Evidence map›Paper›PMID 37315812›Full record

Trial reportThe Journal of allergy and clinical immunology2023

Rapid reduction in Staphylococcus aureus in atopic dermatitis subjects following dupilumab treatment.

Eric L Simpson, Patrick M Schlievert, Takeshi Yoshida, Stephanie Lussier, Mark Boguniewicz, Tissa Hata, Zelma Fuxench, Anna De Benedetto, Peck Y Ong, Justin Ko and 12 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 3 pooled it
21.7field-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.

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

55 citing papers in PubMed, 3 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Correlation betweenFrontiers in immunology · 2026
    Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Article
  9. Article
  10. Review
  11. Review
  12. Addressing potential bias when assessing safety of biologics and JAK inhibitors in atopic dermatitis.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Article
  13. Article
  14. Article
  15. Atopic dermatitis.Nature reviews. Disease primers · 2026
    Review
  16. [Biologics and infections: understand and recognize].Dermatologie (Heidelberg, Germany) · 2026
    Review
  17. Article
  18. [The Relationship Between Interleukin-4, C-reactive Protein, Atopic Dermatitis, and the Therapeutic Effect of Dupilumab].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Article
  19. Multi-Kingdom Synergy ofLife (Basel, Switzerland) · 2026
    Review
  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

22 authors at 10 institutions in 1 country.

Eric L SimpsonDepartment of Dermatology, Oregon Health and Science University, Portland, Ore.
Patrick M SchlievertDepartment of Microbiology and Immunology, University of Iowa, Iowa City, Iowa.
Takeshi YoshidaDepartment of Dermatology, University of Rochester School of Medicine and Dentistry, Rochester, NY.
Stephanie LussierRho, Inc, Durham, NC.
Mark BoguniewiczDivision of Allergy-Immunology, Department of Pediatrics, National Jewish Health and University of Colorado School of Medicine, Denver, Colo.
Tissa HataDepartment of Dermatology, University of California, San Diego, Calif.
Zelma FuxenchDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pa.
Anna De BenedettoDepartment of Dermatology, University of Rochester School of Medicine and Dentistry, Rochester, NY.
Peck Y OngDepartment of Pediatrics, University Southern California, Los Angeles, Calif.
Justin KoDepartment of Dermatology, Stanford University, Stanford, Calif.
Agustin CalatroniRho, Inc, Durham, NC.
Amanda K Rudman SpergelDivision of Allergy, Immunology, and Transplantation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
Marshall PlautDivision of Allergy, Immunology, and Transplantation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
Sally A QuataertCenter for Vaccine Biology and Immunology, University of Rochester Medical Center, Rochester, NY.
Samuel H KilgoreDepartment of Microbiology and Immunology, University of Iowa, Iowa City, Iowa.
Liam PetersonDepartment of Dermatology, University of Rochester School of Medicine and Dentistry, Rochester, NY.
Ann L GillDepartment of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY.
Gloria DavidRho, Inc, Durham, NC.
Tim MosmannCenter for Vaccine Biology and Immunology, University of Rochester Medical Center, Rochester, NY.
Steven R GillDepartment of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY.
Donald Y M LeungDivision of Allergy-Immunology, Department of Pediatrics, National Jewish Health and University of Colorado School of Medicine, Denver, Colo. Electronic address: LeungD@NJHealth.org.
Lisa A BeckDepartment of Dermatology, University of Rochester School of Medicine and Dentistry, Rochester, NY. Electronic address: Lisa_Beck@urmc.rochester.edu.
University of Rochester Medical Center · USUniversity of Rochester · USNational Institutes of Health · USNational Jewish Health · USUniversity of Iowa · USOregon Health & Science University · USStanford University · USUniversity of California San Diego · USUniversity of Pennsylvania · USUniversity of Southern California · US

Funding

Transplantation GroupUM2AI117870 · NIAID · RHO FEDERAL SYSTEMS DIVISION, INC. · PI DAVID, GLORIA · 2015 to 2023
$208.1M
NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
Experimental and Computational Analysis of the Human Epidemiology and Response to SARS-CoV-2 (HEROS) CohortUM1AI151958 · NIAID · NATIONAL JEWISH HEALTH · PI Donald YM Leung · 2020 to 2026
$38.3M
RhoFED AA-SCCCU01AI178772 · NIAID · RHO FEDERAL SYSTEMS DIVISION, INC. · PI Gloria David, Cynthia M Visness · 2023 to 2026
$37.2M
Colorado Clinical and Translational Sciences Institute (CCTSI)UM1TR004399 · NCATS · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS, RONALD J. SOKOL · 2023 to 2026
$30.7M
Targeted Microbiome Transplant in Atopic DermatitisU19AI117673 · NIAID · NATIONAL JEWISH HEALTH · PI GEHA, RAIF SALIM · 2015 to 2019
$30.6M
Biomarker Identification, Viral Susceptibility and Management in S. aureus Colonized AD PatientsU01AI152011 · NIAID · UNIVERSITY OF ROCHESTER · PI Lisa Ann Beck · 2020 to 2026
$3.2M
NCATS NIH HHS UL1 TR002535NCATS NIH HHS UM1 TR004399NIAID NIH HHS U01 AI152011NIAID NIH HHS U01 AI178772NIAID NIH HHS U19 AI117673NIAID NIH HHS UM1 AI151958NIAID NIH HHS UM2 AI117870
6 · The paper itself

Abstract

backgroundAtopic dermatitis (AD) is an inflammatory disorder characterized by dominant type 2 inflammation leading to chronic pruritic skin lesions, allergic comorbidities, and Staphylococcus aureus skin colonization and infections. S aureus is thought to play a role in AD severity.

objectivesThis study characterized the changes in the host-microbial interface in subjects with AD following type 2 blockade with dupilumab.

methodsParticipants (n = 71) with moderate-severe AD were enrolled in a randomized (dupilumab vs placebo; 2:1), double-blind study at Atopic Dermatitis Research Network centers. Bioassays were performed at multiple time points: S aureus and virulence factor quantification, 16s ribosomal RNA microbiome, serum biomarkers, skin transcriptomic analyses, and peripheral blood T-cell phenotyping.

resultsAt baseline, 100% of participants were S aureus colonized on the skin surface. Dupilumab treatment resulted in significant reductions in S aureus after only 3 days (compared to placebo), which was 11 days before clinical improvement. Participants with the greatest S aureus reductions had the best clinical outcomes, and these reductions correlated with reductions in serum CCL17 and disease severity. Reductions (10-fold) in S aureus cytotoxins (day 7), perturbations in T

conclusionsBlockade of IL-4 and IL-13 signaling, very rapidly (day 3) reduces S aureus abundance in subjects with AD, and this reduction correlates with reductions in the type 2 biomarker, CCL17, and measures of AD severity (excluding itch). Immunoprofiling and/or transcriptomics suggest a role for T

Indexed as

Dermatitis, AtopicStaphylococcal InfectionsAntibodies, Monoclonal, HumanizedHumansSeverity of Illness IndexSkinStaphylococcus aureusTreatment OutcomeAntibodies, Monoclonal, HumanizeddupilumabAtopic dermatitisbarriercytotoxinsdupilumabIL-13IL-17IL-4microbiomeStaphylococcus aureustype 2 immunity

Identifiers

PMID37315812
PMCPMC10716365
OpenAlexW4380301245

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.