Evidence map›Paper›PMID 31427775›Full record

ArticleNature immunology2019

IL-1R3 blockade broadly attenuates the functions of six members of the IL-1 family, revealing their contribution to models of disease.

Jesper Falkesgaard Højen, Marie Louise Vindvad Kristensen, Amy S McKee, Megan Taylor Wade, Tania Azam, Lars P Lunding, Dennis M de Graaf, Benjamin J Swartzwelter, Michael Wegmann, Martin Tolstrup and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
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  17. Challenges and Future Trends in Atopic Dermatitis.International journal of molecular sciences · 2023
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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

14 authors at 4 institutions in 4 countries.

Jesper Falkesgaard HøjenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0002-2629-5391
Marie Louise Vindvad KristensenDepartment of Medicine, University of Colorado Denver, Aurora, CO, USA.
Amy S McKeeDepartment of Medicine, University of Colorado Denver, Aurora, CO, USA.
Megan Taylor WadeDepartment of Medicine, University of Colorado Denver, Aurora, CO, USA.
Tania AzamDepartment of Medicine, University of Colorado Denver, Aurora, CO, USA.
Lars P LundingDivision of Asthma Exacerbation & Regulation, Priority Area Asthma and Allergy, Leibniz Lung Center Borstel, Airway Research Center North (ARCN), Member of the German Center for Lung Research (DZL), Borstel, Germany.
Dennis M de GraafDepartment of Medicine, University of Colorado Denver, Aurora, CO, USA.
Benjamin J SwartzwelterDepartment of Medicine, University of Colorado Denver, Aurora, CO, USA.
Michael WegmannDivision of Asthma Exacerbation & Regulation, Priority Area Asthma and Allergy, Leibniz Lung Center Borstel, Airway Research Center North (ARCN), Member of the German Center for Lung Research (DZL), Borstel, Germany.
Martin TolstrupDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-7020-5173
Karsten BeckmanMAB Discovery GmbH, Neuried, Germany.
Mayumi FujitaDepartment of Microbiology and Immunology, University of Colorado Denver, Aurora, CO, USA.
Stephan FischerMAB Discovery GmbH, Neuried, Germany.
Charles A DinarelloDepartment of Medicine, University of Colorado Denver, Aurora, CO, USA. cdinare333@aol.com.ORCID http://orcid.org/0000-0002-5073-8316
University of Colorado Denver · USAarhus University · DKGerman Center for Lung Research · DERadboud University Nijmegen · NL

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Yeast-based HTS Assay Technologies for ProteasesR01AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 1985 to 2025
$8.5M
Investigating paclitaxel treatment in a pre-clinical model of Schistosoma-pulmonary hypertensionR01HL135872 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Brian Barkley Graham · 2017 to 2026
$5.1M
Interactions between antigen-specific effector and regulatory T cells in beryllium-induced diseaseR01ES025534 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI FONTENOT, ANDREW P. · 2016 to 2020
$2.1M
Innate effects of beryllium on pulmonarydendritic cell function in chronic beryllium diseaseR01HL126736 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MCKEE, AMY STRAW · 2016 to 2020
$1.9M
Pathogenesis of Fever in ManR56AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 2016 to 2016
$311k
NCI NIH HHS P30 CA046934NHLBI NIH HHS R01 HL126736NHLBI NIH HHS R01 HL135872NIAID NIH HHS R01 AI015614NIAID NIH HHS R56 AI015614NIEHS NIH HHS R01 ES025534
6 · The paper itself

Abstract

Interleukin (IL)-1R3 is the co-receptor in three signaling pathways that involve six cytokines of the IL-1 family (IL-1α, IL-1β, IL-33, IL-36α, IL-36β and IL-36γ). In many diseases, multiple cytokines contribute to disease pathogenesis. For example, in asthma, both IL-33 and IL-1 are of major importance, as are IL-36 and IL-1 in psoriasis. We developed a blocking monoclonal antibody (mAb) to human IL-1R3 (MAB-hR3) and demonstrate here that this antibody specifically inhibits signaling via IL-1, IL-33 and IL-36 in vitro. Also, in three distinct in vivo models of disease (crystal-induced peritonitis, allergic airway inflammation and psoriasis), we found that targeting IL-1R3 with a single mAb to mouse IL-1R3 (MAB-mR3) significantly attenuated heterogeneous cytokine-driven inflammation and disease severity. We conclude that in diseases driven by multiple cytokines, a single antagonistic agent such as a mAb to IL-1R3 is a therapeutic option with considerable translational benefit.

Indexed as

A549 CellsAnimalsAntibodies, BlockingAntibodies, MonoclonalCell Line, TumorDisease Models, AnimalHEK293 CellsHumansImiquimodInflammationInterleukin-1Interleukin-1betaInterleukin-1 Receptor Accessory ProteinInterleukin-33MaleMiceAntibodies, BlockingAntibodies, MonoclonalIL1B protein, humanIL1RAP protein, humanIL33 protein, humanIL36A protein, humanImiquimodInterleukin-1Interleukin-1betaInterleukin-1 Receptor Accessory ProteinInterleukin-33OvalbuminUric Acid

Identifiers

PMID31427775
PMCPMC6707854
OpenAlexW2968119119

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.