Evidence map›Paper›PMID 22887873›Full record

ArticleEMBO molecular medicine2012

Preventing acute gut wall damage in infectious diarrhoeas with glycosylated dendrimers.

Ian Teo, Steve M Toms, Benoit Marteyn, Teresa S Barata, Peter Simpson, Karen A Johnston, Pamela Schnupf, Andrea Puhar, Tracey Bell, Chris Tang and 5 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2012. 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
2.7field-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

15 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
    Review
  3. Review
  4. Nanomaterials and Their Impact on the Immune System.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Nanoparticles and direct immunosuppression.Experimental biology and medicine (Maywood, N.J.) · 2016
    Review
  11. Article
  12. Article
  13. Review
  14. Applications of nanotechnology for immunology.Nature reviews. Immunology · 2013
    Review
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Ian TeoDepartments of Medicine, Infectious Diseases & Immunity, Imperial College London, Hammersmith Hospital, UK.
Steve M Toms
Benoit Marteyn
Teresa S Barata
Peter Simpson
Karen A Johnston
Pamela Schnupf
Andrea Puhar
Tracey Bell
Chris Tang
Mire Zloh
Steve Matthews
Phillip M Rendle
Philippe J Sansonetti
Sunil Shaunak
Imperial College London · GBInserm · FRHammersmith Hospital · GBInstitut Pasteur · FRUniversity College London · GB

Funding

Dendrimer aminosaccharide drug to modulate inflammatory responses in shigellosisU01AI075351 · NIAID · IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE · PI SHAUNAK, SUNIL · 2007 to 2008
$663k
NIAID NIH HHS U01 5U01AI075351-02NIAID NIH HHS U01 AI075351
6 · The paper itself

Abstract

Intestinal pathogens use the host's excessive inflammatory cytokine response, designed to eliminate dangerous bacteria, to disrupt epithelial gut wall integrity and promote their tissue invasion. We sought to develop a non-antibiotic-based approach to prevent this injury. Molecular docking studies suggested that glycosylated dendrimers block the TLR4-MD-2-LPS complex, and a 13.6 kDa polyamidoamine (PAMAM) dendrimer glucosamine (DG) reduced the induction of human monocyte interleukin (IL)-6 by Gram-negative bacteria. In a rabbit model of shigellosis, PAMAM-DG prevented epithelial gut wall damage and intestinal villous destruction, reduced local IL-6 and IL-8 expression, and minimized bacterial invasion. Computational modelling studies identified a 3.3 kDa polypropyletherimine (PETIM)-DG as the smallest likely bioactive molecule. In human monocytes, high purity PETIM-DG potently inhibited Shigella Lipid A-induced IL-6 expression. In rabbits, PETIM-DG prevented Shigella-induced epithelial gut wall damage, reduced local IL-6 and IL-8 expression, and minimized bacterial invasion. There was no change in β-defensin, IL-10, interferon-β, transforming growth factor-β, CD3 or FoxP3 expression. Small and orally delivered DG could be useful for preventing gut wall tissue damage in a wide spectrum of infectious diarrhoeal diseases.

Indexed as

Interleukin-6 InhibitorsAdministration, OralAnimalsBacterial TranslocationDendrimersDiarrheaDisease Models, AnimalDysentery, BacillaryGastrointestinal AgentsGastrointestinal TractGlucosamineImmunologic FactorsInterleukin-8RabbitsShigellaDendrimersGastrointestinal AgentsGlucosamineImmunologic FactorsInterleukin-6 InhibitorsInterleukin-8polypropyletherimine dendrimer glucosamine

Identifiers

PMID22887873
PMCPMC3491821
OpenAlexW2144453447

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.