Evidence map›Paper›PMID 25346475›Full record

ArticleExperimental dermatology2014

Human skin dendritic cells can be targeted in situ by intradermal injection of antibodies against lectin receptors.

Patrizia Stoitzner, Sandra Schaffenrath, Christoph H Tripp, Daniela Reider, Kerstin Komenda, Barbara Del Frari, Gabriel Djedovic, Susanne Ebner, Nikolaus Romani

Open access · hybridAbstract read
In one paragraph

Article in Experimental dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  8. Combining chemotherapy and autologous peptide-pulsed dendritic cells provides survival benefit in stage IV melanoma patients.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2020
    Article
  9. Article
  10. Review
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  16. Engineering immunity: Modulating dendritic cell subsets and lymph node response to direct immune-polarization and vaccine efficacy.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  17. Review
  18. Regulation of Dendritic Cell Function in Inflammation.Journal of immunology research · 2015
    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

9 authors at 3 institutions in 2 countries.

Patrizia StoitznerDepartment of Dermatology & Venereology, Medical University of Innsbruck, Innsbruck, Austria.
Sandra Schaffenrath
Christoph H Tripp
Daniela Reider
Kerstin Komenda
Barbara Del Frari
Gabriel Djedovic
Susanne Ebner
Nikolaus Romani
Innsbruck Medical University · ATUniversität Innsbruck · ATZero to Three · US

Funding

Austrian Science Fund FWF P 21487
6 · The paper itself

Abstract

Skin dendritic cells (DC) express C-type lectin receptors for the recognition of pathogens. Langerhans cells (LC) express the receptor Langerin/CD207, whereas DEC-205/CD205 is mainly expressed by dermal DC, but can also be detected at low levels on LC. In this study, we tested an ex vivo approach for targeting DC in situ with monoclonal antibodies (mAb) against Langerin and DEC-205. The targeting mAb was injected intradermally into human skin biopsies or added to the medium during skin explant culture. Corresponding to the expression patterns of these lectin receptors on skin DC, Langerin mAb was detected merely in LC in the epidermis and DEC-205 mainly in dermal DC in human skin explants, regardless of the application route. Migratory skin DC bound and carried targeting mAb from skin explants according to their lectin receptor expression profiles. In contrast to the very selective transport of Langerin mAb by LC, DEC-205 mAb was more widely distributed on all CD1a(+) skin DC subsets but almost absent in CD14(+) dermal DC. As effective vaccination requires the addition of adjuvant, we co-administered the toll-like receptor (TLR)-3 ligand poly I:C with the mAb. This adjuvant enhanced binding of DEC-205 mAb to all skin DC subsets, whereas Langerin targeting efficacy remained unchanged. Our findings demonstrate that LC can be preferentially targeted by Langerin mAb. In contrast, DEC-205 mAb can be bound by all CD1a(+) skin DC subsets. The efficacy of DEC-205 mAb targeting strategy can be boosted by addition of poly I:C underlining the potential of this combination for immunotherapeutical interventions.

Indexed as

Adjuvants, ImmunologicAntibodies, MonoclonalAntigen-Antibody ComplexAntigens, CDCells, CulturedHumansImmunizationInjections, IntradermalLangerhans CellsLectins, C-TypeMannose-Binding LectinsMinor Histocompatibility AntigensPoly I-CReceptors, Cell SurfaceReceptors, MitogenToll-Like Receptor 3Adjuvants, ImmunologicAntibodies, MonoclonalAntigen-Antibody ComplexAntigens, CDCD207 protein, humanDEC-205 receptorLectins, C-TypeMannose-Binding LectinsMinor Histocompatibility AntigensPoly I-CReceptors, Cell SurfaceReceptors, MitogenTLR3 protein, humanToll-Like Receptor 3dendritic cellsimmunotherapyLangerhans cellsskin

Identifiers

PMID25346475
PMCPMC4282089
OpenAlexW1977856756

What OpenQuestion holds

Textmetadata
LicenceTDM
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.