Evidence map›Paper›PMID 23875023›Full record

ArticlePloS one2013

IL-10 conditioning of human skin affects the distribution of migratory dendritic cell subsets and functional T cell differentiation.

Jelle J Lindenberg, Dinja Oosterhoff, Claudia C Sombroek, Sinéad M Lougheed, Erik Hooijberg, Anita G M Stam, Saskia J A M Santegoets, Henk J Tijssen, Jan Buter, Herbert M Pinedo and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  9. Review
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  13. Human dendritic cell subsets and function in health and disease.Cellular and molecular life sciences : CMLS · 2015
    Review
  14. Human skin dendritic cells in health and disease.Journal of dermatological science · 2015
    Review
  15. Review
  16. Article
  17. Article
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  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

15 authors at 3 institutions in 1 country.

Jelle J LindenbergDepartment of Medical Oncology, VU University medical center, Amsterdam, The Netherlands.
Dinja Oosterhoff
Claudia C Sombroek
Sinéad M Lougheed
Erik Hooijberg
Anita G M Stam
Saskia J A M Santegoets
Henk J Tijssen
Jan Buter
Herbert M Pinedo
Alfons J M van den Eertwegh
Rik J Scheper
Hans J P M Koenen
Rieneke van de Ven
Tanja D de Gruijl
Amsterdam UMC Location VUmc · NLRadboud University Medical Center · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In cancer patients pervasive systemic suppression of Dendritic Cell (DC) differentiation and maturation can hinder vaccination efficacy. In this study we have extensively characterized migratory DC subsets from human skin and studied how their migration and T cell-stimulatory abilities were affected by conditioning of the dermal microenvironment through cancer-related suppressive cytokines. To assess effects in the context of a complex tissue structure, we made use of a near-physiological skin explant model. By 4-color flow cytometry, we identified migrated Langerhans Cells (LC) and five dermis-derived DC populations in differential states of maturation. From a panel of known tumor-associated suppressive cytokines, IL-10 showed a unique ability to induce predominant migration of an immature CD14(+)CD141(+)DC-SIGN(+) DC subset with low levels of co-stimulatory molecules, up-regulated expression of the co-inhibitory molecule PD-L1 and the M2-associated macrophage marker CD163. A similarly immature subset composition was observed for DC migrating from explants taken from skin overlying breast tumors. Whereas predominant migration of mature CD1a(+) subsets was associated with release of IL-12p70, efficient Th cell expansion with a Th1 profile, and expansion of functional MART-1-specific CD8(+) T cells, migration of immature CD14(+) DDC was accompanied by increased release of IL-10, poor expansion of CD4(+) and CD8(+) T cells, and skewing of Th responses to favor coordinated FoxP3 and IL-10 expression and regulatory T cell differentiation and outgrowth. Thus, high levels of IL-10 impact the composition of skin-emigrated DC subsets and appear to favor migration of M2-like immature DC with functional qualities conducive to T cell tolerance.

Indexed as

Analysis of VarianceAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenCell DifferentiationCell MovementFlow CytometryGene Expression RegulationHumansInterleukin-10Langerhans CellsReal-Time Polymerase Chain ReactionReceptors, Cell SurfaceReverse Transcriptase Polymerase Chain ReactionSkinT-Lymphocyte SubsetsAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenInterleukin-10Receptors, Cell Surface

Identifiers

PMID23875023
PMCPMC3715492
OpenAlexW2040104372

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Registered trials

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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.