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Opinion Review
Copyright: ©Author(s) 2026.
World J Gastroenterol. Oct 28, 2026; 32(40): 119684
Published online Oct 28, 2026. doi: 10.3748/wjg.119684
Table 1 Function of the interleukin-33/suppression of tumorigenicity 2 signaling pathway in different cell types
Cell type
Key molecules
Function
Mast cellTNF-α, IL-1β, IL-6, IL-13, VEGFAmplification of inflammation, vascular responses, and tissue remodeling; increased cell adhesion and immune cell crosstalk
Th2 cellIL-4, IL-5, IL-10, IL-13IL-33 exerts a chemotactic effect on Th2 cells; it promotes the polarization of naive T cells toward the Th2 pathway
Treg cellFoxP3, ST2IL-33/ST2 axis promotes Treg expansion; suppresses IL-17 and IFN-γ production
EosinophilIL-4, IL-5, IL-9, IL-13, GM-CSFDual involvement in pro-inflammatory and immunomodulatory functions
ILC2IL-6, IL-4, IL-5, IL-9, IL-13Central amplifier of Type 2 immune responses
Dendritic cellIL-1β, IL-6, TNF-α, CD80, CD86IL-33 promotes the polarization of naïve T cells toward Th2 cells by activating dendritic cells
FibroblastERK, p38 MAPKIL-33 activates fibroblasts (ERK/p38 MAPK–dependent) to produce chemokines and promote eosinophil infiltration
B cellIL-4RIL-33 activates B cells during delayed-type hypersensitivity and increases IL-4R+ B cells, facilitating IgE production
MacrophageIL-1β, IL-6, IL-10, VEGF, MMP9IL-33-induced STAT1 signaling correlates with IFN-γ output


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