Literature DB >> 33632927

Association of Fusobacterium nucleatum with Specific T-cell Subsets in the Colorectal Carcinoma Microenvironment.

Jennifer Borowsky1,2,3,4, Koichiro Haruki1,5, Mai Chan Lau1,5, Andressa Dias Costa6, Jochen K Lennerz2, Marios Giannakis6,7,8, Jonathan A Nowak9, Shuji Ogino10,5,11,7,12, Juha P Väyrynen1,5,6,13, Tomotaka Ugai1,11, Kota Arima1,5, Annacarolina da Silva5, Kristen D Felt14, Melissa Zhao5, Carino Gurjao6, Tyler S Twombly1,5, Kenji Fujiyoshi1,5, Sara A Väyrynen5,6, Tsuyoshi Hamada1,5, Kosuke Mima5, Susan Bullman15, Tabitha A Harrison16, Amanda I Phipps16,17, Ulrike Peters16,17, Kimmie Ng6, Jeffrey A Meyerhardt6, Mingyang Song18,19,20, Edward L Giovannucci11,18, Kana Wu11,18,21, Xuehong Zhang21, Gordon J Freeman6, Curtis Huttenhower22,7, Wendy S Garrett6,7,23, Andrew T Chan19,20,21,23, Barbara A Leggett3,4,24, Vicki L J Whitehall3,4,25, Neal Walker4,26, Ian Brown4,26, Mark Bettington3,4,26, Reiko Nishihara1,5,11,18,22, Charles S Fuchs27,28,29.   

Abstract

PURPOSE: While evidence indicates that Fusobacterium nucleatum (F. nucleatum) may promote colorectal carcinogenesis through its suppressive effect on T-cell-mediated antitumor immunity, the specific T-cell subsets involved remain uncertain. EXPERIMENTAL
DESIGN: We measured F. nucleatum DNA within tumor tissue by quantitative PCR on 933 cases (including 128 F. nucleatum-positive cases) among 4,465 incident colorectal carcinoma cases in two prospective cohorts. Multiplex immunofluorescence combined with digital image analysis and machine learning algorithms for CD3, CD4, CD8, CD45RO (PTPRC isoform), and FOXP3 measured various T-cell subsets. We leveraged data on Bifidobacterium, microsatellite instability (MSI), tumor whole-exome sequencing, and M1/M2-type tumor-associated macrophages [TAM; by CD68, CD86, IRF5, MAF, and MRC1 (CD206) multimarker assay]. Using the 4,465 cancer cases and inverse probability weighting method to control for selection bias due to tissue availability, multivariable-adjusted logistic regression analysis assessed the association between F. nucleatum and T-cell subsets.
RESULTS: The amount of F. nucleatum was inversely associated with tumor stromal CD3+ lymphocytes [multivariable OR, 0.47; 95% confidence interval (CI), 0.28-0.79, for F. nucleatum-high vs. -negative category; P trend = 0.0004] and specifically stromal CD3+CD4+CD45RO+ cells (corresponding multivariable OR, 0.52; 95% CI, 0.32-0.85; P trend = 0.003). These relationships did not substantially differ by MSI status, neoantigen load, or exome-wide tumor mutational burden. F. nucleatum was not significantly associated with tumor intraepithelial T cells or with M1 or M2 TAMs.
CONCLUSIONS: The amount of tissue F. nucleatum is associated with lower density of stromal memory helper T cells. Our findings provide evidence for the interactive pathogenic roles of microbiota and specific immune cells. ©2021 American Association for Cancer Research.

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Year:  2021        PMID: 33632927      PMCID: PMC8127352          DOI: 10.1158/1078-0432.CCR-20-4009

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   13.801


  54 in total

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Journal:  Br J Cancer       Date:  2020-03-11       Impact factor: 7.640

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4.  Immune cell profiles in the tumor microenvironment of early-onset, intermediate-onset, and later-onset colorectal cancer.

Authors:  Tomotaka Ugai; Jennifer Borowsky; Marios Giannakis; Shuji Ogino; Juha P Väyrynen; Mai Chan Lau; Naohiko Akimoto; Sara A Väyrynen; Melissa Zhao; Rong Zhong; Koichiro Haruki; Andressa Dias Costa; Kenji Fujiyoshi; Kota Arima; Kana Wu; Andrew T Chan; Yin Cao; Mingyang Song; Charles S Fuchs; Molin Wang; Jochen K Lennerz; Kimmie Ng; Jeffrey A Meyerhardt; Jonathan A Nowak
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