Evidence map›Paper›PMID 25636695›Full record

ArticleBMC immunology2015

Elevated levels of dehydroepiandrosterone as a potential mechanism of dendritic cell impairment during pregnancy.

Elena R Chernykh, Olga Yu Leplina, Marina A Tikhonova, Nataliya V Seledtsova, Tamara V Tyrinova, Nataliya A Khonina, Alexandr A Ostanin, Nataliya M Pasman

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. 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

8 authors at 2 institutions in 1 country.

Elena R ChernykhLaboratory of Cellular Immunotherapy, Research Institute of Fundamental and Clinical Immunology, 14, Yadrintsevskaya St., 630099, Novosibirsk, Russia. ct_lab@mail.ru.
Olga Yu LeplinaLaboratory of Cellular Immunotherapy, Research Institute of Fundamental and Clinical Immunology, 14, Yadrintsevskaya St., 630099, Novosibirsk, Russia. oleplina@mail.ru.
Marina A TikhonovaLaboratory of Cellular Immunotherapy, Research Institute of Fundamental and Clinical Immunology, 14, Yadrintsevskaya St., 630099, Novosibirsk, Russia. matrix-59@mail.ru.
Nataliya V SeledtsovaLaboratory of Cellular Immunotherapy, Research Institute of Fundamental and Clinical Immunology, 14, Yadrintsevskaya St., 630099, Novosibirsk, Russia. jewel82@mail.ru.
Tamara V TyrinovaLaboratory of Cellular Immunotherapy, Research Institute of Fundamental and Clinical Immunology, 14, Yadrintsevskaya St., 630099, Novosibirsk, Russia. tyrinova@mail.ru.
Nataliya A KhoninaLaboratory of Cellular Immunotherapy, Research Institute of Fundamental and Clinical Immunology, 14, Yadrintsevskaya St., 630099, Novosibirsk, Russia. nkhonina@mail.ru.
Alexandr A OstaninLaboratory of Cellular Immunotherapy, Research Institute of Fundamental and Clinical Immunology, 14, Yadrintsevskaya St., 630099, Novosibirsk, Russia. ostanin62@mail.ru.
Nataliya M PasmanNovosibirsk State University, 2, Pirogova St., 630090, Novosibirsk, Russia. pasman@mail.ru.
Research Institute of Fundamental and Clinical Immunology · RUNovosibirsk State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to test the hypothesis that immune dysfunction and the increased risk of spontaneous abortion in pregnant women with hyperandrogenia (HA) are caused by the reduced tolerogenic potential of dendritic cells (DCs) that results from elevated levels of dehydroepiandrosterone sulfate (DHEAS).

methodsThe phenotypic and functional properties of monocyte-derived DCs generated from blood monocytes from non-pregnant women, women with a normal pregnancy, or pregnant women with HA, as well as the in vitro effects of DHEAS on DCs in healthy pregnant women were investigated.

resultsIn a normal pregnancy, DCs were shown to be immature and are characterized by a reduced number of CD83(+) and CD25(+) DCs, the ability to stimulate type 2 T cell responses and to induce T cell apoptosis. By contrast, DCs from pregnant women with HA had a mature phenotype, were able to stimulate both type 1 (IFN-γ) and type 2 (IL-4) T cell responses, and were characterized by lower B7-H1 expression and cytotoxic activity against CD8(+) T cells. The addition of DHEAS to cultures of DCs from healthy pregnant women induced the maturation of DCs and increased their ability to activate type 1 T cell responses.

conclusionOur data demonstrated the reduction in the tolerogenic potential of DCs from pregnant women with HA, and revealed new mechanisms involved in the hormonal regulation of DCs mediated by DHEAS.

Indexed as

Abortion, SpontaneousAdultCell DifferentiationCells, CulturedDehydroepiandrosteroneDendritic CellsFemaleHumansHyperandrogenismImmune ToleranceInterferon-gammaInterleukin-4Lymphocyte ActivationPregnancyRiskTh1 CellsDehydroepiandrosteroneInterferon-gammaInterleukin-4

Identifiers

PMID25636695
PMCPMC4322645
OpenAlexW1983958625

What OpenQuestion holds

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LicenceCC BY
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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.