Evidence map›Paper›PMID 39188718›Full record

ReviewFrontiers in immunology2024

Screening NLRP3 drug candidates in clinical development: lessons from existing and emerging technologies.

Isak W Tengesdal, Migachelle Banks, Charles A Dinarello, Carlo Marchetti

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
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  9. Ginsenoside Re mitigates AβJournal of ginseng research · 2026
    Article
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  12. IL-1 family cytokines in inflammation and immunity.Cellular & molecular immunology · 2025
    Review
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  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

4 authors.

Isak W TengesdalDepartment of Medicine, University of Colorado Denver, Aurora, CO, United States.
Migachelle BanksDepartment of Medicine, University of Colorado Denver, Aurora, CO, United States.
Charles A DinarelloDepartment of Medicine, University of Colorado Denver, Aurora, CO, United States.
Carlo MarchettiDepartment of Medicine, University of Colorado Denver, Aurora, CO, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decades of evidence positioned IL-1β as a master regulatory cytokine in acute and chronic inflammatory diseases. Approved biologics aimed at inhibiting IL-1 signaling have shown efficacy but variable safety. More recently, targeting NLRP3 activation, an upstream mediator of IL-1β, has garnered the most attention. Aberrant NLRP3 activation has been demonstrated to participate in the progression of several pathological conditions from neurogenerative diseases to cardio-metabolic syndromes and cancer. Pharmacological and genetic strategies aimed to limit NLRP3 function have proven effective in many preclinical models of diseases. These evidences have lead to a significant effort in the generation and clinical testing of small orally active molecules that can target NLRP3. In this report, we discuss different properties of these molecules with translational potential and describe the technologies currently available to screen NLRP3 targeting molecules highlighting advantages and limitations of each method.

Indexed as

Drug DevelopmentNLR Family, Pyrin Domain-Containing 3 ProteinAnimalsDrug Evaluation, PreclinicalHumansInflammasomesInflammationInterleukin-1betaSignal TransductionInflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanIL-1inflammasomeNLRP3screening methodsmall molecule inhibitor

Identifiers

PMID39188718
PMCPMC11345644

What OpenQuestion holds

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LicenceCC BY
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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.