2022
DOI: 10.1177/15353702221102094
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The role of IL-33/ST2 signaling in the tumor microenvironment and Treg immunotherapy

Abstract: Interleukin (IL)-33 is a tissue-derived nuclear cytokine belonging to the IL-1 family. Stimulation-2 (ST2) is the only known IL-33 receptor. ST2 signals mostly on immune cells found within tissues, such as regulatory T cells (Treg cells), CD8+ T cells, and natural killer (NK) cells. Therefore, the IL-33/ST2 signaling pathway is important in the immune system. IL-33 deficiency impairs Treg cell function. ST2 signaling is also increased in active Treg cells, providing a new approach for Treg-related immunotherap… Show more

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Cited by 4 publications
(2 citation statements)
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References 113 publications
(146 reference statements)
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“…MTE inhibits osteopontin, which is elevated in human CRC, and may function as an immune checkpoint and potent T cell suppressor ( 15 ). MTE downregulates ST2, a factor that drives Tregs to accumulate in the tumor microenvironment ( 16 ), was down regulated by MTE.…”
Section: Resultsmentioning
confidence: 99%
“…MTE inhibits osteopontin, which is elevated in human CRC, and may function as an immune checkpoint and potent T cell suppressor ( 15 ). MTE downregulates ST2, a factor that drives Tregs to accumulate in the tumor microenvironment ( 16 ), was down regulated by MTE.…”
Section: Resultsmentioning
confidence: 99%
“…IL-33, present in the nucleus as a nuclear factor, is rapidly released during cell stress or damage (122). IL-33, in combination with ST2, induces the production of inflammatory factors by DC, macrophages, Th2, Tregs, mast cells, and innate lymphoid cell type 2 (ILC2) (123,124), promotes the proliferation of Tregs and enhances the inhibitory capacity of Tregs (125,126).…”
Section: Th17 and Treg Differentiation And Function In The Sepsismentioning
confidence: 99%