Evidence map›Paper›PMID 23621371›Full record

ReviewImmunology2013

Human dendritic cell subsets.

Matthew Collin, Naomi McGovern, Muzlifah Haniffa

Open access · hybridAbstract readReview
In one paragraph

Review in Immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 248 papers.

0numbers the graph read from it
0cells of the map it votes in
248citing papers in PubMed
18.1field-weighted citation impact, top 1% 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

248 citing papers in PubMed, 496 citations in OpenAlex.

  1. Trial
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  8. Review
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  12. Review
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  16. Article
  17. Inflammatory Cells in Control and Prolapsed Uterosacral Ligament Tissue.Reproductive sciences (Thousand Oaks, Calif.) · 2024
    Article
  18. Article
  19. Review
  20. Review

188 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

3 authors at 1 institution in 1 country.

Matthew CollinHuman Dendritic Cell Laboratory, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK. matthew.collin@ncl.ac.uk
Naomi McGovern
Muzlifah Haniffa
Newcastle University · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Dendritic cells are highly adapted to their role of presenting antigen and directing immune responses. Developmental studies indicate that DCs originate independently from monocytes and tissue macrophages. Emerging evidence also suggests that distinct subsets of DCs have intrinsic differences that lead to functional specialisation in the generation of immunity. Comparative studies are now allowing many of these properties to be more fully understood in the context of human immunology.

Indexed as

Antigens, CD1Cell LineageDendritic CellsGlycoproteinsHumansInflammationLangerhans CellsLipopolysaccharide ReceptorsLymphoid TissueMacrophagesMicrogliaMonocytesAntigens, CD1CD1C protein, humanGlycoproteinsLipopolysaccharide Receptorsdendritic cellshaematologytherapy/immunotherapy

Identifiers

PMID23621371
PMCPMC3809702
OpenAlexW2097581069

What OpenQuestion holds

Textmetadata
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.