Evidence map›Paper›PMID 26242300›Full record

ArticleThe Journal of allergy and clinical immunology2015

Early pediatric atopic dermatitis shows only a cutaneous lymphocyte antigen (CLA)(+) TH2/TH1 cell imbalance, whereas adults acquire CLA(+) TH22/TC22 cell subsets.

Tali Czarnowicki, Hitokazu Esaki, Juana Gonzalez, Dana Malajian, Avner Shemer, Shinji Noda, Sreya Talasila, Adam Berry, Jayla Gray, Lauren Becker and 7 more

Registry-linked trialOpen access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of allergy and clinical immunology, 2015. 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 73 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 2 pooled it
25.8field-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

73 citing papers in PubMed, 2 syntheses or guidelines pooled it, 202 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Circulating CLAJID innovations : skin science from molecules to population health · 2025
    Review
  13. Cytotoxic T Cells: Kill, Memorize, and Mask to Maintain Immune Homeostasis.International journal of molecular sciences · 2025
    Review
  14. Review
  15. Allergen-specific circulating CLAFrontiers in immunology · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. Deficiency of peripheral CLAArthritis research & therapy · 2024
    Article
  20. Review

13 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

17 authors at 4 institutions in 1 country.

Tali CzarnowickiLaboratory for Investigative Dermatology, Rockefeller University, New York, NY.
Hitokazu EsakiLaboratory for Investigative Dermatology, Rockefeller University, New York, NY; Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY.
Juana GonzalezTranslational Technology Core Laboratory, Rockefeller University, New York, NY.
Dana MalajianLaboratory for Investigative Dermatology, Rockefeller University, New York, NY; Columbia University College of Physicians and Surgeons, New York, NY.
Avner ShemerDepartment of Dermatology, Tel-Hashomer Hospital, Tel Aviv, Israel.
Shinji NodaLaboratory for Investigative Dermatology, Rockefeller University, New York, NY.
Sreya TalasilaDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Adam BerryDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Jayla GrayDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Lauren BeckerDepartments of Dermatology and Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Yeriel EstradaDepartment of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY.
Hui XuDepartment of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY.
Xiuzhong ZhengLaboratory for Investigative Dermatology, Rockefeller University, New York, NY.
Mayte Suárez-FariñasDepartment of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY; Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY; Icahn Institute for Genomics and Multiscale Biology, 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-YasskyLaboratory for Investigative Dermatology, Rockefeller University, New York, NY; Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY. Electronic address: Emma.Guttman@mountsinai.org.
Rockefeller University · USNorthwestern University · USIcahn School of Medicine at Mount Sinai · USColumbia 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
TRANSFORMING TRANSLATIONAL SCIENCE AND EDUCATION TO BENEFIT HUMAN HEALTHUL1RR024143 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2006 to 2011
$49.1M
Transforming Translational Science and Education to Benefit Human HealthUL1TR000043 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2012 to 2015
$26.8M
The Role of Keratinocytes as Independent ThermosensorsP30AR057216 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PEREZ WHITE, BETHANY E · 2009 to 2018
$6.0M
NCATS NIH HHS UL1TR0000NCATS NIH HHS UL1 TR000043NCATS NIH HHS UL1 TR001422NCRR NIH HHS 5UL1RR024143-02NCRR NIH HHS UL1 RR024143NIAMS NIH HHS P30 AR057216NIAMS NIH HHS P30AR057216
6 · The paper itself

Abstract

backgroundIdentifying differences and similarities between cutaneous lymphocyte antigen (CLA)(+) polarized T-cell subsets in children versus adults with atopic dermatitis (AD) is critical for directing new treatments toward children.

objectiveWe sought to compare activation markers and frequencies of skin-homing (CLA(+)) versus systemic (CLA(-)) "polar" CD4 and CD8 T-cell subsets in patients with early pediatric AD, adults with AD, and control subjects.

methodsFlow cytometry was used to measure CD69/inducible costimulator/HLA-DR frequency in memory cell subsets, as well as IFN-γ, IL-13, IL-9, IL-17, and IL-22 cytokines, defining TH1/cytotoxic T (TC) 1, TH2/TC2, TH9/TC9, TH17/TC17, and TH22/TC22 populations in CD4 and CD8 cells, respectively. We compared peripheral blood from 19 children less than 5 years old and 42 adults with well-characterized moderate-to-severe AD, as well as age-matched control subjects (17 children and 25 adults).

resultsSelective inducible costimulator activation (P < .001) was seen in children. CLA(+) TH2 T cells were markedly expanded in both children and adults with AD compared with those in control subjects, but decreases in CLA(+) TH1 T-cell numbers were greater in children with AD (17% vs 7.4%, P = .007). Unlike in adults, no imbalances were detected in CLA(-) T cells from pediatric patients with AD nor were there altered frequencies of TH22 T cells within the CLA(+) or CLA(-) compartments. Adults with AD had increased frequencies of IL-22-producing CD4 and CD8 T cells within the skin-homing population, compared with controls (9.5% vs 4.5% and 8.6% vs 2.4%, respectively; P < .001), as well as increased HLA-DR activation (P < .01).

conclusionsThese data suggest that TH2 activation within skin-homing T cells might drive AD in children and that reduced counterregulation by TH1 T cells might contribute to excess TH2 activation. TH22 "spreading" of AD is not seen in young children and might be influenced by immune development, disease chronicity, or recurrent skin infections.

Indexed as

AdolescentAdultAgedAntigens, Differentiation, T-LymphocyteCell SeparationChildChild, PreschoolDermatitis, AtopicFlow CytometryHumansImmunophenotypingInfantInterleukin-22InterleukinsLymphocyte ActivationMembrane GlycoproteinsAntigens, Differentiation, T-LymphocyteCTAGE1 protein, humanInterleukin-22InterleukinsMembrane GlycoproteinsAtopic dermatitisCD69cutaneous lymphocyte antigenHLA-DRIFN-γIL-13IL-22inducible costimulatorT cell

Identifiers

PMID26242300
PMCPMC4946641
OpenAlexW2040342875

What OpenQuestion holds

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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.