Evidence map›Paper›PMID 30619262›Full record

ReviewFrontiers in immunology2018

The Role of Extracellular Vesicles and PIBF in Embryo-Maternal Immune-Interactions.

Julia Szekeres-Bartho, Sandra Šućurović, Biserka Mulac-Jeričević

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 88 citations in OpenAlex.

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  19. Micro- and Nanosized Substances Cause Different Autophagy-Related Responses.International journal of molecular sciences · 2021
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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

3 authors at 2 institutions in 2 countries.

Julia Szekeres-BarthoDepartment of Medical Biology and Central Electron Microscope Laboratory, Medical School, Pécs University, Pécs, Hungary.
Sandra ŠućurovićDepartment of Physiology and Immunology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Biserka Mulac-JeričevićDepartment of Physiology and Immunology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
University of Rijeka · HRUniversity of Pecs · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pregnancy represents a unique immunological situation. Though paternal antigens expressed by the conceptus are recognized by the immune system of the mother, the immune response does not harm the fetus. Progesterone and a progesterone induced protein; PIBF are important players in re-adjusting the functioning of the maternal immune system during pregnancy. PIBF expressed by peripheral pregnancy lymphocytes, and other cell types, participates in the feto-maternal communication, partly, by mediating the immunological actions of progesterone. Several splice variants of PIBF were identified with different physiological activity. The full length 90 kD PIBF protein plays a role in cell cycle regulation, while shorter splice variants are secreted and act as cytokines. Aberrant production of PIBF isoforms lead to the loss of immune-regulatory functions, resulting in and pregnancy failure. By up regulating Th2 type cytokine production and by down-regulating NK activity, PIBF contributes to the altered attitude of the maternal immune system. Normal pregnancy is characterized by a Th2-dominant cytokine balance, which is partly due to the action of the smaller PIBF isoforms. These bind to a novel form of the IL-4 receptor, and induce increased production of IL-3, IL-4, and IL-10. The communication between the conceptus and the mother is established via extracellular vesicles (EVs). Pre-implantation embryos produce EVs both

Indexed as

AnimalsEmbryo, MammalianExtracellular VesiclesFemaleFetusHumansImmune ToleranceInterleukin-10Maternal-Fetal ExchangeMicePregnancyPregnancy ProteinsProgesteroneSuppressor Factors, ImmunologicTh2 CellsInterleukin-10PIBF1 protein, humanPibf1 protein, mousePregnancy ProteinsProgesteroneSuppressor Factors, Immunologiccytokinesextracellular vesiclesNK cellsPIBFpregnancyprogesterone

Identifiers

PMID30619262
PMCPMC6300489
OpenAlexW2904780259

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.