Evidence map›Paper›PMID 28120642›Full record

ArticleInnate immunity2017

A novel mouse model of conditional IRAK-M deficiency in myeloid cells: application in lung Pseudomonas aeruginosa infection.

Di Jiang, Jennifer Matsuda, Reena Berman, Niccolette Schaefer, Connor Stevenson, James Gross, Bicheng Zhang, Amelia Sanchez, Liwu Li, Hong Wei Chu

Abstract read
In one paragraph

Article in Innate immunity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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

10 authors.

Di Jiang1 Department of Medicine, National Jewish Health, Denver, CO, USA.
Jennifer Matsuda2 Office of Academic Affairs and Department of Biomedical Research, National Jewish Health, Denver, CO, USA.
Reena Berman1 Department of Medicine, National Jewish Health, Denver, CO, USA.
Niccolette Schaefer1 Department of Medicine, National Jewish Health, Denver, CO, USA.
Connor Stevenson1 Department of Medicine, National Jewish Health, Denver, CO, USA.
James Gross2 Office of Academic Affairs and Department of Biomedical Research, National Jewish Health, Denver, CO, USA.
Bicheng Zhang2 Office of Academic Affairs and Department of Biomedical Research, National Jewish Health, Denver, CO, USA.
Amelia Sanchez1 Department of Medicine, National Jewish Health, Denver, CO, USA.
Liwu Li3 Department of Biological Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Hong Wei Chu1 Department of Medicine, National Jewish Health, Denver, CO, USA.

Funding

Tollip inhibits IL-33 signaling during airway influenza virus infectionU19AI125357 · NIAID · UNIVERSITY OF ARIZONA · PI VOELKER, DENNIS R. · 2016 to 2025
$14.7M
IRAK-M in lung defense against rhinovirus infectionR01AI106287 · NIAID · NATIONAL JEWISH HEALTH · PI CHU, HONG W, LI, LIWU · 2014 to 2018
$2.0M
SPLUNC1 in Severe AsthmaR01HL125128 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHU, HONG W, DI, YUANPU PETER · 2015 to 2018
$1.9M
Novel function of MUC18: amplification of inflammation in allergic lungsR01HL122321 · NHLBI · NATIONAL JEWISH HEALTH · PI CHU, HONG W · 2015 to 2018
$1.6M
NHLBI NIH HHS R01 HL122321NHLBI NIH HHS R01 HL125128NIAID NIH HHS R01 AI106287NIAID NIH HHS U19 AI125357
6 · The paper itself

Abstract

Myeloid cells such as macrophages are critical to innate defense against infection. IL-1 receptor-associated kinase M (IRAK-M) is a negative regulator of TLR signaling during bacterial infection, but the role of myeloid cell IRAK-M in bacterial infection is unclear. Our goal was to generate a novel conditional knockout mouse model to define the role of myeloid cell IRAK-M during bacterial infection. Myeloid cell-specific IRAK-M knockout mice were generated by crossing IRAK-M floxed mice with LysM-Cre knock-in mice. The resulting LysM-Cre

Indexed as

AnimalsBacteriolysisCell MovementCells, CulturedDisease Models, AnimalHumansImmunity, InnateInterleukin-1 Receptor-Associated KinasesLungLung DiseasesMacrophagesMiceMice, Inbred C57BLMice, KnockoutNeutrophilsPeroxidaseInterleukin-1 Receptor-Associated KinasesIrak3 protein, mousePeroxidaseinfectionIRAK-MlungLysM–CrePseudomonas aeruginosa

Identifiers

PMID28120642
PMCPMC5612436

What OpenQuestion holds

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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.