Evidence map›Paper›PMID 21576952›Full record

ReviewCurrent problems in dermatology2011

The role of regulatory T cells in atopic dermatitis.

Rachana Agrawal, Julia A Wisniewski, Judith A Woodfolk

Open access · greenAbstract readReview
In one paragraph

Review in Current problems in dermatology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
22.7field-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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. MicroRNAs in atopic dermatitis: A systematic review.Journal of cellular and molecular medicine · 2020
    Pooled it
  3. Article
  4. Article
  5. The Role of MicroRNA in the Pathogenesis of Atopic Dermatitis.International journal of molecular sciences · 2025
    Review
  6. Immunomodulating Effects of Heat-KilledVeterinary sciences · 2025
    Article
  7. Review
  8. Review
  9. Review
  10. Neutrophils in Atopic Dermatitis.Clinical reviews in allergy & immunology · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Rachana Agrawal
Julia A Wisniewski
Judith A Woodfolk
University of Virginia Health System · US

Funding

Mechanisms of airways pH deviation in asthma and chronic coughU19AI070364 · NIAID · UNIVERSITY OF VIRGINIA · PI HUNT, JOHN F · 2006 to 2010
$6.0M
Immune Response to Cat: Regulatory and Effector T CellsR01AI052196 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI WOODFOLK, JUDITH A · 2004 to 2013
$2.9M
NIAID NIH HHS AI-052196NIAID NIH HHS AI-070364NIAID NIH HHS R01 AI052196NIAID NIH HHS U19 AI070364
6 · The paper itself

Abstract

Regulatory T (T(reg)) cells play a pivotal role in immune suppression and are integral to the control of allergic responses. The chronic inflammatory skin condition atopic dermatitis (AD) is severest in patients who are sensitized to allergens from diverse sources including foods, pollens and animal danders, as well as skin-colonizing organisms. These individuals typically present with eczematous skin eruptions in early childhood, and evolution of the disease is thought to reflect an underlying dysregulated T-cell response to allergens that manifests as a Th2 response. Studying T(reg) cells in the context of AD from infancy into adulthood could yield insight into their role in disease pathogenesis and reveal new strategies for exploiting these cells for therapeutic purposes. Such studies are challenging in humans owing to the heterogeneous nature of T(reg) cells, lack of a reliable surface marker, and the paucity of knowledge surrounding the emergence of specialized T cells in early life. Moreover, the blurred distinction between activated effector T cells and T(reg) cells further complicates studies in the context of inflammatory disorders such as AD. There is emerging evidence to suggest that T(reg) cells can convert to Th2 cells and that this pathway is bidirectional. This phenomenon may be a double-edged sword with important implications not only for subverting T(reg) cells in disease, but also for potential treatments designed to amplify these cells in order to suppress the allergic inflammatory cascade in AD.

Indexed as

AllergensBiomarkersDermatitis, AtopicForkhead Transcription FactorsHumansHypersensitivityInflammation MediatorsModels, ImmunologicalTh2 CellsT-Lymphocytes, RegulatoryAllergensBiomarkersForkhead Transcription FactorsFOXP3 protein, humanInflammation Mediators

Identifiers

PMID21576952
PMCPMC4547455
OpenAlexW1502240335

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.