Evidence map›Paper›PMID 40133410›Full record

ArticleCommunications medicine2025

Fluctuations in serogroup B meningococcal vaccine antigens prior to routine MenB vaccination in France.

Michaël Falguières, Eva Hong, Mélanie Denizon, Aude Terrade, Muhamed-Kheir Taha, Ala-Eddine Deghmane

Abstract read
In one paragraph

Article in Communications medicine, 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. 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

6 authors.

Michaël FalguièresInvasive Bacterial Infections Unit and National Reference Centre for Meningococci and Haemophilus Influnezae, Institut Pasteur and Université Paris Cité, Paris, France.
Eva HongInvasive Bacterial Infections Unit and National Reference Centre for Meningococci and Haemophilus Influnezae, Institut Pasteur and Université Paris Cité, Paris, France.
Mélanie DenizonInvasive Bacterial Infections Unit and National Reference Centre for Meningococci and Haemophilus Influnezae, Institut Pasteur and Université Paris Cité, Paris, France.
Aude TerradeInvasive Bacterial Infections Unit and National Reference Centre for Meningococci and Haemophilus Influnezae, Institut Pasteur and Université Paris Cité, Paris, France.
Muhamed-Kheir TahaInvasive Bacterial Infections Unit and National Reference Centre for Meningococci and Haemophilus Influnezae, Institut Pasteur and Université Paris Cité, Paris, France.
Ala-Eddine DeghmaneInvasive Bacterial Infections Unit and National Reference Centre for Meningococci and Haemophilus Influnezae, Institut Pasteur and Université Paris Cité, Paris, France. ala-eddine.deghmane@pasteur.fr.ORCID http://orcid.org/0000-0003-2887-1732

Funding

Institut Pasteur 24519E
6 · The paper itself

Abstract

backgroundInvasive meningococcal disease (IMD) of serogroup B is preventable by protein-based vaccines targeting one (Bivalent rLP2086 vaccine) or several variable proteins (4CMenB vaccine) at the bacterial surface. The 4CMenB was licensed in Europe in 2013 but has been recommended and reimbursed in France for infants over 2 months old since April 2022. The bivalent rLP2086 vaccine was licensed in Europe in 2017 for subjects of 10 years and older. Evaluating strain coverage and fluctuations prior to large scale vaccine use is highly informative.

methodsWe analysed invasive isolates at the French National Reference Centre for meningococci between 1975 and 2022. The 1691 recovered isolates were sequenced. We scored sex, and age groups of subjects. We also scored clonal complexes (CC) and the predicted coverage rates of the corresponding isolates using the genetic Meningococcal Antigen Typing System (gMATS) and the Meningococcal Deduced Vaccine Antigen Reactivity (MenDeVAR).

resultsThe period was divided into four periods 1975-1986, 1987-1998-1999-2010 and 2011-2022. Our data clearly show significant differences in the distribution of alleles encoding the vaccine-covered antigens between these four periods. The clonal complex (CC) distribution also differed between the two periods with the disappearance of CC8 since 2011 and drastic decreases in CC11 since 1999. MenDeVar-predicted coverage fluctuated between 46.8% and 60.6% during the four periods for the 4CMenB and between 63.4% and 81.3% for rLP2086. For 4CMenB, coverage was higher using gMATS and varied between 74.5% and 85.0%. Fluctuations were also observed for all age groups.

conclusionsIMD epidemiology is continuously changing with fluctuation in vaccine strain coverage over the 48 years prior to the routine implementation of the vaccines.

Identifiers

PMID40133410
PMCPMC11937567

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