Evidence map›Paper›PMID 25634359›Full record

ArticleThe Journal of investigative dermatology2015

NKG2D-dependent activation of dendritic epidermal T cells in contact hypersensitivity.

Morten M Nielsen, Beatrice Dyring-Andersen, Jonas D Schmidt, Deborah Witherden, Paola Lovato, Anders Woetmann, Niels Ødum, Steen S Poulsen, Wendy L Havran, Carsten Geisler and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  11. Epidermal resident γδ T cell development and function in skin.Cellular and molecular life sciences : CMLS · 2021
    Review
  12. AHR Signaling Dampens Inflammatory Signature in Neonatal Skin γδ T Cells.International journal of molecular sciences · 2020
    Article
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  20. Emerging Skin T-Cell Functions in Response to Environmental Insults.The Journal of investigative dermatology · 2017
    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

11 authors at 3 institutions in 2 countries.

Morten M NielsenDepartment of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Skin Inflammation Pharmacology, LEO Pharma A/S, Ballerup, Denmark.
Beatrice Dyring-AndersenDepartment of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Dermato-Allergology, Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.
Jonas D SchmidtDepartment of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Deborah WitherdenDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, California, USA.
Paola LovatoDepartment of Skin Inflammation Pharmacology, LEO Pharma A/S, Ballerup, Denmark.
Anders WoetmannDepartment of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Niels ØdumDepartment of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Steen S PoulsenDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Wendy L HavranDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, California, USA.
Carsten GeislerDepartment of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Charlotte M BonefeldDepartment of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. Electronic address: cmenne@sund.ku.dk.
University of Copenhagen · DKScripps Research Institute · USLeo Pharma (Denmark) · DK

Funding

JAML: A New Costimulatory Molecule for Gamma Delta T CellsR01AI064811 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI HAVRAN, WENDY L. · 2006 to 2016
$4.8M
EPITHELIAL T CELL SECRETION OF TISSUE SPECIFIC CYTOKINESR01AI036964 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI HAVRAN, WENDY L. · 1996 to 2012
$3.7M
NIAID NIH HHS AI36964NIAID NIH HHS AI64811NIAID NIH HHS R01 AI036964NIAID NIH HHS R01 AI064811
6 · The paper itself

Abstract

The interaction between keratinocytes (KCs) and skin-resident immune cells has an important role in induction of contact hypersensitivity. A specific subset of γδ T cells termed dendritic epidermal T cells (DETCs) are located in mouse epidermis, and we have recently shown that DETCs become activated and produce IL-17 in an IL-1β-dependent manner during contact hypersensitivity. Various receptors on DETCs, including NKG2D, are involved in DETC responses against tumors and during wound healing. The ligands for NKG2D (NKG2DL) are stress-induced proteins such as mouse UL16-binding protein-like transcript 1 (Mult-1), histocompatibility 60 (H60), and retinoic acid early inducible-1 (Rae-1) in mice and major histocompatibility complex (MHC) class I-chain-related A (MICA), MHC class I-chain-related B, and UL16-binding protein in humans. Here, we show that allergens upregulate expression of the NKG2DL Mult-1, H60, and Rae-1 in cultured mouse KCs and of MICA in primary human KCs. We demonstrate that Mult-1 is expressed in mouse skin exposed to allergen. Furthermore, we find that the vast majority of DETCs in murine epidermis and skin-homing cutaneous lymphocyte-associated antigen positive γδ T cells in humans express NKG2D. Finally, we demonstrate that blocking of NKG2D partially inhibits allergen-induced DETC activation. These findings demonstrate that NKG2D and NKG2DL are involved in allergen-induced activation of DETCs and indicate that the NKG2D/NKG2DL pathway might be a potential target for treatment of contact hypersensitivity.

Indexed as

AllergensAnimalsAntibodies, Anti-IdiotypicCarrier ProteinsCell LineCells, CulturedDermatitis, ContactDisease Models, AnimalFemaleHistocompatibility Antigens Class IHumansKeratinocytesLangerhans CellsMembrane ProteinsMiceMice, Inbred C57BLAllergensAntibodies, Anti-IdiotypicCarrier ProteinsHistocompatibility Antigens Class IKLRK1 protein, humanKlrk1 protein, mouseMembrane ProteinsMHC class I-related chain Aminor H antigen H60Minor Histocompatibility AntigensNK Cell Lectin-Like Receptor Subfamily KNuclear Matrix-Associated ProteinsNucleocytoplasmic Transport ProteinsRae1 protein, mouseUL16 binding protein 1, mouse

Identifiers

PMID25634359
PMCPMC4402141
OpenAlexW2063186735

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.