Evidence map›Paper›PMID 30046157›Full record

ArticleScientific reports2018

Neutrophils enhance early Trypanosoma brucei infection onset.

Guy Caljon, Dorien Mabille, Benoît Stijlemans, Carl De Trez, Massimiliano Mazzone, Fabienne Tacchini-Cottier, Marie Malissen, Jo A Van Ginderachter, Stefan Magez, Patrick De Baetselier and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-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

25 citing papers in PubMed, 32 citations in OpenAlex.

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  20. Frontiers in immunology · 2020
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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

11 authors at 6 institutions in 4 countries.

Guy CaljonLaboratory of Microbiology, Parasitology and Hygiene (LMPH), University of Antwerp, Wilrijk, Belgium. Guy.Caljon@uantwerpen.be.
Dorien MabilleLaboratory of Microbiology, Parasitology and Hygiene (LMPH), University of Antwerp, Wilrijk, Belgium.
Benoît StijlemansMyeloid Cell Immunology Lab, VIB Center for Inflammation Research, Ghent, Belgium.ORCID 0000-0003-0082-9751
Carl De TrezUnit of Cellular and Molecular Immunology, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Massimiliano MazzoneLaboratory of Tumor Inflammation and Angiogenesis, Center for Cancer Biology, VIB, Leuven, Belgium.
Fabienne Tacchini-CottierDepartment of Biochemistry, WHO-Immunology Research and Training Center, University of Lausanne, Epalinges, Switzerland.ORCID 0000-0003-3561-0207
Marie MalissenCentre d'Immunologie de Marseille-Luminy, Aix Marseille Université UM2, Inserm U1104, CNRS UMR7280, F-13288, Marseille, France.
Jo A Van GinderachterMyeloid Cell Immunology Lab, VIB Center for Inflammation Research, Ghent, Belgium.
Stefan MagezUnit of Cellular and Molecular Immunology, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Patrick De BaetselierMyeloid Cell Immunology Lab, VIB Center for Inflammation Research, Ghent, Belgium.
Jan Van Den AbbeeleUnit of Veterinary Protozoology, Department of Biomedical Sciences, Institute of Tropical Medicine Antwerp (ITM), Antwerp, Belgium. jvdabbeele@itg.be.
Vrije Universiteit Brussel · BEUniversity of Antwerp · BECentre National de la Recherche Scientifique · FRInstituut voor Tropische Geneeskunde · BEUniversity of Lausanne · CHVIB-KU Leuven Center for Cancer Biology · BE

Funding

EC | European Research Council (ERC) 282312European Research Council 282312Federaal Wetenschapsbeleid (Politique scientifique fédérale) P7/41Fonds Wetenschappelijk Onderzoek (Research Foundation Flanders) G031312NUniversiteit Antwerpen (University of Antwerp) 34775Universiteit Antwerpen (University of Antwerp) TT-ZAPBOF 33049
6 · The paper itself

Abstract

In this study, Trypanosoma brucei was naturally transmitted to mice through the bites of infected Glossina morsitans tsetse flies. Neutrophils were recruited rapidly to the bite site, whereas monocytes were attracted more gradually. Expression of inflammatory cytokines (il1b, il6), il10 and neutrophil chemokines (cxcl1, cxcl5) was transiently up-regulated at the site of parasite inoculation. Then, a second influx of neutrophils occurred that coincided with the previously described parasite retention and expansion in the ear dermis. Congenital and experimental neutropenia models, combined with bioluminescent imaging, indicate that neutrophils do not significantly contribute to dermal parasite control and elicit higher systemic parasitemia levels during the infection onset. Engulfment of parasites by neutrophils in the skin was rarely observed and was restricted to parasites with reduced motility/viability, whereas live parasites escaped phagocytosis. To our knowledge, this study represents the first description of a trypanosome infection promoting role of early innate immunological reactions following an infective tsetse fly bite. Our data indicate that the trypanosome is not hindered in its early development and benefits from the host innate responses with the neutrophils being important regulators of the early infection, as already demonstrated for the sand fly transmitted Leishmania parasite.

Indexed as

AnimalsChemokine CXCL1Chemokine CXCL5DermisGene Expression RegulationInsect Bites and StingsInsect VectorsInterleukin-10Interleukin-1betaInterleukin-6Luminescent MeasurementsMiceNeutrophilsTrypanosoma brucei bruceiTrypanosomiasis, AfricanTsetse FliesChemokine CXCL1Chemokine CXCL5Cxcl1 protein, mouseCxcl5 protein, mouseIL1B protein, mouseInterleukin-10Interleukin-1betaInterleukin-6interleukin-6, mouse

Identifiers

PMID30046157
PMCPMC6060092
OpenAlexW2883887661

What OpenQuestion holds

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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.