Evidence map›Paper›PMID 27311059›Full record

ArticlePloS one2016

CD1c-Expression by Monocytes - Implications for the Use of Commercial CD1c+ Dendritic Cell Isolation Kits.

Martine Schrøder, Guro Reinholt Melum, Ole J B Landsverk, Anna Bujko, Sheraz Yaqub, Einar Gran, Henrik Aamodt, Espen S Bækkevold, Frode L Jahnsen, Lisa Richter

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Prevalence of hybrid TLR4Frontiers in immunology · 2024
    Article
  6. Article
  7. Article
  8. Functionally Mature CD1cFrontiers in immunology · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Subsets of CD1cFrontiers in immunology · 2020
    Review
  14. Two distinct colonic CD14Mucosal immunology · 2019
    Article
  15. Article
  16. The CD14Frontiers in immunology · 2019
    Review
  17. Review
  18. Review
  19. Article
  20. 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

10 authors at 2 institutions in 1 country.

Martine SchrøderDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Guro Reinholt MelumDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Ole J B LandsverkDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Anna BujkoDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Sheraz YaqubDepartment of Gastrointestinal Surgery, Oslo University Hospital, Oslo, Norway.
Einar GranDepartment of Otolaryngology, Lovisenberg Diakonale Hospital, Oslo, Norway.
Henrik AamodtDepartment of Cardiothoracic Surgery, Oslo University Hospital, Oslo, Norway.
Espen S BækkevoldDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Frode L JahnsenDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Lisa RichterDepartment of Pathology, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0002-0769-619X
Oslo University Hospital · NOLovisenberg Diakonale Sykehus · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conventional dendritic cells (cDCs) comprise a heterogeneous population of cells that are important regulators of immunity and homeostasis. CD1c+ cDCs are present in human blood and tissues, and found to efficiently activate naïve CD4+ T cells. While CD1c is thought to specifically identify this subset of human cDCs, we show here that also classical and intermediate monocytes express CD1c. Accordingly, the commercial CD1c (BDCA-1)+ Dendritic Cell Isolation Kit isolates two distinct cell populations from blood: CD1c+CD14- cDCs and CD1c+CD14+ monocytes. CD1c+ cDCs and CD1c+ monocytes exhibited strikingly different properties, including their differential regulation of surface marker expression, their levels of cytokine production, and their ability to stimulate naïve CD4+ T cells. These results demonstrate that a commercial CD1c (BDCA-1)+ Dendritic Cell Isolation Kit isolates two functionally different cell populations, which has important implications for the interpretation of previously generated data using this kit to characterize CD1c+ cDCs.

Indexed as

Antigens, CD1CD4-Positive T-LymphocytesCell CommunicationCell SeparationCoculture TechniquesDendritic CellsFlow CytometryGene ExpressionGlycoproteinsHumansLymphocyte ActivationMonocytesPrimary Cell CultureReagent Kits, DiagnosticAntigens, CD1CD1C protein, humanGlycoproteinsReagent Kits, Diagnostic

Identifiers

PMID27311059
PMCPMC4911075
OpenAlexW2429235535

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.