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GM-CSF promotes antitumor immunity by inducing Th9 cell responses

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dc.contributor.authorKim, Il-Kyu-
dc.contributor.authorKoh, Choong-Hyun-
dc.contributor.authorJeon, Insu-
dc.contributor.authorShin, Kwang-Soo-
dc.contributor.authorKang, Tae-Seung-
dc.contributor.authorBae, Eun-Ah-
dc.contributor.authorSeo, Hyungseok-
dc.contributor.authorKo, Hyun-Ja-
dc.contributor.authorKim, Byung-Seok-
dc.contributor.authorChung, Yeonseok-
dc.contributor.authorKang, Chang-Yuil-
dc.date.accessioned2023-05-08T08:25:35Z-
dc.date.available2023-05-08T08:25:35Z-
dc.date.created2019-10-23-
dc.date.created2019-10-23-
dc.date.created2019-10-23-
dc.date.created2019-10-23-
dc.date.created2019-10-23-
dc.date.created2019-10-23-
dc.date.issued2019-03-
dc.identifier.citationCancer Immunology Research, Vol.7 No.3, pp.498-509-
dc.identifier.issn2326-6066-
dc.identifier.urihttps://hdl.handle.net/10371/192154-
dc.description.abstractGM-CSF as an adjuvant has been shown to promote anti-tumor immunity in mice andhumans; however, theunderlying mechanism ofGM-CSF-induced antitumorimmunity remains incompletely understood. In this study, we demonstrate that GM-CSF potentiates the efficacy of cancer vaccines through IL9-producing Th (Th9) cells. GM-CSF selectively enhanced Th9 cell differentiation by regulating theCOX2-PGE2 pathway while inhibiting the differentiation of induced regulatory T (iTreg) cells in vitro and in vivo. GM-CSF-activated monocyte-derived dendritic cells converted tumor-specific naive Th cells into Th9 cells, and delayed tumor growth by inducing antitumor CTLs in an IL9-dependent manner. Our findings reveal a mechanism for the adjuvanticity of GM-CSF and provide a rationale for the use of GM-CSF in cancer vaccines.-
dc.language영어-
dc.publisherAmerican Association for Cancer Research Inc.-
dc.titleGM-CSF promotes antitumor immunity by inducing Th9 cell responses-
dc.typeArticle-
dc.identifier.doi10.1158/2326-6066.CIR-18-0518-
dc.citation.journaltitleCancer Immunology Research-
dc.identifier.wosid000460097000014-
dc.identifier.scopusid2-s2.0-85062269619-
dc.citation.endpage509-
dc.citation.number3-
dc.citation.startpage498-
dc.citation.volume7-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorSeo, Hyungseok-
dc.contributor.affiliatedAuthorChung, Yeonseok-
dc.contributor.affiliatedAuthorKang, Chang-Yuil-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCD4(+) T-CELLS-
dc.subject.keywordPlusCOLONY-STIMULATING FACTORS-
dc.subject.keywordPlusDENDRITIC CELLS-
dc.subject.keywordPlusMETASTATIC MELANOMA-
dc.subject.keywordPlusTUMOR-IMMUNITY-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusIMMUNOTHERAPY-
dc.subject.keywordPlusSYNERGIZES-
dc.subject.keywordPlusINDUCTION-
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  • Department of Manufacturing Pharmacy
Research Area Gene Signalling, Immunology, Transcriptional Networking, 면역유전체, 면역학, 항암면역학

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