Evidence map›Paper›PMID 30404092›Full record

ReviewJournal of innate immunity2018

Extracellular RNA Sensing by Pattern Recognition Receptors.

Megumi Tatematsu, Kenji Funami, Tsukasa Seya, Misako Matsumoto

Open access · goldAbstract readReview
In one paragraph

Review in Journal of innate immunity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

59 citing papers in PubMed, 88 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. The strategies and advances of mRNA translation booster.Asian journal of pharmaceutical sciences · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. The Pestivirus RNase EViruses · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Autoimmune myasthenia gravis and COVID-19. A case report-based review.The Journal of international medical research · 2023
    Review
  18. Article
  19. Review
  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 2 institutions in 2 countries.

Megumi TatematsuDepartment of Vaccine Immunology, Hokkaido University Graduate School of Medicine, Sapporo, Japan, Megumi.Tatematsu@med.uni-muenchen.de.
Kenji FunamiDepartment of Vaccine Immunology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Tsukasa SeyaDepartment of Vaccine Immunology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Misako MatsumotoDepartment of Vaccine Immunology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Hokkaido University · JPLudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA works as a genome and messenger in RNA viruses, and it sends messages in most of the creatures of the Earth, including viruses, bacteria, fungi, plants, and animals. The human innate immune system has evolved to detect single- and double-stranded RNA molecules from microbes by pattern recognition receptors and induce defense reactions against infections such as the production of type I interferons and inflammatory cytokines. To avoid cytokine toxicity causing chronic inflammation or autoimmunity by sensing self-RNA, the activation of RNA sensors is strictly regulated. All of the Toll-like receptors that recognize RNA are localized to endosomes/lysosomes, which require internalization of RNA for sensing through an endocytic pathway. RIG-I-like receptors sense RNA in cytosol. These receptors are expressed in a cell type-specific fashion, enabling sensing of RNA for a wide range of microbial invasions. At the same time, both endosomal and cytoplasmic receptors have strategies to respond only to RNA of pathogenic microorganisms or dying cells. RNA are potential vaccine adjuvants for immune enhancement against cancer and provide a benefit for vaccinations. Understanding the detailed molecular mechanisms of the RNA-sensing system will help us to broaden the clinical utility of RNA adjuvants for patients with incurable diseases.

Indexed as

Adjuvants, ImmunologicAnimalsDEAD Box Protein 58Extracellular SpaceHumansInfectionsInterferon Type IReceptors, ImmunologicReceptors, Pattern RecognitionRNAVaccinesAdjuvants, ImmunologicDEAD Box Protein 58Interferon Type IReceptors, ImmunologicReceptors, Pattern RecognitionRIGI protein, humanRNAVaccinesEndosomeExtracellular RNAInnate immune signalingRNA uptakeToll-like receptor

Identifiers

PMID30404092
PMCPMC6784046
OpenAlexW2899835491

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.