Evidence map›Paper›PMID 25159465›Full record

ArticleThe Journal of allergy and clinical immunology2014

Identification of novel gene signatures in patients with atopic dermatitis complicated by eczema herpeticum.

Lianghua Bin, Michael G Edwards, Ryan Heiser, Joanne E Streib, Brittany Richers, Clifton F Hall, Donald Y M Leung

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01429311 (Investigation of Reduced Interferon Responses in Peripheral Blood Mononuclear Cells of Participants With Atopic Dermatitis and a History of Eczema Herpeticum), which is not on this map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
9.0field-weighted citation impact, top 2% 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.

NCT01429311 completednot on this map

Investigation of Reduced Interferon Responses in Peripheral Blood Mononuclear Cells of Participants With Atopic Dermatitis and a History of Eczema Herpeticum (ADRN-01)

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2011 to 2016Enrolled84ConditionsAtopic Dermatitis, Eczema Herpeticum, Herpes Simplex Infections, Eczema Vaccinatum
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Classifying atopic dermatitis: a systematic review of phenotypes and associated characteristics.Journal of the European Academy of Dermatology and Venereology : JEADV · 2022
    Pooled it
  2. Guideline
  3. Trial
  4. Review
  5. Article
  6. Genetic and Immunological Pathogenesis of Atopic Dermatitis.The Journal of investigative dermatology · 2024
    Review
  7. Article
  8. Review
  9. The Genetics of Eczema Herpeticum.Clinical reviews in allergy & immunology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Interferon-Lambda 1 InhibitsFrontiers in pharmacology · 2021
    Article
  14. Eczema Herpeticum: Clinical and Pathophysiological Aspects.Clinical reviews in allergy & immunology · 2020
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

7 authors at 2 institutions in 1 country.

Lianghua BinDepartment of Pediatrics, National Jewish Health, Denver, Colo.
Michael G EdwardsDivision of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado Denver, Aurora, Colo.
Ryan HeiserDepartment of Pediatrics, National Jewish Health, Denver, Colo.
Joanne E StreibDepartment of Pediatrics, National Jewish Health, Denver, Colo.
Brittany RichersDepartment of Pediatrics, National Jewish Health, Denver, Colo.
Clifton F HallDepartment of Pediatrics, National Jewish Health, Denver, Colo.
Donald Y M LeungDepartment of Pediatrics, National Jewish Health, Denver, Colo; Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colo. Electronic address: leungd@njhealth.org.
National Jewish Health · USUniversity of Colorado Denver · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Colorado Clinical and Translational Science Institute (UL1)UL1TR000154 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2012 to 2013
$20.4M
NCATS NIH HHS UL1 TR000154NCATS NIH HHS UL1 TR001082NCRR NIH HHS UL1 RR025780NIAID NIH HHS HHSN272201000020C
6 · The paper itself

Abstract

backgroundA subset of patients with atopic dermatitis (AD) is prone to disseminated herpes simplex virus (HSV) infection (ie, atopic dermatitis with a history of eczema herpeticum [ADEH+]). Biomarkers that identify ADEH+ are lacking.

objectiveWe sought to search for novel ADEH+ gene signatures in PBMCs.

methodsAn RNA-sequencing approach was applied to evaluate global transcriptional changes by using PBMCs from patients with ADEH+ and patients with atopic dermatitis without a history of eczema herpeticum (ADEH-). Candidate genes were confirmed by means of quantitative PCR or ELISA.

resultsPBMCs from patients with ADEH+ had distinct changes to the transcriptome when compared with those from patients with ADEH- after HSV-1 stimulation: 792 genes were differentially expressed at a false discovery rate of less than 0.05 (ANOVA), and 15 type I and type III interferon genes were among the top 20 most downregulated genes in patients with ADEH+. We further validated that IFN-α and IL-29 mRNA and protein levels were significantly decreased in HSV-1-stimulated PBMCs from patients with ADEH+ compared with those from patients with ADEH- and healthy subjects. Ingenuity Pathway Analysis demonstrated that the upstream regulators of type I and type III interferons, interferon regulatory factor (IRF) 3 and IRF7, were significantly inhibited in patients with ADEH+ based on the downregulation of their target genes. Furthermore, we found that gene expression of IRF3 and IRF7 was significantly decreased in HSV-1-stimulated PBMCs from patients with ADEH+.

conclusionsPBMCs from patients with ADEH+ have a distinct immune response after HSV-1 exposure compared with those from patients with ADEH-. Inhibition of the IRF3 and IRF7 innate immune pathways in patients with ADEH+ might be an important mechanism for increased susceptibility to disseminated viral infection.

Indexed as

TranscriptomeAdolescentAdultAgedAnimalsCells, CulturedChildDermatitis, AtopicDown-RegulationFemaleGenetic MarkersHerpesvirus 1, HumanHumansImmunity, InnateInterferon LambdaInterferon Regulatory Factor-3Genetic MarkersInterferon Lambdainterferon-lambda, humanInterferon Regulatory Factor-3Interferon Regulatory Factor-7InterferonsInterferon Type IInterleukinsIRF3 protein, humanIRF7 protein, humanAtopic dermatitiseczema herpeticumherpes simplex virusinterferon regulatory factor 3interferon regulatory factor 7type III interferontype I interferon

Identifiers

PMID25159465
PMCPMC4186924
OpenAlexW2032848177

What OpenQuestion holds

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Registered trials

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.