Evidence map›Paper›PMID 31309143›Full record

ArticleScience advances2019

Control of TLR7-mediated type I IFN signaling in pDCs through CXCR4 engagement-A new target for lupus treatment.

Nikaïa Smith, Mathieu P Rodero, Nassima Bekaddour, Vincent Bondet, Yasser B Ruiz-Blanco, Mirja Harms, Benjamin Mayer, Brigitte Bader-Meunier, Pierre Quartier, Christine Bodemer and 13 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.2field-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

32 citing papers in PubMed, 52 citations in OpenAlex.

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  5. Disruption of constitutive CXCR4 oligomers impairs oncogenic properties in lymphoid neoplasms.Proceedings of the National Academy of Sciences of the United States of America · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 8 institutions in 2 countries.

Nikaïa SmithCNRS UMR-8601, CICB, 45 rue des Saints-Pères, 75006 Paris, France.ORCID 0000-0002-0202-612X
Mathieu P RoderoCNRS UMR-8601, CICB, 45 rue des Saints-Pères, 75006 Paris, France.ORCID 0000-0002-1300-0187
Nassima BekaddourCNRS UMR-8601, CICB, 45 rue des Saints-Pères, 75006 Paris, France.ORCID 0000-0001-7777-5929
Vincent BondetImmunobiology of Dendritic Cells, Institut Pasteur, Paris, France.ORCID 0000-0002-6534-0984
Yasser B Ruiz-BlancoComputational Biochemistry and Center of Medical Biotechnology, University of Duisburg-Essen, 45141 Essen, Germany.ORCID 0000-0001-5400-4427
Mirja HarmsInstitute of Molecular Virology, Ulm University Medical Center, Ulm 89081, Germany.
Benjamin MayerInstitute for Epidemiology and Medical Biometry, Ulm University, Ulm, Germany.
Brigitte Bader-MeunierUniversité Paris Descartes, Sorbonne Paris Cité, Paris, France.
Pierre QuartierUniversité Paris Descartes, Sorbonne Paris Cité, Paris, France.
Christine BodemerUniversité Paris Descartes, Sorbonne Paris Cité, Paris, France.
Véronique BaudouinHôpital Universitaire Robert Debré, Néphrologie pédiatrique, Paris, France.
Yannick DieudonnéCNRS UPR 3572 "Immunopathology and Therapeutic Chemistry"/Laboratory of Excellence Médalis, Institute of Molecular and Cellular Biology (IBMC), Strasbourg, France.
Frank KirchhoffInstitute of Molecular Virology, Ulm University Medical Center, Ulm 89081, Germany.ORCID 0000-0002-7052-2360
Elsa Sanchez GarciaComputational Biochemistry and Center of Medical Biotechnology, University of Duisburg-Essen, 45141 Essen, Germany.ORCID 0000-0002-9211-5803
Bruno CharbitCentre for Translational Research, Institut Pasteur, Paris, France.ORCID 0000-0002-5478-482X
Nicolas LeboulangerUniversité Paris Descartes, Sorbonne Paris Cité, Paris, France.ORCID 0000-0003-3466-6903
Bernd JahrsdörferInstitute of Transfusion Medicine and Immunogenetics (IKT) Ulm, Helmholtzstr. 10, 89081 Ulm, Germany.
Yolande RichardUniversité Paris Descartes, Sorbonne Paris Cité, Paris, France.ORCID 0000-0001-8560-9250
Anne-Sophie KorganowCNRS UPR 3572 "Immunopathology and Therapeutic Chemistry"/Laboratory of Excellence Médalis, Institute of Molecular and Cellular Biology (IBMC), Strasbourg, France.
Jan MünchInstitute of Molecular Virology, Ulm University Medical Center, Ulm 89081, Germany.ORCID 0000-0001-7316-7141
Sébastien NisoleIRIM, Université de Montpellier, CNRS UMR, 9004 Montpellier, France.ORCID 0000-0001-9793-419X
Darragh DuffyImmunobiology of Dendritic Cells, Institut Pasteur, Paris, France.ORCID 0000-0002-8875-2308
Jean-Philippe HerbeuvalCNRS UMR-8601, CICB, 45 rue des Saints-Pères, 75006 Paris, France.ORCID 0000-0001-8114-8012
Délégation Paris 5 · FRUniversität Ulm · DECentre National de la Recherche Scientifique · FRInserm · FRUniversity of Duisburg-Essen · DEHôpital Robert-Debré · FRImmungenetics (Germany) · DEInstitut Pasteur · FR

Funding

CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

Type I interferons are highly potent cytokines essential for self-protection against tumors and infections. Deregulations of type I interferon signaling are associated with multiple diseases that require novel therapeutic options. Here, we identified the small molecule, IT1t, a previously described CXCR4 ligand, as a highly potent inhibitor of Toll-like receptor 7 (TLR7)-mediated inflammation. IT1t inhibits chemical (R848) and natural (HIV) TLR7-mediated inflammation in purified human plasmacytoid dendritic cells from blood and human tonsils. In a TLR7-dependent lupus-like model, in vivo treatment of mice with IT1t drives drastic reduction of both systemic inflammation and anti-double-stranded DNA autoantibodies and prevents glomerulonephritis. Furthermore, IT1t controls inflammation, including interferon α secretion, in resting and stimulated cells from patients with systemic lupus erythematosus. Our findings highlight a groundbreaking immunoregulatory property of CXCR4 signaling that opens new therapeutic perspectives in inflammatory settings and autoimmune diseases.

Indexed as

Signal TransductionAnimalsCytokinesDendritic CellsDisease Models, AnimalDisease ProgressionDisease SusceptibilityGene Expression ProfilingHumansInterferon Type ILigandsLupus Erythematosus, SystemicMiceProtein BindingReceptors, CXCR4Toll-Like Receptor 7CXCR4 protein, humanCytokinesInterferon Type ILigandsReceptors, CXCR4TLR7 protein, humanToll-Like Receptor 7

Identifiers

PMID31309143
PMCPMC6620093
OpenAlexW2961373581

What OpenQuestion holds

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LicenceCC BY-NC
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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.