Evidence map›Paper›PMID 25774883›Full record

ArticlePLoS neglected tropical diseases2015

Drug-induced exposure of Schistosoma mansoni antigens SmCD59a and SmKK7.

Natalie Reimers, Arne Homann, Beate Höschler, Kristina Langhans, R Alan Wilson, Christine Pierrot, Jamal Khalife, Christoph G Grevelding, Iain W Chalmers, Maria Yazdanbakhsh and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. 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
2.1field-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, 34 citations in OpenAlex.

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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

14 authors at 6 institutions in 4 countries.

Natalie ReimersDivision of Cellular Allergology, Priority Area Asthma & Allergy, Research Center Borstel (RCB), Borstel, Germany.
Arne HomannDivision of Cellular Allergology, Priority Area Asthma & Allergy, Research Center Borstel (RCB), Borstel, Germany.
Beate HöschlerDivision of Cellular Allergology, Priority Area Asthma & Allergy, Research Center Borstel (RCB), Borstel, Germany.
Kristina LanghansDivision of Cellular Allergology, Priority Area Asthma & Allergy, Research Center Borstel (RCB), Borstel, Germany.
R Alan WilsonCentre for Immunology and Infection, Department of Biology, University of York, York, United Kingdom.
Christine PierrotCenter for Infection and Immunity of Lille, Inserm U1019, CNRS 8204, Institut Pasteur de Lille, Lille, France.
Jamal KhalifeCenter for Infection and Immunity of Lille, Inserm U1019, CNRS 8204, Institut Pasteur de Lille, Lille, France.
Christoph G GreveldingInstitute for Parasitology, University of Giessen, Giessen, Germany.
Iain W ChalmersInstitute of Biological, Environmental & Rural Sciences (IBERS), Aberystwyth University, Aberystwyth, United Kingdom.
Maria YazdanbakhshDepartment of Parasitology, Leiden University Medical Center, Leiden, Netherlands.
Karl F HoffmannInstitute of Biological, Environmental & Rural Sciences (IBERS), Aberystwyth University, Aberystwyth, United Kingdom.
Cornelis H HokkeDepartment of Parasitology, Leiden University Medical Center, Leiden, Netherlands.
Helmut HaasDivision of Cellular Allergology, Priority Area Asthma & Allergy, Research Center Borstel (RCB), Borstel, Germany; helminGuard, Suelfeld, Germany.
Gabriele SchrammDivision of Cellular Allergology, Priority Area Asthma & Allergy, Research Center Borstel (RCB), Borstel, Germany.
Research Center Borstel - Leibniz Lung Center · DEAberystwyth University · GBInstitut Pasteur de Lille · FRLeiden University Medical Center · NLUniversity of Giessen · DEUniversity of York · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchistosomiasis is a serious health problem especially in developing countries and affects more than 243 million people. Only few anthelmintic drugs are available up to now. A major obstacle for drug treatment is the different developmental stages and the varying host compartments during worm development. Anthelmintic drugs have been tested mainly on adult schistosomes or freshly transformed cercariae. Knowledge concerning the larval stages is lacking. METHODOLOGY/PRINCIPAL

findingsIn this study, we used in vitro-grown schistosomula (aged between 2 to 14 days) to investigate drug effects of the three anthelmintics praziquantel, artemether, and oxamniquine. Further, we analyzed the antibody accessibility of two exemplary schistosome antigens SmCD59a and SmKK7, before and after drug treatment. Our results demonstrated that praziquantel applied at a concentration of 1 μM inhibited development of all life stages. Application of 10 μM praziquantel led to dramatic morphological changes of all schistosomula. Artemether at 1 and 10 μM had differential effects depending on whether it was applied to 2-day as compared to 7- and 14-day schistosomula. While 2-day schistosomula were not killed but inhibited from further development, severe morphological damage was seen in 7- and 14-day schistosomula. Oxamniquine (1 and 10 μM) led to severe morphological impairment in all life stages. Analyzing the accessibility of the antigens SmCD59a and SmKK7 before drug treatment showed no antibody binding on living intact schistosomula. However, when schistosomula were treated with anthelmintics, both antigens became exposed on the larvae. Oxamniquine turned out to be most effective in promoting antibody binding to all schistosomula stages.

conclusionThis study has revealed marked differences in anthelmintic drug effects against larvae. Drug treatment increases surface antigen presentation and renders larvae accessible to antibody attack.

Indexed as

AnimalsAnthelminticsAntigens, HelminthArtemetherArtemisininsCD59 AntigensHumansMalePraziquantelRatsRats, Inbred BNRats, Inbred F344Schistosoma mansoniAnthelminticsAntigens, HelminthArtemetherArtemisininsCD59 AntigensPraziquantel

Identifiers

PMID25774883
PMCPMC4361651
OpenAlexW2021169613

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.