Evidence map›Paper›PMID 32182225›Full record

ArticleThe Journal of clinical investigation2020

OX40+ plasmacytoid dendritic cells in the tumor microenvironment promote antitumor immunity.

Kate Poropatich, Donye Dominguez, Wen-Ching Chan, Jorge Andrade, Yuanyuan Zha, Brian Wray, Jason Miska, Lei Qin, Lisa Cole, Sydney Coates and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 81 citations in OpenAlex.

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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

13 authors at 5 institutions in 3 countries.

Kate PoropatichDepartment of Pathology.
Donye DominguezDivision of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Wen-Ching ChanCenter for Research Informatics and.
Jorge AndradeCenter for Research Informatics and.
Yuanyuan ZhaHuman Immunologic Monitoring Facility, Office of Shared Research Facilities, University of Chicago, Chicago, Illinois, USA.
Brian WrayDepartment of Biochemistry and Molecular Genetics.
Jason MiskaDepartment of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Lei QinDivision of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Lisa ColeDepartment of Chemistry, Northwestern University, Evanston, Illinois, USA.
Sydney CoatesHead and Neck Surgery, Department of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Urjeet PatelRobert H. Lurie Comprehensive Cancer Center, and.
Sandeep SamantRobert H. Lurie Comprehensive Cancer Center, and.
Bin ZhangRobert H. Lurie Comprehensive Cancer Center, and.
Northwestern University · USTranslational Research Informatics Center (Japan) · JPIllinois Department of Human Services · USLaboratory of Molecular Genetics · PLRobert H. Lurie Comprehensive Cancer Center of Northwestern University

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Project 3: Spherical Nucleic Acids as Immunotherapeutic Agents for Prostate CancerU54CA199091 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A. · 2015 to 2019
$11.7M
The distinct role of cysteinyl leukotriene receptor for myeloid-derived suppressive cellsR01CA250101 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2020 to 2025
$2.5M
WEE1 inhibition and tumor immunityR01CA222963 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2018 to 2023
$2.2M
The role of GPSM3 in tumor-promoting emergency myelopoiesisR01CA208354 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, BIN · 2017 to 2021
$1.8M
FACSAria SORP Cell SorterS10OD011996 · OD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GOOLSBY, CHARLES L. · 2012 to 2012
$482k
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA208354NCI NIH HHS R01 CA222963NCI NIH HHS R01 CA250101NCI NIH HHS U54 CA199091NIH HHS S10 OD011996
6 · The paper itself

Abstract

Plasmacytoid DCs (pDCs), the major producers of type I interferon, are principally recognized as key mediators of antiviral immunity. However, their role in tumor immunity is less clear. Depending on the context, pDCs can promote or suppress antitumor immune responses. In this study, we identified a naturally occurring pDC subset expressing high levels of OX40 (OX40+ pDC) enriched in the tumor microenvironment (TME) of head and neck squamous cell carcinoma. OX40+ pDCs were distinguished by a distinct immunostimulatory phenotype, cytolytic function, and ability to synergize with conventional DCs (cDCs) in generating potent tumor antigen-specific CD8+ T cell responses. Transcriptomically, we found that they selectively utilized EIF2 signaling and oxidative phosphorylation pathways. Moreover, depletion of pDCs in the murine OX40+ pDC-rich tumor model accelerated tumor growth. Collectively, we present evidence of a pDC subset in the TME that favors antitumor immunity.

Indexed as

AnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesCell Line, TumorDendritic CellsEukaryotic Initiation Factor-2FemaleHumansMaleMiceNeoplasms, ExperimentalReceptors, OX40Tumor MicroenvironmentAntigens, NeoplasmEukaryotic Initiation Factor-2Receptors, OX40TNFRSF4 protein, humanTnfrsf4 protein, mouseAntigen presenting cellsDendritic cellsHead and neck cancerImmunologyOncology

Identifiers

PMID32182225
PMCPMC7324178
OpenAlexW3011884918

What OpenQuestion holds

Textmetadata
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.