Evidence map›Paper›PMID 39790077›Full record

ArticleEuro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin2025

Monitoring SARS-CoV-2 variants with complementary surveillance systems: risk evaluation of the Omicron JN.1 variant in France, August 2023 to January 2024.

Adriana Traore, Kelly Charniga, Sophie Grellet, Garance Terpant, Héléna Da Cruz, Anais Lamy, Nathalie Thomas, Gwladys Gbaguidi, Alizé Mercier, Julie Prudhomme and 20 more

Abstract read
In one paragraph

Article in Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Interim vaccine effectiveness against influenza virus among outpatients, France, October 2025 to January 2026.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Influenza vaccine effectiveness against detected infection in the community, France, October 2024 to February 2025.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2025
    Article
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

30 authors.

Adriana TraoreDirection des Maladies Infectieuses, Santé publique France, Saint-Maurice, France.
Kelly CharnigaMathematical Modelling of Infectious Diseases Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 2000, Paris, France.
Sophie GrelletThese authors have contributed equally to this work.
Garance TerpantThese authors have contributed equally to this work.
Héléna Da CruzThese authors have contributed equally to this work.
Anais LamyThese authors have contributed equally to this work.
Nathalie ThomasThese authors have contributed equally to this work.
Gwladys GbaguidiThese authors have contributed equally to this work.
Alizé MercierThese authors have contributed equally to this work.
Julie PrudhommeThese authors have contributed equally to this work.
Benoit VisseauxCerba, Infectiology Department, Saint-Ouen-l'Aumône, France.
Vincent VieillefondBPO-BIOEPINE-Biogroup, Levallois-Perret, France.
Stéphanie Haim-BoukobzaLaboratoires Cerballiance, Issy-Les-Moulineaux, France.
Jean-Marc GiannoliLABAC, Villeurbanne, France.
RELAB Study GroupThe members of RELAB Study Group are listed under Collaborators and at the end of the article.
Laboratory groupThe members of the Laboratory Group are listed under Collaborators.
Javier Castro-AlvarezDirection des Maladies Infectieuses, Santé publique France, Saint-Maurice, France.
Alain-Claude KouamenDirection des Maladies Infectieuses, Santé publique France, Saint-Maurice, France.
Marie-Anne Rameix-WeltiNational Reference Center for Respiratory Viruses, M3P, Institut Pasteur, Université Paris Cité, Paris, France.
Samar Beirrera-IbraimNational Reference Center for Respiratory Viruses, M3P, Institut Pasteur, Université Paris Cité, Paris, France.
Gregory DestrasNational Reference Center for Respiratory Viruses, Hospices Civils de Lyon, CIRI, INSERM U1111, University Claude Bernard Lyon 1, Lyon, France.
Laurence JossetNational Reference Center for Respiratory Viruses, Hospices Civils de Lyon, CIRI, INSERM U1111, University Claude Bernard Lyon 1, Lyon, France.
Simon CauchemezMathematical Modelling of Infectious Diseases Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 2000, Paris, France.
Bruno LinaNational Reference Center for Respiratory Viruses, Hospices Civils de Lyon, CIRI, INSERM U1111, University Claude Bernard Lyon 1, Lyon, France.
Bruno CoignardDirection des Maladies Infectieuses, Santé publique France, Saint-Maurice, France.
Justine SchaefferDirection des Maladies Infectieuses, Santé publique France, Saint-Maurice, France.
Vincent EnoufNational Reference Center for Respiratory Viruses, M3P, Institut Pasteur, Université Paris Cité, Paris, France.
Antonin BalNational Reference Center for Respiratory Viruses, Hospices Civils de Lyon, CIRI, INSERM U1111, University Claude Bernard Lyon 1, Lyon, France.
Members of the Laboratory Group
Members of the RELAB Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundEarly detection and characterisation of SARS-CoV-2 variants have been and continue to be essential for assessing their public health impact. In August 2023, Santé publique France implemented enhanced surveillance for BA.2.86 and sub-lineage JN.1 because of their genetic divergence from other variants and increased prevalence.AimTo detail how combining epidemiological and laboratory data sources, targeted investigations and modelling enabled comprehensive characterisation of sub-lineage JN.1.MethodsData were collected from epidemiological investigations using a standardised questionnaire and from routine and novel (RELAB network) surveillance systems. JN.1 cases were compared with cases infected with previously circulating variants, such as EG.5, BA.4/BA.5 and other BA.2.86 sub-lineages. The growth rate and doubling time of JN.1 were estimated.ResultsJN.1 was first detected in September 2023 in the Île-de-France region, France, and spread widely across the country. By late November, doubling time was estimated to be 8.6 to 26.4 days depending on the region. For all data sources, cases infected by JN.1 showed similar demographics, rates of hospitalisation and RT-PCR cycle threshold values compared with those infected by previous variants. JN.1 cases also had older median age (54 years; 40-71 vs 47 years; 30-59), more frequent reports of feverish feeling and less frequent cough or nausea compared with BA.4/BA.5 cases. JN.1 cases had significantly higher frequency of anosmia compared with other BA.2.86 cases.ConclusionCombining different data sources played a key role in detecting emerging variant JN.1, for which no evidence of increased public health impact was found despite its genetic divergence.

Indexed as

COVID-19SARS-CoV-2AdolescentAdultAgedAged, 80 and overChildChild, PreschoolFemaleFranceHumansInfantMaleMiddle AgedPopulation SurveillanceRisk AssessmentBA.2.86COVID-19genomic surveillanceJN.1laboratory networkSARS-CoV-2 variant

Identifiers

PMID39790077
PMCPMC11719805

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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.