Evidence map›Paper›PMID 28115575›Full record

ArticleThe Journal of experimental medicine2017

The EGR2 targets LAG-3 and 4-1BB describe and regulate dysfunctional antigen-specific CD8+ T cells in the tumor microenvironment.

Jason B Williams, Brendan L Horton, Yan Zheng, Yukan Duan, Jonathan D Powell, Thomas F Gajewski

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 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed
10.2field-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

113 citing papers in PubMed, 206 citations in OpenAlex.

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  20. T-Cell Senescence in Human Metabolic Diseases.Diabetes & metabolism journal · 2024
    Review

53 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Jason B WilliamsDepartments of Pathology, Section of Hematology/Oncology, the University of Chicago, Chicago, IL 60637.ORCID 0000-0002-8386-6285
Brendan L HortonDepartments of Pathology, Section of Hematology/Oncology, the University of Chicago, Chicago, IL 60637.
Yan ZhengDepartments of Pathology, Section of Hematology/Oncology, the University of Chicago, Chicago, IL 60637.ORCID 0000-0001-9426-4127
Yukan DuanDepartment of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, MD 21287.ORCID 0000-0001-9614-8402
Jonathan D PowellSidney Kimmel Comprehensive Cancer Research Center, Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21231.
Thomas F GajewskiDepartments of Pathology, Section of Hematology/Oncology, the University of Chicago, Chicago, IL 60637 tgajewsk@medicine.bsd.uchicago.edu.ORCID 0000-0001-5727-3972
University of Chicago · USJohns Hopkins University · US

Funding

INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
EGR2 in T cell toleranceR01CA161005 · NCI · UNIVERSITY OF CHICAGO · PI GAJEWSKI, THOMAS F · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA161005NIAID NIH HHS T32 AI007090
6 · The paper itself

Abstract

Although the presence of tumor-infiltrating lymphocytes (TILs) indicates an endogenous antitumor response, immune regulatory pathways can subvert the effector phase and enable tumor escape. Negative regulatory pathways include extrinsic suppression mechanisms, but also a T cell-intrinsic dysfunctional state. A more detailed study has been hampered by a lack of cell surface markers defining tumor-specific dysfunctional TILs, and PD-1 alone is not sufficient. Recently, we identified the transcription factor Egr2 as a critical component in controlling the anergic state in vitro. In this study, we show that the Egr2-driven cell surface proteins LAG-3 and 4-1BB can identify dysfunctional tumor antigen-specific CD8

Indexed as

Tumor MicroenvironmentAnimalsAntibodies, MonoclonalAntigens, CDAntigens, NeoplasmCD8-Positive T-LymphocytesEarly Growth Response Protein 2FemaleFingolimod HydrochlorideInterferon-gammaInterleukin-2Lymphocyte Activation Gene 3 ProteinLymphocytes, Tumor-InfiltratingMiceMice, Inbred C57BLTumor Necrosis Factor Receptor Superfamily, Member 9Antibodies, MonoclonalAntigens, CDAntigens, NeoplasmEarly Growth Response Protein 2Egr2 protein, mouseFingolimod HydrochlorideInterferon-gammaInterleukin-2Lag3 protein, mouseLymphocyte Activation Gene 3 ProteinTumor Necrosis Factor Receptor Superfamily, Member 9

Identifiers

PMID28115575
PMCPMC5294847
OpenAlexW2580464105

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.