Evidence map›Paper›PMID 20718816›Full record

ArticleClinical and translational science2010

A new class of human mast cell and peripheral blood basophil stabilizers that differentially control allergic mediator release.

Sarah K Norton, Anthony Dellinger, Zhiguo Zhou, Robert Lenk, Darren Macfarland, Becky Vonakis, Daniel Conrad, Christopher L Kepley

Open access · greenAbstract read
In one paragraph

Article in Clinical and translational science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. IL-33/ST2 axis promotes mast cell survival via BCLXL.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  13. From immunotoxicity to nanotherapy: the effects of nanomaterials on the immune system.Toxicological sciences : an official journal of the Society of Toxicology · 2014
    Review
  14. Engineered nanomaterial exposure and the risk of allergic disease.Current opinion in allergy and clinical immunology · 2014
    Review
  15. Twenty-first century mast cell stabilizers.British journal of pharmacology · 2013
    Review
  16. Review
  17. Functionalization of gadolinium metallofullerenes for detecting atherosclerotic plaque lesions by cardiovascular magnetic resonance.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2013
    Article
  18. Article
  19. Review
  20. Mediators released during human anaphylaxis.Current allergy and asthma reports · 2012
    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

8 authors at 2 institutions in 1 country.

Sarah K NortonDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, USA.
Anthony Dellinger
Zhiguo Zhou
Robert Lenk
Darren Macfarland
Becky Vonakis
Daniel Conrad
Christopher L Kepley
Luna Innovations (United States) · USVirginia Commonwealth University · US

Funding

Using Nanomaterials to Inhibit Mast Cell/Basophil-Associated DiseaseR01GM083274 · NIGMS · LUNA INNOVATIONS, INC. · PI KEPLEY, CHRIS L · 2008 to 2012
$1.5M
Prevention of Allergic Disease Using NanomaterialsR21ES015696 · NIEHS · LUNA INNOVATIONS, INC. · PI KEPLEY, CHRIS L · 2009 to 2010
$556k
Development of Novel Cholesteryl-Derivatized Endohedral Metallofullerenes for ImaR43HL087578 · NHLBI · LUNA INNOVATIONS, INC. · PI LENK, ROBERT · 2007 to 2008
$400k
NHLBI NIH HHS 1R43HL087578NHLBI NIH HHS R43 HL087578NIEHS NIH HHS 1 R21 ES015696NIEHS NIH HHS R21 ES015696NIGMS NIH HHS 1R01GM083274NIGMS NIH HHS R01 GM083274
6 · The paper itself

Abstract

Treatments for allergic disease block the effects of mediators released from activated mast cells and blood basophils. A panel of fullerene derivatives was synthesized and tested for their ability to preempt the release of allergic mediators in vitro and in vivo. The fullerene C(70)-tetraglycolic acid significantly inhibited degranulation and cytokine production from mast cells and basophils, while C(70)-tetrainositol blocked only cytokine production in mast cells and degranulation and cytokine production in basophils. The early phase of FcepsilonRI inhibition was dependent on the blunted release of intracellular calcium stores, elevations in reactive oxygen species, and several signaling molecules. Gene microarray studies further showed the two fullerene derivatives inhibited late phase responses in very different ways. C(70)-tetraglycolic acid was able to block mast cell-driven anaphylaxis in vivo, while C(70)-tetrainositol did not. No toxicity was observed with either compound. These findings demonstrate the biological effects of fullerenes critically depends on the moieties added to the carbon cage and suggest they act on different FcepsilonRI-specific molecules in mast cells and basophils. These next generation fullerene derivatives represent a new class of compounds that interfere with FcepsilonRI signaling pathways to stabilize mast cells and basophils. Thus, fullerene-based therapies may be a new approach for treating allergic diseases.

Indexed as

AnaphylaxisAnimalsBasophil Degranulation TestBasophilsDisease Models, AnimalDrug DesignFemaleFullerenesGene Expression ProfilingHumansHypersensitivityImmunomodulationIntracellular Signaling Peptides and ProteinsMast CellsMiceMice, Inbred C57BLFcRI protein, humanfullerene C70FullerenesIntracellular Signaling Peptides and Proteins

Identifiers

PMID20718816
PMCPMC5350695
OpenAlexW2115267404

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.