Evidence map›Paper›PMID 21930765›Full record

ArticleThe Journal of experimental medicine2011

Host type I IFN signals are required for antitumor CD8+ T cell responses through CD8{alpha}+ dendritic cells.

Mercedes B Fuertes, Aalok K Kacha, Justin Kline, Seng-Ryong Woo, David M Kranz, Kenneth M Murphy, Thomas F Gajewski

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04212377 (An Exploratory Study), which is not on this map. Cited by 777 papers.

0numbers the graph read from it
0cells of the map it votes in
777citing papers in PubMed
17.0field-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.

NCT04212377 phase2completednot on this mapstarted 2019, after this paper: background citation

An Exploratory Study: Dendritic Cells for Immunotherapy of Metastatic Endometrial Cancer Patients

TypeinterventionalSponsorRadboud University Medical CenterRan2019 to 2021Enrolled8ConditionsEndometrial CancerArmsDendritic Cells for endometrial cancer
3 · Its place in the literature

Who cites it

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

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  20. Nanovaccines with ferroptosis, necroptosis and STING-activation for synergistic immunotherapy.Journal of experimental & clinical cancer research : CR · 2026
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Mercedes B FuertesDepartment of Pathology and Department of Medicine, Section of Hematology/Oncology, the University of Chicago, Chicago, IL, USA.
Aalok K Kacha
Justin Kline
Seng-Ryong Woo
David M Kranz
Kenneth M Murphy
Thomas F Gajewski
University of Chicago · USUniversity of Illinois Urbana-Champaign · USWashington University in St. Louis · US

Funding

Protein Expression and Peptide CoreP01CA097296 · NCI · UNIVERSITY OF CHICAGO · PI SCHREIBER, HANS · 2003 to 2012
$15.0M
NCI NIH HHS P01 CA097296NCI NIH HHS P01 CA97296Wellcome Trust
6 · The paper itself

Abstract

Despite lack of tumor control in many models, spontaneous T cell priming occurs frequently in response to a growing tumor. However, the innate immune mechanisms that promote natural antitumor T cell responses are undefined. In human metastatic melanoma, there was a correlation between a type I interferon (IFN) transcriptional profile and T cell markers in metastatic tumor tissue. In mice, IFN-β was produced by CD11c(+) cells after tumor implantation, and tumor-induced T cell priming was defective in mice lacking IFN-α/βR or Stat1. IFN signaling was required in the hematopoietic compartment at the level of host antigen-presenting cells, and selectively for intratumoral accumulation of CD8α(+) dendritic cells, which were demonstrated to be essential using Batf3(-/-) mice. Thus, host type I IFNs are critical for the innate immune recognition of a growing tumor through signaling on CD8α(+) DCs.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell Line, TumorDendritic CellsHumansImmunity, InnateInterferon Type ILymphatic MetastasisLymph NodesLymphocyte SubsetsMelanomaMiceMice, Inbred C57BLMice, KnockoutSignal TransductionSTAT1 Transcription FactorInterferon Type ISTAT1 Transcription Factor

Identifiers

PMID21930765
PMCPMC3182064
OpenAlexW2143523733

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.