Evidence map›Paper›PMID 37603180›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

In Vitro Study of TLR4-NLRP3-Inflammasome Activation in Innate Immune Response.

Letizia Mezzasoma, Carsten B Schmidt-Weber, Francesca Fallarino

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

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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

3 authors at 2 institutions in 2 countries.

Letizia MezzasomaDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy. letizia.mezzasoma@unipg.it.
Carsten B Schmidt-WeberCenter for Allergy and Environment (ZAUM), Technical University and Helmholtz Center Munich-Biedersteiner, Munich, Germany.
Francesca FallarinoDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
University of Perugia · ITHelmholtz Zentrum München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) are pivotal players in mediating immune responses. TLR4 is the main receptor for LPS, a strong activator of immune cells. LPS/TLR4-dependent pathway, by inducing NF-κB activation, is responsible for the release of several mediators, including IL-1β, one of the most powerful cytokines deeply involved in inflammatory and immune responses. The same pathway is also involved in NLRP3-inflammasome activation, essential for IL-1β maturation. NLRP3 is a major component of innate immune responses, being a crucial player of host immune defense against virus, bacterial, or fungal infections. NLRP3-inflammasome and IL-1β hyperactivation have been associated to the pathogenesis of a wide range of disorders and represent therapeutic targets for the development of new treatments of inflammasome-driven inflammatory and autoimmune diseases.Here, we describe an in vitro protocol to induce LPS/TLR4-dependent NLRP3-inflammasome/IL-1β activation in immune cells, in order to provide a useful assay to study the efficacy of different anti-inflammatory/immune-modulatory agents.

Indexed as

InflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinImmunity, InnateLipopolysaccharidesRadiopharmaceuticalsToll-Like Receptor 4InflammasomesLipopolysaccharidesNLR Family, Pyrin Domain-Containing 3 ProteinRadiopharmaceuticalsToll-Like Receptor 4Autoimmune diseasesIL-1βInflammatory diseasesLPSNF-κBNLRP3-inflammasomeToll-like receptor 4

Identifiers

PMID37603180
OpenAlexW4386019748

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.