Evidence map›Paper›PMID 24048123›Full record

ReviewNature immunology2013

Innate and adaptive immune cells in the tumor microenvironment.

Thomas F Gajewski, Hans Schreiber, Yang-Xin Fu

3 registry-linked trialsAbstract readReview
In one paragraph

Review in Nature immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 2,492 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2,492citing papers in PubMed, 2 pooled it
75.6field-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.

NCT02758314 unknown statusnot on this mapstarted 2017, after this paper: background citation

Clinical Pathological Features Associated With the Expression of PD1 / PD-L1 in Subpopulations of Peripheral Blood and Tumor Tissue in Patients With Advanced Non-small Cell Lung Cancer, Their Role as Prognostic and Therapeutic Targets

TypeobservationalSponsorInstituto Nacional de Cancerologia de MexicoRan2017 to 2018Enrolled150ConditionsNon-Small Cell Lung CancerArmsEvaluation of PD-1/PDL-1 expression.
NCT03330834 phase1terminatednot on this mapstarted 2017, after this paper: background citation

Safety and Toxicity of CAR-T Cell Immunotherapy in Patients With Advanced Lung Cancer After Standard Treatment Failure: A Single-Arm and Single-Center Phase I Clinical Study

TypeinterventionalSponsorSun Yat-sen UniversityRan2017 to 2020Enrolled1ConditionsAdvanced Lung CancerArmsCAR-T cells to treat advanced lung cancer
NCT05349227 narecruitingnot on this mapstarted 2022, after this paper: background citation

Comprehensive Outcomes for After Cancer Health (COACH): the Feasibility and Impact of an MHealth Augmented Coaching Program for Self-Management in Cancer Survivors

TypeinterventionalSponsorPack HealthRan2022 to 2027Enrolled625ConditionsOvarian Cancer, Breast Cancer, Lung Cancer, Gastric CancerArmsDigital Health Coaching Program, Fitbit
3 · Its place in the literature

Who cites it

2,492 citing papers in PubMed, 2 syntheses or guidelines pooled it, 4,168 citations in OpenAlex.

  1. Pooled it
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  13. Universal off-the-shelf TGF-Acta pharmaceutica Sinica. B · 2026
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  16. Green nanomedicine for cancer therapy.Chinese medical journal · 2026
    Review
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2,432 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

3 authors at 1 institution in 1 country.

Thomas F GajewskiUniversity of Chicago, Chicago, Illinois, USA.
Hans Schreiber
Yang-Xin Fu
University of Chicago · US

Funding

EGR2 in T cell toleranceR01CA161005 · NCI · UNIVERSITY OF CHICAGO · PI GAJEWSKI, THOMAS F · 2012 to 2016
$1.6M
Countering immune resistance in the melanoma tumor microenvironmentR01CA127475 · NCI · UNIVERSITY OF CHICAGO · PI GAJEWSKI, THOMAS F · 2007 to 2011
$1.4M
T Cell Responsiveness and Homeostasis in Anti-TumorR01CA118153 · NCI · UNIVERSITY OF CHICAGO · PI GAJEWSKI, THOMAS F · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA118153NCI NIH HHS R01 CA127475NCI NIH HHS R01 CA161005
6 · The paper itself

Abstract

Most tumor cells express antigens that can mediate recognition by host CD8(+) T cells. Cancers that are detected clinically must have evaded antitumor immune responses to grow progressively. Recent work has suggested two broad categories of tumor escape based on cellular and molecular characteristics of the tumor microenvironment. One major subset shows a T cell-inflamed phenotype consisting of infiltrating T cells, a broad chemokine profile and a type I interferon signature indicative of innate immune activation. These tumors appear to resist immune attack through the dominant inhibitory effects of immune system-suppressive pathways. The other major phenotype lacks this T cell-inflamed phenotype and appears to resist immune attack through immune system exclusion or ignorance. These two major phenotypes of tumor microenvironment may require distinct immunotherapeutic interventions for maximal therapeutic effect.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsDendritic CellsHumansLymphocyte ActivationNeoplasmsStromal CellsT-Lymphocyte SubsetsTumor Microenvironment

Identifiers

PMID24048123
PMCPMC4118725
OpenAlexW2042699075

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.