Evidence map›Paper›PMID 25227985›Full record

ArticleMucosal immunology2015

Dendritic cell-bound IgE functions to restrain allergic inflammation at mucosal sites.

B Platzer, K Baker, M P Vera, K Singer, M Panduro, W S Lexmond, D Turner, S O Vargas, J-P Kinet, D Maurer and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 70 citations in OpenAlex.

  1. Mouse Models of Food Allergies: Where Do They Take Us?Clinical reviews in allergy & immunology · 2026
    Review
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  12. World journal of gastroenterology · 2022
    Article
  13. Review
  14. The 10,000-Year Success Story of Wheat!Foods (Basel, Switzerland) · 2021
    Review
  15. Article
  16. 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

13 authors at 4 institutions in 2 countries.

B PlatzerDivision of Gastroenterology and Nutrition, Boston Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
K BakerDivision of Gastroenterology, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
M P VeraDivision of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
K SingerDivision of Gastroenterology and Nutrition, Boston Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
M PanduroDivision of Gastroenterology and Nutrition, Boston Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
W S LexmondDivision of Gastroenterology and Nutrition, Boston Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
D TurnerDepartment of Pathology, Harvard Medical School and Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
S O VargasDepartments of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
J-P KinetDepartment of Pathology, Harvard Medical School and Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
D MaurerDivision of Immunology, Allergy and Infectious Diseases, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
R M BaronDivision of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
R S BlumbergDivision of Gastroenterology, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
E FiebigerDivision of Gastroenterology and Nutrition, Boston Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
Harvard University · USBoston Children's Hospital · USBrigham and Women's Hospital · USMedical University of Vienna · AT

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI JONATHAN C KAGAN · 1986 to 2026
$32.4M
INTESTINAL TRANSCYTOSIS OF IGG IN ADULT LIFER01DK053056 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BLUMBERG, RICHARD S · 1997 to 2021
$10.6M
Molecular analysis of FCERI signaling and functionR37GM053950 · NIGMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KINET, JEAN-PIERRE M · 2004 to 2013
$4.2M
Role of NOS2 in Sepsis-Induced ARDSR01HL091957 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI BARON, REBECCA M · 2009 to 2013
$2.2M
Studies of Fc-epsilon-RI as an antigen presentation structure at mucosal surfacesR01AI075037 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI FIEBIGER, ELISABETH EDDA · 2009 to 2013
$2.0M
Impact of aryl hydrocarbon receptor ligand ingestion on gastrointestinal immunityK01DK093597 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI PLATZER, BARBARA · 2012 to 2015
$625k
Studies on Fc-epsilon-RI as an antigen presentation structure at mucosal surfacesR56AI075037 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI FIEBIGER, ELISABETH EDDA · 2008 to 2008
$423k
Intestinal Immune Regulation by IgG and FcRnR56DK053056 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BLUMBERG, RICHARD S · 2017 to 2017
$100k
CIHRNHLBI NIH HHS R01 HL091957NHLBI NIH HHS R01HL091957NIAID NIH HHS AI075037NIAID NIH HHS R01 AI075037NIAID NIH HHS R56 AI075037NIDDK NIH HHS DK53056NIDDK NIH HHS K01 DK093597NIDDK NIH HHS K01DK093597NIDDK NIH HHS P30 DK034854NIDDK NIH HHS P30DK034854NIDDK NIH HHS R01 DK053056NIDDK NIH HHS R56 DK053056NIGMS NIH HHS R37 GM053950NIGMS NIH HHS R37GM053950
6 · The paper itself

Abstract

Antigen-mediated cross-linking of Immunoglobulin E (IgE) bound to mast cells/basophils via FcɛRI, the high affinity IgE Fc-receptor, is a well-known trigger of allergy. In humans, but not mice, dendritic cells (DCs) also express FcɛRI that is constitutively occupied with IgE. In contrast to mast cells/basophils, the consequences of IgE/FcɛRI signals for DC function remain poorly understood. We show that humanized mice that express FcɛRI on DCs carry IgE like non-allergic humans and do not develop spontaneous allergies. Antigen-specific IgE/FcɛRI cross-linking fails to induce maturation or production of inflammatory mediators in human DCs and FcɛRI-humanized DCs. Furthermore, conferring expression of FcɛRI to DCs decreases the severity of food allergy and asthma in disease-relevant models suggesting anti-inflammatory IgE/FcɛRI signals. Consistent with the improved clinical parameters in vivo, antigen-specific IgE/FcɛRI cross-linking on papain or lipopolysaccharide-stimulated DCs inhibits the production of pro-inflammatory cytokines and chemokines. Migration assays confirm that the IgE-dependent decrease in cytokine production results in diminished recruitment of mast cell progenitors; providing a mechanistic explanation for the reduced mast cell-dependent allergic phenotype observed in FcɛRI-humanized mice. Our study demonstrates a novel immune regulatory function of IgE and proposes that DC-intrinsic IgE signals serve as a feedback mechanism to restrain allergic tissue inflammation.

Indexed as

AllergensAnimalsAsthmaCell Migration AssaysCell MovementCross-Linking ReagentsCytokinesDendritic CellsEgg HypersensitivityFeedback, PhysiologicalGene Expression RegulationHumansImmunity, MucosalImmunoglobulin ELipopolysaccharidesMast CellsAllergensCross-Linking ReagentsCytokinesFcepsilonRI alpha-chain, humanImmunoglobulin ELipopolysaccharidesOvalbuminPapainReceptors, IgE

Identifiers

PMID25227985
PMCPMC4363306
OpenAlexW2014013261

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.