Evidence map›Paper›PMID 23087431›Full record

ArticleThe Journal of infectious diseases2013

T-helper 17 cells are associated with pathology in human schistosomiasis.

Moustapha Mbow, Bridget M Larkin, Lynn Meurs, Linda J Wammes, Sanne E de Jong, Lucja A Labuda, Makhtar Camara, Hermelijn H Smits, Katja Polman, Tandakha N Dieye and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Schistosomiasis.Advances in experimental medicine and biology · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Phenotypic Characterization of CD4Frontiers in immunology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

13 authors at 4 institutions in 4 countries.

Moustapha MbowImmunology Unit, Laboratory of Bacteriology and Virology, Aristide Le Dantec Teaching Hospital, Dakar, Senegal. moustaphazero@yahoo.fr
Bridget M Larkin
Lynn Meurs
Linda J Wammes
Sanne E de Jong
Lucja A Labuda
Makhtar Camara
Hermelijn H Smits
Katja Polman
Tandakha N Dieye
Souleymane Mboup
Miguel J Stadecker
Maria Yazdanbakhsh
Leiden University Medical Center · NLHôpital Aristide Le Dantec · SNInstituut voor Tropische Geneeskunde · BETufts University · US

Funding

Immunoregulation of SchistosomiasisR01AI018919 · NIAID · TUFTS UNIVERSITY BOSTON · PI KALANTARI, PARISA, STADECKER, MIGUEL J. · 1992 to 2020
$8.2M
NIAID NIH HHS R01 AI018919PHS HHS R01-18919
6 · The paper itself

Abstract

backgroundSchistosome infections are often clinically silent, but some individuals develop severe pathological reactions. In several disease processes, T-helper 17 (Th17) cells have been linked to tissue injuries, while regulatory T cells (Tregs) are thought to downmodulate inflammatory reactions. We assessed whether bladder pathology in human Schistosoma haematobium infection is related to the balance of Th17 cells and Tregs. We used a murine model of Schistosoma mansoni infection to further investigate whether the peripheral profiles reflected ongoing events in tissues.

methodsWe characterized T-helper cell subsets in the peripheral blood of children residing in a S. haematobium-endemic area and in the peripheral blood, spleen, and hepatic granulomas of S. mansoni-infected high-pathology CBA mice and low-pathology C57BL/6 mice.

resultsS. haematobium-infected children with bladder pathology had a significantly higher percentage of Th17 cells than those without pathology. Moreover, the Th17/Treg ratios were significantly higher in infected children with pathology, compared with infected children without pathology. Percentages of interleukin 17-producing cells were significantly higher in spleen and granulomas of CBA mice, compared with C57BL/6 mice. This difference was also reflected in the peripheral blood.

conclusionsThis is the first study to indicate that Th17 cells may be involved in the pathogenesis of human schistosomiasis.

Indexed as

AdolescentAdultAnimalsChildChild, PreschoolCytokinesFemaleGranulocytesHost-Parasite InteractionsHumansInterleukin-17MaleMiceMice, Inbred C57BLMice, Inbred CBAMiddle AgedCytokinesInterleukin-17

Identifiers

PMID23087431
PMCPMC3571236
OpenAlexW2112174079

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.