Evidence map›Paper›PMID 24352044›Full record

ArticleThe Journal of investigative dermatology2014

A three-dimensional atlas of human dermal leukocytes, lymphatics, and blood vessels.

Xiao-Nong Wang, Naomi McGovern, Merry Gunawan, Connor Richardson, Martin Windebank, Tee-Wei Siah, Hwee-Ying Lim, Katja Fink, Jackson L Yao Li, Lai G Ng and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
12.3field-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

68 citing papers in PubMed, 138 citations in OpenAlex.

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  8. Hidden immune memory niches in inflammatory skin diseases.bioRxiv : the preprint server for biology · 2026
    Article
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  19. Exploiting Unique Features of Microneedles to Modulate Immunity.Advanced materials (Deerfield Beach, Fla.) · 2023
    Review
  20. Article

8 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

14 authors at 5 institutions in 2 countries.

Xiao-Nong WangInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Naomi McGovernInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Merry GunawanInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Connor RichardsonInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Martin WindebankInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Tee-Wei SiahDepartment of Dermatology, Royal Victoria Infirmary, Newcastle upon Tyne, UK.
Hwee-Ying LimNational University of Singapore, Singapore, Singapore.
Katja FinkSingapore Immunology Network, A*Star, Singapore, Singapore.
Jackson L Yao LiSingapore Immunology Network, A*Star, Singapore, Singapore.
Lai G NgSingapore Immunology Network, A*Star, Singapore, Singapore.
Florent GinhouxSingapore Immunology Network, A*Star, Singapore, Singapore.
Veronique AngeliNational University of Singapore, Singapore, Singapore.
Matthew CollinInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Muzlifah HaniffaInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK. Electronic address: m.a.haniffa@ncl.ac.uk.
Newcastle University · GBSingapore Immunology Network · SGNational University of Singapore · SGAgency for Science, Technology and Research · SGRoyal Victoria Infirmary · GB

Funding

Wellcome Trust 088555
6 · The paper itself

Abstract

Dendritic cells (DCs), macrophages (Mφ), and T cells are major components of the skin immune system, but their interstitial spatial organization is poorly characterized. Using four-channel whole-mount immunofluorescence staining of the human dermis, we demonstrated the three-dimensional distribution of CD31(+) blood capillaries, LYVE-1(+) lymphatics, discrete populations of CD11c(+) myeloid DCs, FXIIIa(+) Mφ, and lymphocytes. We showed phenotypic and morphological differences in situ between DCs and Mφ. DCs formed the first dermal cellular layer (0-20 μm beneath the dermoepidermal junction), Mφ were located deeper (40-60 μm), and CD3(+) lymphocytes were observed throughout (0-60 μm). Below this level, DCs, T cells, and the majority of Mφ formed stable perivascular sheaths. Whole-mount imaging revealed the true extent of dermal leukocytes previously underestimated from cross-section views. The total area of apical dermis (0-30 μm) contained approximately 10-fold more myeloid DCs than the entire blood volume of an average individual. Surprisingly, <1% of dermal DCs occupied lymphatics in freshly isolated skin. Dermal DCs rapidly accumulated within lymphatics, but Mφ remained fixed in skin explants cultured ex vivo. The leukocyte architecture observed in normal skin was distorted in inflammation and disease. These studies illustrate the micro-anatomy of dermal leukocytes and provide further insights into their functional organization.

Indexed as

AdolescentAdultAgedAnisotropyCarrier ProteinsCD11c AntigenCell MovementDermisFemaleFlow CytometryHumansLangerhans CellsLeukocytesLymphatic SystemLymphatic VesselsLymphocytesCarrier ProteinsCD11c AntigenfascinMicrofilament ProteinsPlatelet Endothelial Cell Adhesion Molecule-1

Identifiers

PMID24352044
PMCPMC3961477
OpenAlexW2077967428

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.