Evidence map›Paper›PMID 22029446›Full record

ReviewJournal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research2011

Intracellular nucleic acid sensors and autoimmunity.

Argyrios N Theofilopoulos, Dwight H Kono, Bruce Beutler, Roberto Baccala

Abstract readReview
In one paragraph

Review in Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. The solute carrier SLC15A4 is required for optimal trafficking of nucleic acid-sensing TLRs and ligands to endolysosomes.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Review
  8. Review
  9. Modulation of toll-like receptor signaling by antimicrobial peptides.Seminars in cell & developmental biology · 2019
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  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

4 authors at 1 institution in 1 country.

Argyrios N TheofilopoulosDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, California 92137, USA. argyrio@scripps.edu
Dwight H Kono
Bruce Beutler
Roberto Baccala
Scripps Research Institute · US

Funding

Genetic Basis of Systemic AutoimmunityR37AR039555 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 2003 to 2012
$4.2M
Defining the effector gene repertoire in systemic autoimmunity by ENU mutagenesisR01AR053731 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI KONO, DWIGHT H · 2007 to 2011
$2.5M
TYPE I INTERFERONS IN LUPUSR01AR053228 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 2006 to 2010
$2.0M
T CELL ANTIGEN RECEPTOR GENES IN AUTOIMMUNITYR01AR039555 · NIAMS · SCRIPPS RESEARCH INSTITUTE · PI THEOFILOPOULOS, ARGYRIOS N · 1988 to 2002
$1.4M
NIAMS NIH HHS AR053228NIAMS NIH HHS AR053731NIAMS NIH HHS AR30103NIAMS NIH HHS AR39555NIAMS NIH HHS R37 AR039555
6 · The paper itself

Abstract

A collection of molecular sensors has been defined by studies in the last decade that can recognize a diverse array of pathogens and initiate protective immune and inflammatory responses. However, if the molecular signatures recognized are shared by both foreign and self-molecules, as is the case of nucleic acids, then the responses initiated by these sensors may have deleterious consequences. Notably, this adverse occurrence may be of primary importance in autoimmune disease pathogenesis. In this case, microbe-induced damage or mishandled physiologic processes could lead to the generation of microparticles containing self-nucleic acids. These particles may inappropriately gain access to the cytosol or endolysosomes and, hence, engage resident RNA and DNA sensors. Evidence, as reviewed here, strongly indicates that these sensors are primary contributors to autoimmune disease pathogenesis, spearheading efforts toward development of novel therapeutics for these disorders.

Indexed as

AutoantigensAutoimmune DiseasesAutoimmunityCytosolHumansModels, ImmunologicalNucleic AcidsOrganellesReceptors, ImmunologicSignal TransductionAutoantigensNucleic AcidsReceptors, Immunologic

Identifiers

PMID22029446
PMCPMC3234494
OpenAlexW2066035628

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.