaptive immune system. Originally, the IL-33/ST2 signaling axis was studied in the context of inducing type 2 immune responses with the expression of ST2 by T helper 2 (TH2) cells. However, the role of IL-33 is not limited to TH2 responses. Rather, IL-33 is a potent activator of TH1 cells, group 2 innate lymphoid cells (ILC2s), regulatory T (Treg) cells, and CD8+ T cells. The intestine is uniquely important in this discussion, as the intestinal epithelium is distinctively positioned to interact with both pathogens and the immune cells housed in the mucosa. In the intestine, IL-33 is expressed by the pericryptal fibroblasts and its expression is increased particularly in disease states. Moreover, IL-33/ST2 signaling aberrancy is implicated in the pathogenesis of inflammatory bowel disease (IBD). Accordingly, for this review, we will focus on the role of IL-33 in the regulation of intestinal immunity, involvement in intestinal disease, and implication in potential therapeutics.

Original languageEnglish
Pages (from-to)1-10
Number of pages10
JournalCytokine
Volume100
DOIs
StatePublished - Dec 2017

Keywords

  • Inflammatory bowel disease
  • Interleukin-33
  • Intestinal immunity
  • Microbiome
  • T cells

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