Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33951
Title: TCF-1 limits intraepithelial lymphocyte antitumor immunity in colorectal carcinoma.
Austin Authors: Yakou, Marina H;Ghilas, Sonia;Tran, Kelly;Liao, Yang;Afshar-Sterle, Shoukat ;Kumari, Anita;Schmid, Kevin;Dijkstra, Christine ;Inguanti, Chantelle;Ostrouska, Simone;Wilcox, Jordan;Smith, Maxine;Parathan, Pavitha;Allam, Amr;Xue, Hai-Hui;Belz, Gabrielle T;Mariadason, John M ;Behren, Andreas;Drummond, Grant R;Ruscher, Roland;Williams, David S ;Pal, Bhupinder;Shi, Wei;Ernst, Matthias ;Raghu, Dinesh;Mielke, Lisa A
Affiliation: Olivia Newton-John Cancer Research Institute
La Trobe University School of Cancer Medicine, Heidelberg, Victoria 3084, Australia.
Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia.
Center for Discovery and Innovation, Hackensack University Medical Center, Nutley, NJ, USA.;New Jersey Veterans Affairs Health Care System, East Orange, NJ, USA.
University of Queensland Frazer Institute, Faculty of Medicine, University of Queensland, Woolloongabba, Queensland 4102, Australia.
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.
Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia.
Issue Date: 13-Oct-2023
Date: 2023
Publication information: Science Immunology 2023-10-13; 8(88)
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.
URI: https://ahro.austin.org.au/austinjspui/handle/1/33951
DOI: 10.1126/sciimmunol.adf2163
ORCID: 0009-0006-4618-4118
0000-0002-0164-2860
0009-0006-3318-7280
0000-0003-2678-7297
0009-0004-1763-1914
0000-0001-7582-3990
0000-0002-0585-9573
0000-0002-8743-3639
0000-0002-9163-7669
0000-0002-9660-9587
0000-0001-9123-7684
0000-0001-5329-280X
0000-0001-8556-9738
0000-0002-8600-6985
0000-0002-3684-4331
0000-0003-1182-7735
0000-0002-6399-1177
0000-0002-8960-6222
0000-0002-9522-9320
Journal: Science Immunology
Start page: eadf2163
PubMed URL: 37801516
ISSN: 2470-9468
Type: Journal Article
Appears in Collections:Journal articles

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