Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/33951
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yakou, Marina H | - |
dc.contributor.author | Ghilas, Sonia | - |
dc.contributor.author | Tran, Kelly | - |
dc.contributor.author | Liao, Yang | - |
dc.contributor.author | Afshar-Sterle, Shoukat | - |
dc.contributor.author | Kumari, Anita | - |
dc.contributor.author | Schmid, Kevin | - |
dc.contributor.author | Dijkstra, Christine | - |
dc.contributor.author | Inguanti, Chantelle | - |
dc.contributor.author | Ostrouska, Simone | - |
dc.contributor.author | Wilcox, Jordan | - |
dc.contributor.author | Smith, Maxine | - |
dc.contributor.author | Parathan, Pavitha | - |
dc.contributor.author | Allam, Amr | - |
dc.contributor.author | Xue, Hai-Hui | - |
dc.contributor.author | Belz, Gabrielle T | - |
dc.contributor.author | Mariadason, John M | - |
dc.contributor.author | Behren, Andreas | - |
dc.contributor.author | Drummond, Grant R | - |
dc.contributor.author | Ruscher, Roland | - |
dc.contributor.author | Williams, David S | - |
dc.contributor.author | Pal, Bhupinder | - |
dc.contributor.author | Shi, Wei | - |
dc.contributor.author | Ernst, Matthias | - |
dc.contributor.author | Raghu, Dinesh | - |
dc.contributor.author | Mielke, Lisa A | - |
dc.date | 2023 | - |
dc.date.accessioned | 2023-10-11T06:21:16Z | - |
dc.date.available | 2023-10-11T06:21:16Z | - |
dc.date.issued | 2023-10-13 | - |
dc.identifier.citation | Science Immunology 2023-10-13; 8(88) | en_US |
dc.identifier.issn | 2470-9468 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/33951 | - |
dc.description.abstract | Intraepithelial 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.iso | eng | - |
dc.title | TCF-1 limits intraepithelial lymphocyte antitumor immunity in colorectal carcinoma. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Science Immunology | en_US |
dc.identifier.affiliation | Olivia Newton-John Cancer Research Institute | en_US |
dc.identifier.affiliation | La Trobe University School of Cancer Medicine, Heidelberg, Victoria 3084, Australia. | en_US |
dc.identifier.affiliation | Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia. | en_US |
dc.identifier.affiliation | Center 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.affiliation | University of Queensland Frazer Institute, Faculty of Medicine, University of Queensland, Woolloongabba, Queensland 4102, Australia. | en_US |
dc.identifier.affiliation | Centre 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.affiliation | Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia. | en_US |
dc.identifier.doi | 10.1126/sciimmunol.adf2163 | en_US |
dc.type.content | Text | en_US |
dc.identifier.orcid | 0009-0006-4618-4118 | en_US |
dc.identifier.orcid | 0000-0002-0164-2860 | en_US |
dc.identifier.orcid | 0009-0006-3318-7280 | en_US |
dc.identifier.orcid | 0000-0003-2678-7297 | en_US |
dc.identifier.orcid | 0009-0004-1763-1914 | en_US |
dc.identifier.orcid | 0000-0001-7582-3990 | en_US |
dc.identifier.orcid | 0000-0002-0585-9573 | en_US |
dc.identifier.orcid | 0000-0002-8743-3639 | en_US |
dc.identifier.orcid | 0000-0002-9163-7669 | en_US |
dc.identifier.orcid | 0000-0002-9660-9587 | en_US |
dc.identifier.orcid | 0000-0001-9123-7684 | en_US |
dc.identifier.orcid | 0000-0001-5329-280X | en_US |
dc.identifier.orcid | 0000-0001-8556-9738 | en_US |
dc.identifier.orcid | 0000-0002-8600-6985 | en_US |
dc.identifier.orcid | 0000-0002-3684-4331 | en_US |
dc.identifier.orcid | 0000-0003-1182-7735 | en_US |
dc.identifier.orcid | 0000-0002-6399-1177 | en_US |
dc.identifier.orcid | 0000-0002-8960-6222 | en_US |
dc.identifier.orcid | 0000-0002-9522-9320 | en_US |
dc.identifier.pubmedid | 37801516 | - |
dc.description.volume | 8 | - |
dc.description.issue | 88 | - |
dc.description.startpage | eadf2163 | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
Appears in Collections: | Journal articles |
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