Evidence map›Paper›PMID 33712643›Full record

ArticleScientific reports2021

Primary ectocervical epithelial cells display lower permissivity to Chlamydia trachomatis than HeLa cells and a globally higher pro-inflammatory profile.

Chongfa Tang, Chang Liu, Benoit Maffei, Béatrice Niragire, Henri Cohen, Aminata Kane, Anne-Claire Donnadieu, Yael Levy-Zauberman, Thomas Vernay, Juliette Hugueny and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  8. mBio · 2024
    Article
  9. Review
  10. Review
  11. Frontiers in cellular and infection microbiology · 2022
    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

14 authors at 3 institutions in 3 countries.

Chongfa Tang *Unité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France.
Chang Liu *Unité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France.
Benoit MaffeiUnité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France.
Béatrice NiragireUnité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France.
Henri CohenService de Chirurgie gynécologique, Institut Mutualiste Montsouris, 75014, Paris, France.
Aminata KaneService de Gynécologie, Clinique Saint Jean de Dieu, 75007, Paris, France.
Anne-Claire DonnadieuService de Chirurgie gynécologique, Institut Mutualiste Montsouris, 75014, Paris, France.
Yael Levy-ZaubermanService de Chirurgie gynécologique, Institut Mutualiste Montsouris, 75014, Paris, France.
Thomas VernayUnité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France.
Juliette HuguenyUnité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France.
Etienne VincensService de Gynécologie, Clinique Saint Jean de Dieu, 75007, Paris, France.
Christine Louis-SylvestreService de Chirurgie gynécologique, Institut Mutualiste Montsouris, 75014, Paris, France.
Agathe SubtilUnité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France. asubtil@pasteur.fr.
Yongzheng WuUnité de Biologie cellulaire de l'infection microbienne, Institut Pasteur, UMR3691 CNRS, 75015, Paris, France. wuyzh@pasteur.fr.
Biology of Infection · FRInstitute Mutualiste Montsouris · FRClinique Saint Jean Languedoc · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumoral origin and extensive passaging of HeLa cells, a most commonly used cervical epithelial cell line, raise concerns on their suitability to study the cell responses to infection. The present study was designed to isolate primary epithelial cells from human ectocervix explants and characterize their susceptibility to C. trachomatis infection. We achieved a high purity of isolation, assessed by the expression of E-cadherin and cytokeratin 14. The infectious progeny in these primary epithelial cells was lower than in HeLa cells. We showed that the difference in culture medium, and the addition of serum in HeLa cultures, accounted for a large part of these differences. However, all things considered the primary ectocervical epithelial cells remained less permissive than HeLa cells to C. trachomatis serovar L2 or D development. Finally, the basal level of transcription of genes coding for pro-inflammatory cytokines was globally higher in primary epithelial cells than in HeLa cells. Transcription of several pro-inflammatory genes was further induced by infection with C. trachomatis serovar L2 or serovar D. In conclusion, primary epithelial cells have a strong capacity to mount an inflammatory response to Chlamydia infection. Our simplified purification protocol from human explants should facilitate future studies to understand the contribution of this response to limiting the spread of the pathogen to the upper female genital tract.

Indexed as

Cell ProliferationCell SeparationCell ShapeCervix UteriChlamydia InfectionsChlamydia trachomatisEpithelial CellsFemaleFibroblastsHeLa CellsHumansImmunityInflammation

Identifiers

PMID33712643
PMCPMC7955086
OpenAlexW3134605561

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.