Evidence map›Paper›PMID 39589546›Full record

ArticleHistochemistry and cell biology2024

PD-L1 expression and characterization of its carrier macrophages in placentas with acute and specifically post-SARS-CoV-2 infection.

Marina C Seefried, Johanna Mittelberger, Manuela Franitza, Fabian Garrido, Carl Mathis Wild, Nina Ditsch, Oleksii Protsepko, Christina Kuhn, Christian Dannecker, Peter Altevogt and 2 more

Abstract read
In one paragraph

Article in Histochemistry and cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
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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

12 authors.

Marina C SeefriedGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Johanna MittelbergerGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Manuela FranitzaGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Fabian GarridoGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Carl Mathis WildGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Nina DitschGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Oleksii ProtsepkoGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Christina KuhnGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Christian DanneckerGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany.
Peter AltevogtDKFZ and University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg, Heidelberg, Germany.
Udo JeschkeGynecology and Obstetrics, Augsburg University Hospital, Augsburg, Bavaria, Germany. udo.jeschke@med.uni-augsburg.de.
Marei SammarDepartment of Biotechnology Engineering, Braude College of Engineering, Karmiel, Israel. sammar@braude.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At the beginning of the coronavirus disease 2019 (COVID-19) pandemic, uncertainties about the virus and its dangers during pregnancy caused great uncertainty and fear, especially among pregnant women. New data suggest an increased risk of obstetric complications, including maternal complications, preterm labor, intrauterine growth restriction, hypertensive disorders, stillbirths, gestational diabetes and risk, of neonatal developmental disorders. In addition, preeclampsia (PE)-like syndromes were also induced by severe COVID-19 infection. Therefore, the aim of this study was to investigate the expression of CD68 and CD163 and PD-L1 on placental tissues from acute covid patients, patients who survived a covid-19 infection and normal term controls that are known to be dysregulated in preeclampsia cases. We examined a total of 60 placentas from women that had given birth to female or male offspring in the University Hospital Augsburg. We investigated ten acute COVID-19 females, ten acute COVID-19 males, ten post-COVID-19 females, ten post-COVID-19 males, ten female term controls, and ten male term controls. Immunohistochemical staining against CD68, CD163, and PD-L1 was performed and the expression of the markers was evaluated with an immunoreactive score (percentage score). Identity of CD163- or PD-L1 expressing cells was analyzed by double immune fluorescence analyses. In opposite to PE, CD163 positive maternal macrophages are significantly upregulated in the decidua of male acute COVID-19 placentas. PD-L1 is significantly upregulated on male acute- and post-COVID-19 decidual immune cells and on male post-COVID-19 extravillous trophoblast cells. Surprisingly the observed effects are related to the fetal gender as they were not observed in female offsprings. Further investigation is necessary to analyze especially the imprinting effect of this infection.

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticB7-H1 AntigenCOVID-19MacrophagesPlacentaSARS-CoV-2AdultCD163 AntigenCD68 MoleculeFemaleHumansMalePregnancyPregnancy Complications, InfectiousReceptors, Cell SurfaceAntigens, CDAntigens, Differentiation, MyelomonocyticB7-H1 AntigenCD163 AntigenCD274 protein, humanCD68 antigen, humanCD68 MoleculeReceptors, Cell SurfaceCD163Extravillous trophoblastMacrophagesPD-L1SARS-CoV-2 infection

Identifiers

PMID39589546
PMCPMC11599338

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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.