Evidence map›Paper›PMID 20421491›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Requirement of CCL17 for CCR7- and CXCR4-dependent migration of cutaneous dendritic cells.

Susanne Stutte, Thomas Quast, Nancy Gerbitzki, Terhi Savinko, Nina Novak, Julia Reifenberger, Bernhard Homey, Waldemar Kolanus, Harri Alenius, Irmgard Förster

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

64 citing papers in PubMed, 118 citations in OpenAlex.

  1. Trial
  2. Hidden immune memory niches in inflammatory skin diseases.bioRxiv : the preprint server for biology · 2026
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  4. Article
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  9. Article
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  12. Article
  13. Article
  14. Article
  15. Antibiotics (Basel, Switzerland) · 2023
    Review
  16. Testis exposure to unopposed/elevated activin AFrontiers in endocrinology · 2023
    Article
  17. Article
  18. CC Chemokine Receptor 4 (CCR4) as a Possible New Target for Therapy.International journal of molecular sciences · 2022
    Review
  19. How cell migration helps immune sentinels.Frontiers in cell and developmental biology · 2022
    Review
  20. Review

4 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

10 authors at 4 institutions in 2 countries.

Susanne StutteMolecular Immunology, Leibniz Institut fuer Umweltmedizinische Forschung, Düsseldorf, Germany.
Thomas Quast
Nancy Gerbitzki
Terhi Savinko
Nina Novak
Julia Reifenberger
Bernhard Homey
Waldemar Kolanus
Harri Alenius
Irmgard Förster
Leibniz Institute of Environmental Medicine · DEUniversity of Bonn · DEFinnish Institute of Occupational Health · FIHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokines are known to regulate the steady-state and inflammatory migration of cutaneous dendritic cells (DCs). The beta-chemokine CCL17, a ligand of CCR4, is inducibly expressed in a subset of DCs and is strongly up-regulated in atopic diseases. Using an atopic dermatitis model, we show that CCL17-deficient mice develop acanthosis as WT mice, whereas dermal inflammation, T helper 2-type cytokine production, and the allergen-specific humoral immune response are significantly decreased. Notably, CCL17-deficient mice retained Langerhans cells (LCs) in the lesional skin after chronic allergen exposure, whereas most LCs emigrated from the epidermis of allergen-treated WT controls into draining lymph nodes (LNs). Moreover, CCL17-deficient LCs showed impaired emigration from the skin after exposure to a contact sensitizer. In contrast, the absence of CCR4 had no effect on cutaneous DC migration and development of atopic dermatitis symptoms. As an explanation for the major migratory defect of CCL17-deficient DCs in vivo, we demonstrate impaired mobility of CCL17-deficient DCs to CCL19/21 in 3D in vitro migration assays and a blockade of intracellular calcium release in response to CCR7 ligands. In addition, responsiveness of CCL17-deficient DCs to CXCL12 was impaired as well. We demonstrate that the inducible chemokine CCL17 sensitizes DCs for CCR7- and CXCR4-dependent migration to LN-associated homeostatic chemokines under inflammatory conditions and thus plays an important role in cutaneous DC migration.

Indexed as

AllergensAnimalsCell MovementChemokine CCL17Dermatitis, ContactDermisImmunity, HumoralInflammationLangerhans CellsLigandsMiceReceptors, CCR7Receptors, CXCR4AllergensCcl17 protein, mouseCcr7 protein, mouseChemokine CCL17CXCR4 protein, mouseLigandsReceptors, CCR7Receptors, CXCR4

Identifiers

PMID20421491
PMCPMC2889308
OpenAlexW2082651651

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.