Evidence map›Paper›PMID 28745029›Full record

ArticleAllergy2018

ADAM10 and Notch1 on murine dendritic cells control the development of type 2 immunity and IgE production.

S R Damle, R K Martin, C L Cockburn, J C Lownik, J A Carlyon, A D Smith, D H Conrad

Open access · greenAbstract read
In one paragraph

Article in Allergy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Type 2 immunity in allergic diseases.Cellular & molecular immunology · 2025
    Review
  3. Review
  4. Article
  5. Genes · 2022
    Article
  6. Article
  7. Article
  8. TAO-kinase 3 governs the terminal differentiation of NOTCH2-dependent splenic conventional dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Review
  10. Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  11. Loci Associated With Antibody Response in Feral Swine (Frontiers in veterinary science · 2020
    Article
  12. Cell-autonomous FLT3L shedding via ADAM10 mediates conventional dendritic cell development in mouse spleen.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. 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

7 authors at 2 institutions in 1 country.

S R DamleDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
R K MartinDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
C L CockburnDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
J C LownikCenter for Clinical and Translational Research, Virginia Commonwealth University, Richmond, VA, USA.
J A CarlyonDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
A D SmithUnited States Department of Agriculture, Diet, Genomics, and Immunology Laboratory, Agricultural Research Service, Beltsville Human Nutrition Research Center, Beltsville, MD, USA.
D H ConradDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.ORCID http://orcid.org/0000-0002-4791-2694
Virginia Commonwealth University · USAgricultural Research Service · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
Virginia Commonwealth University IRADCAK12GM093857 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIEL C BULLARD, John J Ryan · 2010 to 2026
$7.0M
STRUCTURE/FUNCTION OF THE LYMPHOCYTE FCE RECEPTORR01AI018697 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI MARTIN, REBECCA KELLEY · 1985 to 2018
$6.5M
VCU Neuroscience Center Core GrantP30NS047463 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI POVLISHOCK, JOHN T · 2003 to 2013
$5.0M
NCI NIH HHS P30 CA016059NIAID NIH HHS R01 AI018697NIGMS NIH HHS K12 GM093857NINDS NIH HHS P30 NS047463
6 · The paper itself

Abstract

backgroundAllergy and allergic asthma are significant health burdens in developed countries and are increasing in prevalence. Dendritic cells (DCs) initiate immune responses to common aeroallergens, and ADAM10 has been demonstrated to be important for the development of adaptive responses. This study's objective was to understand the role of ADAM10 on DCs in the development of allergic and anaphylactic responses.

methodsIn this study, we used mouse models of allergic airway inflammation (house dust mice and Alternaria alternata) and OVA-induced models of active anaphylaxis to determine the DC-specific function of ADAM10 and Notch signaling. To examine T

resultsMice, which have ADAM10 deleted from DCs, have dramatic reductions in IgE production and do not develop significant T

conclusionsTargeting ADAM10 and Notch1 on DCs represent a novel strategy for modulating T

Indexed as

ADAM10 ProteinAmyloid Precursor Protein SecretasesAnaphylaxisAnimalsBiomarkersDendritic CellsDisease Models, AnimalGene ExpressionHypersensitivityImmunoglobulin EImmunoglobulin GInterleukin-6Kruppel-Like Factor 4Kruppel-Like Transcription FactorsMembrane ProteinsMiceADAM10 ProteinAdam10 protein, mouseAmyloid Precursor Protein SecretasesBiomarkersImmunoglobulin EImmunoglobulin GInterleukin-6Kruppel-Like Factor 4Kruppel-Like Transcription FactorsMembrane ProteinsNotch1 protein, mouseReceptor, Notch1animal modelsasthmadendritic cellsIgE

Identifiers

PMID28745029
PMCPMC5739941
OpenAlexW2738786339

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.