Evidence map›Paper›PMID 21458658›Full record

ArticleThe Journal of allergy and clinical immunology2011

Human atopic dermatitis complicated by eczema herpeticum is associated with abnormalities in IFN-γ response.

Donald Y M Leung, Pei-Song Gao, Dmitry N Grigoryev, Nicholas M Rafaels, Joanne E Streib, Michael D Howell, Patricia A Taylor, Mark Boguniewicz, Jennifer Canniff, Brian Armstrong and 7 more

Erratum issued Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT01737710 (A Randomized Open Label Mechanistic Study in Atopic Dermatitis to Assess the Immunogenicity of Fluzone® Intradermal and Intramuscular Vaccines), which is not on this map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
15.0field-weighted citation impact, top 1% 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.

NCT01737710 nacompletednot on this mapstarted 2012, after this paper: background citation

A Randomized Open Label Mechanistic Study in Atopic Dermatitis to Assess the Immunogenicity of Fluzone® Intradermal and Intramuscular Vaccines

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2012 to 2013Enrolled368ConditionsDermatitis, AtopicArmsFluzone® Intradermal Vaccine, Fluzone® (Intramuscular) vaccine
3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
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  7. TThe Journal of allergy and clinical immunology · 2024
    Review
  8. Article
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  11. Genetic/Protein Association of Atopic Dermatitis and Tooth Agenesis.International journal of molecular sciences · 2023
    Review
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  14. Article
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7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

17 authors at 9 institutions in 2 countries.

Donald Y M LeungDepartment of Pediatrics, National Jewish Health, Denver, CO 80206, USA. leungd@njhealth.org
Pei-Song Gao
Dmitry N Grigoryev
Nicholas M Rafaels
Joanne E Streib
Michael D Howell
Patricia A Taylor
Mark Boguniewicz
Jennifer Canniff
Brian Armstrong
Daniel J Zaccaro
Lynda C Schneider
Tissa R Hata
Jon M Hanifin
Lisa A Beck
Adriana Weinberg
Kathleen C Barnes
University of Colorado Denver · USJohns Hopkins University · USNational Jewish Health · USRho (United States) · USBoston Children's Museum · USJohns Hopkins Medicine · USOregon Health & Science University · USUniversity of California San Diego Medical Center · USUniversity of Rochester Medical Center · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
SEAL (Stopping Atopic dermatitis and ALlergy) Study: Prevent allergy by enhancing the skin barrierU01AI147462 · NIAID · STANFORD UNIVERSITY · PI Mary Johnson, GIDEON LACK · 2020 to 2026
$14.0M
Statistical and Data Coordinating Center for the ADVNN01AI40033 · NIAID · RHO FEDERAL SYSTEMS DIVISION, INC. · PI ATHEY, CAROL · 2008 to 2014
$6.2M
THE ROLE OF BACTERIAL TOXINS IN HUMAN SKIN DISEASER01AR041256 · NIAMS · NATIONAL JEWISH HEALTH · PI GOLEVA, ELENA, LEUNG, DONALD YM · 1992 to 2020
$5.9M
ATOPIC DERMITITIS VACCINIA NETWORK /ADVN/-266040029N01AI040029 · NIAID · NATIONAL JEWISH MEDICAL AND RESEARCH CEN · PI LEUNG, DONALD YM · 2006 to 2006
–
NCRR NIH HHS UL1 RR025780NIAID NIH HHS HHSN266200400029CNIAID NIH HHS N01 AI040029NIAID NIH HHS N01 AI040030NIAID NIH HHS N01 AI040033NIAID NIH HHS N01 AI40033NIAID NIH HHS U01 AI147462NIAMS NIH HHS AR41256NIAMS NIH HHS R01 AR041256
6 · The paper itself

Abstract

backgroundThe basis for increased susceptibility of patients with atopic dermatitis (AD) to develop disseminated viral skin infections such as eczema herpeticum (AD with a history of eczema herpeticum, ADEH(+)) is poorly understood.

objectiveWe sought to determine whether subjects with AD prone to disseminated viral skin infections have defects in their IFN responses.

methodsGeneChip profiling was used to identify differences in gene expression of PBMCs from patients with ADEH(+) compared with patients with AD without a history of eczema herpeticum (ADEH(-)) and nonatopic controls. Key differences in protein expression were verified by enzyme-linked immunosorbent spot assay and/or ELISA. Clinical relevance was further demonstrated by a mouse model of disseminated viral skin infection and genetic association analysis for genetic variants in IFNG and IFNGR1 and ADEH among 435 cases and controls.

resultsWe demonstrate by global gene expression analysis selective transcriptomic changes within the IFN superfamily of PBMCs from subjects with ADEH(+) reflecting low IFN-γ and IFN-γ receptor gene expression. IFN-γ protein production was also significantly lower in patients with ADEH(+) (n = 24) compared with patients with ADEH(-) (n = 20) and nonatopic controls (n = 20). IFN-γ receptor knockout mice developed disseminated viral skin infection after epicutaneous challenge with vaccinia virus. Genetic variants in IFNG and IFNGR1 single nucleotide polymorphisms (SNPs) were significantly associated with ADEH (112 cases, 166 controls) and IFN-γ production: a 2-SNP (A-G) IFNGR1 haplotype (rs10457655 and rs7749390) showed the strongest association with a reduced risk of ADEH+ (13.2% ADEH(+) vs 25.5% ADEH(-); P = .00057).

conclusionPatients with ADEH(+) have reduced IFN-γ production, and IFNG and IFNGR1 SNPs are significantly associated with ADEH(+) and may contribute to an impaired immune response to herpes simplex virus.

Indexed as

AnimalsDermatitis, AtopicEnzyme-Linked Immunosorbent AssayGene Expression ProfilingGenetic Predisposition to DiseaseHumansInterferon-gammaInterferon gamma ReceptorKaposi Varicelliform EruptionMiceMice, KnockoutOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideReceptors, InterferonInterferon-gammaInterferon gamma ReceptorReceptors, Interferon

Identifiers

PMID21458658
PMCPMC3074534
OpenAlexW1989945566

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.