Evidence map›Paper›PMID 28679751›Full record

ArticlemBio2017

AIM2-Like Receptors Positively and Negatively Regulate the Interferon Response Induced by Cytosolic DNA.

Yuki Nakaya, Jingtao Lilue, Spyridon Stavrou, Eileen A Moran, Susan R Ross

Open access · goldAbstract read
In one paragraph

Article in mBio, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

45 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Activation of host nucleic acid sensors byCritical reviews in microbiology · 2024
    Review
  11. Review
  12. Review
  13. Article
  14. Lupus Nephritis in Children: Novel Perspectives.Medicina (Kaunas, Lithuania) · 2023
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

5 authors at 3 institutions in 2 countries.

Yuki NakayaDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Jingtao LilueWellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, United Kingdom.
Spyridon StavrouDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Eileen A MoranDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Susan R RossDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA srross@uic.edu.
University of Illinois Chicago · USUniversity of Pennsylvania · USWellcome Sanger Institute · GB

Funding

Role of APOBEC3 in in vivo Restriction of Retrovirus InfectionR01AI085015 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROSS, SUSAN R · 2010 to 2019
$3.9M
Role of DNA sensors in host anti-retroviral defenseR01AI121275 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ROSS, SUSAN R · 2016 to 2020
$2.0M
NIAID NIH HHS R01 AI085015NIAID NIH HHS R01 AI121275
6 · The paper itself

Abstract

Cytosolic DNAs derived from retrotransposons serve as pathogen-associated molecular patterns for pattern recognition receptors (PRRs) that stimulate the induction of interferons (IFNs) and other cytokines, leading to autoimmune disease. Cyclic GMP-AMP synthase is one PRR that senses retrotransposon DNA, activating type I IFN responses through the stimulator of IFN genes (STING). Absent in melanoma 2 (AIM2)-like receptors (ALRs) have also been implicated in these pathways. Here we show that the mouse ALR IFI205 senses cytosolic retrotransposon DNA independently of cyclic GMP-AMP production. AIM2 antagonizes IFI205-mediated IFN induction activity by sequestering it from STING. We also found that the complement of genes located in the ALR locus in C57BL/6 and AIM2 knockout mice are different and unique, which has implications for interpretation of the sensing of pathogens in different mouse strains. Our data suggest that members of the ALR family are critical to the host IFN response to endogenous DNA.

Indexed as

AnimalsAntiviral AgentsAutoimmunityCytosolDNADNA-Binding ProteinsExodeoxyribonucleasesHEK293 CellsHumansImmunity, InnateInterferon-betaInterferon Type IMacrophagesMiceMice, Inbred C57BLMice, KnockoutAim2 protein, mouseAntiviral AgentsDNADNA-Binding ProteinsExodeoxyribonucleasesIfi205 protein, mouseInterferon-betaInterferon Type IPathogen-Associated Molecular Pattern MoleculesPhosphoproteinsRetroelementsthree prime repair exonuclease 1Tumor Suppressor ProteinsAim2ALRendogenous retrovirusretrotransposonself DNATrex1

Identifiers

PMID28679751
PMCPMC5573678
OpenAlexW2724149674

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.