Evidence map›Paper›PMID 24492801›Full record

ArticleImmunology and cell biology

Innate and adaptive type 2 immune cell responses in genetically controlled resistance to intestinal helminth infection.

Kara J Filbey, John R Grainger, Katherine A Smith, Louis Boon, Nico van Rooijen, Yvonne Harcus, Stephen Jenkins, James P Hewitson, Rick M Maizels

Open access · hybridAbstract read
In one paragraph

Article in Immunology and cell biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
11.7field-weighted citation impact, top 1% 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

75 citing papers in PubMed, 132 citations in OpenAlex.

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  14. Genetic mapping revealsScience immunology · 2023
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  19. Trickle infection withFrontiers in immunology · 2022
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  20. Review

15 more citing papers are in PubMed but not listed here.

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.

Kara J FilbeyInstitute for Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
John R GraingerInstitute for Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
Katherine A SmithInstitute for Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
Louis BoonBioceros BV, Utrecht, The Netherlands.
Nico van RooijenDepartment of Molecular Cell Biology and Immunology, VU Medical Center, Amsterdam, The Netherlands.
Yvonne HarcusInstitute for Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
Stephen JenkinsInstitute for Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
James P HewitsonInstitute for Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
Rick M MaizelsInstitute for Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
University of Edinburgh · GBCentre for Immunity, Infection and Evolution · GBAmsterdam UMC Location VUmc · NLPolpharma Biologics (Netherlands) · NL

Funding

Medical Research Council G0901697Wellcome Trust 076561Wellcome Trust 095831
6 · The paper itself

Abstract

The nematode Heligmosomoides polygyrus is an excellent model for intestinal helminth parasitism. Infection in mice persists for varying lengths of time in different inbred strains, with CBA and C57BL/6 mice being fully susceptible, BALB/c partially so and SJL able to expel worms within 2-3 weeks of infection. We find that resistance correlates not only with the adaptive Th2 response, including IL-10 but with activation of innate lymphoid cell and macrophage populations. In addition, the titer and specificity range of the serum antibody response is maximal in resistant mice. In susceptible strains, Th2 responses were found to be counterbalanced by IFN-γ-producing CD4(+) and CD8(+) cells, but these are not solely responsible for susceptibility as mice deficient in either CD8(+) T cells or IFN-γ remain unable to expel the parasites. Foxp3(+) Treg numbers were comparable in all strains, but in the most resistant SJL strain, this population does not upregulate CD103 in infection, and in the lamina propria the frequency of Foxp3(+)CD103(+) T cells is significantly lower than in susceptible mice. The more resistant SJL and BALB/c mice develop macrophage-rich IL-4Rα-dependent Type 2 granulomas around intestinal sites of larval invasion, and expression of alternative activation markers Arginase-1, Ch3L3 (Ym1) and RELM-α within the intestine and the peritoneal lavage was also strongly correlated with helminth elimination in these strains. Clodronate depletion of phagocytic cells compromises resistance of BALB/c mice and slows expulsion in the SJL strain. Thus, Type 2 immunity involves IL-4Rα-dependent innate cells including but not limited to a phagocyte population, the latter likely involving the action of specific antibodies.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsAntibodies, HelminthClodronic AcidDisease ResistanceFemaleGranulomaHelminthiasisHelminthiasis, AnimalHelminthsImmunity, CellularInterferon-gammaIntestinal DiseasesIntestinal Diseases, ParasiticMacrophage ActivationAntibodies, HelminthClodronic AcidInterferon-gammaReceptors, Interleukin-4

Identifiers

PMID24492801
PMCPMC4038150
OpenAlexW2141897776

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.