Evidence map›Paper›PMID 14563683›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2003

Discovery of a potent nanoparticle P-selectin antagonist with anti-inflammatory effects in allergic airway disease.

Alison E John, Nicholas W Lukacs, Aaron A Berlin, Aiyappa Palecanda, Robert F Bargatze, Lloyd M Stoolman, Jon O Nagy

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Recent Advances in Nanomaterials for Asthma Treatment.International journal of molecular sciences · 2022
    Review
  3. Review
  4. Article
  5. Review
  6. Microvascular targets for anti-fibrotic therapeutics.The Yale journal of biology and medicine · 2013
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Pulmonary applications and toxicity of engineered nanoparticles.American journal of physiology. Lung cellular and molecular physiology · 2008
    Review
  13. Review
  14. Review
  15. Nanomaterials, inflammation, and tissue engineering.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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.

Alison E JohnDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109-0602, USA.
Nicholas W Lukacs
Aaron A Berlin
Aiyappa Palecanda
Robert F Bargatze
Lloyd M Stoolman
Jon O Nagy
University of Michigan–Ann Arbor · USIncyte (United States) · US

Funding

RATIONAL DESIGN OF ADHESION BLOCKING ANTI-INFLAMMATORIESR44AI043789 · NIAID · TAKEDA VACCINES, INC. · PI BARGATZE, ROBERT FROST · 2000 to 2008
$8.1M
RATIONAL DESIGN OF ADHESION BLOCKING ANTIINFLAMMATORIESR43AI043789 · NIAID · LIGOCYTE PHARMACEUTICALS, INC. · PI NAGY, JON O · 1998 to 1998
–
NIAID NIH HHS R43 AI043789NIAID NIH HHS R44 AI043789
6 · The paper itself

Abstract

The severity of allergic asthma is dependent, in part, on the intensity of peribronchial inflammation. P-selectin is known to play a role in the development of allergen-induced peribronchial inflammation and airway hyperreactivity. Selective inhibitors of P-selectin-mediated leukocyte endothelial-cell interactions may therefore attenuate the inflammatory processes associated with allergic airway disease. Novel P-selectin inhibitors were created using a polyvalent polymer nanoparticle capable of displaying multiple synthetic, low molecular weight ligands. By assembling a particle that presents an array of groups, which as monomers interact with only low affinity, we created a construct that binds extremely efficiently to P-selectin. The ligands acted as mimetics of the key binding elements responsible for the high-avidity adhesion of P-selectin to the physiologic ligand, PSGL-1. The inhibitors were initially evaluated using an in vitro shear assay system in which interactions between circulating cells and P-selectin-coated capillary tubes were measured. The nanoparticles were shown to preferentially bind to selectins expressed on activated endothelial cells. We subsequently demonstrated that nanoparticles displaying P-selectin blocking arrays were functionally active in vivo, significantly reducing allergen-induced airway hyperreactivity and peribronchial eosinophilic inflammation in a murine model of asthma.

Indexed as

AllergensAnimalsAnti-Inflammatory AgentsAsthmaBiopolymersBronchial HyperreactivityBronchitisCell AdhesionLeukocyte RollingLeukocytesLigandsLipidsLungMembrane GlycoproteinsMiceMice, KnockoutAllergensAnti-Inflammatory AgentsBiopolymersLigandsLipidsMembrane GlycoproteinsP-SelectinP-selectin ligand protein

Identifiers

PMID14563683
PMCPMC2839900
OpenAlexW2143147838

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.