Evidence map›Paper›PMID 26617829›Full record

ArticleInternational journal of clinical and experimental pathology2015

IL-17 producing innate lymphoid cells 3 (ILC3) but not Th17 cells might be the potential danger factor for preeclampsia and other pregnancy associated diseases.

Prince A Barnie, Xin Lin, Yueqin Liu, Huaxi Xu, Zhaoliang Su

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In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy.International journal of biological sciences · 2020
    Review
  12. Article
  13. Innate Lymphoid Cells in Human Pregnancy.Frontiers in immunology · 2020
    Review
  14. Article
  15. Immunology of hepatic diseases during pregnancy.Seminars in immunopathology · 2016
    Review
  16. HYPOTHYROXINAEMIA AND BRAIN DEVELOPMENT.Acta endocrinologica (Bucharest, Romania : 2005)
    Article
  17. Article
  18. 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

5 authors at 1 institution in 2 countries.

Prince A BarnieDepartment of Immunology, School of Medicine, Jiangsu University Zhenjiang 212013, PR China ; Department of Biomedical and Forensic Sciences, School of Biological Sciences, University of Cape Coast Ghana.
Xin LinDepartment of Laboratory Medicine, The Fourth Affiliated Hospital of Jiangsu University Zhenjiang 212001, PR China.
Yueqin LiuDepartment of Laboratory Medicine, The Fourth Affiliated Hospital of Jiangsu University Zhenjiang 212001, PR China.
Huaxi XuDepartment of Immunology, School of Medicine, Jiangsu University Zhenjiang 212013, PR China.
Zhaoliang SuDepartment of Immunology, School of Medicine, Jiangsu University Zhenjiang 212013, PR China ; Department of Laboratory Medicine, The Fourth Affiliated Hospital of Jiangsu University Zhenjiang 212001, PR China.
Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In pregnancy, the immunologic system plays an important role that ensures normal pregnancy development and can as well promote the development of complications. Pregnancy success appears to rely on a discrete balance between the Th cytokines, which are involved in fetal growth and development. Preeclampsia and gestational diabetes are known complications associated with pregnancy. However, the source of the increased IL-17 cytokine in preeclampsia and other pregnancy associated diseases still remains unclear amidst numerous inconsistencies. The recent identification of innate lymphoid cells (ILC) has raised more doubts about the sources of most of the Th associated cytokines. We investigated the source of peripheral IL-17 levels in preeclamptic, gestational diabetics and chronic diabetics compared to healthy pregnancy subjects. To evaluate the source of the increased IL-17 cytokine among preeclampsia, chronic diabetic and gestational diabetic patients we investigated the proportion of Th17 cell populations in peripheral blood mononuclear cells using flow cytometry as well as analyzing levels of IFN-γ, IL-17, IL-1β and HMGB1. This study found that the Th17 cell populations in peripheral blood of preeclamptic, gestational nor chronic diabetes during pregnancy did not correlate with the increased IL-17. We report that the increased IL-17 levels observed in patients with preeclampsia, gestational diabetes and chronic diabetes are associated with innate lymphoid cells 3 (ILC3) and may pose threats to the fetus if disregulated.

Indexed as

Immunity, InnateAdultBiomarkersCase-Control StudiesDiabetes, GestationalFemaleHMGB1 ProteinHumansInterferon-gammaInterleukin-17Interleukin-1betaLymphocytesPre-EclampsiaPregnancyPregnancy in DiabeticsRisk FactorsBiomarkersHMGB1 ProteinHMGB1 protein, humanIFNG protein, humanIL1B protein, humanInterferon-gammaInterleukin-17Interleukin-1betaGestational diabetesinnate lymphoid cellspreeclampsiaTh17 cells

Identifiers

PMID26617829
PMCPMC4637644
OpenAlexW2414254774

What OpenQuestion holds

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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.