Evidence map›Paper›PMID 31730667›Full record

ArticlePLoS pathogens2019

Trickle infection and immunity to Trichuris muris.

Maya Glover, Stefano A P Colombo, David J Thornton, Richard K Grencis

Abstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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  5. Article
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  7. Article
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  10. Cooperation of ILC2s and TNature reviews. Immunology · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Trickle infection withFrontiers in immunology · 2022
    Article
  20. NKp46Frontiers in immunology · 2022
    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

4 authors.

Maya GloverLydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, United Kingdom.ORCID 0000-0001-6737-3555
Stefano A P ColomboLydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, United Kingdom.ORCID 0000-0002-3346-3437
David J ThorntonLydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, United Kingdom.ORCID 0000-0001-7148-1970
Richard K GrencisLydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, United Kingdom.ORCID 0000-0002-7592-0085

Funding

Wellcome Trust 103132/Z/13/ZWellcome Trust 203128/Z/16/ZWellcome Trust 210661/Z/18/ZWellcome Trust Z10661/Z/18/Z
6 · The paper itself

Abstract

The majority of experiments investigating the immune response to gastrointestinal helminth infection use a single bolus infection. However, in situ individuals are repeatedly infected with low doses. Therefore, to model natural infection, mice were repeatedly infected (trickle infection) with low doses of Trichuris muris. Trickle infection resulted in the slow acquisition of immunity reflected by a gradual increase in worm burden followed by partial expulsion. Flow cytometry revealed that the CD4+ T cell response shifted from Th1 dominated to Th2 dominated, which coincided with an increase in Type 2 cytokines. The development of resistance following trickle infection was associated with increased worm expulsion effector mechanisms including goblet cell hyperplasia, Muc5ac production and increased epithelial cell turn over. Depletion of CD4+ T cells reversed resistance confirming their importance in protective immunity following trickle infection. In contrast, depletion of group 2 innate lymphoid cells did not alter protective immunity. T. muris trickle infection resulted in a dysbiotic mircrobiota which began to recover alpha diversity following the development of resistance. These data establish trickle infection as a robust and informative model for analysis of immunity to chronic intestinal helminth infection more akin to that observed under natural infection conditions and confirms the importance of CD4+ T cell adaptive immunity in host protection.

Indexed as

Adaptive ImmunityAnimalsAntibodies, HelminthCD4-Positive T-LymphocytesHypersensitivityImmunity, InnateIntestinesLungMaleMiceMice, Inbred C57BLTh2 CellsTrichuriasisTrichurisAntibodies, Helminth

Identifiers

PMID31730667
PMCPMC6881069

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.