Evidence map›Paper›PMID 29969603›Full record

ReviewImmunology letters2018

Taking the lead - how keratinocytes orchestrate skin T cell immunity.

M M Klicznik, A B Szenes-Nagy, D J Campbell, I K Gratz

Open access · greenAbstract readReview
In one paragraph

Review in Immunology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Oral Manifestation of Viral-Induced Erythema Multiforme Major: A Rare Presentation.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2024
    Article
  12. Review
  13. Article
  14. T helper 1 effector memory CD4Cell reports · 2023
    Article
  15. Review
  16. Review
  17. Review
  18. Inflammatory Microenvironment of Skin Wounds.Frontiers in immunology · 2022
    Review
  19. Inflammatory Response AgainstFrontiers in immunology · 2022
    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

4 authors at 2 institutions in 2 countries.

M M KlicznikDepartment of Biosciences, University of Salzburg, Salzburg, Austria.
A B Szenes-NagyDepartment of Biosciences, University of Salzburg, Salzburg, Austria.
D J CampbellBenaroya Research Institute, Seattle, WA, 98101, USA; Department of Immunology, University of Washington School of Medicine, Seattle, WA, 98195, USA.
I K GratzDepartment of Biosciences, University of Salzburg, Salzburg, Austria; Benaroya Research Institute, Seattle, WA, 98101, USA; EB House Austria, Department of Dermatology, University Hospital of the Paracelsus Medical University, Salzburg, Austria. Electronic address: iris.gratz@sbg.ac.at.
University of Salzburg · ATUniversity of Washington · US

Funding

Regulation of cutaneous immunity and tissue-repair by a specialized population of CD4+ T cellsR01AI127726 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J, GRATZ, IRIS KARINA · 2017 to 2021
$2.8M
NIAID NIH HHS R01 AI127726
6 · The paper itself

Abstract

The skin comprises a complex coordinated system of epithelial tissue cells and immune cells that ensure adequate immune reactions against trauma, toxins and pathogens, while maintaining tissue homeostasis. Keratinocytes form the outermost barrier of the skin, and sense changes in barrier integrity, intrusion of microbial components and stress molecules. Thus, they act as sentinels that continuously communicate the status of the organ to the cutaneous immune system. Upon damage the keratinocytes initiate a pro-inflammatory signaling cascade that leads to the activation of resident immune cells. Simultaneously, the tissue mediates and supports immune-suppressive functions to contain inflammation locally. After resolution of inflammation, the skin provides a niche for regulatory and effector memory T cells that can quickly respond to reoccurring antigens. In this review we discuss the central role of keratinocyte-derived signals in controlling cutaneous T cell immunity.

Indexed as

ImmunomodulationSkin Physiological PhenomenaAnimalsCell CommunicationCytokinesEnvironmentHomeostasisHost-Pathogen InteractionsHumansImmunologic MemoryImmunologic SurveillanceKeratinocytesMicrobiotaSignal TransductionSkinStress, PhysiologicalCytokines

Identifiers

PMID29969603
PMCPMC7032065
OpenAlexW2873855610

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.