Evidence map›Paper›PMID 30700015›Full record

ArticleInternational journal of molecular sciences2019

Involvement of the PD-1/PD-L1 Co-Inhibitory Pathway in the Pathogenesis of the Inflammatory Stage of Early-Onset Preeclampsia.

Matyas Meggyes, Eva Miko, Adrienn Lajko, Beata Csiszar, Barbara Sandor, Peter Matrai, Peter Tamas, Laszlo Szereday

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Immune checkpoint for pregnancy.Seminars in immunopathology · 2025
    Review
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  20. Insulin-mediated immune dysfunction in the development of preeclampsia.Journal of molecular medicine (Berlin, Germany) · 2021
    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.

Matyas Meggyes.Department of Medical Microbiology and Immunology, Medical School, University of Pecs, 12 Szigeti Street, 7624 Pecs, Hungary. meggyes.matyas@pte.hu.
Eva Miko.Department of Medical Microbiology and Immunology, Medical School, University of Pecs, 12 Szigeti Street, 7624 Pecs, Hungary. miko.eva@pte.hu.
Adrienn Lajko.Department of Medical Microbiology and Immunology, Medical School, University of Pecs, 12 Szigeti Street, 7624 Pecs, Hungary. lajko.adri@gmail.com.
Beata Csiszar.1st Department of Internal Medicine, Medical School, University of Pecs, 13 Ifjusag Street, 7624 Pecs, Hungary. csiszar.beata@pte.hu.
Barbara Sandor.1st Department of Internal Medicine, Medical School, University of Pecs, 13 Ifjusag Street, 7624 Pecs, Hungary. sandor.barbara@pte.hu.
Peter Matrai.Institute of Bioanalysis, Medical School, University of Pecs, 12 Szigeti Street, 7624 Pecs, Hungary. matraip@gamma.ttk.pte.hu.
Peter Tamas.Department of Obstetrics and Gynaecology, Medical School, University of Pecs, 17 Edesanyak street, 7624 Pecs, Hungary. tamas.peter@pte.hu.
Laszlo Szereday.Department of Medical Microbiology and Immunology, Medical School, University of Pecs, 12 Szigeti Street, 7624 Pecs, Hungary. szereday.laszlo@pte.hu.
University of Pecs · HUSzent János Kórház · HU

Funding

National Research, Development, and Innovation Office K119529National Research, Development, and Innovation Office PD112465PTE ÁOK KA Research Grant KA-2018-07PTE ÁOK KA Research Grant KA-2019-Miko
6 · The paper itself

Abstract

The programmed cell death protein 1 (PD-1) receptor has been reported to downregulate T cell activation effectively via binding to its ligands PD-L1 or PD-L2 in a negative co-stimulatory manner. Little is known about the involvement of PD-1 mediated immunoregulation in pregnancy and in pregnancy-related disorders. In this work, we investigated the possible role of the PD-1 co-stimulatory pathway in the pathogenesis of the clinical phase of early-onset preeclampsia characterized by a systemic maternal inflammatory response. We performed a cross-sectional study for comparative analysis of phenotypic and functional characteristics of peripheral blood mononuclear cells in women with early-onset preeclampsia and third-trimester healthy pregnant controls. According to our findings, enhanced expression of either PD-1 or its ligand PD-L1, or both, on the cell surface of effector cells (T cells, natural killer (NK) cells, natural killer T (NKT)-like cells) and Tregs could be observed, but PD-1 expression did not correlate with effector cells exhaustion. These results suggest the failure of the axis to downregulate Th1 responses, contributing thereby to the exaggerated immunoactivation observed in early-onset preeclampsia.

Indexed as

B7-H1 AntigenCross-Sectional StudiesFemaleHumansInflammationPre-EclampsiaPregnancyProgrammed Cell Death 1 Ligand 2 ProteinProgrammed Cell Death 1 ReceptorB7-H1 AntigenCD274 protein, humanPDCD1LG2 protein, humanProgrammed Cell Death 1 Ligand 2 ProteinProgrammed Cell Death 1 Receptorearly-onsetimmune checkpointinflammationPD-1PD-L1preeclampsia

Identifiers

PMID30700015
PMCPMC6386834
OpenAlexW2912703087

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.