Evidence map›Paper›PMID 30782114›Full record

ArticleBMC pregnancy and childbirth2019

The importance of the PD-1/PD-L1 pathway at the maternal-fetal interface.

Matyas Meggyes, Eva Miko, Brigitta Szigeti, Nelli Farkas, Laszlo Szereday

Open access · goldAbstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

55 citing papers in PubMed, 99 citations in OpenAlex.

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  10. Immune Cells in Preeclampsia.International journal of molecular sciences · 2025
    Review
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  14. Differential Immune Checkpoint Expression in CD4International journal of molecular sciences · 2025
    Article
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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

5 authors at 1 institution in 1 country.

Matyas MeggyesDepartment of Medical Microbiology and Immunology, University of Pecs, Medical School, 7624 Pecs, 12 Szigeti Street, Pecs, Hungary. meggyes.matyas@pte.hu.ORCID http://orcid.org/0000-0002-9913-2024
Eva MikoDepartment of Medical Microbiology and Immunology, University of Pecs, Medical School, 7624 Pecs, 12 Szigeti Street, Pecs, Hungary.
Brigitta SzigetiDepartment of Medical Microbiology and Immunology, University of Pecs, Medical School, 7624 Pecs, 12 Szigeti Street, Pecs, Hungary.
Nelli FarkasInstitute of Bioanalysis, University of Pecs, Medical School, 7624 Pecs, 12 Szigeti Street, Pecs, Hungary.
Laszlo SzeredayDepartment of Medical Microbiology and Immunology, University of Pecs, Medical School, 7624 Pecs, 12 Szigeti Street, Pecs, Hungary.
University of Pecs · HU

Funding

Általános Orvostudományi Kar, Pécsi Tudományegyetem KA-2018-07Általános Orvostudományi Kar, Pécsi Tudományegyetem KA-2018-18Development of scientific workshops of medical, health sciences and pharmaceutical educations EFOP-3.6.3-VEKOP-16-2017-00009National Research, Development and Innovation Office NKFIH K119529
6 · The paper itself

Abstract

backgroundOur goal with this study was to investigate the contribution of PD-1/PD-L1 immune-checkpoint pathway to maternal immunotolerance mechanisms.

methodsThirteen healthy pregnant women and 10 non-pregnant controls were involved in this project. PBMCs and DICs were isolated from peripheral blood and from decidual tissues. After the characterization of different immune cell subsets, we used fluorochrome-conjugated monoclonal antibodies to measure the expression level of PD-1, PD-L1, NKG2D, and CD107a molecules by flow cytometry.

resultsWe measured significant alternations in the proportion of decidual immune cell subsets compared to the periphery. Elevated PD-1 expression by decidual CD8+ T, CD4+ T, and NKT-like cells were also detected accompanied by the increased PD-L1 expression by decidual CD4+ T, Treg, NKT-like and CD56 + NK cell subsets compared to peripheral blood. The cytotoxic potential was significantly higher in PD-1- decidual immune cells compared to the periphery, however we measured a significantly lower cytotoxicity in the decidual PD-1+ CD8+ T cells compared with the peripheral subsets. An activation receptor NKG2D expression was decreased by the PD-1+ CD8+ T subsets in the first trimester compared to non-pregnant condition but the expression level of the decidual counterparts was significantly elevated compared to the periphery. The cytotoxic potential of decidual PD1/NKG2D double positive CD8+ T cells was significantly decreased compared to the peripheral subsets.

conclusionsBased on our results we assume that PD-1/PD-L1 pathway might have a novel role in the maintaining of the local immunological environment. Accompanied by NKG2D activating receptor this checkpoint interaction could regulate decidual CD8 Tc cell subsets and may contribute maternal immunotolerance.

Indexed as

AdultAntibodiesB7-H1 AntigenCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDeciduaFemaleFlow CytometryHistocompatibility, Maternal-FetalHumansLeukocytes, MononuclearLysosomal-Associated Membrane Protein 1NK Cell Lectin-Like Receptor Subfamily KPregnancyProgrammed Cell Death 1 ReceptorSignal TransductionAntibodiesB7-H1 AntigenCD274 protein, humanLysosomal-Associated Membrane Protein 1NK Cell Lectin-Like Receptor Subfamily KPDCD1 protein, humanProgrammed Cell Death 1 ReceptorMaternal-fetal interfaceMaternal immunotolerancePD-1PD-L1Pregnancy

Identifiers

PMID30782114
PMCPMC6381664
OpenAlexW2943225208

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.