The DOI matches its Crossref record; 50 of the 51 references it cites were found in a registry or an index.
Longitudinal analysis reveals high prevalence of Epstein-Barr virus associated with multiple sclerosis
Abstract
Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system of unknown etiology. We tested the hypothesis that MS is caused by Epstein-Barr virus (EBV) in a cohort comprising more than 10 million young adults on active duty in the US military, 955 of whom were diagnosed with MS during their period of service. Risk of MS increased 32-fold after infection with EBV but was not increased after infection with other viruses, including the similarly transmitted cytomegalovirus. Serum levels of neurofilament light chain, a biomarker of neuroaxonal degeneration, increased only after EBV seroconversion. These findings cannot be explained by any known risk factor for MS and suggest EBV as the leading cause of MS.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“This phenomenon is particularly relevant considering recent data demonstrating that EBV infection is a necessary risk factor for MS and that cross-reactive immune responses between EBV antigens and CNS proteins may contribute to disease initiation [211, 212].”
From Insights and challenges on animal models for progressive multiple sclerosis (2026) · cites this paper as [212]
In the citing paper
“For example, type 1 diabetes mellitus was linked to enterovirus infections185 and multiple sclerosis to Epstein–Barr virus (EBV) infections186.”
From COVID-19 and cellular senescence (2023) · cites this paper as [186]
Citations
Cites
Sensitivity analysis in observational research: Introducing the E-value
VanderWeele, T. J., & Ding, P. (2017) · Annals of Internal Medicine · doi:10.7326/m16-2607 · Cited by 6,350
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
The International Multiple Sclerosis Genetics Consortium & The Wellcome Trust Case Control Consortium 2 (2011) · Nature · doi:10.1038/nature10251 · Cited by 2,697
Reich, D. S., Lucchinetti, C. F., & Calabresi, P. A. (2018) · New England Journal of Medicine · doi:10.1056/nejmra1401483 · Cited by 2,491
The Immune Epitope Database (IEDB): 2018 update
Vita, R., Mahajan, S., Overton, J. A., Dhanda, S. K., Martini, S. R., Cantrell, J. R., Wheeler, D. K., Sette, A., & Peters, B. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1006 · Cited by 2,194
Ocrelizumab versus Interferon Beta-1a in Relapsing Multiple Sclerosis
Hauser, S. L., Bar-Or, A., Comi, G., Giovannoni, G., Hartung, H.-P., Hemmer, B., Lublin, F., Montalban, X., Rammohan, K. W., Selmaj, K., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1601277 · Cited by 2,021
Neurofilaments as biomarkers in neurological disorders
Khalil, M., Teunissen, C. E., Otto, M., Piehl, F., Sormani, M. P., Gattringer, T., Barro, C., Kappos, L., Comabella, M., Fazekas, F., et al. (2018) · Nature Reviews Neurology · doi:10.1038/s41582-018-0058-z · Cited by 1,988
Negative Controls: A Tool for Detecting Confounding and Bias in Observational Studies
Lipsitch, M., Tchetgen Tchetgen, E., & Cohen, T. (2010) · Epidemiology · doi:10.1097/ede.0b013e3181d61eeb · Cited by 1,583
Interactions between genetic, lifestyle and environmental risk factors for multiple sclerosis
Olsson, T. P., Barcellos, L. F., & Alfredsson, L. S. (2016) · Nature Reviews Neurology · doi:10.1038/nrneurol.2016.187 · Cited by 1,263
Serum neurofilament light: a biomarker of neuronal damage in multiple sclerosis
Disanto, G., Barro, C., Benkert, P., Naegelin, Y., Schädelin, S., Giardiello, A., Zecca, C., Blennow, K., Zetterberg, H., Leppert, D., et al. (2017) · Annals of Neurology · doi:10.1002/ana.24954 · Cited by 1,164
Epstein-Barr virus: exploiting the immune system
Thorley‐Lawson, D. A. (2001) · Nature reviews. Immunology · doi:10.1038/35095584 · Cited by 942
Flagged first, then by citations
1 of the 51 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 801–900 of 1,001
Greater humoral EBV response may be associated with choroid plexus inflammation in progressive MS
Jakimovski, D., Zivadinov, R., Ramanathan, M. K., Weinstock‐Guttman, B., Tavazzi, E., Dwyer, M. G., & Bergsland, N. (2024) · Journal of NeuroVirology · doi:10.1007/s13365-024-01231-w · Cited by 8
“(Bjornevik et al. 2022 ; Guan et al. 2019 ) However, the role of EBV after the disease initiation and its potential effect towards further disease propagation and how it may impact the MS pathophysiological process have not been extensively investigated.”
Blackmer‐Raynolds, L., & Sampson, T. R. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.02.013 · Cited by 8
Henríquez, K., Molt, F., Gajardo, J., Cortés, B., & Ramírez-Santana, M. (2022) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2022.103750 · Cited by 9
B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet’s Disease
Maghrebi, O., Belghith, M., Jeridi, C., Rachdi, A., Nabli, F., Saied, Z., Belal, S., Sassi, S. B., & Barbouche, M. (2022) · Cells · doi:10.3390/cells11081306 · Cited by 8
Gremese, E., Tolusso, B., Bruno, D., Alivernini, S., & Ferraccioli, G. (2022) · Autoimmunity Reviews · doi:10.1016/j.autrev.2022.103102 · Cited by 8
Langhorst, S. E., Frahm, N., Hecker, M., Mashhadiakbar, P., Streckenbach, B., Baldt, J., Heidler, F., & Zettl, U. K. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12050677 · Cited by 9
Bezzini, D., Gualdani, E., Razzanelli, M., Battaglia, M. A., Cortese, R., Francesconi, P., & Ulivelli, M. (2022) · Neurological Sciences · doi:10.1007/s10072-022-06345-9 · Cited by 8
Drosophila as a Model for Human Viral Neuroinfections
Benoit, I., Curzio, D. L. D., Civetta, A., & Douville, R. N. (2022) · Cells · doi:10.3390/cells11172685 · Cited by 8
Bevens, W., Reece, J. C., Jelinek, P. L., Weiland, T. J., Nag, N., Simpson, S., Gray, K. M., Jelinek, G., & Neate, S. L. (2022) · Digital Health · doi:10.1177/20552076221123713 · Cited by 8
Sedaghat, N., & Etemadifar, M. (2022) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2022.104155 · Cited by 8
Gold, J., Holden, D., Parratt, J. D. E., Yiannikas, C., Ahmad, R., Sedhom, M. A. K., & Giovannoni, G. (2022) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2022.104377 · Cited by 8
Agrafiotis, A., Dizerens, R., Vincenti, I., Wagner, I., Kuhn, R., Shlesinger, D., Manero-Carranza, M., Cotet, T., Hong, K., Pagé, N., et al. (2023) · Acta Neuropathologica · doi:10.1007/s00401-023-02537-5 · Cited by 9
Activated immune cells drive neurodegeneration in an Alzheimer’s model
Guldner, I. H., & Wyss‐Coray, T. (2023) · Nature · doi:10.1038/d41586-023-00600-5 · Cited by 8
Goldin, K., Riemann-Lorenz, K., Daubmann, A., Pöttgen, J., Krause, N., Schröder, H., & Heesen, C. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1172419 · Cited by 9
Uribe, F. R., González, V. P. I., Kalergis, A. M., Soto, J. A., & Böhmwald, K. (2024) · Brain Sciences · doi:10.3390/brainsci14010059 · Cited by 8
Cervical lymph node diameter reflects disease progression in multiple sclerosis
Tuulasvaara, A., Kurdo, G., Martola, J., & Laakso, S. M. (2024) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2024.105496 · Cited by 9
New Evidence for Epstein-Barr Virus Infection as a Cause of Multiple Sclerosis
Hacohen, Y., & Ciccarelli, O. (2022) · Neurology · doi:10.1212/wnl.0000000000200243 · Cited by 8
Single Cell Transcriptomics Reveals the Hidden Microbiomes of Human TissuesPreprint
Mahmoudabadi, G., Crasta, S., & Quake, S. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.11.511790 · Cited by 8
Liu, Z., Luo, Y., Kirimunda, S., Verboom, M., Onabajo, O. O., Gouveia, M. H., Ogwang, M. D., Kerchan, P., Reynolds, S. J., Tenge, C., et al. (2024) · Communications Biology · doi:10.1038/s42003-023-05701-5 · Cited by 7
“Additionally, both rs2040406(G) and HLA-DQA1 * 04:01 have pleiotropic effects against multiple sclerosis 30,31 , which is EBV-linked 32 .”
Lukač, J. K., Baronica, K. B., Šućur, A., Sremec, J., Tomasović, S., Baronica, R., Kelava, T., Grčević, D., & Kovačić, N. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158064 · Cited by 9
“Infection with EBV has, for a long time, been considered as an important contributor for the development of MS, and a recent assessment by Bjornevik et al. reports a 32-fold increase in the risk for MS development [51,52].”
Górska, A., Canziani, L. M., Rinaldi, E., Pana, Z. D., Beale, S., Bai, F., Klerk, B. M. B., de Bruijn, S., Donà, D., Ekkelenkamp, M. B., et al. (2024) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2024.12.001 · Cited by 7
Yiu, S. P. T., Liao, Y., Yan, J., Weekes, M. P., & Gewurz, B. E. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2400167122 · Cited by 7
Infectious mononucleosis is a more realistic target for preventing multiple sclerosis
Giovannoni, G., Hawkes, C. H., Lechner‐Scott, J., Yeh, E. A., & Levy, M. (2025) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2025.106337 · Cited by 7
Yuasa‐Kawada, J., Kinoshita-Kawada, M., Hiramoto, M., Yamagishi, S., Mishima, T., Yasunaga, S., Tsuboi, Y., Hattori, N., & Wu, J. Y. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-01330 · Cited by 10
Aubry, A., François, C., Demey, B., Louchet-Ducoroy, M., Pannier, C., Segard, C., Brochot, É., & Castelain, S. (2025) · Microorganisms · doi:10.3390/microorganisms13040733 · Cited by 7
“…primary EBV infections occur at an earlier age due to different hygienic and social conditions [12–14], whereas delayed primary infection is associated with an increased risk of infectious mononucleosis and, consequently, a higher risk of Hodgkin’s lymphoma [15] or multiple sclerosis [16,17].”
Wang, M., Otto, C., Fernández‐Zapata, C., Dehlinger, A., Gallaccio, G., Diekmann, L., Niederschweiberer, M. A., Schindler, P., Körtvelyessy, P., Kunkel, D., et al. (2025) · iScience · doi:10.1016/j.isci.2025.112383 · Cited by 9
Role of soluble biomarkers in treating multiple sclerosis and neuroinflammatory conditions
Bose, G., Thebault, S., Fadda, G., Brooks, J., & Freedman, M. S. (2025) · Neurotherapeutics · doi:10.1016/j.neurot.2025.e00588 · Cited by 8
“A large cohort from the United States identi fi ed that infection with Epstein-Barr virus (EBV) increased the risk of developing MS by 30-fold, and that it was essentially necessary in order for MS to occur [10].”
Multiple sclerosis: what have we learned and can we still learn from electron microscopy
Oost, W., Meilof, J. F., & Baron, W. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05690-0 · Cited by 7
Ganta, K. K., McManus, M. M., Blanc, R., Wang, Q., Jung, W., Brody, R., Carrington, M. N., Paris, R., Chandramouli, S., McNamara, R. P., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115709 · Cited by 7
“3,7 In particular, high levels of antibodies that target a region of EBNA-1 (aa 365–459) with known homology to several human proteins have been linked to an elevated risk of developing MS 3 ; risk is especially high (15-fold) in individuals who have at least one HLA-DRB1*15:01 allele and who are…”
Filipek, B., Macieja, A., Binda, A., Szelenberger, R., Gorniak, L., Miller, E. D., Matysiak, M., Stasiołek, M., Majsterek, I., & Popławski, T. (2025) · Biomolecules · doi:10.3390/biom15060756 · Cited by 9
“Although the precise etiology of MS remains elusive, its pathogenesis involves a complex interplay between genetic susceptibility and environmental exposures such as Epstein–Barr virus (EBV) infection, smoking, obesity, and vitamin D deficiency [4–7].”
Embodiment of structural racism and multiple sclerosis risk and outcomes in the USA
Langer-Gould, A. M., Cepon‐Robins, T. J., Torres, J. B., Yeh, E. A., & Gildner, T. E. (2025) · Nature Reviews Neurology · doi:10.1038/s41582-025-01096-5 · Cited by 9
“Another possibility is that EBV reactivation reflects a more general deficit in cell-mediated immunity; however, this scenario seems unlikely, as other ubiquitous herpes viruses, such as cytomegalovirus and varicella zoster virus, do not show similar associations with MS 93 .”
Latent EBV enhances the efficacy of anti-CD3 mAb in Type 1 diabetes
Lledó-Delgado, A., Preston‐Hurlburt, P., Higdon, L. E., Hu, A. K., James, E. A., Lim, N., Long, S. A., McNamara, J., Nguyen, H. D., Serti, E., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60276-5 · Cited by 10
“1C; II) showing separate donors should be provided for all cells, CD4+ , CD8+ T cells, B cells, monocytes.”
Bingöl, F. G., Koçyiğit, E., Çelik, E., Ağagündüz, D., & Budán, F. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26125464 · Cited by 8
“Additionally, the Epstein–Barr virus infection, particularly when contracted later in life, is a recognized risk factor [10,18,19].”
Bourgonje, A. R., Andreu‐Sánchez, S., Gaćeša, R., Innocenti, G., Kalka, I. N., Klompus, S., Leviatan, S., Schlesinger, Y., Krongauz, D. L., Weinberger, A., et al. (2025) · Gut · doi:10.1136/gutjnl-2024-334362 · Cited by 7
“…EBV peptides were reported to be cross-reactive with this motif (BRFF2 and HFM NS2PC, which were not identified in the present study), the role of EBV reactivity and immune control in early multiple sclerosis pathogenesis is well-documented 45 and supported by strong epidemiological evidence.”
The Latent Membrane Protein 1 (LMP1): Biological Functions and Molecular Mechanisms
Kieser, A. (2025) · Current topics in microbiology and immunology · doi:10.1007/82_2025_321 · Cited by 7
Ghezzi, A., D’Alfonso, S., Pugliatti, M., Pilotto, S., Tosi, M., Corona, A., Zollo, A., Pomella, N., Amato, M. P., Cocco, E. E., et al. (2025) · Neurological Sciences · doi:10.1007/s10072-025-08385-3 · Cited by 7
“Among viruses [23] large body of evidence suggests the role of EBV, considered as a prerequisite for MS development [24–26], supported by three main findings: a) in a longitudinal study of subjects initially seronegative for EBV, MS risk increased more than 30-fold after EBV infection, b) a history…”
Epstein-Barr virus (EBV) infection and its sequelae in the immunocompetent host
Meirhaeghe, M. R., & BalfourJr., H. H. (2025) · Journal of Clinical Virology · doi:10.1016/j.jcv.2025.105854 · Cited by 7
Autoimmunity, epitope analysis, and molecular mimicry
Rojas, M., Acosta‐Ampudia, Y., Monsalve, D. M., Ramı́rez-Santana, C., Heuer, L. S., Ridgway, W. M., Anaya, J., Lian, Z.-X., & Gershwin, M. E. (2025) · Current Opinion in Immunology · doi:10.1016/j.coi.2025.102681 · Cited by 8
Crammond, P., Hastak, P., Delaney, A. P., & Sasson, S. C. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1761361 · Cited by 8
Antibodies to blood coagulation components are implicated in patients with multiple sclerosis
Hadjiagapiou, M. S., Krashias, G., Deeba, E., Christodoulou, C., Pantzaris, M., & Lambrianides, A. (2022) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2022.103775 · Cited by 7
Immune checkpoints in T cells during oncogenic γ‐herpesvirus infections
Münz, C. (2022) · Journal of Medical Virology · doi:10.1002/jmv.27840 · Cited by 7
Antisense modulation of IL7R splicing to control sIL7R expression in human CD4 + T cells
Galarza-Muñoz, G., Kennedy-Boone, D., Schott, G., Bradrick, S. S., & García-Blanco, M. A. (2022) · RNA · doi:10.1261/rna.079137.122 · Cited by 7
The adaptation model of immunity: A new insight into aetiology and treatment of multiple sclerosis
Manjili, M. H. (2023) · Scandinavian Journal of Immunology · doi:10.1111/sji.13255 · Cited by 7
Autologous Hematopoietic Stem Cell Transplantation to Treat Multiple Sclerosis
Ross, L. A., Stropp, L. M., & Cohen, J. A. (2023) · Neurologic Clinics · doi:10.1016/j.ncl.2023.06.002 · Cited by 7
Language impairments in people with autoimmune neurological diseases: A scoping review
Rook, J., Llufriú, S., de Kok, D., & Rofes, A. (2023) · Journal of Communication Disorders · doi:10.1016/j.jcomdis.2023.106368 · Cited by 8
Salmen, A., Hoepner, R., Fleischer, V., Heldt, M. B. O. T., Gisevius, B., Motte, J., Ruprecht, K., Schneider, R., Fisse, A. L., Grüter, T., et al. (2023) · Therapeutic Advances in Neurological Disorders · doi:10.1177/17562864231197309 · Cited by 7
The role of autophagy protein Atg5 in multiple sclerosis
Baeva, M.-E., & Camara-Lemarroy, C. R. (2023) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2023.105029 · Cited by 7
Epstein–Barr Virus Encoded BCL2, BHRF1, Downregulates Autophagy by Noncanonical Binding of BECN1
Wyatt, S., Glover, K., Dasanna, S., Lewison, M., González‐García, M., Colbert, C. L., & Sinha, S. C. (2023) · Biochemistry · doi:10.1021/acs.biochem.3c00225 · Cited by 8
Brain Virome in Neurodegenerative Disorders: Insights from Transcriptomic Data Analysis
Balakrishnan, B., Arul, S. S., Ravindran, A., & Venkataraman, S. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00432 · Cited by 7
Sarcoidosis and its relation to other immune-mediated diseases: Epidemiological insights
Arkema, E. V., Rossides, M., & Cozier, Y. C. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2023.103127 · Cited by 7
Baccianti, F., Masson, C., Delécluse, S., Li, Z., Poirey, R., & Delecluse, H. (2023) · mBio · doi:10.1128/mbio.01784-23 · Cited by 7
A new computational workflow to guide personalized drug therapy
Pernice, S., Maglione, A., Tortarolo, D., Sirovich, R., Clerico, M., Rolla, S., Beccuti, M., & Cordero, F. (2023) · Journal of Biomedical Informatics · doi:10.1016/j.jbi.2023.104546 · Cited by 7
Mageau, A., Helary, A., Ruckly, S., Strukov, A., Papo, T., Timsit, J., & Sacré, K. (2023) · Journal of Internal Medicine · doi:10.1111/joim.13745 · Cited by 7
Smith, G. D., Albert Hofman, D., & Brennan, P. (2023) · European Journal of Epidemiology · doi:10.1007/s10654-023-01090-5 · Cited by 7
Drosu, N. C., & Levy, M. (2024) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2023.105396 · Cited by 7
Yin, R., Melton, S., Huseby, E. S., Mehran Kardar, A., & Chakraborty, A. K. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2318599121 · Cited by 7
Follow-up of cognitive impairment and inflammatory profile in individuals with mild COVID-19
Silva, N. G. S. E., Rosa, D. V., de Paula, J. J., Coimbra, R. S., de Miranda, D. M., & Romano‐Silva, M. A. (2024) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2024.578327 · Cited by 7
HLA Associations of Intrathecal IgG Production against Specific Viruses in Multiple Sclerosis
Neidhart, S., Vlad, B., Hilty, M., Högelin, K. A., Ziegler, M., Berenjeno‐Correa, E., Reichen, I., Stridh, P., Jelčić, I., Khademi, M., et al. (2024) · Annals of Neurology · doi:10.1002/ana.26921 · Cited by 7
Andreu‐Sánchez, S., Ripoll-Cladellas, A., Culinscaia, A., Bulut, O. P., Bourgonje, A. R., Netea, M. G., Lansdorp, P. M., Aubert, G., Bonder, M. J., Franke, L., et al. (2024) · iScience · doi:10.1016/j.isci.2024.109981 · Cited by 7
Histone methylation in Epstein–Barr virus-associated diseases
Chen, G., Zhang, L., Wang, R., & Xie, Z. (2024) · Epigenomics · doi:10.1080/17501911.2024.2345040 · Cited by 7
Mastering Death: The Roles of Viral Bcl-2 in dsDNA Viruses
Suraweera, C. D., Espinoza, B., Hinds, M. G., & Kvansakul, M. (2024) · Viruses · doi:10.3390/v16060879 · Cited by 7
“EBV infections have recently been correlated with multiple sclerosis [112].”
BackgroundMultiple sclerosis: the NLRP3 inflammasome, gasdermin D, and therapeutics
Brint, A. A., Greene, S., Fennig-Victor, A. R., & Wang, S. (2024) · Annals of Translational Medicine · doi:10.21037/atm-23-1960 · Cited by 8
“Evidence that EBV, a herpesvirus, may be responsible for triggering the autoimmune response and lead to demyelination (5).”
An Overview of Multiple Sclerosis In Vitro Models
Czpakowska, J., Kałuża, M., Szpakowski, P., & Głąbiński, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147759 · Cited by 7
“It has been indicated that the risk of MS development after such an event increases 32-fold in comparison to other infections, even if the route of viral transmission is similar [24].”
BackgroundChen, J., Wei, C., Huang, S., Wu, S., He, R., Chen, T., Qin, X., Wei, W., Qin, B., Wu, S., et al. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113027 · Cited by 7
Moloney, E., Mashayekhi, A., Sharma, S., Kontogiannis, V., Ansaripour, A., Brownlee, W. J., Paling, D., & Javanbakht, M. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1479476 · Cited by 7
Ghaffary, E. M., Bjørklund, G., Bhat, R. S., & Mirmosayyeb, O. (2025) · Autoimmunity Reviews · doi:10.1016/j.autrev.2025.103825 · Cited by 7
Romeo, M. A., Montani, M. S. G., Benedetti, R., Arena, A., Gaeta, A., & Cirone, M. (2022) · Virus Research · doi:10.1016/j.virusres.2022.198726 · Cited by 7
Predictors of progression from a first demyelinating event to clinically definite multiple sclerosis
Chapman, C., Lucas, R. M., Ponsonby, A., Taylor, B. V., Ausimmune Investigator Group, Chapman, C., Coulthard, A., Dear, K. B. G., Dwyer, T., Kilpatrick, T. J., et al. (2022) · Brain Communications · doi:10.1093/braincomms/fcac181 · Cited by 8
Uchida, A. M., Ro, G., Garber, J. J., Roelstraete, B., & Ludvigsson, J. F. (2022) · United European Gastroenterology Journal · doi:10.1002/ueg2.12324 · Cited by 7
Contribution of Intravital Neuroimaging to Study Animal Models of Multiple Sclerosis
Buttigieg, E., Scheller, A., Waly, B. E., Kirchhoff, F., & Debarbieux, F. C. (2023) · Neurotherapeutics · doi:10.1007/s13311-022-01324-6 · Cited by 7
Lucas, R. M., Lay, M. J., Grant, J. W., Cherbuin, N., Toi, C. S., Dear, K. B. G., Taylor, B. V., Dwyer, D. E., Ausimmune Investigator Group, & Ponsonby, A. (2023) · European Journal of Neurology · doi:10.1111/ene.15919 · Cited by 7
Abou‐Mrad, T., Naja, K., Khoury, S. J., & Hannoun, S. (2023) · European Journal of Neurology · doi:10.1111/ene.15922 · Cited by 8
Grimaldi‐Bensouda, L., Papeix, C., Hamon, Y., Bénichou, J., & Abenhaim, L. (2023) · Journal of Neurology · doi:10.1007/s00415-023-11822-y · Cited by 13
Cladribine Tablets Mode of Action, Learning from the Pandemic: A Narrative Review
Carlini, F., Lusi, V., Rizzi, C., Assogna, F., & Laroni, A. (2023) · Neurology and Therapy · doi:10.1007/s40120-023-00520-6 · Cited by 7
Salvetti, M., Wray, S. E., Nelles, G., Belviso, N., Kumar, A., Koster, T. M., Castro-Borrero, W., Vignos, M., & on behalf of the POP Investigators (2024) · Multiple Sclerosis Journal - Experimental Translational and Clinical · doi:10.1177/20552173241238632 · Cited by 7
Multiple sclerosis and the intestine: Chasing the microbial offender
Peters, A., Gerdes, L. A., & Wekerle, H. (2024) · Immunological Reviews · doi:10.1111/imr.13357 · Cited by 7
“This observation opens up new opportunities for addressing important unsolved questions related to the prodromal (clinically non-apparent) stage of MS.”
InfluentialDobson, R., Holden, D., Vickaryous, N. K., Bestwick, J. P., George, K., Sayali, T., Bianchi, L., Wafa, M., Gold, J., & Giovannoni, G. (2023) · Multiple Sclerosis Journal · doi:10.1177/13524585231215268 · Cited by 6
Yang, N. Y., Hsieh, A. Y. Y., Chen, Z., Campbell, A. R., Gadawska, I., Kakkar, F., Sauve, L. J., Bitnun, A., Brophy, J. C., Murray, M. C. M., et al. (2024) · Viruses · doi:10.3390/v16050755 · Cited by 8
Domínguez‐Mozo, M. I., Galán, V., Ramió‐Torrentà, L., Quiroga, A., Quintana, E., Villar, L. M., Costa‐Frossard, L., Fernández-Velasco, J. I., Villarrubia, N., García‐Martínez, M. Á., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1384411 · Cited by 6
Evolution from viral encephalitis to autoimmune encephalitis to multiple sclerosis: a case report
Wurdack, K., Prüß, H., & Finke, C. (2024) · Journal of Neurology · doi:10.1007/s00415-024-12659-9 · Cited by 8
“Viral infections may represent an influential external element that, taken together with individual susceptibility to immune system dysregulation, could trigger neuroimmunological disease [2, 11, 14, 15].”
Epstein-Barr virus infection in patients with MOGAD
Maniscalco, G. T., Dinoto, A., Foglia, M. C., Battista, M. E. D., Moreggia, O., Cesare, D. D. G., Williams, M., Rossi, F. W., Carta, S., Chiodega, V., et al. (2024) · Multiple Sclerosis Journal · doi:10.1177/13524585241298065 · Cited by 6
Animal models of post-acute COVID-19 syndrome: a call for longitudinal animal studies
Dai, J., He, F., Chen, Q., Li, Q., Zhao, L., & Du, Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1521029 · Cited by 9
Nova, A., Gentilini, D., Caprio, G. D., Bourguiba, S., Vince, N., Gourraud, P., Bernardinelli, L., & Fazia, T. (2025) · European Journal of Neurology · doi:10.1111/ene.70131 · Cited by 10
Decoding the etiology of immune-mediated inflammatory diseases statistically
ElAbd, H., & Mahdy, A. K. H. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1610662 · Cited by 7
Comprehensive resolution and classification of the Epstein Barr virus transcriptome
Nguyen, T. D., Wang, J., Lam, M., McFerrin, H., O’Grady, T. M., Roberts, C., Otterloo, N. V., Nguyen, T. T., Baddoo, M., Wyczechowska, D. D., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-61870-3 · Cited by 6
“Since early genes are defined by having a late transcription component of less than 20% (BALF2 ratio > 0.8), a contribution of vPIC to their transcription of up to 20% would be expected.”
InfluentialLi, J., Vas, N., Amezcua, L., & Rotstein, D. L. (2025) · CNS Drugs · doi:10.1007/s40263-025-01205-4 · Cited by 6
“Furthermore, Epstein–Barr virus (EBV) infection is a risk factor for MS [79], and EBV reactivation may be implicated in MS pathophysiology and disease activity [80].”
Gupta, N. S., Shrivastav, S. K., Singh, I. K., Kumari, S., Jha, N. K., & Gupta, R. (2025) · Brain Research · doi:10.1016/j.brainres.2025.149844 · Cited by 6
Riel, M., & Johannsen, E. (2025) · Current topics in microbiology and immunology · doi:10.1007/82_2025_330 · Cited by 8
Alterations of the nasal and oral microbiota in multiple sclerosis
Li, S., Montini, F., Song, A., Willocq, V., Chan, E., Shamah, R., Weiner, M., Glanz, B. I., Weiner, H. L., & Cox, L. M. (2025) · EBioMedicine · doi:10.1016/j.ebiom.2025.105959 · Cited by 6
“23 While Epstein–Barr virus (EBV) infection is strongly associated with the development of MS, 24–26 only a small proportion of EBV infected individuals develop MS, suggesting other environmental factors may be important.”
Fitzjerrells, R. L., Meza, L. A., Yadav, M., Olalde, H. M., Hoang, J., Paullus, M., Cherwin, C. H., Cho, T. A., Brown, G., Ganesan, S. M., et al. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00787-7 · Cited by 7
Towards primary prevention of multiple sclerosis
Dobson, R., Kreft, K. L., Jacobs, B. M., Brown, J. W. L., Thomson, A., Nicholas, R. S., Walton, C., Narendran, P., Taskforce, O. B. O. T. U. M. P., Braithwaite, T., et al. (2025) · Nature Reviews Neurology · doi:10.1038/s41582-025-01164-w · Cited by 8
Hirabayashi, M., Georges, D., Combes, J., & Clifford, G. M. (2026) · International Journal of Cancer · doi:10.1002/ijc.70468 · Cited by 6
“Primary EBV infection is often asymptomatic but may present as infectious mononucleosis in young adults, and has been causally linked with the autoimmune disease multiple sclerosis [4] and other immunoproliferative disorders.”
Advances in Multiple Sclerosis
Hauser, S. L. (2026) · New England Journal of Medicine · doi:10.1056/nejmra2501195 · Cited by 7
Understanding the neurological implications of acute and long COVID using brain organoids
García‐González, L., Martí-Sarrias, A., Puertas, M. C., Bayón-Gil, Á., Resa‐Infante, P., Martínez‐Picado, J., Navarro, A., & Acosta, S. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.050049 · Cited by 7
Herrera, P., & Cauchi, R. J. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166818 · Cited by 6
Stem Cells from Dental Pulp of Deciduous Teeth: Twenty Years of Experience
Kerkis, I., Wenceslau, C. V., & Araldi, R. P. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1003850 · Cited by 6
Association between multiple sclerosis and cancer risk: A two-sample Mendelian randomization study
Liu, Z., Fan, T., Mo, X., Kan, J., & Zhang, B. (2024) · PLoS ONE · doi:10.1371/journal.pone.0298271 · Cited by 6
Antigen-specific immunotherapy via delivery of tolerogenic dendritic cells for multiple sclerosis
Li, V., Binder, M. D., Purcell, A. W., & Kilpatrick, T. J. (2024) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2024.578347 · Cited by 7
EBV-RELATED LYMPHOPROLIFERATIVE DISEASES: A REVIEW IN LIGHT OF NEW CLASSIFICATIONS
Tralongo, P., Bakacs, A., & Larocca, L. M. (2024) · Mediterranean Journal of Hematology and Infectious Diseases · doi:10.4084/mjhid.2024.042 · Cited by 6
Ojo, T. O., Elegbeleye, O. E., Bolaji, O. Q., Adelusi, T. I., Oladipo, E. K., Olawuyi, M. O., Afolayan, B. O., Oyaronbi, A. O., Ogunjobi, T. T., Oyewole, M. P., et al. (2024) · Neurogenetics · doi:10.1007/s10048-024-00764-w · Cited by 6
“It also results in the elevated IgG level of EBNA-1 in the CSF which is the hallmark of MS [9, 10].”
Metadata
- Authors
- Bjornevik, K., Cortese, M., Healy, B. C., Kuhle, J., Mina, M. J., Leng, Y., Elledge, S. J., Niebuhr, D. W., Scher, A. I., Munger, K. L., & Ascherio, A.
- Affiliations
- Department of Nutrition, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
- Harvard University (US)
- Brigham and Women's Hospital (US)
- Neurologic Clinic and Policlinic, MS Center and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel, University of Basel, Basel, Switzerland.
- Uniformed Services University of the Health Sciences (US)
- Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
- Corresponding author
- Cortese, Marianna
- Munger, Kassandra L.
- Ascherio, Alberto
- ORCID
- Venue
- Science
- Published
- 2022-01-21
- Volume
- 375
- Issue
- 6578
- Pages
- 296-301
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W4205972999
- Cited by
- 2,049
- References
- 51
- Citations by year
- 2026: 354 · 2025: 412 · 2024: 461 · 2023: 432 · 2022: 388
- FWCI
- 289.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute of Neurological Disorders and Stroke (R01NS042194, R01NS046635, R01NS103891)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Health Sciences › Medicine › Oncology › Viral-associated cancers and disorders
- Health Sciences › Medicine › Epidemiology › Cytomegalovirus and herpesvirus research
- Keywords
- multiple sclerosis, Epstein-Barr virus, viral etiology, neurofilament light chain, neuroaxonal degeneration, cytomegalovirus, demyelinating disease, military personnel
- MeSH terms
- Antibodies, Viral, Cytomegalovirus, Herpesvirus 4, Human, Female, Humans, Longitudinal Studies, Male, Military Personnel, Multiple Sclerosis, Risk Factors, Cohort Studies, Biomarkers, Prevalence, Neurofilament Proteins, Age of Onset, Epstein-Barr Virus Infections, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review