Evidence map›Paper›PMID 37415975›Full record

ArticleFrontiers in immunology2023

NOD2 in monocytes negatively regulates macrophage development through TNFalpha.

Camille Chauvin, Daniel Alvarez-Simon, Katarina Radulovic, Olivier Boulard, William Laine, Myriam Delacre, Nadine Waldschmitt, Elodie Segura, Jérome Kluza, Mathias Chamaillard and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 8 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

11 authors at 7 institutions in 2 countries.

Camille ChauvinU1019, Institut Pasteur de Lille, Univ. Lille, Centre National de la Recherche Scientifique, Inserm, Centre Hospitalo- Universitaire Lille, Lille, France.
Daniel Alvarez-SimonU1019, Institut Pasteur de Lille, Univ. Lille, Centre National de la Recherche Scientifique, Inserm, Centre Hospitalo- Universitaire Lille, Lille, France.
Katarina RadulovicUnité de Recherche Clinique, Centre Hospitalier de Valenciennes, Valenciennes CEDEX, France.
Olivier BoulardU1003, Univ. Lille Inserm, Lille, France.
William LaineUMR9020-U1277 - CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, University Lille, Lille, France.
Myriam DelacreU1019, Institut Pasteur de Lille, Univ. Lille, Centre National de la Recherche Scientifique, Inserm, Centre Hospitalo- Universitaire Lille, Lille, France.
Nadine WaldschmittChair of Nutrition and Immunology, School of Life Sciences, Technische Universität München, Freising-Weihenstephan, Germany.
Elodie SeguraINSERM U932, Institut Curie, Paris Sciences et Lettres Research University, Paris, France.
Jérome KluzaUMR9020-U1277 - CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, University Lille, Lille, France.
Mathias ChamaillardU1003, Univ. Lille Inserm, Lille, France.
Lionel F PoulinU1003, Univ. Lille Inserm, Lille, France.
Inserm · FRCANTHER - Hétérogénéité, Plasticité et Résistance aux Thérapies des CancersCentre Hospitalier de Valenciennes · FRInstitut Curie · FRInstitut Pasteur de Lille · FRTechnical University of Munich · DEUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: It is believed that intestinal recruitment of monocytes from Crohn's Disease (CD) patients who carry NOD2 risk alleles may repeatedly give rise to recruitment of pathogenic macrophages. We investigated an alternative possibility that NOD2 may rather inhibit their differentiation from intravasating monocytes. Design: The monocyte fate decision was examined by using germ-free mice, mixed bone marrow chimeras and a culture system yielding macrophages and monocyte-derived dendritic cells (mo-DCs). Results: We observed a decrease in the frequency of mo-DCs in the colon of Conclusion: NOD2 negatively regulates a macrophage developmental program through a feed-forward loop that could be exploited for overcoming resistance to anti-TNF therapy in CD.

Indexed as

Crohn DiseaseMonocytesAcetylmuramyl-Alanyl-IsoglutamineAnimalsMacrophagesMiceNod2 Signaling Adaptor ProteinTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAcetylmuramyl-Alanyl-IsoglutamineNod2 protein, mouseNod2 Signaling Adaptor ProteinTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitorscolitismacrophagesmicrobiotamo-DCsmonocytesmTORNOD2TNF-α

Identifiers

PMID37415975
PMCPMC10320732
OpenAlexW4381662057

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.