Evidence map›Paper›PMID 21285515›Full record

ArticleThe Journal of clinical investigation2011

Particulate allergens potentiate allergic asthma in mice through sustained IgE-mediated mast cell activation.

Cong Jin, Christopher P Shelburne, Guojie Li, Erin N Potts, Kristina J Riebe, Gregory D Sempowski, W Michael Foster, Soman N Abraham

Expression of concernErratum issuedOpen 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. It carries an expression of concern. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Impact of PMEnvironmental science and pollution research international · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. PM2.5 in Beijing - temporal pattern and its association with influenza.Environmental health : a global access science source · 2014
    Article
  15. Review
  16. Nanotoxicity overview: nano-threat to susceptible populations.International journal of molecular sciences · 2014
    Review
  17. Article
  18. Article
  19. Tetraspanins in mast cells.Frontiers in immunology · 2012
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 3 countries.

Cong JinDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27514, USA.
Christopher P Shelburne
Guojie Li
Erin N Potts
Kristina J Riebe
Gregory D Sempowski
W Michael Foster
Soman N Abraham
Duke University · USNational University of Singapore · SG

Funding

Yessinia autotransporters (Yaps): Structure, function, and host responseU54AI057157 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GOLDMAN, WILLIAM E · 2003 to 2013
$91.4M
Regional Biocontainment Laboratory (RBL)UC6AI058607 · NIAID · DUKE UNIVERSITY · PI WILLIAMS, R SANDERS · 2003 to 2005
$16.3M
Duke University Center for Translational ResearchP30AI051445 · NIAID · DUKE UNIVERSITY · PI FROTHINGHAM, RICHARD · 2002 to 2006
$8.1M
Surfactant Protein-A Regulation of Innate Immunityin AsthmaP01AI081672 · NIAID · DUKE UNIVERSITY · PI SUNDY, JOHN S · 2009 to 2013
$7.4M
LIGAND RECEPTOR INTERACTIONS IN UTISR37DK050814 · NIDDK · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 1999 to 2008
$2.7M
Modulation of Bladder cAMP to combat UTI'sR01DK077159 · NIDDK · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 2007 to 2011
$1.7M
Dependency of O-3 Induced Lung Mucus Hypersecretion on NQ01R01ES016347 · NIEHS · DUKE UNIVERSITY · PI FOSTER, W MICHAEL · 2008 to 2010
$1.0M
Development of Efficacious Vaccine Against UTI'sR21DK077307 · NIDDK · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 2008 to 2010
$529k
Small cationic antimicrobial peptides: activators of innate & adaptive immunityR56AI074751 · NIAID · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 2008 to 2008
$390k
Proteome Mining in Caveolae of the Bladder EpitheliumR21AI056101 · NIAID · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 2004 to 2005
$308k
2020 Antibody Biology & Engineering Gordon Research Conference and Gordon Research SeminarR13AI150021 · NIAID · GORDON RESEARCH CONFERENCES · PI LEUSEN, JEANETTE · 2020 to 2020
$8k
LIGAND RECEPTOR INTERACTIONS IN UTISR01DK050814 · NIDDK · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 1995 to 1998
–
NIAID NIH HHS AI056101NIAID NIH HHS AI074751NIAID NIH HHS AI081672NIAID NIH HHS AI150021NIAID NIH HHS P01 AI081672NIAID NIH HHS P30 AI051445NIAID NIH HHS P30-AI051445NIAID NIH HHS R13 AI150021NIAID NIH HHS R21 AI056101NIAID NIH HHS R56 AI074751NIAID NIH HHS U54 AI057157NIAID NIH HHS U54-AI057157NIAID NIH HHS UC6 AI058607NIAID NIH HHS UC6-AI058607NIDDK NIH HHS DK050814NIDDK NIH HHS DK077159NIDDK NIH HHS DK077307NIDDK NIH HHS R01 DK077159NIDDK NIH HHS R21 DK077307NIDDK NIH HHS R37 DK050814NIEHS NIH HHS ES016347NIEHS NIH HHS R01 ES016347
6 · The paper itself

Abstract

Allergic asthma is characterized by airway hyperresponsiveness, inflammation, and a cellular infiltrate dominated by eosinophils. Numerous epidemiological studies have related the exacerbation of allergic asthma with an increase in ambient inhalable particulate matter from air pollutants. This is because inhalable particles efficiently deliver airborne allergens deep into the airways, where they can aggravate allergic asthma symptoms. However, the cellular mechanisms by which inhalable particulate allergens (pAgs) potentiate asthmatic symptoms remain unknown, in part because most in vivo and in vitro studies exploring the pathogenesis of allergic asthma use soluble allergens (sAgs). Using a mouse model of allergic asthma, we found that, compared with their sAg counterparts, pAgs triggered markedly heightened airway hyperresponsiveness and pulmonary eosinophilia in allergen-sensitized mice. Mast cells (MCs) were implicated in this divergent response, as the differences in airway inflammatory responses provoked by the physical nature of the allergens were attenuated in MC-deficient mice. The pAgs were found to mediate MC-dependent responses by enhancing retention of pAg/IgE/FcεRI complexes within lipid raft–enriched, CD63(+) endocytic compartments, which prolonged IgE/FcεRI-initiated signaling and resulted in heightened cytokine responses. These results reveal how the physical attributes of allergens can co-opt MC endocytic circuitry and signaling responses to aggravate pathological responses of allergic asthma in mice.

Indexed as

Gene Expression RegulationAir PollutantsAllergensAnimalsAntigens, CDAsthmaBronchial HyperreactivityDisease Models, AnimalEndocytosisHypersensitivityImmunoglobulin EInflammationLipidsMaleMast CellsMembrane MicrodomainsAir PollutantsAllergensAntigens, CDCd63 protein, mouseImmunoglobulin ELipidsPlatelet Membrane GlycoproteinsTetraspanin 30

Identifiers

PMID21285515
PMCPMC3049384
OpenAlexW1977445502

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.