Evidence map›Paper›PMID 32345968›Full record

ArticleNature communications2020

Engineered niches support the development of human dendritic cells in humanized mice.

Giorgio Anselmi, Kristine Vaivode, Charles-Antoine Dutertre, Pierre Bourdely, Yoann Missolo-Koussou, Evan Newell, Oliver Hickman, Kristie Wood, Alka Saxena, Julie Helft and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Human CD34Frontiers in immunology · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Development of an Inflammatory CD14Frontiers in immunology · 2021
    Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Identification of novel molecular markers of mastitis caused byJournal of animal science and biotechnology · 2020
    Article
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

12 authors at 5 institutions in 3 countries.

Giorgio AnselmiCentre for Inflammation Biology and Cancer Immunology, The Peter Gorer Department of Immmunobiology, King's College London, London, UK.
Kristine VaivodeCentre for Inflammation Biology and Cancer Immunology, The Peter Gorer Department of Immmunobiology, King's College London, London, UK.
Charles-Antoine DutertreSingapore Immunology Network (SIgN), A*STAR, Singapore, Singapore.
Pierre BourdelyCentre for Inflammation Biology and Cancer Immunology, The Peter Gorer Department of Immmunobiology, King's College London, London, UK.
Yoann Missolo-KoussouParis-Sciences-Lettres University, Institut Curie Research Center, INSERM U932 & SiRIC, Translational Immunotherapy Team, Paris, France.ORCID http://orcid.org/0000-0002-3815-3980
Evan NewellSingapore Immunology Network (SIgN), A*STAR, Singapore, Singapore.
Oliver HickmanCentre for Inflammation Biology and Cancer Immunology, The Peter Gorer Department of Immmunobiology, King's College London, London, UK.
Kristie WoodNational Institute of Health Research Biomedical Research Centre at Guy's and St Thomas' Hospital and King's College London, London, UK.
Alka SaxenaNational Institute of Health Research Biomedical Research Centre at Guy's and St Thomas' Hospital and King's College London, London, UK.
Julie HelftParis-Sciences-Lettres University, Institut Curie Research Center, INSERM U932 & SiRIC, Translational Immunotherapy Team, Paris, France.ORCID http://orcid.org/0000-0002-2733-1972
Florent GinhouxSingapore Immunology Network (SIgN), A*STAR, Singapore, Singapore.ORCID http://orcid.org/0000-0002-2857-7755
Pierre GuermonprezCentre for Inflammation Biology and Cancer Immunology, The Peter Gorer Department of Immmunobiology, King's College London, London, UK. pierre.guermonprez@kcl.ac.uk.
King's College London · GBAgency for Science, Technology and Research · SGInserm · FRSt Thomas' Hospital · GBCentre National de la Recherche Scientifique · FR

Funding

Biotechnology and Biological Sciences Research Council BB/M029735/1Cancer Research UK (CRUK) C57672/A22369
6 · The paper itself

Abstract

Classical dendritic cells (cDCs) are rare sentinel cells specialized in the regulation of adaptive immunity. Modeling cDC development is crucial to study cDCs and harness their therapeutic potential. Here we address whether cDCs could differentiate in response to trophic cues delivered by mesenchymal components of the hematopoietic niche. We find that mesenchymal stromal cells engineered to express membrane-bound FLT3L and stem cell factor (SCF) together with CXCL12 induce the specification of human cDCs from CD34

Indexed as

Stem Cell NicheAnimalsBiomarkersBone Marrow CellsCell DifferentiationCell MembraneChemokine CXCL12Cluster AnalysisCollagenDendritic CellsDrug CombinationsHumansLamininMembrane ProteinsMiceOrganoidsBiomarkersChemokine CXCL12CollagenDrug Combinationsflt3 ligand proteinLamininmatrigelMembrane ProteinsProteoglycans

Identifiers

PMID32345968
PMCPMC7189247
OpenAlexW3018586675

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.