Evidence map›Paper›PMID 24331381›Full record

Trial reportThe Journal of allergy and clinical immunology2014

Transcutaneous yellow fever vaccination of subjects with or without atopic dermatitis.

Mark K Slifka, Donald Y M Leung, Erika Hammarlund, Hans-Peter Raué, Eric L Simpson, Susan Tofte, Shahana Baig-Lewis, Gloria David, Henry Lynn, Rob Woolson and 3 more

Registry-linked trialOpen access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report 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 NCT05374317 (An Exploratory, Pilot Study of the Safety and Immunogenicity of Reduced Doses of the US Yellow Fever Vaccine), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% 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.

NCT05374317 phase4completednot on this mapstarted 2021, after this paper: background citation

An Exploratory, Pilot Study of the Safety and Immunogenicity of Reduced Doses of the US Yellow Fever Vaccine

TypeinterventionalSponsorUS Army Medical Research Institute of Infectious DiseasesRan2021 to 2022Enrolled88ConditionsYellow Fever Vaccination ReactionArmsYellow Fever Vaccine
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Review
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  11. Article
  12. Article
  13. Lessons from Ebola and readiness for new emerging infectious threats.The Journal of allergy and clinical immunology · 2015
    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

13 authors at 5 institutions in 1 country.

Mark K SlifkaOregon National Primate Research Center, Oregon Health & Science University, Beaverton, Ore. Electronic address: slifkam@ohsu.edu.
Donald Y M LeungDepartment of Pediatrics, National Jewish Health, Denver, Colo.
Erika HammarlundOregon National Primate Research Center, Oregon Health & Science University, Beaverton, Ore.
Hans-Peter RauéOregon National Primate Research Center, Oregon Health & Science University, Beaverton, Ore.
Eric L SimpsonDepartment of Dermatology, Oregon Health & Science University, Portland, Ore.
Susan TofteDepartment of Dermatology, Oregon Health & Science University, Portland, Ore.
Shahana Baig-LewisDepartment of Dermatology, Oregon Health & Science University, Portland, Ore.
Gloria DavidRho, Inc, Chapel Hill, NC.
Henry LynnRho, Inc, Chapel Hill, NC.
Rob WoolsonRho, Inc, Chapel Hill, NC.
Tissa HataDivision of Dermatology, University of California San Diego, La Jolla, Calif.
Henry MilgromDepartment of Pediatrics, National Jewish Health, Denver, Colo.
Jon HanifinDepartment of Dermatology, Oregon Health & Science University, Portland, Ore.
Oregon Health & Science University · USRho (United States) · USUniversity of Colorado Denver · USOregon National Primate Research Center · USUniversity of California, San Diego · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
ATOPIC DERMITITIS VACCINIA NETWORK /ADVN/-266040029N01AI040029 · NIAID · NATIONAL JEWISH MEDICAL AND RESEARCH CEN · PI LEUNG, DONALD YM · 2006 to 2006
–
NIAID NIH HHS HHSN266200400029CNIAID NIH HHS N01 AI040029NIH HHS 8P51 OD011092-53NIH HHS P51 OD011092
6 · The paper itself

Abstract

backgroundAtopic dermatitis (AD) is a common inflammatory skin disease with a global prevalence ranging from 3% to 20%. Patients with AD have an increased risk for complications after viral infection (eg, herpes simplex virus), and vaccination of patients with AD with live vaccinia virus is contraindicated because of a heightened risk of eczema vaccinatum, a rare but potentially lethal complication associated with smallpox vaccination.

objectiveWe sought to develop a better understanding of immunity to cutaneous viral infection in patients with AD.

methodsIn a double-blind randomized study we investigated the safety and immunogenicity of live attenuated yellow fever virus (YFV) vaccination of nonatopic subjects and patients with AD after standard subcutaneous inoculation or transcutaneous vaccination administered with a bifurcated needle. Viremia, neutralizing antibody, and antiviral T-cell responses were analyzed for up to 30 days after vaccination.

resultsYFV vaccination administered through either route was well tolerated. Subcutaneous vaccination resulted in higher seroconversion rates than transcutaneous vaccination but elicited similar antiviral antibody levels and T-cell responses in both the nonatopic and AD groups. After transcutaneous vaccination, both groups mounted similar neutralizing antibody responses, but patients with AD demonstrated lower antiviral T-cell responses by 30 days after vaccination. Among transcutaneously vaccinated subjects, a significant inverse correlation between baseline IgE levels and the magnitude of antiviral antibody and CD4(+) T-cell responses was observed.

conclusionsYFV vaccination of patients with AD through the transcutaneous route revealed that high baseline IgE levels provide a potential biomarker for predicting reduced virus-specific immune memory after transcutaneous infection with a live virus.

Indexed as

Administration, CutaneousAdultAntibodies, ViralCells, CulturedDermatitis, AtopicDouble-Blind MethodFemaleHumansImmunoglobulin ELeukocytes, MononuclearMaleRNA, ViralT-LymphocytesVaccinationViremiaYellow FeverAntibodies, ViralImmunoglobulin ERNA, ViralYellow Fever VaccineADAdverse eventAEantibodyatopic dermatitisAtopic dermatitisIgELNILog neutralizing indexNeutralizing titer 50NT(50)T-cell memoryYellow fever virusYFV

Identifiers

PMID24331381
PMCPMC3960337
OpenAlexW2059712141

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.