Evidence map›Paper›PMID 27641636›Full record

ArticleCellular immunology2016

Significant role for IRF3 in both T cell and APC effector functions during T cell responses.

Zacharey Guinn, Anna T Lampe, Deborah M Brown, Thomas M Petro

Open access · greenAbstract read
In one paragraph

Article in Cellular immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. International journal of biological sciences · 2026
    Article
  2. Review
  3. Article
  4. Transcriptional signature of CD56Frontiers in immunology · 2024
    Article
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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

4 authors at 1 institution in 1 country.

Zacharey GuinnSchool of Biological Sciences, University of Nebraska-Lincoln, United States.
Anna T LampeSchool of Biological Sciences, University of Nebraska-Lincoln, United States.
Deborah M BrownSchool of Biological Sciences, University of Nebraska-Lincoln, United States; Nebraska Center for Virology, University of Nebraska-Lincoln, United States.
Thomas M PetroNebraska Center for Virology, University of Nebraska-Lincoln, United States; Department of Oral Biology, University of Nebraska Medical Center, Lincoln, NE, United States. Electronic address: tpetro@unmc.edu.
University of Nebraska–Lincoln · US

Funding

Research Pilot Project ProgramP30GM106397 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WAHL, JAMES K · 2013 to 2017
$4.9M
Nebraska Center for VirologyP30GM103509 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI WOOD, CHARLES · 2012 to 2014
$3.3M
Nebraska Center for Cellular SignalingP20GM103489 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JOHNSON, KEITH R · 2012 to 2012
$2.0M
Molecular Mechanisms of DiseaseT32GM107001 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI BECKER, DONALD F, BLACK, PAUL N. · 2015 to 2019
$1.0M
NIGMS NIH HHS P20 GM103489NIGMS NIH HHS P30 GM103509NIGMS NIH HHS P30 GM106397NIGMS NIH HHS T32 GM107001
6 · The paper itself

Abstract

Interferon Regulatory Factor (IRF)3 is a crucial transcription factor during innate immune responses. Here we show IRF3 also has a role in adaptive T cell immune responses. Expression of IFN-γ, IL-17, and Granzyme B (GrB) during in vitro T cell responses was impaired when either dendritic cells (DCs) or T cells were derived from IRF3KO mice. Unexpectedly, IRF3-dependent NK-activating molecule (INAM), which is an NK cell activating factor of the DC innate immune response, was induced during the T cell response. Additionally, supernatants from responding T cells induced ISG54 in the RAW264.7 macrophage cell line in an IRF3 dependent manner. Moreover, addition of anti-IFN-γ prevented supernatant induction of ISG54 and recombinant IFN-γ stimulated ISG54 expression. Thus, IRF3 in APCs and T cells is required for optimal T-cell effector function and the ability of T cells to influence innate immune function of APCs.

Indexed as

Adaptive ImmunityAnimalsAntigen-Presenting CellsDendritic CellsFemaleInterferon-gammaInterferon Regulatory Factor-3MacrophagesMembrane GlycoproteinsMiceMice, Inbred C57BLMice, KnockoutRAW 264.7 CellsT-LymphocytesTranscription FactorsINAM protein, mouseInterferon-gammaInterferon Regulatory Factor-3Irf3 protein, mouseISG54 protein, mouseMembrane GlycoproteinsTranscription FactorsDendritic cellsGranzyme-BInnate immunityInterferon Regulatory Factor-3Interferon stimulated gene-54Interferon-γInterleukin-17T cells

Identifiers

PMID27641636
PMCPMC5125847
OpenAlexW2512695823

What OpenQuestion holds

Textmetadata
LicenceTDM
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.