Evidence map›Paper›PMID 25023063›Full record

ReviewCytokine & growth factor reviews2014

Regulation of RIG-I-like receptor signaling by host and viral proteins.

Jessica J Chiang, Meredith E Davis, Michaela U Gack

Open access · greenAbstract readReview
In one paragraph

Review in Cytokine & growth factor reviews, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

69 citing papers in PubMed, 123 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Porcine Teschovirus 2 3CMicroorganisms · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The lncRNAs involved in regulating the RIG-I signaling pathway.Frontiers in cellular and infection microbiology · 2022
    Review
  19. Review
  20. Host-pathogen protein-nucleic acid interactions: A comprehensive review.Computational and structural biotechnology journal · 2022
    Review

9 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 1 institution in 1 country.

Jessica J ChiangDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, United States.
Meredith E DavisDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, United States.
Michaela U GackDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, United States. Electronic address: michaela_gack@hms.harvard.edu.
Harvard University · US

Funding

Regulation of Host Innate Immunity Against Viral InfectionR01AI087846 · NIAID · UNIVERSITY OF CHICAGO · PI GACK, MICHAELA ULRIKE · 2010 to 2020
$3.9M
Regulation of Host Innate Immunity Against Viral InfectionR37AI087846 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI Michaela Ulrike Gack · 2021 to 2026
$2.8M
Regulatory mechanisms of the MDA5-mediated antiviral interferon responseR21AI097699 · NIAID · HARVARD MEDICAL SCHOOL · PI GACK, MICHAELA ULRIKE · 2012 to 2013
$481k
NIAID NIH HHS AI087846NIAID NIH HHS AI097699NIAID NIH HHS R01 AI087846NIAID NIH HHS R21 AI097699NIAID NIH HHS R37 AI087846
6 · The paper itself

Abstract

Vertebrate innate immunity is characterized by an effective immune surveillance apparatus, evolved to sense foreign structures, such as proteins or nucleic acids of invading microbes. RIG-I-like receptors (RLRs) are key sensors of viral RNA species in the host cell cytoplasm. Activation of RLRs in response to viral RNA triggers an antiviral defense program through the production of hundreds of antiviral effector proteins including cytokines, chemokines, and host restriction factors that directly interfere with distinct steps in the virus life cycle. To avoid premature or abnormal antiviral and proinflammatory responses, which could have harmful consequences for the host, the signaling activities of RLRs and their common adaptor molecule, MAVS, are delicately controlled by cell-intrinsic regulatory mechanisms. Furthermore, viruses have evolved multiple strategies to modulate RLR-MAVS signal transduction to escape from immune surveillance. Here, we summarize recent progress in our understanding of the regulation of RLR signaling through host factors and viral antagonistic proteins.

Indexed as

Host-Pathogen InteractionsSignal TransductionAnimalsDEAD Box Protein 58DEAD-box RNA HelicasesHumansImmunity, InnateModels, BiologicalReceptors, ImmunologicViral ProteinsDEAD Box Protein 58DEAD-box RNA HelicasesReceptors, ImmunologicRIGI protein, humanViral ProteinsInnate immunityMDA5RIG-IType-I interferonViral immune evasion

Identifiers

PMID25023063
PMCPMC7108356
OpenAlexW2061578670

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.