Evidence map›Paper›PMID 39251813›Full record

ReviewNature reviews. Immunology2025

Inflammasome components as new therapeutic targets in inflammatory disease.

Rebecca C Coll, Kate Schroder

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing 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

80 citing papers in PubMed.

  1. Trial
  2. Article
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  5. Article
  6. Review
  7. Review
  8. Structure-Activity Relationship for Inflammasome Inhibition by Thiomuscimol.International journal of molecular sciences · 2026
    Article
  9. Structural and molecular principles of DAMP biology.Nature structural & molecular biology · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Targeting FAPActa pharmaceutica Sinica. B · 2026
    Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Rebecca C CollWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK. R.Coll@qub.ac.uk.ORCID http://orcid.org/0000-0002-7359-6023
Kate SchroderInstitute for Molecular Bioscience (IMB), The University of Queensland, St Lucia, Queensland, Australia. K.Schroder@imb.uq.edu.au.ORCID http://orcid.org/0000-0001-9261-3805

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation drives pathology in many human diseases for which there are no disease-modifying drugs. Inflammasomes are signalling platforms that can induce pathological inflammation and tissue damage, having potential as an exciting new class of drug targets. Small-molecule inhibitors of the NLRP3 inflammasome that are now in clinical trials have demonstrated proof of concept that inflammasomes are druggable, and so drug development programmes are now focusing on other key inflammasome molecules. In this Review, we describe the potential of inflammasome components as candidate drug targets and the novel inflammasome inhibitors that are being developed. We discuss how the signalling biology of inflammasomes offers mechanistic insights for therapeutic targeting. We also discuss the major scientific and technical challenges associated with drugging these molecules during preclinical development and clinical trials.

Indexed as

InflammasomesInflammationNLR Family, Pyrin Domain-Containing 3 ProteinSignal TransductionAnimalsHumansMolecular Targeted TherapyInflammasomesNLR Family, Pyrin Domain-Containing 3 Protein

Identifiers

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.