Evidence map›Paper›PMID 35857588›Full record

ArticleScience (New York, N.Y.)2022

TCR-Vγδ usage distinguishes protumor from antitumor intestinal γδ T cell subsets.

Bernardo S Reis, Patrick W Darcy, Iasha Z Khan, Christine S Moon, Adam E Kornberg, Vanessa S Schneider, Yelina Alvarez, Olawale Eleso, Caixia Zhu, Marina Schernthanner and 8 more

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
9.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

91 citing papers in PubMed, 124 citations in OpenAlex.

  1. Trial
  2. Review
  3. γδ T cells in colorectal and liver cancer.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  4. γδ T cells and cancer.The Journal of clinical investigation · 2026
    Review
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31 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 5 institutions in 2 countries.

Bernardo S ReisLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-6841-116X
Patrick W DarcyLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-7696-3212
Iasha Z KhanLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Christine S MoonDepartment of Medicine, Division of Digestive and Liver Diseases, Columbia University, New York, NY 10032, USA.ORCID 0000-0001-8717-2435
Adam E KornbergDepartment of Medicine, Division of Digestive and Liver Diseases, Columbia University, New York, NY 10032, USA.ORCID 0000-0002-8099-9699
Vanessa S SchneiderLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-7734-9150
Yelina AlvarezLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0003-0778-5683
Olawale ElesoLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-9210-9585
Caixia ZhuLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Marina SchernthannerLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Ainsley LockhartLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0003-0304-4618
Aubrey ReedLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-8613-3167
Juliana BortolattoLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Tiago B R CastroLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-0359-0611
Angelina M BilateLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0003-4575-786X
Sergei GrivennikovDepartment of Medicine and Department of Biomedical Sciences, Cedars-Sinai Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.ORCID 0000-0003-2987-0555
Arnold S HanDepartment of Medicine, Division of Digestive and Liver Diseases, Columbia University, New York, NY 10032, USA.ORCID 0000-0002-2667-5335
Daniel MucidaLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-0000-0452
Rockefeller University · USColumbia University Irving Medical Center · USCedars-Sinai Medical Center · USHoward Hughes Medical Institute · USUniversidade Federal do Paraná · BR

Funding

Developing, Demonstrating, and Disseminating Innovative Programs to Achieve Translational SuccessUL1TR001866 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY, KRUEGER, JAMES G · 2016 to 2025
$40.6M
The Organoid and Cell Culture CoreP30DK132710 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Robert F. Schwabe · 2022 to 2026
$7.2M
INTESTINAL REGULATION OF ThPOK EXPRESSION AND CD4 HELPER T CELL FUNCTIONR01DK093674 · NIDDK · ROCKEFELLER UNIVERSITY · PI Daniel S Mucida · 2013 to 2026
$7.0M
Intestinal surveillance by intraepithelial lymphocytesR01DK113375 · NIDDK · ROCKEFELLER UNIVERSITY · PI Semir Beyaz, Daniel S Mucida · 2017 to 2026
$5.5M
Mechanisms of cytokine driven tumor elicited inflammation in colorectal cancerR01CA218133 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GRIVENNIKOV, SERGEI I · 2018 to 2022
$2.4M
Columbia University Graduate Training Program in Microbiology and ImmunologyT32AI106711 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Nicholas Arpaia, Uttiya Basu · 2014 to 2026
$2.1M
EPA EP-W-17-011NCATS NIH HHS UL1 TR001866NCI NIH HHS R01 CA218133NIAID NIH HHS T32 AI106711NIDDK NIH HHS P30 DK132710NIDDK NIH HHS R01 DK093674NIDDK NIH HHS R01 DK113375
6 · The paper itself

Abstract

γδ T cells represent a substantial fraction of intestinal lymphocytes at homeostasis, but they also constitute a major lymphocyte population infiltrating colorectal cancers (CRCs); however, their temporal contribution to CRC development or progression remains unclear. Using human CRC samples and murine CRC models, we found that most γδ T cells in premalignant or nontumor colons exhibit cytotoxic markers, whereas tumor-infiltrating γδ T cells express a protumorigenic profile. These contrasting T cell profiles were associated with distinct T cell receptor (TCR)-Vγδ gene usage in both humans and mice. Longitudinal intersectional genetics and antibody-dependent strategies targeting murine γδ T cells enriched in the epithelium at steady state led to heightened tumor development, whereas targeting γδ subsets that accumulate during CRC resulted in reduced tumor growth. Our results uncover temporal pro- and antitumor roles for γδ T cell subsets.

Indexed as

Colorectal NeoplasmsCytotoxicity, ImmunologicIntestinesIntraepithelial LymphocytesReceptors, Antigen, T-Cell, gamma-deltaAnimalsHumansMiceReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID35857588
PMCPMC9326786
OpenAlexW4285385773

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.