Evidence map›Paper›PMID 39640372›Full record

ArticleWellcome open research2024

Human placental cells are resistant to SARS-CoV-2 infection and replication.

Nagisa Yoshida, Jake R Thomas, Anna Appios, Matthew P Brember, Irving L M H Aye, James R Edgar, Andrew E Firth, Betty Y W Chung, Naomi McGovern, Hazel Stewart

Abstract read
In one paragraph

Article in Wellcome open research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Trophoblast ferroptosis restricts SARS-CoV-2 spread in the placenta.bioRxiv : the preprint server for biology · 2026
    Article
  2. 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

10 authors.

Nagisa YoshidaDepartment of Pathology, University of Cambridge, Cambridge, England, UK.
Jake R ThomasDepartment of Pathology, University of Cambridge, Cambridge, England, UK.
Anna AppiosDepartment of Pathology, University of Cambridge, Cambridge, England, UK.
Matthew P BremberDepartment of Pathology, University of Cambridge, Cambridge, England, UK.
Irving L M H AyeCentre for Trophoblast Research, University of Cambridge, Cambridge, England, UK.
James R EdgarDepartment of Pathology, University of Cambridge, Cambridge, England, UK.
Andrew E FirthDepartment of Pathology, University of Cambridge, Cambridge, England, UK.
Betty Y W ChungDepartment of Pathology, University of Cambridge, Cambridge, England, UK.
Naomi McGovernDepartment of Pathology, University of Cambridge, Cambridge, England, UK.ORCID https://orcid.org/0000-0001-5200-2698
Hazel StewartDepartment of Pathology, University of Cambridge, Cambridge, England, UK.ORCID https://orcid.org/0000-0003-1438-1089

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Infection during pregnancy with SARS-CoV-2 can have a serious impact on both maternal and foetal health. Clinical studies have shown that SARS-CoV-2 transmission from the mother to the foetus typically does not occur. However, there is evidence that SARS-CoV-2 can infect the placenta Methods: By using publicly available single-cell RNA sequencing (scRNAseq) data sets and confocal microscopy we compared ACE2 transcript and protein expression across human first trimester and term placental cells. We also used Results: ACE2 transcripts are found in a range of placental cell types across gestation, including trophoblast. However, ACE2 protein expression does not significantly change across placental cell types from first trimester to term. We find that 0.5±0.15 % of term trophoblast cells can be infected with SARS-CoV-2 while primary placental fibroblasts and macrophages, and JEG-3, JAR and HUVEC cell lines are resistant to infection. Furthermore, primary trophoblast cells poorly support viral release while JEG-3 cells allow relatively high levels of viral release. Conclusions: The low level of viral release by primary placental cells provides insight into how the virus is impaired from crossing the placenta to the foetus.

Indexed as

placentaSARS-CoV-2trophoblast

Identifiers

PMID39640372
PMCPMC11617822

What OpenQuestion holds

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Registered trials

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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.