Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33951
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dc.contributor.authorYakou, Marina H-
dc.contributor.authorGhilas, Sonia-
dc.contributor.authorTran, Kelly-
dc.contributor.authorLiao, Yang-
dc.contributor.authorAfshar-Sterle, Shoukat-
dc.contributor.authorKumari, Anita-
dc.contributor.authorSchmid, Kevin-
dc.contributor.authorDijkstra, Christine-
dc.contributor.authorInguanti, Chantelle-
dc.contributor.authorOstrouska, Simone-
dc.contributor.authorWilcox, Jordan-
dc.contributor.authorSmith, Maxine-
dc.contributor.authorParathan, Pavitha-
dc.contributor.authorAllam, Amr-
dc.contributor.authorXue, Hai-Hui-
dc.contributor.authorBelz, Gabrielle T-
dc.contributor.authorMariadason, John M-
dc.contributor.authorBehren, Andreas-
dc.contributor.authorDrummond, Grant R-
dc.contributor.authorRuscher, Roland-
dc.contributor.authorWilliams, David S-
dc.contributor.authorPal, Bhupinder-
dc.contributor.authorShi, Wei-
dc.contributor.authorErnst, Matthias-
dc.contributor.authorRaghu, Dinesh-
dc.contributor.authorMielke, Lisa A-
dc.date2023-
dc.date.accessioned2023-10-11T06:21:16Z-
dc.date.available2023-10-11T06:21:16Z-
dc.date.issued2023-10-13-
dc.identifier.citationScience Immunology 2023-10-13; 8(88)en_US
dc.identifier.issn2470-9468-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33951-
dc.description.abstractIntraepithelial lymphocytes (IELs), including αβ and γδ T cells (T-IELs), constantly survey and play a critical role in maintaining the gastrointestinal epithelium. We show that cytotoxic molecules important for defense against cancer were highly expressed by T-IELs in the small intestine. In contrast, abundance of colonic T-IELs was dependent on the microbiome and displayed higher expression of TCF-1/TCF7 and a reduced effector and cytotoxic profile, including low expression of granzymes. Targeted deletion of TCF-1 in γδ T-IELs induced a distinct effector profile and reduced colon tumor formation in mice. In addition, TCF-1 expression was significantly reduced in γδ T-IELs present in human colorectal cancers (CRCs) compared with normal healthy colon, which strongly correlated with an enhanced γδ T-IEL effector phenotype and improved patient survival. Our work identifies TCF-1 as a colon-specific T-IEL transcriptional regulator that could inform new immunotherapy strategies to treat CRC.en_US
dc.language.isoeng-
dc.titleTCF-1 limits intraepithelial lymphocyte antitumor immunity in colorectal carcinoma.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleScience Immunologyen_US
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen_US
dc.identifier.affiliationLa Trobe University School of Cancer Medicine, Heidelberg, Victoria 3084, Australia.en_US
dc.identifier.affiliationCentre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia.en_US
dc.identifier.affiliationCenter for Discovery and Innovation, Hackensack University Medical Center, Nutley, NJ, USA.;New Jersey Veterans Affairs Health Care System, East Orange, NJ, USA.en_US
dc.identifier.affiliationUniversity of Queensland Frazer Institute, Faculty of Medicine, University of Queensland, Woolloongabba, Queensland 4102, Australia.en_US
dc.identifier.affiliationCentre for Cardiovascular Biology and Disease Research; Department of Microbiology, Anatomy, Physiology and Pharmacology; and School of Agriculture, Biomedicine, and Environment, La Trobe University, Bundoora, Victoria, Australia.en_US
dc.identifier.affiliationCentre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia.en_US
dc.identifier.doi10.1126/sciimmunol.adf2163en_US
dc.type.contentTexten_US
dc.identifier.orcid0009-0006-4618-4118en_US
dc.identifier.orcid0000-0002-0164-2860en_US
dc.identifier.orcid0009-0006-3318-7280en_US
dc.identifier.orcid0000-0003-2678-7297en_US
dc.identifier.orcid0009-0004-1763-1914en_US
dc.identifier.orcid0000-0001-7582-3990en_US
dc.identifier.orcid0000-0002-0585-9573en_US
dc.identifier.orcid0000-0002-8743-3639en_US
dc.identifier.orcid0000-0002-9163-7669en_US
dc.identifier.orcid0000-0002-9660-9587en_US
dc.identifier.orcid0000-0001-9123-7684en_US
dc.identifier.orcid0000-0001-5329-280Xen_US
dc.identifier.orcid0000-0001-8556-9738en_US
dc.identifier.orcid0000-0002-8600-6985en_US
dc.identifier.orcid0000-0002-3684-4331en_US
dc.identifier.orcid0000-0003-1182-7735en_US
dc.identifier.orcid0000-0002-6399-1177en_US
dc.identifier.orcid0000-0002-8960-6222en_US
dc.identifier.orcid0000-0002-9522-9320en_US
dc.identifier.pubmedid37801516-
dc.description.volume8-
dc.description.issue88-
dc.description.startpageeadf2163-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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