Evidence map›Paper›PMID 25446897›Full record

ArticleCancer cell2014

Dissecting the tumor myeloid compartment reveals rare activating antigen-presenting cells critical for T cell immunity.

Miranda L Broz, Mikhail Binnewies, Bijan Boldajipour, Amanda E Nelson, Joshua L Pollack, David J Erle, Andrea Barczak, Michael D Rosenblum, Adil Daud, Diane L Barber and 5 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03792724 (Phase I-II Study of Intratumoral Urelumab Combined With Nivolumab in Patients With Solid Tumors), which is not on this map. Cited by 694 papers.

0numbers the graph read from it
0cells of the map it votes in
694citing papers in PubMed
20.8field-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.

NCT03792724 phase1 / phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Phase I-II Study of Intratumoral Urelumab Combined With Nivolumab in Patients With Solid Tumors

TypeinterventionalSponsorClinica Universidad de Navarra, Universidad de NavarraRan2019 to 2023Enrolled32ConditionsNeoplasmsArmsUrelumab + Nivolumab
3 · Its place in the literature

Who cites it

694 citing papers in PubMed, 1,167 citations in OpenAlex.

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  5. CD4Oncoimmunology · 2026
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634 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 2 countries.

Miranda L BrozDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143, USA.
Mikhail BinnewiesDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143, USA.
Bijan BoldajipourDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143, USA.
Amanda E NelsonDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143, USA.
Joshua L PollackLung Biology Center, University of California San Francisco, San Francisco, CA 94143, USA.
David J ErleLung Biology Center, University of California San Francisco, San Francisco, CA 94143, USA.
Andrea BarczakLung Biology Center, University of California San Francisco, San Francisco, CA 94143, USA.
Michael D RosenblumDepartment of Dermatology, University of California San Francisco, San Francisco, CA 94143, USA.
Adil DaudMelanoma Clinical Research Unit, University of California San Francisco, San Francisco, CA 94143, USA.
Diane L BarberDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA 94143, USA.
Sebastian AmigorenaINSERM U932, Immunity and Cancer, Institut Curie, 75248 Paris Cedex 05, France.
Laura J Van't VeerDepartment of Laboratory Medicine, University of California San Francisco, San Francisco, CA 94143, USA.
Anne I SperlingCommittee on Immunology, University of Chicago, 924 E. 57th Street, Chicago, IL 60637, USA.
Denise M WolfDepartment of Laboratory Medicine, University of California San Francisco, San Francisco, CA 94143, USA.
Matthew F KrummelDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143, USA. Electronic address: matthew.krummel@ucsf.edu.
University of California, San Francisco · USInserm · FRUniversity of Chicago · US

Funding

Understanding Asthma EndotypesU19AI077439 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Nirav Rati Bhakta · 2008 to 2026
$41.1M
Tools for Analysis of Airway InflammationP01HL024136 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CAUGHEY, GEORGE H · 1985 to 2014
$23.3M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
PREDOCTORAL TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007470 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Todd Nystul · 1994 to 2026
$7.7M
Immune Enhancement and Therapy of CancerU01CA105379 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HANAHAN, DOUGLAS · 2004 to 2008
$2.9M
Collaborative Innate-Adaptive Immune Regulation of Tumor ProgressionU01CA141451 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 2009 to 2013
$2.2M
Leukocyte Biomarkers for Predicting Human Breast Cancer OutcomesU54CA163123 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COUSSENS, LISA M., KRUMMEL, MATTHEW F · 2011 to 2015
$2.0M
Mechanisms of immune regulation in the skinK08AR062064 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSENBLUM, MICHAEL DAVID · 2012 to 2016
$670k
NCATS NIH HHS UL1 TR000430NCI NIH HHS U01 CA105379NCI NIH HHS U01CA105379NCI NIH HHS U01 CA141451NCI NIH HHS U54 CA163123NHLBI NIH HHS P01 HL024136NIAID NIH HHS T32 AI007334NIAID NIH HHS U19 AI077439NIAMS NIH HHS K08 AR062064NICHD NIH HHS T32 HD007470
6 · The paper itself

Abstract

It is well understood that antigen-presenting cells (APCs) within tumors typically do not maintain cytotoxic T cell (CTL) function, despite engaging them. Across multiple mouse tumor models and human tumor biopsies, we have delineated the intratumoral dendritic cell (DC) populations as distinct from macrophage populations. Within these, CD103(+) DCs are extremely sparse and yet remarkably capable CTL stimulators. These are uniquely dependent on IRF8, Zbtb46, and Batf3 transcription factors and are generated by GM-CSF and FLT3L cytokines. Regressing tumors have higher proportions of these cells, T-cell-dependent immune clearance relies on them, and abundance of their transcripts in human tumors correlates with clinical outcome. This cell type presents opportunities for prognostic and therapeutic approaches across multiple cancer types.

Indexed as

AnimalsAntigens, CDCoculture TechniquesDendritic CellsFemaleHumansImmunotherapy, AdoptiveMacrophagesMammary Neoplasms, ExperimentalMice, Inbred C57BLMyeloid CellsT-LymphocytesTumor Cells, CulturedTumor MicroenvironmentAntigens, CD

Identifiers

PMID25446897
PMCPMC4254577
OpenAlexW1976199086

What OpenQuestion holds

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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.