Evidence map›Paper›PMID 30824528›Full record

ArticleScience immunology2019

Tissue clonality of dendritic cell subsets and emergency DCpoiesis revealed by multicolor fate mapping of DC progenitors.

Mar Cabeza-Cabrerizo, Janneke van Blijswijk, Stephan Wienert, Daniel Heim, Robert P Jenkins, Probir Chakravarty, Neil Rogers, Bruno Frederico, Sophie Acton, Evelyne Beerling and 9 more

Abstract read
In one paragraph

Article in Science immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 124 citations in OpenAlex.

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6 more citing papers are in PubMed but not listed here.

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

19 authors at 5 institutions in 5 countries.

Mar Cabeza-CabrerizoImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. caetano@crick.ac.uk mar.cabeza-cabrerizo@crick.ac.uk jannekevanblijswijk@gmail.com frederick.klauschen@charite.de.ORCID 0000-0001-9061-058X
Janneke van BlijswijkImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. caetano@crick.ac.uk mar.cabeza-cabrerizo@crick.ac.uk jannekevanblijswijk@gmail.com frederick.klauschen@charite.de.
Stephan WienertInstitute of Pathology, Charité University Medicine Berlin, Charitéplatz 1, D-10117 Berlin, Germany.
Daniel HeimInstitute of Pathology, Charité University Medicine Berlin, Charitéplatz 1, D-10117 Berlin, Germany.ORCID 0000-0002-3809-1417
Robert P JenkinsTumour Cell Biology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.ORCID 0000-0002-6186-7746
Probir ChakravartyBioinformatics, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.ORCID 0000-0003-1146-8824
Neil RogersImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Bruno FredericoImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.ORCID 0000-0002-6985-3090
Sophie ActonImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.ORCID 0000-0003-2704-716X
Evelyne BeerlingHubrecht Institute, Uppsalalaan 8, 3584 CT Utrecht, Netherlands.
Jacco van RheenenHubrecht Institute, Uppsalalaan 8, 3584 CT Utrecht, Netherlands.
Hans CleversHubrecht Institute, Uppsalalaan 8, 3584 CT Utrecht, Netherlands.ORCID 0000-0002-3077-5582
Barbara U SchramlImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.ORCID 0000-0002-5801-0151
Marc BajénoffAix-Marseille University Centre, National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), Centre d'Immunologie de Marseille-Luminy (CIML), Marseille, France.
Michael GernerLaboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0001-5406-8308
Ronald N GermainLaboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Erik SahaiTumour Cell Biology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.ORCID 0000-0002-3932-5086
Frederick KlauschenInstitute of Pathology, Charité University Medicine Berlin, Charitéplatz 1, D-10117 Berlin, Germany. caetano@crick.ac.uk mar.cabeza-cabrerizo@crick.ac.uk jannekevanblijswijk@gmail.com frederick.klauschen@charite.de.
Caetano Reis e SousaImmunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. caetano@crick.ac.uk mar.cabeza-cabrerizo@crick.ac.uk jannekevanblijswijk@gmail.com frederick.klauschen@charite.de.ORCID 0000-0001-7392-2119
The Francis Crick Institute · GBCharité - Universitätsmedizin Berlin · DEHubrecht Institute for Developmental Biology and Stem Cell Research · NLNational Institutes of Health · USCentre National de la Recherche Scientifique · FR

Funding

Multiscale Analysis of Immune ResponsesZIAAI000545 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GERMAIN, RONALD N · 2009 to 2025
$29.4M
Functional Biology Of T CellsZIAAI000758 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GERMAIN, RONALD N · 2009 to 2025
$15.4M
Cancer Research UK 19763Cancer Research UK FC001136Medical Research Council FC001136Wellcome Trust FC001136
6 · The paper itself

Abstract

Conventional dendritic cells (cDCs) are found in all tissues and play a key role in immune surveillance. They comprise two major subsets, cDC1 and cDC2, both derived from circulating precursors of cDCs (pre-cDCs), which exited the bone marrow. We show that, in the steady-state mouse, pre-cDCs entering tissues proliferate to give rise to differentiated cDCs, which themselves have residual proliferative capacity. We use multicolor fate mapping of cDC progenitors to show that this results in clones of sister cDCs, most of which comprise a single cDC1 or cDC2 subtype, suggestive of pre-cDC commitment. Upon infection, a surge in the influx of pre-cDCs into the affected tissue dilutes clones and increases cDC numbers. Our results indicate that tissue cDCs can be organized in a patchwork of closely positioned sister cells of the same subset whose coexistence is perturbed by local infection, when the bone marrow provides additional pre-cDCs to meet increased tissue demand.

Indexed as

Influenza A virusAnimalsCell DifferentiationDendritic CellsHumansInfluenza, HumanLungLymph NodesMice, Inbred C57BLMice, TransgenicOrthomyxoviridae InfectionsSpleenStem Cells

Identifiers

PMID30824528
PMCPMC6420147
OpenAlexW2918516172

What OpenQuestion holds

Textmetadata
LicenceTDM
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.