Evidence map›Paper›PMID 29038367›Full record

ArticleThe Journal of experimental medicine2017

A nonimmune function of T cells in promoting lung tumor progression.

Jesse A Green, Nicholas Arpaia, Michail Schizas, Anton Dobrin, Alexander Y Rudensky

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Foxp3Research square · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Treg-tissue cell interactions in repair and regeneration.The Journal of experimental medicine · 2024
    Review
  10. Article
  11. Article
  12. Amphiregulin couples IL1RL1Science advances · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Tumor resident regulatory T cells.Seminars in immunology · 2021
    Review
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jesse A GreenHoward Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY.
Nicholas ArpaiaHoward Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID http://orcid.org/0000-0002-0657-0528
Michail SchizasHoward Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY.
Anton DobrinHoward Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID http://orcid.org/0000-0002-9751-0677
Alexander Y RudenskyHoward Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY rudenska@mskcc.org.ORCID http://orcid.org/0000-0003-1280-2898
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor-specific T cell state dynamics and heterogeneity in early tumorigenesisU54CA209975 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LESLIE, CHRISTINA S, RUDENSKY, ALEXANDER Y · 2016 to 2021
$11.8M
Self Peptides Bound to MHC Class II In T Cell SelectionR37AI034206 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI RUDENSKY, ALEXANDER Y · 2009 to 2018
$4.8M
Mechanisms mediating tissue repair by leukocytes during influenza virus infectionK22AI127847 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ARPAIA, NICHOLAS · 2017 to 2018
$266k
NCI NIH HHS P30 CA008748NCI NIH HHS U54 CA209975NIAID NIH HHS K22 AI127847NIAID NIH HHS R37 AI034206
6 · The paper itself

Abstract

The involvement of effector T cells and regulatory T (T reg) cells in opposing and promoting solid organ carcinogenesis, respectively, is viewed as a shifting balance between a breach versus establishment of tolerance to tumor or self-antigens. We considered that tumor-associated T cells might promote malignancy via distinct mechanisms used by T cells in nonlymphoid organs to assist in their maintenance upon injury or stress. Recent studies suggest that T reg cells can participate in tissue repair in a manner separable from their immunosuppressive capacity. Using transplantable models of lung tumors in mice, we found that amphiregulin, a member of the epidermal growth factor family, was prominently up-regulated in intratumoral T reg cells. Furthermore, T cell-restricted amphiregulin deficiency resulted in markedly delayed lung tumor progression. This observed deterrence in tumor progression was not associated with detectable changes in T cell immune responsiveness or T reg and effector T cell numbers. These observations suggest a novel "nonimmune" modality for intratumoral T reg and effector T cells in promoting tumor growth through the production of factors normally involved in tissue repair and maintenance.

Indexed as

Disease ProgressionAmphiregulinAnimalsCell Line, TumorCell ProliferationLung NeoplasmsLymphocyte ActivationMice, Inbred C57BLMice, TransgenicNeovascularization, PathologicSignal TransductionT-Lymphocytes, RegulatoryAmphiregulinAreg protein, mouse

Identifiers

PMID29038367
PMCPMC5716034
OpenAlexW2765728936

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.