Evidence map›Paper›PMID 40473628›Full record

ArticleNPJ vaccines2025

Characterization of a suspension Vero cell line for viral vaccine production.

Léa Bourigault, Corinne Bresson, Christian Jean, Christophe Chevalard, Mathilde Kloutz, Damien Soulet, Fleurine Pelissier, Stéphanie Richard, Isabelle Bassard, Nicolas Sève and 2 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2025. 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. Article
  2. Article
  3. 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

12 authors.

Léa BourigaultUniversity of Lyon, Université Lyon 1, INSERM, INRAE, Stem Cell and Brain Research Institute U1208, Bron, France.
Corinne BressonSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Christian JeanUniversity of Lyon, Université Lyon 1, INSERM, INRAE, Stem Cell and Brain Research Institute U1208, Bron, France.
Christophe ChevalardSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Mathilde KloutzSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Damien SouletSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Fleurine PelissierSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Stéphanie RichardSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Isabelle BassardSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Nicolas SèveSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Cédric CharretierSanofi Vaccines, VCDS Global Bioprocess Development, Marcy L'Etoile, France.
Bertrand PainUniversity of Lyon, Université Lyon 1, INSERM, INRAE, Stem Cell and Brain Research Institute U1208, Bron, France. bertrand.pain@inserm.fr.ORCID http://orcid.org/0000-0002-1210-8444

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vero cells, as approved by the World Health Organization, have been the most commonly used continuous cell line for viral vaccine production over the last 25 years, but their adherent phenotype continues to limit productivity. Adapting to a suspension culture would overcome this restriction and reduce production costs. First, a Vero suspension isolate was obtained and metabolically characterized. Second, RNA sequencing analysis was used to identify differentially expressed genes between adherent and suspension cells, which revealed complete downregulation of adhesion and matrix-associated genes. Additionally, signaling pathways involving Wnt and other tyrosine kinase receptors were identified as potential leads for growth optimization. In particular, supplementation with fibroblast growth factor 2 allowed for a 20% increase in cell density. Finally, a comparative viral productivity assay revealed a 30% increase in poliovirus production in suspension Vero cells compared to adherent cells depending on the serotype, as well as a 140% increase in respiratory syncytial virus production and a 150% increase in yellow fever virus production. This work establishes the potential of the suspension Vero cell line as a new cell platform for viral vaccine production.

Identifiers

PMID40473628
PMCPMC12141672

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LicenceCC BY-NC-ND
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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.