Evidence map›Paper›PMID 31626841›Full record

ArticleThe Journal of allergy and clinical immunology2020

Evolution of pathologic T-cell subsets in patients with atopic dermatitis from infancy to adulthood.

Tali Czarnowicki, Helen He, Talia Canter, Joseph Han, Rachel Lefferdink, Taylor Erickson, Stephanie Rangel, Naoya Kameyama, Hyun Je Kim, Ana B Pavel and 4 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05719649 (The Efficacy of NTU 101 Lactic Acid Bacteria Powder in the Adjuvant Improvement of Atopic Dermatitis - A Double-blind, Multi-center Randomized, Placebo-controlled Clinical Trial), which is not on this map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
10.5field-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.

NCT05719649 naunknown statusnot on this mapstarted 2023, after this paper: background citation

The Efficacy of NTU 101 Lactic Acid Bacteria Powder in the Adjuvant Improvement of Atopic Dermatitis - A Double-blind, Multi-center Randomized, Placebo-controlled Clinical Trial

TypeinterventionalSponsorSunWay Biotech Co., LTD.Ran2023 to 2023Enrolled72ConditionsAtopic Dermatitis, Atopic Dermatitis EczemaArmsLactic acid bacteria NTU 101, Placebo
3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 115 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Circulating CLAJID innovations : skin science from molecules to population health · 2025
    Review
  10. Cytotoxic T Cells: Kill, Memorize, and Mask to Maintain Immune Homeostasis.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Allergen-specific circulating CLAFrontiers in immunology · 2025
    Article
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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

14 authors at 3 institutions in 1 country.

Tali CzarnowickiDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY; Laboratory for Investigative Dermatology, Rockefeller University, New York, NY.
Helen HeDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Talia CanterDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Joseph HanDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Rachel LefferdinkDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Taylor EricksonDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Stephanie RangelDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Naoya KameyamaDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Hyun Je KimDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Ana B PavelDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Yeriel EstradaDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
James G KruegerLaboratory for Investigative Dermatology, Rockefeller University, New York, NY.
Amy S PallerDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Emma Guttman-YasskyDepartment of Dermatology and the Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY. Electronic address: emma.guttman@mountsinai.org.
Icahn School of Medicine at Mount Sinai · USNorthwestern University · USRockefeller University · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Northwestern University Skin Disease Research Center Resource-based CenterP30AR075049 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Irina Budunova · 2019 to 2026
$6.6M
The Role of Keratinocytes as Independent ThermosensorsP30AR057216 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PALLER, AMY S · 2009 to 2018
$6.0M
NCATS NIH HHS UL1 TR001422NIAMS NIH HHS P30 AR057216NIAMS NIH HHS P30 AR075049
6 · The paper itself

Abstract

backgroundThe circulating immune phenotype was defined in adults and young children with early atopic dermatitis (AD), but chronologic changes in the blood of infants and children with AD through adolescence have not been explored.

objectiveWe sought to compare immune activation and cytokine polarization in the blood of 0- to 5-year-old (n = 39), 6- to 11-year-old (n = 26), 12- to 17-year-old (n = 21) and 18-year-old or older (n = 43) patients with AD versus age-matched control subjects.

methodsFlow cytometry was used to measure IFN-γ, IL-9, IL-13, IL-17, and IL-22 cytokine levels in CD4

resultsAlthough CLA

conclusionsThe adult AD phenotype is achieved only in adulthood. Unique cytokine signatures characterizing individual pediatric endotypes might require age-specific therapies. Future longitudinal studies, comparing the profile of patients with cleared versus persistent pediatric AD, might define age-specific changes that predict AD clearance.

Indexed as

AdolescentAdultChildChild, PreschoolCytokinesDermatitis, AtopicFemaleHLA-DR AntigensHumansInfantInfant, NewbornMaleTh1 CellsTh2 CellsCytokinesHLA-DR AntigensAtopic dermatitiscutaneous lymphocyte antigenendotypesHLA-DRIFN-γIL-13IL-22inducible costimulator moleculeT cell

Identifiers

PMID31626841
PMCPMC6957229
OpenAlexW2980556682

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.