Evidence map›Paper›PMID 19776740›Full record

ArticleNature2009

STING regulates intracellular DNA-mediated, type I interferon-dependent innate immunity.

Hiroki Ishikawa, Zhe Ma, Glen N Barber

Open access · greenAbstract read
In one paragraph

Article in Nature, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,637 papers.

0numbers the graph read from it
0cells of the map it votes in
1,637citing papers in PubMed
23.5field-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.

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

1,637 citing papers in PubMed, 2,663 citations in OpenAlex.

  1. Trial
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  4. A Fish MDA5 Integrates Canonical RIG-I and MDA5 Ligand Recognition.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  17. Precision tuning of STING signaling: a mutational blueprint.Signal transduction and targeted therapy · 2026
    Article
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  19. Article
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1,577 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 2 institutions in 1 country.

Hiroki IshikawaDepartment of Medicine and Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Zhe Ma
Glen N Barber
Sylvester Comprehensive Cancer Center · USUniversity of Miami · US

Funding

The Role of STING in Innate ImmunityR01AI079336 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BARBER, GLEN N. · 2008 to 2019
$3.9M
The role of STING in innate immunityR56AI079336 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BARBER, GLEN N. · 2014 to 2014
$384k
NIAID NIH HHS AI079336NIAID NIH HHS R01 AI079336NIAID NIH HHS R56 AI079336
6 · The paper itself

Abstract

The innate immune system is critical for the early detection of invading pathogens and for initiating cellular host defence countermeasures, which include the production of type I interferon (IFN). However, little is known about how the innate immune system is galvanized to respond to DNA-based microbes. Here we show that STING (stimulator of interferon genes) is critical for the induction of IFN by non-CpG intracellular DNA species produced by various DNA pathogens after infection. Murine embryonic fibroblasts, as well as antigen presenting cells such as macrophages and dendritic cells (exposed to intracellular B-form DNA, the DNA virus herpes simplex virus 1 (HSV-1) or bacteria Listeria monocytogenes), were found to require STING to initiate effective IFN production. Accordingly, Sting-knockout mice were susceptible to lethal infection after exposure to HSV-1. The importance of STING in facilitating DNA-mediated innate immune responses was further evident because cytotoxic T-cell responses induced by plasmid DNA vaccination were reduced in Sting-deficient animals. In the presence of intracellular DNA, STING relocalized with TANK-binding kinase 1 (TBK1) from the endoplasmic reticulum to perinuclear vesicles containing the exocyst component Sec5 (also known as EXOC2). Collectively, our studies indicate that STING is essential for host defence against DNA pathogens such as HSV-1 and facilitates the adjuvant activity of DNA-based vaccines.

Indexed as

AnimalsAntigen-Presenting CellsCytoplasmic VesiclesDNA, BacterialDNA, ViralEndoplasmic ReticulumFibroblastsHerpesvirus 1, HumanImmunity, InnateInterferon Type IIntracellular SpaceListeria monocytogenesMembrane ProteinsMiceMice, KnockoutPlasmidsDNA, BacterialDNA, ViralExoc2 protein, mouseInterferon Type IMembrane ProteinsProtein Serine-Threonine KinasesSting1 protein, mouseSTING ProteinTbk1 protein, mouseVaccines, DNAVesicular Transport Proteins

Identifiers

PMID19776740
PMCPMC4664154
OpenAlexW1968178474

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.