Evidence map›Paper›PMID 25622194›Full record

ReviewAnnual review of immunology2015

Structural biology of innate immunity.

Qian Yin, Tian-Min Fu, Jixi Li, Hao Wu

Abstract readReview
In one paragraph

Review in Annual review of immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 2 pooled it
–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

76 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Supramolecular Assemblies Drive Activation of Inflammasomes.Advances in experimental medicine and biology · 2026
    Review
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  7. Review
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  11. Article
  12. Review
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  16. Article
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  19. Listerin promotes cGAS protein degradation through the ESCRT pathway to negatively regulate cGAS-mediated immune response.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. Review

16 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

4 authors.

Qian YinDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, and.
Tian-Min Fu
Jixi Li
Hao Wu

Funding

Structural Studies of TNF Receptor Associated Factors (TRAFs)R01AI045937 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI WU, HAO · 1999 to 2016
$5.9M
Structural & Functional Studies of TLR/IL-1R SignalingR37AI050872 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI WU, HAO · 2012 to 2021
$4.7M
Structural Studies of Protein Caspase InhibitorsR01AI050872 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI WU, HAO · 2002 to 2012
$3.6M
Molecular elucidation of the CBM complex in NF-kappaB activation by antigen recepR01AI089882 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI WU, HAO · 2010 to 2014
$1.9M
Dissecting inflammasome anatomy: mechanistic studies and potential interventionK99AI108793 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI YIN, QIAN · 2014 to 2014
$120k
NIAID NIH HHS AI045937NIAID NIH HHS AI089882NIAID NIH HHS K99 AI108793NIAID NIH HHS R01 AI045937NIAID NIH HHS R01 AI050872NIAID NIH HHS R01 AI089882NIAID NIH HHS R37 AI050872
6 · The paper itself

Abstract

Innate immune responses depend on timely recognition of pathogenic or danger signals by multiple cell surface or cytoplasmic receptors and transmission of signals for proper counteractions through adaptor and effector molecules. At the forefront of innate immunity are four major signaling pathways, including those elicited by Toll-like receptors, RIG-I-like receptors, inflammasomes, or cGAS, each with its own cellular localization, ligand specificity, and signal relay mechanism. They collectively engage a number of overlapping signaling outcomes, such as NF-κB activation, interferon response, cytokine maturation, and cell death. Several proteins often assemble into a supramolecular complex to enable signal transduction and amplification. In this article, we review the recent progress in mechanistic delineation of proteins in these pathways, their structural features, modes of ligand recognition, conformational changes, and homo- and hetero-oligomeric interactions within the supramolecular complexes. Regardless of seemingly distinct interactions and mechanisms, the recurring themes appear to consist of autoinhibited resting-state receptors, ligand-induced conformational changes, and higher-order assemblies of activated receptors, adaptors, and signaling enzymes through conserved protein-protein interactions.

Indexed as

AnimalsHumansImmunity, InnateInflammasomesMembrane ProteinsProtein BindingReceptors, Pattern RecognitionSignal TransductionStructure-Activity RelationshipInflammasomesMembrane ProteinsReceptors, Pattern RecognitioncGASdeath domain superfamilyhigher-order assemblyinflammasomeRIG-I-like receptorSTINGToll-like receptor

Identifiers

PMID25622194
PMCPMC4394028

What OpenQuestion holds

Textmetadata
LicenceTDM
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.