Evidence map›Paper›PMID 19436711›Full record

ArticlePLoS pathogens2009

Natural killer T cells activated by a lipopeptidophosphoglycan from Entamoeba histolytica are critically important to control amebic liver abscess.

Hannelore Lotter, Nestor González-Roldán, Buko Lindner, Florian Winau, Armando Isibasi, Martha Moreno-Lafont, Artur J Ulmer, Otto Holst, Egbert Tannich, Thomas Jacobs

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Genetic and immune determinants ofProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Genetic and immune determinants ofbioRxiv : the preprint server for biology · 2023
    Article
  9. Sex Difference in Amebiasis.Current topics in microbiology and immunology · 2023
    Article
  10. Frontiers in immunology · 2023
    Review
  11. Membranes · 2022
    Review
  12. Review
  13. Article
  14. NKT Cells Contribute to the Control of Microbial Infections.Frontiers in cellular and infection microbiology · 2021
    Review
  15. Article
  16. Antileishmanial Effects of SyntheticAntimicrobial agents and chemotherapy · 2020
    Article
  17. Article
  18. Article
  19. Review
  20. 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

10 authors at 5 institutions in 3 countries.

Hannelore LotterBernhard-Nocht-Institute for Tropical Medicine, Hamburg, Germany. lotter@bni-hamburg.de
Nestor González-Roldán
Buko Lindner
Florian Winau
Armando Isibasi
Martha Moreno-Lafont
Artur J Ulmer
Otto Holst
Egbert Tannich
Thomas Jacobs
Bernhard Nocht Institute for Tropical Medicine · DEResearch Center Borstel - Leibniz Lung Center · DEMexican Social Security Institute · MXHarvard University · USInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate immune response is supposed to play an essential role in the control of amebic liver abscess (ALA), a severe form of invasive amoebiasis due to infection with the protozoan parasite Entamoeba histolytica. In a mouse model for the disease, we previously demonstrated that Jalpha18(-/-) mice, lacking invariant natural killer T (iNKT) cells, suffer from more severe abscess development. Here we show that the specific activation of iNKT cells using alpha-galactosylceramide (alpha-GalCer) induces a significant reduction in the sizes of ALA lesions, whereas CD1d(-/-) mice develop more severe abscesses. We identified a lipopeptidophosphoglycan from E. histolytica membranes (EhLPPG) as a possible natural NKT cell ligand and show that the purified phosphoinositol (PI) moiety of this molecule induces protective IFN-gamma but not IL-4 production in NKT cells. The main component of EhLPPG responsible for NKT cell activation is a diacylated PI, (1-O-[(28:0)-lyso-glycero-3-phosphatidyl-]2-O-(C16:0)-Ins). IFN-gamma production by NKT cells requires the presence of CD1d and simultaneously TLR receptor signalling through MyD88 and secretion of IL-12. Similar to alpha-GalCer application, EhLPPG treatment significantly reduces the severity of ALA in ameba-infected mice. Our results suggest that EhLPPG is an amebic molecule that is important for the limitation of ALA development and may explain why the majority of E. histolytica-infected individuals do not develop amebic liver abscess.

Indexed as

AnimalsAntigen-Presenting CellsAntigens, CD1dAntigens, ProtozoanAntigens, SurfaceCells, CulturedDisease Models, AnimalEntamoeba histolyticaGalactosylceramidesInterferon-gammaLiver Abscess, AmebicLymphocyte ActivationMiceMice, Inbred C57BLNatural Killer T-CellsPeptidoglycanalpha-galactosylceramideAntigens, CD1dAntigens, ProtozoanAntigens, SurfaceCd1d1 protein, mouseGalactosylceramidesInterferon-gammalipopeptidophosphoglycanPeptidoglycanPhosphatidylinositolsPhospholipids

Identifiers

PMID19436711
PMCPMC2674934
OpenAlexW2112990445

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.