Evidence map›Paper›PMID 26431538›Full record

ArticlePLoS pathogens2015

Antigen-Specific Th17 Cells Are Primed by Distinct and Complementary Dendritic Cell Subsets in Oropharyngeal Candidiasis.

Kerstin Trautwein-Weidner, André Gladiator, Florian R Kirchner, Simone Becattini, Thomas Rülicke, Federica Sallusto, Salomé LeibundGut-Landmann

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  9. Immunity to fungi in the lung.Seminars in immunology · 2023
    Review
  10. Article
  11. Review
  12. Review
  13. TheScience signaling · 2022
    Article
  14. The Role of IL-17-Producing Cells in Cutaneous Fungal Infections.International journal of molecular sciences · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

7 authors at 3 institutions in 2 countries.

Kerstin Trautwein-WeidnerInstitute of Microbiology, ETH Zürich, Zürich, Switzerland.
André GladiatorInstitute of Microbiology, ETH Zürich, Zürich, Switzerland.
Florian R KirchnerInstitute of Microbiology, ETH Zürich, Zürich, Switzerland; Section of Immunology, Institute of Virology, University of Zürich, Zürich, Switzerland.
Simone BecattiniInstitute of Microbiology, ETH Zürich, Zürich, Switzerland; Institute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona, Switzerland.
Thomas RülickeInstitute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Vienna, Austria.
Federica SallustoInstitute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona, Switzerland.
Salomé LeibundGut-LandmannInstitute of Microbiology, ETH Zürich, Zürich, Switzerland; Section of Immunology, Institute of Virology, University of Zürich, Zürich, Switzerland.
ETH Zurich · CHUniversità della Svizzera italiana · CHUniversity of Veterinary Medicine Vienna · AT

Funding

Swiss National Science Foundation 123342Swiss National Science Foundation 150758
6 · The paper itself

Abstract

Candida spp. can cause severe and chronic mucocutaneous and systemic infections in immunocompromised individuals. Protection from mucocutaneous candidiasis depends on T helper cells, in particular those secreting IL-17. The events regulating T cell activation and differentiation toward effector fates in response to fungal invasion in different tissues are poorly understood. Here we generated a Candida-specific TCR transgenic mouse reactive to a novel endogenous antigen that is conserved in multiple distant species of Candida, including the clinically highly relevant C. albicans and C. glabrata. Using TCR transgenic T cells in combination with an experimental model of oropharyngeal candidiasis (OPC) we investigated antigen presentation and Th17 priming by different subsets of dendritic cells (DCs) present in the infected oral mucosa. Candida-derived endogenous antigen accesses the draining lymph nodes and is directly presented by migratory DCs. Tissue-resident Flt3L-dependent DCs and CCR2-dependent monocyte-derived DCs collaborate in antigen presentation and T cell priming during OPC. In contrast, Langerhans cells, which are also present in the oral mucosa and have been shown to prime Th17 cells in the skin, are not required for induction of the Candida-specific T cell response upon oral challenge. This highlights the functional compartmentalization of specific DC subsets in different tissues. These data provide important new insights to our understanding of tissue-specific antifungal immunity.

Indexed as

AnimalsAntigen PresentationAntigens, FungalCandidiasis, OralDendritic CellsDisease Models, AnimalEpitopes, T-LymphocyteFlow CytometryLymphocyte ActivationMiceMice, Inbred C57BLMice, TransgenicReceptors, Antigen, T-CellTh17 CellsAntigens, FungalEpitopes, T-LymphocyteReceptors, Antigen, T-Cell

Identifiers

PMID26431538
PMCPMC4591991
OpenAlexW2173485226

What OpenQuestion holds

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LicenceCC BY
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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.