Evidence map›Paper›PMID 39749987›Full record

Observational studyClinical infectious diseases : an official publication of the Infectious Diseases Society of America2025

Clinical Characterization and Outcomes of Human Clade IIb Mpox Virus Disease: A European Multicenter Mpox Observational Cohort Study (MOSAIC).

Elise Pesonel, Cédric Laouénan, Laetitia Guiraud, Josephine Bourner, Isabelle Hoffmann, Diana Molino, Coralie Tardivon, Delphine Bachelet, France Mentré, Alain Amstutz and 18 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Review
  7. Article
  8. From neglected to notoriety: a review of Mpox clinical features, virology, epidemiology, treatment and prevention strategies.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Review
  9. Review
  10. 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

28 authors.

Elise PesonelInternational Severe Acute Respiratory and Emerging Infection Consortium-Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.ORCID 0009-0009-0133-5009
Cédric LaouénanDepartment of Epidemiology Biostatistics and Clinical Research, Assistance Publique-Hôpitaux de Paris (AP-HP) Nord, Hôpital Bichat, Paris, France.
Laetitia GuiraudHIV/AIDS Unit, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.ORCID 0000-0002-3230-934X
Josephine BournerInternational Severe Acute Respiratory and Emerging Infection Consortium-Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-4687-8380
Isabelle HoffmannDepartment of Epidemiology Biostatistics and Clinical Research, Assistance Publique-Hôpitaux de Paris (AP-HP) Nord, Hôpital Bichat, Paris, France.ORCID 0000-0002-3861-8768
Diana MolinoINSERM, National Agency for Research on AIDS and Viral Hepatitis-Emerging Infectious Diseases, Paris, France.ORCID 0000-0002-2188-3880
Coralie TardivonDepartment of Epidemiology Biostatistics and Clinical Research, Assistance Publique-Hôpitaux de Paris (AP-HP) Nord, Hôpital Bichat, Paris, France.ORCID 0000-0002-2304-9910
Delphine BacheletDepartment of Epidemiology Biostatistics and Clinical Research, Assistance Publique-Hôpitaux de Paris (AP-HP) Nord, Hôpital Bichat, Paris, France.ORCID 0000-0003-0547-008X
France MentréDepartment of Epidemiology Biostatistics and Clinical Research, Assistance Publique-Hôpitaux de Paris (AP-HP) Nord, Hôpital Bichat, Paris, France.ORCID 0000-0002-7045-1275
Alain AmstutzDivision of Clinical Epidemiology, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.ORCID 0000-0003-1716-993X
Laura MersonInternational Severe Acute Respiratory and Emerging Infection Consortium-Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-4168-1960
Amanda RojekInternational Severe Acute Respiratory and Emerging Infection Consortium-Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-3948-0756
Minerva Cervantes GonzalezDepartment of Epidemiology Biostatistics and Clinical Research, Assistance Publique-Hôpitaux de Paris (AP-HP) Nord, Hôpital Bichat, Paris, France.ORCID 0000-0003-2813-2219
Andrea AntinoriNational Institute for Infectious Diseases Lazzaro Spallanzani, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.ORCID 0000-0003-2121-4684
Antonella CastagnaInfectious Diseases Unit, Vita-Salute University, Milan, Italy.ORCID 0000-0001-6481-4570
Silvia NozzaInfectious Diseases Unit, Vita-Salute University, Milan, Italy.ORCID 0000-0002-2673-2731
Valérie PourcherInfectious Diseases Department, Sorbonne University, Pitié-Salpêtrière Hospital, AP-HP, Pierre-Louis Epidemiology and Public Health Institute, INSERM U1136, Paris, France.ORCID 0000-0002-3879-1480
Agnès LiboisDepartment of Infectious Diseases, Centre hospitalier universitaire Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.ORCID 0000-0002-6078-878X
Jake DunningInternational Severe Acute Respiratory and Emerging Infection Consortium-Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-4035-4562
Evelina TacconelliInfectious Diseases, Department of Diagnostic and Public Health, University of Verona, Italy.ORCID 0000-0003-2010-4977
Maya HitesHôpital Universitaire de Bruxelles-Érasme, Université Libre de Bruxelles, Brussels, Belgium.ORCID 0000-0001-6961-6039
Fernando De La Calle PrietoNational Reference Centre for Imported Diseases and International Health, High-Level Isolation Unit, La Paz-Carlos III University Hospital, CIBERINFEC, Madrid, Spain.ORCID 0000-0003-2544-3492
Peter HorbyInternational Severe Acute Respiratory and Emerging Infection Consortium-Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9822-1586
Yazdan YazdanpanahINSERM, National Agency for Research on AIDS and Viral Hepatitis-Emerging Infectious Diseases, Paris, France.ORCID 0009-0004-2402-643X
Alexandra CalmyHIV/AIDS Unit, Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.ORCID 0000-0002-1137-6826
François-Xavier LescureInfections, Antimicrobials, Modelling, Evolution (IAME) Research Centre, Unité mixte de recherche(UMR) 1137,Université Paris Cité, Institut national de la santé et de la recherche médicale (INSERM), Paris, France.ORCID 0000-0002-2828-125X
Piero OlliaroInternational Severe Acute Respiratory and Emerging Infection Consortium-Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-1426-3680
Mpox ObServAtIonal Cohort (MOSAIC) Study Group

Funding

Bill & Melinda Gates Foundation OPP1209135MPX-Response 101115188UK Foreign, Commonwealth and Development OfficeWellcome 215091/Z/18/ZWellcome Trust
6 · The paper itself

Abstract

backgroundThe global mpox outbreak that started in May 2022 was caused by a novel clade IIb variant of the mpox virus (Orthopoxvirus monkeypox, MPXV). It differed from the traditional Western and Central Africa disease in transmission patterns and clinical presentation.

methodsTo address the need for detailed clinical and virologic data, we conducted an observational cohort study (MOSAIC) during May 2022-July 2023 in individuals with confirmed MPXV infection enrolled in 6 European countries. Case management decisions were left to the attending physician. Participants were monitored for up to 6 months for clinical signs/symptoms and clinical and virologic outcomes through hospital visits, phone interviews, and self-administered questionnaires. Outcomes included time to lesion resolution, clinical status, and virus clearance.

resultsThe 518 participants not receiving any specific treatment ("untreated") were diagnosed a median 5 days from symptom onset; 90% were managed as outpatients. Lesions were mostly cutaneous (88%) and perigenital (74%). By day 14 from the first polymerase chain reaction (PCR)-positive sample, 39% had resolved lesions. Time to 95% unculturable virus was longest in cutaneous lesions (52 days). A putative systemic antiviral was available for 57 participants, 44% as inpatients; 34% and 58% had resolved lesions by day 14 from the first PCR-positive sample and from treatment start, respectively. Time to 95% unculturable virus was 60 days in skin and oropharynx. No death or recrudescence occurred by day 180.

conclusionsMOSAIC provides comprehensive insights into the clinical and virologic characteristics of mpox caused by the clade IIb variant. The study forms the basis of clinical characterization for ongoing mpox outbreaks.

Indexed as

Monkeypox virusMpox, MonkeypoxAdolescentAdultAgedChildChild, PreschoolCohort StudiesDisease OutbreaksEuropeFemaleHumansMaleMiddle AgedYoung Adultclade IIblesion resolutionmpoxobservational cohortviral load

Identifiers

PMID39749987
PMCPMC12135908

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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.