Evidence map›Paper›PMID 19075398›Full record

ArticleThe Journal of clinical investigation2009

IL-21R is essential for epicutaneous sensitization and allergic skin inflammation in humans and mice.

Haoli Jin, Michiko K Oyoshi, Yi Le, Teresa Bianchi, Suresh Koduru, Clinton B Mathias, Lalit Kumar, Séverine Le Bras, Deborah Young, Mary Collins and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Probing the Skin-Brain Axis: New Vistas Using Mouse Models.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. IL-22 promotes allergic airway inflammation in epicutaneously sensitized mice.The Journal of allergy and clinical immunology · 2019
    Article
  17. Article
  18. Review
  19. Article
  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

17 authors at 4 institutions in 2 countries.

Haoli JinDivision of Immunology, Children's Hospital and Harvard Medical SChool, Boston, MA 02115, USA.
Michiko K Oyoshi
Yi Le
Teresa Bianchi
Suresh Koduru
Clinton B Mathias
Lalit Kumar
Séverine Le Bras
Deborah Young
Mary Collins
Michael J Grusby
Joerg Wenzel
Thomas Bieber
Marianne Boes
Leslie E Silberstein
Hans C Oettgen
Raif S Geha
Boston Children's Hospital · USHarvard University · USUniversity of Bonn · DEBrigham and Women's Hospital · US

Funding

IMMUNOLOGIC MECHANISMS OF ATOPIC DERMATITISR01AR047417 · NIAMS · CHILDREN'S HOSPITAL BOSTON · PI GEHA, RAIF SALIM · 2001 to 2011
$3.5M
Class II MHC & CD1d antigen presentation pathways in skin-derived dendritic cellsR01AR052810 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI FUHLBRIGGE, ROBERT C · 2007 to 2011
$1.0M
NIAID NIH HHS AI-05447NIAID NIH HHS N01 AI040030NIAMS NIH HHS AR-047417NIAMS NIH HHS AR-052810NIAMS NIH HHS R01 AR047417NIAMS NIH HHS R01 AR052810PHS HHS HHSN26620040029C
6 · The paper itself

Abstract

Atopic dermatitis (AD) is a common allergic inflammatory skin disease caused by a combination of intense pruritus, scratching, and epicutaneous (e.c.) sensitization with allergens. To explore the roles of IL-21 and IL-21 receptor (IL-21R) in AD, we examined skin lesions from patients with AD and used a mouse model of allergic skin inflammation. IL-21 and IL-21R expression was upregulated in acute skin lesions of AD patients and in mouse skin subjected to tape stripping, a surrogate for scratching. The importance of this finding was highlighted by the fact that both Il21r-/- mice and WT mice treated with soluble IL-21R-IgG2aFc fusion protein failed to develop skin inflammation after e.c. sensitization of tape-stripped skin. Adoptively transferred OVA-specific WT CD4+ T cells accumulated poorly in draining LNs (DLNs) of e.c. sensitized Il21r-/- mice. This was likely caused by both DC-intrinsic and nonintrinsic effects, because trafficking of skin DCs to DLNs was defective in Il21r-/- mice and, to a lesser extent, in WT mice reconstituted with Il21r-/- BM. More insight into this defect was provided by the observation that skin DCs from tape-stripped WT mice, but not Il21r-/- mice, upregulated CCR7 and migrated toward CCR7 ligands. Treatment of epidermal and dermal cells with IL-21 activated MMP2, which has been implicated in trafficking of skin DCs. These results suggest an important role for IL-21R in the mobilization of skin DCs to DLNs and the subsequent allergic response to e.c. introduced antigen.

Indexed as

Dermatitis, AtopicImmunizationSkinAdoptive TransferAnimalsCells, CulturedDisease Models, AnimalEnzyme ActivationFemaleHumansInflammationInterleukin-21InterleukinsMatrix Metalloproteinase 2MiceMice, Inbred BALB CInterleukin-21InterleukinsMatrix Metalloproteinase 2OvalbuminReceptors, CCR7Receptors, Interleukin-21Recombinant Fusion Proteins

Identifiers

PMID19075398
PMCPMC2613448
OpenAlexW2032596171

What OpenQuestion holds

Textmetadata
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.