Evidence map›Paper›PMID 28490801›Full record

ArticleScientific reports2017

Dendritic cells provide a therapeutic target for synthetic small molecule analogues of the parasitic worm product, ES-62.

Felicity E Lumb, James Doonan, Kara S Bell, Miguel A Pineda, Marlene Corbet, Colin J Suckling, Margaret M Harnett, William Harnett

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Mining Helminths for Novel Therapeutics.Trends in molecular medicine · 2021
    Review
  6. Review
  7. Frontiers in immunology · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. 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.

Felicity E LumbStrathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK.
James DoonanStrathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK.
Kara S BellStrathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK.
Miguel A PinedaInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Marlene CorbetInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Colin J SucklingDepartment of Pure & Applied Chemistry, University of Strathclyde, Glasgow, UK.
Margaret M HarnettInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK. Margaret.Harnett@glasgow.ac.uk.ORCID 0000-0001-5740-3028
William HarnettStrathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK. w.harnett@strath.ac.uk.
University of Strathclyde · GBUniversity of Glasgow · GB

Funding

Medical Research Council MC_PC_13063Wellcome Trust
6 · The paper itself

Abstract

ES-62, a glycoprotein secreted by the parasitic filarial nematode Acanthocheilonema viteae, subverts host immune responses towards anti-inflammatory phenotypes by virtue of covalently attached phosphorylcholine (PC). The PC dictates that ES-62 exhibits protection in murine models of inflammatory disease and hence a library of drug-like PC-based small molecule analogues (SMAs) was synthesised. Four sulfone-containing SMAs termed 11a, 11e, 11i and 12b were found to reduce mouse bone marrow-derived dendritic cell (DC) pathogen-associated molecular pattern (PAMP)-induced pro-inflammatory cytokine production, inhibit NF-κB p65 activation, and suppress LPS-induced up-regulation of CD40 and CD86. Active SMAs also resulted in a DC phenotype that exhibited reduced capacity to prime antigen (Ag)-specific IFN-γ production during co-culture with naïve transgenic TCR DO.11.10 T cells in vitro and reduced their ability, following adoptive transfer, to prime the expansion of Ag-specific T lymphocytes, specifically T

Indexed as

AnimalsAnthelminticsArthritis, ExperimentalBone Marrow CellsCytokinesDendritic CellsHelminth ProteinsHelminthsInterleukin-17Interleukin-1betaMice, Inbred BALB CMice, Inbred C57BLSmall Molecule LibrariesTh17 CellsTh1 CellsAnthelminticsCytokinesES-62 protein, Acanthocheilonema viteaeHelminth ProteinsInterleukin-17Interleukin-1betaSmall Molecule Libraries

Identifiers

PMID28490801
PMCPMC5431997
OpenAlexW2611605104

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.