Evidence map›Paper›PMID 35216502›Full record

ArticleInternational journal of molecular sciences2022

Pro- and Anti-Inflammatory Cytokines in the Context of NK Cell-Trophoblast Interactions.

Valentina Mikhailova, Polina Grebenkina, Evgeniia Khokhlova, Alina Davydova, Zeina Salloum, Elizaveta Tyshchuk, Valeria Zagainova, Kseniia Markova, Igor Kogan, Sergey Selkov and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Natural Killer Cells and Immunotherapy.International journal of molecular sciences · 2023
    Article
  9. Article
  10. 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

11 authors at 2 institutions in 1 country.

Valentina MikhailovaDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.ORCID 0000-0003-1328-8157
Polina GrebenkinaDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.
Evgeniia KhokhlovaDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.
Alina DavydovaDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.
Zeina SalloumDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.
Elizaveta TyshchukDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.ORCID 0000-0001-6051-9048
Valeria ZagainovaDepartment of Artificial Reproduction Technologies, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology, and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.
Kseniia MarkovaDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.ORCID 0000-0003-2748-3543
Igor KoganDepartment of Artificial Reproduction Technologies, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology, and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.
Sergey SelkovDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.
Dmitry SokolovDepartment of Immunology and Intercellular Interactions, Federal State Budgetary Scientific Institution, Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, 199034 St. Petersburg, Russia.ORCID 0000-0002-5749-2531
Research Institute of Obstetrics and Gynecology named after D.O. Ott · RUFirst Pavlov State Medical University of St. Petersburg · RU

Funding

the Ministry of Science and Higher Education of the Russian Federation, Research Program 1021062512052-5-3.2.2the Russian Foundation for Basic Research Grant 20-015-00014the Russian Science Foundation Grant 21-15-00021
6 · The paper itself

Abstract

During pregnancy, uterine NK cells interact with trophoblast cells. In addition to contact interactions, uterine NK cells are influenced by cytokines, which are secreted by the cells of the decidua microenvironment. Cytokines can affect the phenotypic characteristics of NK cells and change their functional activity. An imbalance of pro- and anti-inflammatory signals can lead to the development of reproductive pathology. The aim of this study was to assess the effects of cytokines on NK cells in the presence of trophoblast cells in an in vitro model. We used TNFα, IFNγ, TGFβ and IL-10; the NK-92 cell line; and peripheral blood NK cells (pNKs) from healthy, non-pregnant women. For trophoblast cells, the JEG-3 cell line was used. In the monoculture of NK-92 cells, TNFα caused a decrease in CD56 expression. In the coculture of NK cells with JEG-3 cells, TNFα increased the expression of NKG2C and NKG2A by NK-92 cells. Under the influence of TGFβ, the expression of CD56 increased and the expression of NKp30 decreased in the monoculture. After the preliminary cultivation of NK-92 cells in the presence of TGFβ, their cytotoxicity increased. In the case of adding TGFβ to the PBMC culture, as well as coculturing PBMCs and JEG-3 cells, the expression of CD56 and NKp44 by pNK cells was reduced. The differences in the effects of TGFβ in the model using NK-92 cells and pNK cells may be associated with the possible influence of monocytes or other lymphoid cells from the mononuclear fraction.

Indexed as

AdultAnti-Inflammatory AgentsCell LineCell Line, TumorCoculture TechniquesCytokinesFemaleHumansKiller Cells, NaturalLeukocytes, MononuclearPregnancyTransforming Growth Factor betaTrophoblastsTumor Necrosis Factor-alphaUterusAnti-Inflammatory AgentsCytokinesTransforming Growth Factor betaTumor Necrosis Factor-alphaCD56JEG-3NK-92NK cellsPBMCpNKTGFβTNFαtrophoblast

Identifiers

PMID35216502
PMCPMC8878424
OpenAlexW4213042535

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.