Evidence map›Paper›PMID 39666032›Full record

ArticleJournal of neurology2024

Increased EBNA1-specific antibody response in primary-progressive multiple sclerosis.

Manuel Comabella, Harald Hegen, Luisa M Villar, Konrad Rejdak, Augusto Sao-Avilés, Malina Behrens, Jaume Sastre-Garriga, Neus Mongay, Klaus Berek, Sergio Martínez-Yelamos and 22 more

Abstract read
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Article in Journal of neurology, 2024. 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.

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  6. 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

32 authors.

Manuel ComabellaServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Harald HegenDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Luisa M VillarDepartments of Neurology and Immunology, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigacion Sanitaria, Madrid, Spain.
Konrad RejdakDepartment of Neurology, Medical University of Lublin, Lublin, Poland.
Augusto Sao-AvilésServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Malina BehrensDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Jaume Sastre-GarrigaServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Neus MongayServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Klaus BerekDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Sergio Martínez-YelamosDepartment of Neurology, Bellvitge University Hospital, Barcelona, Spain.
Francisco Pérez-MirallesNeuroimmunology Unit, València University and Polytechnic Hospital La Fe, València, Spain.
Ahmed AbdelhakDepartment of Neurology, Ulm University, Ulm, Germany.
Franziska BachhuberDepartment of Neurology, Ulm University, Ulm, Germany.
Hayrettin TumaniDepartment of Neurology, Ulm University, Ulm, Germany.
Jan LyckeFundación INCE (Iniciativa Para Las Neurociencias), Madrid, Spain.
Pere Carbonell-MirabentServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Adrián Valls-CarbóFundación INCE (Iniciativa Para Las Neurociencias), Madrid, Spain.
Igal RosensteinDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology at Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Roberto Alvarez-LafuenteEnvironmental Factors in Degenerative Diseases Research Group, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain.
Tamara Castillo-TriviñoCenter for Networked Biomedical Research on Neurodegenerative Diseases (CIBERNED)-ISCIII, Madrid, Spain.
David OtaeguiCenter for Networked Biomedical Research on Neurodegenerative Diseases (CIBERNED)-ISCIII, Madrid, Spain.
Sara LlufriuNeuroimmunology and Multiple Sclerosis Unit, Service of Neurology, Hospital Clinic and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Yolanda BlancoNeuroimmunology and Multiple Sclerosis Unit, Service of Neurology, Hospital Clinic and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Antonio J Sánchez-LópezNeuroimmunology Unit, Puerta de Hierro-Segovia de Arana Health Research Institute, Madrid, Spain.
Antonio García-MerinoNeuroimmunology Unit, Puerta de Hierro-Segovia de Arana Health Research Institute, Madrid, Spain.
Nicolás FissoloServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Lucía GutiérrezServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Javier Villacieros-ÁlvarezServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Enric MonrealDepartment of Neurology, Hospital Universitario Ramón y Cajal, REEM, IRYCIS, Universidad de Alcalá, Madrid, Spain.
Heinz WiendlDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.
Xavier MontalbanServei de Neurologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Jan D LünemannDepartment of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany. Jan.Luenemann@ukmuenster.de.ORCID http://orcid.org/0000-0002-3007-708X

Funding

HORIZON EUROPE Framework Programme 101137235
6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe impact of viral infections on disease susceptibility and progression has predominantly been studied in patients with relapse-onset MS (RMS). Here, we determined immune responses to ubiquitous viruses in patients with primary progressive MS (PPMS).

methodsAntibody responses to Epstein-Barr virus (EBV), specifically to the latent EBV nuclear antigen 1 and the lytic viral capsid antigen VCA, human herpesvirus 6 (HHV-6), human cytomegalovirus (HCMV), and measles virus were determined in a cohort of 68 PPMS patients with a mean follow-up of 8 years and compared with 66 healthy controls matched for sex and age.

resultsCompared with controls, PPMS patients showed increased humoral immune responses to the EBV-encoded nuclear antigen-1 (EBNA1), but not to the lytic EBV capsid antigen (VCA) or to other viral antigens. Seroprevalence rates for HCMV were significantly higher in PPMS. Antiviral immune responses at baseline did not correlate with disability progression over time. DISCUSSION: Elevated immune responses toward EBNA1 are selectively increased in people with primary progressive disease, indicating a link between EBNA1-targeting immune responses and the development of both RMS and PPMS. Our data also suggest that chronic HCMV infection is associated with progressive MS.

Indexed as

Antibodies, ViralEpstein-Barr Virus InfectionsEpstein-Barr Virus Nuclear AntigensMultiple Sclerosis, Chronic ProgressiveCase-Control StudiesCytomegalovirusDisease SusceptibilityFemaleFollow-Up StudiesHerpesvirus 4, HumanHerpesvirus 6, HumanHumansImmunity, HumoralMaleMeasles virusSeroepidemiologic StudiesAntibodies, ViralEBV-encoded nuclear antigen 1Epstein-Barr Virus Nuclear AntigensEpstein–Barr virusHuman cytomegalovirusMultiple sclerosisPrimary progressiveVirus

Identifiers

PMID39666032
PMCPMC11638268

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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.