Evidence map›Paper›PMID 37208336›Full record

ArticleNature communications2023

Impaired expression of metallothioneins contributes to allergen-induced inflammation in patients with atopic dermatitis.

Sofia Sirvent, Andres F Vallejo, Emma Corden, Ying Teo, James Davies, Kalum Clayton, Eleanor G Seaby, Chester Lai, Sarah Ennis, Rfeef Alyami and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. T-cell mechanisms in atopic dermatitis.Allergologie select · 2026
    Review
  4. Effect of Topical Corticosteroid Treatment on microRNA Expression in Infants with Atopic Dermatitis.JID innovations : skin science from molecules to population health · 2025
    Article
  5. Review
  6. Microorganisms · 2024
    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

22 authors at 5 institutions in 2 countries.

Sofia Sirvent *Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0003-0050-8579
Andres F Vallejo *Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0002-4688-0598
Emma CordenUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Ying TeoClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
James DaviesClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Kalum ClaytonClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0002-1143-3931
Eleanor G SeabyHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.
Chester LaiClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Sarah EnnisHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0003-2648-0869
Rfeef AlyamiClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Gemma DouilhetClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Lareb S N DeanClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0002-8703-9236
Matthew LoxhamClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0001-6459-538X
Sarah HorswillUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Eugene HealyClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0001-5591-6970
Graham RobertsUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Nigel J HallUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Peter S FriedmannClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Harinder SinghDepartments of Immunology and Computational and Systems Biology, The University of Pittsburgh, Pittsburgh, USA.ORCID 0000-0002-6330-8526
Clare L BennettDepartment of Haematology, University College London (UCL) Cancer Institute, London, WC1E 6DD, UK.ORCID 0000-0001-9146-2347
Michael R Ardern-JonesClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0003-1466-2016
Marta E PolakClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK. m.e.polak@soton.ac.uk.ORCID 0000-0003-2878-476X
University of Southampton · GBUniversity Hospital Southampton NHS Foundation Trust · GBSpringhouse · USUniversity College London · GBUniversity of Pittsburgh · US

Funding

Biotechnology and Biological Sciences Research Council BB/V004573/1Cancer Research UK A27179Medical Research Council MR/W03039X/1Wellcome TrustWellcome Trust 109377/Z/15/Z
6 · The paper itself

Abstract

Regulation of cutaneous immunity is severely compromised in inflammatory skin disease. To investigate the molecular crosstalk underpinning tolerance versus inflammation in atopic dermatitis, we utilise a human in vivo allergen challenge study, exposing atopic dermatitis patients to house dust mite. Here we analyse transcriptional programmes at the population and single cell levels in parallel with immunophenotyping of cutaneous immunocytes revealed a distinct dichotomy in atopic dermatitis patient responsiveness to house dust mite challenge. Our study shows that reactivity to house dust mite was associated with high basal levels of TNF-expressing cutaneous Th17 T cells, and documents the presence of hub structures where Langerhans cells and T cells co-localised. Mechanistically, we identify expression of metallothioneins and transcriptional programmes encoding antioxidant defences across all skin cell types, that appear to protect against allergen-induced inflammation. Furthermore, single nucleotide polymorphisms in the MTIX gene are associated with patients who did not react to house dust mite, opening up possibilities for therapeutic interventions modulating metallothionein expression in atopic dermatitis.

Indexed as

Dermatitis, AtopicAllergensAnimalsHumansInflammationPyroglyphidaeSkinAllergens

Identifiers

PMID37208336
PMCPMC10199008
OpenAlexW4377087413

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.