Evidence map›Paper›PMID 25548226›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Antibody-mediated trapping of helminth larvae requires CD11b and Fcγ receptor I.

Julia Esser-von Bieren, Beatrice Volpe, Manuel Kulagin, Duncan B Sutherland, Romain Guiet, Arne Seitz, Benjamin J Marsland, J Sjef Verbeek, Nicola L Harris

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  12. Trickle infection withFrontiers in immunology · 2022
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  14. Review
  15. Review
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  18. Epithelial-Cell-Derived Phospholipase ACell host & microbe · 2017
    Article
  19. Article
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

9 authors at 4 institutions in 2 countries.

Julia Esser-von BierenSwiss Vaccine Research Institute, Global Health Institute, Swiss Federal Institute of Technology, Lausanne, 1015 Lausanne, Switzerland;
Beatrice VolpeSwiss Vaccine Research Institute, Global Health Institute, Swiss Federal Institute of Technology, Lausanne, 1015 Lausanne, Switzerland;
Manuel KulaginSwiss Vaccine Research Institute, Global Health Institute, Swiss Federal Institute of Technology, Lausanne, 1015 Lausanne, Switzerland;
Duncan B SutherlandSwiss Vaccine Research Institute, Global Health Institute, Swiss Federal Institute of Technology, Lausanne, 1015 Lausanne, Switzerland;
Romain GuietBioimaging and Optics Core Facility, Swiss Federal Institute of Technology, Lausanne, 1015 Lausanne, Switzerland;
Arne SeitzBioimaging and Optics Core Facility, Swiss Federal Institute of Technology, Lausanne, 1015 Lausanne, Switzerland;
Benjamin J MarslandFaculty of Biology and Medicine, Respiratory Division, University Hospital, Vaud, University of Lausanne, 1011 Lausanne, Switzerland; and.
J Sjef VerbeekDepartment of Human Genetics, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.
Nicola L HarrisSwiss Vaccine Research Institute, Global Health Institute, Swiss Federal Institute of Technology, Lausanne, 1015 Lausanne, Switzerland; nicola.harris@epfl.ch.
École Polytechnique Fédérale de Lausanne · CHSwiss Vaccine Research Institute · CHLeiden University Medical Center · NLUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infections with intestinal helminths severely impact on human and veterinary health, particularly through the damage that these large parasites inflict when migrating through host tissues. Host immunity often targets the motility of tissue-migrating helminth larvae, which ideally should be mimicked by anti-helminth vaccines. However, the mechanisms of larval trapping are still poorly defined. We have recently reported an important role for Abs in the rapid trapping of tissue-migrating larvae of the murine parasite Heligmosomoides polygyrus bakeri. Trapping was mediated by macrophages (MΦ) and involved complement, activating FcRs, and Arginase-1 (Arg1) activity. However, the receptors and Ab isotypes responsible for MΦ adherence and Arg1 induction remained unclear. Using an in vitro coculture assay of H. polygyrus bakeri larvae and bone marrow-derived MΦ, we now identify CD11b as the major complement receptor mediating MΦ adherence to the larval surface. However, larval immobilization was largely independent of CD11b and instead required the activating IgG receptor FcγRI (CD64) both in vitro and during challenge H. polygyrus bakeri infection in vivo. FcγRI signaling also contributed to the upregulation of MΦ Arg1 expression in vitro and in vivo. Finally, IgG2a/c was the major IgG subtype from early immune serum bound by FcγRI on the MΦ surface, and purified IgG2c could trigger larval immobilization and Arg1 expression in MΦ in vitro. Our findings reveal a novel role for IgG2a/c-FcγRI-driven MΦ activation in the efficient trapping of tissue-migrating helminth larvae and thus provide important mechanistic insights vital for anti-helminth vaccine development.

Indexed as

AnimalsAntibodies, HelminthArginaseCD11b AntigenComplement System ProteinsGene ExpressionHelminthiasis, AnimalHelminthsImmune SeraImmunoglobulin GInterleukin-33InterleukinsLarvaMacrophage ActivationMacrophagesMice, KnockoutAntibodies, HelminthArg1 protein, mouseArginaseCD11b AntigenComplement System ProteinsIl33 protein, mouseImmune SeraImmunoglobulin GInterleukin-33InterleukinsReceptors, IgGReceptors, Interleukin-4

Identifiers

PMID25548226
PMCPMC4298127
OpenAlexW2097741386

What OpenQuestion holds

Textmetadata
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.