Evidence map›Paper›PMID 21537081›Full record

ArticleThe Journal of clinical investigation2011

Epicutaneous challenge of orally immunized mice redirects antigen-specific gut-homing T cells to the skin.

Michiko K Oyoshi, Abdallah Elkhal, Jordan E Scott, Marc-Andre Wurbel, Jason L Hornick, James J Campbell, Raif S Geha

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Skin Aging and the Upcoming Role of Ferroptosis in Geroscience.International journal of molecular sciences · 2024
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Biological therapies for eosinophilic gastrointestinal diseases.The Journal of allergy and clinical immunology · 2018
    Review
  12. Article
  13. Role of neural barriers in the pathogenesis and outcome ofExperimental and therapeutic medicine · 2017
    Article
  14. Review
  15. Article
  16. Article
  17. Commensal bacteria and cutaneous immunity.Seminars in immunopathology · 2015
    Review
  18. Article
  19. Article
  20. Review
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

7 authors at 2 institutions in 1 country.

Michiko K OyoshiDivision of Immunology, Children's Hospital, Boston, Massachusetts 02115, USA.
Abdallah Elkhal
Jordan E Scott
Marc-Andre Wurbel
Jason L Hornick
James J Campbell
Raif S Geha
Boston Children's Hospital · USBrigham 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
The Role of CCR4 in Skin Lymphocyte Homing and ImmunityR01AI046784 · NIAID · CHILDREN'S HOSPITAL BOSTON · PI CAMPBELL, JAMES J. · 2001 to 2010
$3.2M
CCR4 IN SKIN LYMPHOCYTE HOMING AND IMMUNITYR21AI046784 · NIAID · CHILDREN'S HOSPITAL BOSTON · PI CAMPBELL, JAMES J. · 2000 to 2000
$218k
NIAID NIH HHS AI-046784NIAID NIH HHS N01 AI040030NIAID NIH HHS R01 AI046784NIAID NIH HHS R21 AI046784NIAMS NIH HHS AR-047417NIAMS NIH HHS R01 AR047417
6 · The paper itself

Abstract

Patients with atopic dermatitis (AD) often suffer from food allergy and develop flares upon skin contact with food allergens. However, it is unclear whether T cells sensitized to allergens in the gut promote this skin inflammation. To address this question, we orally immunized WT mice and mice lacking the skin-homing chemokine receptor Ccr4 (Ccr4-/- mice) with OVA and then challenged them epicutaneously with antigen. Allergic skin inflammation developed in the WT mice but not in the mutants and was characterized by epidermal thickening, dermal infiltration by eosinophils and CD4+ T cells, and upregulation of Th2 cytokines. T cells purified from mesenteric lymph nodes (MLNs) of orally immunized WT mice transferred allergic skin inflammation to naive recipients cutaneously challenged with antigen, but this effect was lost in T cells purified from Ccr4-/- mice. In addition, the ability of adoptively transferred OVA-activated T cells to home to the skin following cutaneous OVA challenge was ablated in mice that lacked lymph nodes. These results indicate that cutaneous exposure to food antigens can reprogram gut-homing effector T cells in LNs to express skin-homing receptors, eliciting skin lesions upon food allergen contact in orally sensitized AD patients.

Indexed as

Chemotaxis, LeukocyteImmunizationAdministration, CutaneousAdministration, OralAdoptive TransferAllergensAnimalsCholera ToxinDermatitis, Allergic ContactFood HypersensitivityIntegrinsMiceMice, Inbred BALB CMice, Inbred C57BLOvalbuminReceptors, CCR4AllergensCcr4 protein, mouseCholera Toxincysteine-rich fibroblast growth factor receptorintegrin alpha4beta7IntegrinsOvalbuminReceptors, CCR4Receptors, Fibroblast Growth FactorReceptors, Lymphocyte HomingSialoglycoproteins

Identifiers

PMID21537081
PMCPMC3105371
OpenAlexW2109015683

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.