Evidence map›Paper›PMID 20442861›Full record

ArticlePLoS pathogens2010

Keratinocytes determine Th1 immunity during early experimental leishmaniasis.

Jan M Ehrchen, Kirsten Roebrock, Dirk Foell, Nadine Nippe, Esther von Stebut, Johannes M Weiss, Niels-Arne Münck, Dorothee Viemann, Georg Varga, Carsten Müller-Tidow and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. DNA Methylation in macrophages infected withEmerging microbes & infections · 2025
    Article
  5. Review
  6. Human sand fly challenge elicits saliva-specific innate and TbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Immune Responses in Leishmaniasis: An Overview.Tropical medicine and infectious disease · 2022
    Review
  13. Dissection of the macrophage response towards infection by theFrontiers in cellular and infection microbiology · 2022
    Article
  14. Review
  15. Article
  16. Early Leukocyte Responses inFrontiers in cellular and infection microbiology · 2021
    Article
  17. Article
  18. Article
  19. Review
  20. Article
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

13 authors at 4 institutions in 1 country.

Jan M EhrchenInstitute of Immunology, University of Muenster, Muenster, Germany.
Kirsten Roebrock
Dirk Foell
Nadine Nippe
Esther von Stebut
Johannes M Weiss
Niels-Arne Münck
Dorothee Viemann
Georg Varga
Carsten Müller-Tidow
Hans-Joachim Schuberth
Johannes Roth
Cord Sunderkötter
University of Münster · DEJohannes Gutenberg University Mainz · DEUniversität Ulm · DEUniversity of Veterinary Medicine Hannover, Foundation · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental leishmaniasis is an excellent model system for analyzing Th1/Th2 differentiation. Resistance to Leishmania (L.) major depends on the development of a L. major specific Th1 response, while Th2 differentiation results in susceptibility. There is growing evidence that the microenvironment of the early affected tissue delivers the initial triggers for Th-cell differentiation. To analyze this we studied differential gene expression in infected skin of resistant and susceptible mice 16h after parasite inoculation. Employing microarray technology, bioinformatics, laser-microdissection and in-situ-hybridization we found that the epidermis was the major source of immunomodulatory mediators. This epidermal gene induction was significantly stronger in resistant mice especially for several genes known to promote Th1 differentiation (IL-12, IL-1beta, osteopontin, IL-4) and for IL-6. Expression of these cytokines was temporally restricted to the crucial time of Th1/2 differentiation. Moreover, we revealed a stronger epidermal up-regulation of IL-6 in the epidermis of resistant mice. Accordingly, early local neutralization of IL-4 in resistant mice resulted in a Th2 switch and mice with a selective IL-6 deficiency in non-hematopoietic cells showed a Th2 switch and dramatic deterioration of disease. Thus, our data indicate for the first time that epidermal cytokine expression is a decisive factor in the generation of protective Th1 immunity and contributes to the outcome of infection with this important human pathogen.

Indexed as

AnimalsCell DifferentiationDisease Models, AnimalGene ExpressionGene Expression ProfilingImmunohistochemistryIn Situ HybridizationInterleukin-12Interleukin-1betaInterleukin-4Interleukin-6KeratinocytesLasersLeishmaniasis, CutaneousMiceMice, Inbred BALB CInterleukin-12Interleukin-1betaInterleukin-4Interleukin-6Osteopontin

Identifiers

PMID20442861
PMCPMC2861693
OpenAlexW1964188013

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.