Evidence map›Paper›PMID 38688934›Full record

ArticleNature communications2024

Genomic deletion of Bcl6 differentially affects conventional dendritic cell subsets and compromises Tfh/Tfr/Th17 cell responses.

Hongkui Xiao, Isabel Ulmert, Luisa Bach, Johanna Huber, Hamsa Narasimhan, Ilia Kurochkin, Yinshui Chang, Signe Holst, Urs Mörbe, Lili Zhang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. RORγt-expressing dendritic cells are functionally versatile and evolutionarily conserved antigen-presenting cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. B Cell Lymphoma 6 (BCL6): A Conserved Regulator of Immunity and Beyond.International journal of molecular sciences · 2024
    Review
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

15 authors at 6 institutions in 6 countries.

Hongkui Xiao *Section for Experimental and Translational Immunology, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0003-3633-3299
Isabel Ulmert *Section for Experimental and Translational Immunology, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0003-1908-4913
Luisa BachMedical Clinic III for Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital Bonn, University of Bonn, Bonn, Germany.
Johanna HuberInstitute for Immunology, Biomedical Center, Faculty of Medicine, LMU Munich, Planegg-Martinsried, Munich, Germany.
Hamsa NarasimhanBiomedical Center, Institute of Cardiovascular Physiology and Pathophysiology, Faculty of Medicine, Ludwig-Maximillians-Universität München, Planegg-Martinsried, Munich, Germany.
Ilia KurochkinCell Reprogramming in Hematopoiesis and Immunity Laboratory, Lund Stem Cell Center, Molecular Medicine and Gene Therapy, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0003-3100-0903
Yinshui ChangMedical Clinic III for Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital Bonn, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0003-3538-6663
Signe HolstSection for Experimental and Translational Immunology, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0002-8617-7194
Urs MörbeSection for Experimental and Translational Immunology, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0001-8747-437X
Lili ZhangQuantitative Systems Biology, Life and Medical Sciences (LIMES) Institute, University of Bonn, Bonn, Germany.
Andreas SchlitzerQuantitative Systems Biology, Life and Medical Sciences (LIMES) Institute, University of Bonn, Bonn, Germany.
Carlos-Filipe PereiraCell Reprogramming in Hematopoiesis and Immunity Laboratory, Lund Stem Cell Center, Molecular Medicine and Gene Therapy, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0002-9724-1382
Barbara U SchramlBiomedical Center, Institute of Cardiovascular Physiology and Pathophysiology, Faculty of Medicine, Ludwig-Maximillians-Universität München, Planegg-Martinsried, Munich, Germany.ORCID http://orcid.org/0000-0002-5801-0151
Dirk BaumjohannMedical Clinic III for Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital Bonn, University of Bonn, Bonn, Germany. dirk.baumjohann@uni-bonn.de.ORCID http://orcid.org/0000-0001-8385-8288
Katharina LahlSection for Experimental and Translational Immunology, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens, Lyngby, Denmark. katharina.lahl@ucalgary.ca.ORCID http://orcid.org/0000-0003-4919-331X
University of Bonn · DETechnical University of Denmark · DKCentre of Experimental Medicine of the Slovak Academy of Sciences · SKLund University · SEUniversity of Calgary · CAUrologische Klinik München · DE

Funding

Cancerfonden (Swedish Cancer Society) 21 1826 PjDeutsche Forschungsgemeinschaft (German Research Foundation) 210592381Deutsche Forschungsgemeinschaft (German Research Foundation) 252623821Deutsche Forschungsgemeinschaft (German Research Foundation) 322359157-FOR2599-A03Deutsche Forschungsgemeinschaft (German Research Foundation) 360372040Deutsche Forschungsgemeinschaft (German Research Foundation) 390873048Deutsche Forschungsgemeinschaft (German Research Foundation) BA 5132/1Deutsche Forschungsgemeinschaft (German Research Foundation) Schr 1444/1-1EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) ERC-2016-STG-715182Lundbeckfonden (Lundbeck Foundation) R215-2015-4100Vetenskapsrådet (Swedish Research Council) 2020-01977
6 · The paper itself

Abstract

Conventional dendritic cells (cDC) play key roles in immune induction, but what drives their heterogeneity and functional specialization is still ill-defined. Here we show that cDC-specific deletion of the transcriptional repressor Bcl6 in mice alters the phenotype and transcriptome of cDC1 and cDC2, while their lineage identity is preserved. Bcl6-deficient cDC1 are diminished in the periphery but maintain their ability to cross-present antigen to CD8

Indexed as

Citrobacter rodentiumDendritic CellsProto-Oncogene Proteins c-bcl-6Th17 CellsAnimalsCD8-Positive T-LymphocytesGene DeletionMiceMice, Inbred C57BLMice, KnockoutSpleenT Follicular Helper CellsT-Lymphocytes, RegulatoryBcl6 protein, mouseProto-Oncogene Proteins c-bcl-6

Identifiers

PMID38688934
PMCPMC11061177
OpenAlexW4396519608

What OpenQuestion holds

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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.