Evidence map›Paper›PMID 35844602›Full record

ArticleFrontiers in immunology2022

CT-M8 Mice: A New Mouse Model Demonstrates That Basophils Have a Nonredundant Role in Lupus-Like Disease Development.

John Tchen, Quentin Simon, Léa Chapart, Christophe Pellefigues, Hajime Karasuyama, Kensuke Miyake, Ulrich Blank, Marc Benhamou, Eric Daugas, Nicolas Charles

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 13 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

10 authors at 3 institutions in 2 countries.

John TchenUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Quentin SimonUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Léa ChapartUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Christophe PellefiguesUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Hajime KarasuyamaInflammation, Infection and Immunity Laboratory, TMDU Advanced Research Institute, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Kensuke MiyakeInflammation, Infection and Immunity Laboratory, TMDU Advanced Research Institute, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Ulrich BlankUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Marc BenhamouUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Eric DaugasUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Nicolas CharlesUniversité Paris Cité, Centre de Recherche sur l'Inflammation, Institut National de la Santé Et de la Recherche Médicale (INSERM) UMR1149, Centre National de la Recherche Scientifique (CNRS). EMR8252, Faculté de Médecine site Bichat, Paris, France.
Centre National de la Recherche Scientifique · FRUniversité Paris Cité · FRTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue-specific mouse models are essential tools to decipher the role of each cell compartment and/or their expressed genes in the pathophysiology of diseases. Here, we describe a new knock-in mouse model allowing expression of both the fluorescent protein tdTomato and the CRE recombinase selectively in the basophil compartment under the control of the Mcpt8 gene. These "CT-M8" mice did not show any abnormalities in their peripheral distribution of major immune cell populations nor their basophil function. CT-M8 mice allowed the identification of basophils by immunofluorescence and flow cytometry and basophil-specific Cre-mediated floxed gene deletion. Breeding of our CT-M8 mice with the

Indexed as

BasophilsLupus Erythematosus, SystemicAnimalsDisease Models, AnimalLeukocyte CountMiceTomography, X-Ray Computedautoimmunitybasophilslupus nephritismouse modelsystemic lupus erythematosusTH2

Identifiers

PMID35844602
PMCPMC9277511
OpenAlexW4283687528

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.