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10.1016/j.ccell.2015.07.014

http://scihub22266oqcxt.onion/10.1016/j.ccell.2015.07.014
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C4573903!4573903!26321222
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suck abstract from ncbi


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pmid26321222      Cancer+Cell 2015 ; 28 (3): 296-306
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  • IL-36? transforms the tumor microenvironment and promotes type 1 lymphocyte-mediated antitumor immune responses #MMPMID26321222
  • Wang X; Zhao X; Feng C; Weinstein A; Xia R; Wen W; Lv Q; Zuo S; Tang P; Yang X; Chen X; Wang H; Zang S; Stollings L; Denning TL; Jiang J; Fan J; Zhang G; Zhang X; Zhu Y; Storkus W; Lu B
  • Cancer Cell 2015[Sep]; 28 (3): 296-306 PMID26321222show ga
  • Cytokines play a pivotal role in regulating tumor immunogenicity and antitumor immunity. IL-36? is important for the IL-23/IL-17-dominated inflammation and anti-BCG Th1 immune responses. However, the impact of IL-36? on tumor immunity is unknown. Here, we found IL-36? stimulated CD8+ T cells, NK cells, and ?? T cells synergistically with TCR signaling and/or IL-12. Importantly, IL-36? exerted profound antitumor effects in vivo and transformed the tumor microenvironment in favor of tumor eradication. Furthermore, IL-36? strongly increased the efficacy of tumor vaccination. Moreover, IL-36? expression inversely correlated with progression of human melanoma and lung cancer. Our study establishes a role of IL-36? in promoting antitumor immune responses and suggests its potential clinical translation in cancer immunotherapy.
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