Evidence map›Paper›PMID 29551141›Full record

ReviewAdvances in virus research2018

Intracellular Antiviral Immunity.

Maria Bottermann, Leo C James

Abstract readReview
In one paragraph

Review in Advances in virus research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. ENKD1 attenuates antibacterial immunity by facilitating TRIM21-mediated RUBCN degradation to suppress LC3-associated phagocytosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  12. Immune Functions of Astrocytes in Viral Neuroinfections.International journal of molecular sciences · 2023
    Review
  13. Multiple Roles of TRIM21 in Virus Infection.International journal of molecular sciences · 2023
    Review
  14. Review
  15. Article
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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

2 authors.

Maria BottermannMRC Laboratory of Molecular Biology, Cambridge, United Kingdom.
Leo C JamesMRC Laboratory of Molecular Biology, Cambridge, United Kingdom. Electronic address: lcj@mrc-lmb.cam.ac.uk.

Funding

Medical Research Council MC_U105181010Wellcome Trust 200594/Z/16/Z
6 · The paper itself

Abstract

Innate immunity is traditionally thought of as the first line of defense against pathogens that enter the body. It is typically characterized as a rather weak defense mechanism, designed to restrict pathogen replication until the adaptive immune response generates a tailored response and eliminates the infectious agent. However, intensive research in recent years has resulted in better understanding of innate immunity as well as the discovery of many effector proteins, revealing its numerous powerful mechanisms to defend the host. Furthermore, this research has demonstrated that it is simplistic to strictly separate adaptive and innate immune functions since these two systems often work synergistically rather than sequentially. Here, we provide a broad overview of innate pattern recognition receptors in antiviral defense, with a focus on the TRIM family, and discuss their signaling pathways and mechanisms of action with special emphasis on the intracellular antibody receptor TRIM21.

Indexed as

AnimalsHumansImmunity, InnateImmunomodulationIntracellular SpacePathogen-Associated Molecular Pattern MoleculesReceptors, Pattern RecognitionSignal TransductionTripartite Motif ProteinsVirus DiseasesPathogen-Associated Molecular Pattern MoleculesReceptors, Pattern RecognitionTripartite Motif ProteinsInnate immunityPAMPsPRRsSignalingTRIMs

Identifiers

PMID29551141
PMCPMC7172442

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.