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Commensal microbiota and myelin autoantigen cooperate to trigger autoimmune demyelination
Abstract
Active multiple sclerosis lesions show inflammatory changes suggestive of a combined attack by autoreactive T and B lymphocytes against brain white matter. These pathogenic immune cells derive from progenitors that are normal, innocuous components of the healthy immune repertoire but become autoaggressive upon pathological activation. The stimuli triggering this autoimmune conversion have been commonly attributed to environmental factors, in particular microbial infection. However, using the relapsing-remitting mouse model of spontaneously developing experimental autoimmune encephalomyelitis, here we show that the commensal gut flora-in the absence of pathogenic agents-is essential in triggering immune processes, leading to a relapsing-remitting autoimmune disease driven by myelin-specific CD4(+) T cells. We show further that recruitment and activation of autoantibody-producing B cells from the endogenous immune repertoire depends on availability of the target autoantigen, myelin oligodendrocyte glycoprotein (MOG), and commensal microbiota. Our observations identify a sequence of events triggering organ-specific autoimmune disease and these processes may offer novel therapeutic targets.
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“Similar to psoriasis, IL-17 pathway inhibitors (secukinumab and ixekizumab) have been shown to be effective in the treatment of PsA [141, 142].”
From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [142]
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“in a laboratory model of multiple sclerosis, mice sensitized to the autoantigen, myelin oligodendrocyte glycoprotein, only developed experimental autoimmune encephalitis in the presence of commensal bacteria.45”
From The Gut Microbiome and the Brain (2014) · cites this paper as [45]
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Cites
Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554
Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species
Atarashi, K., Tanoue, T., Shima, T., Imaoka, A., Kuwahara, T., Momose, Y., Cheng, G., Yamasaki, S., Saito, T., Ohba, Y., et al. (2011) · Science · doi:10.1126/science.1198469 · Cited by 3,752
Kaser, A., Zeissig, S., & Blumberg, R. S. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101225 · Cited by 1,806
Ivanov, I. I., Frutos, R. D. L., Manel, N., Yoshinaga, K., Rifkin, D. B., Sartor, R. B., Finlay, B. B., & Littman, D. R. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.09.009 · Cited by 1,770
Gaboriau-Routhiau, V., Rakotobe, S., Lécuyer, E., Mulder, I., Lan, A., Bridonneau, C., Rochet, V., Pisi, A., De Paepe, M., Brandi, G., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.08.020 · Cited by 1,452
Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis
Lee, Y. K., Menezes, J. S., Umesaki, Y., & Mazmanian, S. K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000082107 · Cited by 1,323
Environmental risk factors for multiple sclerosis. Part I: The role of infection
Ascherio, A., & Munger, K. L. (2007) · Annals of Neurology · doi:10.1002/ana.21117 · Cited by 1,036
Epitope spreading initiates in the CNS in two mouse models of multiple sclerosis
McMahon, E. J., Bailey, S. L., Castenada, C. V., Waldner, H., & Miller, S. D. (2005) · Nature Medicine · doi:10.1038/nm1202 · Cited by 694
Goverman, J. M., Woods, A., Larson, L., Weiner, L. P., Hood, L., & Zaller, D. M. (1993) · Cell · doi:10.1016/0092-8674(93)90074-z · Cited by 684
Intestinal Bacteria and the Regulation of Immune Cell Homeostasis
Hill, D. A., & Artis, D. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101330 · Cited by 600
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Sepulveda, M., Rasic, M., Lei, Y. M., Kwan, M., Chen, L., Chen, Y., Perkins, D. L., & Alegre, M. (2024) · American Journal of Transplantation · doi:10.1016/j.ajt.2024.03.020 · Cited by 6
Metatranscriptomics, Metaproteomics, and Metabolomics Approaches for Microbiome Characterization
Mathuria, A., Jain, K., Saini, A., Verma, C., & Mani, I. (2024) · Springer eBooks · doi:10.1007/978-981-97-1844-3_6 · Cited by 7
Role of T cells in neuromyelitis optica
Weiner, H. L. (2012) · Annals of Neurology · doi:10.1002/ana.23669 · Cited by 6
Causal clarity and deeper dimensions in microbiota-gut-brain research
Hooks, K. B., Konsman, J. P., & O’Malley, M. A. (2019) · Behavioral and Brain Sciences · doi:10.1017/s0140525x19000050 · Cited by 6
The influence of aging and the microbiome in multiple sclerosis and other neurologic diseases
Fettig, N. M., Pu, A., Osborne, L. C., & Gommerman, J. L. (2024) · Immunological Reviews · doi:10.1111/imr.13361 · Cited by 7
MalarImDB: an open-access literature-based malaria immunology database
Deroost, K., Opdenakker, G., & den Steen, P. E. V. (2014) · Trends in Parasitology · doi:10.1016/j.pt.2014.04.006 · Cited by 6
Looveren, K. V., & Libert, C. (2018) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2018.1539078 · Cited by 6
Impact of Probiotics in Human Health and Disease Treatment
Tingirikari, J. M. R., Sarathy, M. V., & Karthigarani, A. K. (2018) · Advances in human services and public health (AHSPH) book series · doi:10.4018/978-1-5225-3267-5.ch002 · Cited by 6
T Cells and their Subsets in Autoimmunity
Burkett, P. R., Lee, Y., Peters, A., & Kuchroo, V. K. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-384929-8.00006-x · Cited by 6
Microbial Translocation Disorders: Assigning an Etiology to Idiopathic Illnesses
Sfera, A., Hazan, S., Klein, C. A., del Campo, C. M. Z.-M., Sasannia, S., Anton, J. J., Rahman, L., Andronescu, C. V., Sfera, D. O., Kozlakidis, Z., et al. (2023) · Applied Microbiology · doi:10.3390/applmicrobiol3010015 · Cited by 6
Fournier, A. P., Baudron, E., Wagnon, I., Aubert, P., Vivien, D., Neunlist, M., Bardou, I., & Docagne, F. (2020) · Multiple Sclerosis Journal - Experimental Translational and Clinical · doi:10.1177/2055217320959806 · Cited by 6
Gut-Brain Axis: Probiotic Interactions and Implications for Human Mental Health
Gayathri, D., Vasudha, M., & Prashantkumar, C. S. (2022) · Springer eBooks · doi:10.1007/978-981-16-1626-6_11 · Cited by 6
Gut Microbiome-Brain Communications Regulate Host Physiology and Behavior
Serre, C. B. D. L. (2015) · Journal of Nutritional Health & Food Science · doi:10.15226/jnhfs.2015.00141 · Cited by 6
Positive Effect on Multiple Sclerosis With Treatment of Metabolic Syndrome
Haghikia, A., & Gold, R. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2015.5050 · Cited by 6
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Vijitha, N., & Engel, D. R. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.1ce0219-072r · Cited by 6
Ghafoor, D. D., Ahmad, D. O., Najmuldeen, H. H. R., Mohammed, S. J., Jalal, P. J., Mustafa, F. S., Alghofaili, F., Zangana, B. A., & Al-Bajalan, S. J. (2025) · Inflammopharmacology · doi:10.1007/s10787-025-02012-5 · Cited by 5
Suzuki, S., Miyamoto, K., Tojo, A. O., Yoshimatsu, Y., Teratani, T., Uchida, H., Nemoto, Y., Okamoto, R., Sihombing, A. M., Sato, T., et al. (2026) · Science Immunology · doi:10.1126/sciimmunol.aec1627 · Cited by 5
Ladakis, D. C., & Bhargava, P. (2023) · CNS Drugs · doi:10.1007/s40263-023-00986-w · Cited by 6
Developing Connections among B Lymphocytes and Deregulated Pathways in Autoimmunity
Zouali, M., & Tsay, G. J. (2016) · Molecular Medicine · doi:10.2119/molmed.2016.00206 · Cited by 5
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Buruş, A., Çeltikçi, B., & Aksoy, Y. (2021) · Acta Medica · doi:10.32552/2021.actamedica.548 · Cited by 5
Lung microbes mediate spinal-cord autoimmunity
Schonhoff, A. M., & Mazmanian, S. K. (2022) · Nature · doi:10.1038/d41586-022-00468-x · Cited by 5
Amarjeet, Babu, R., Mohapatra, A., Pancholi, B., Garabadu, D., Sharma, A., Sharma, A., & Azad, A. (2023) · Acta Neurologica Scandinavica · doi:10.1155/2023/7398037 · Cited by 5
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El-Sayed, M. M., Mohak, S., Gala, D., Fabian, R., Péterfi, Z., & Fábián, Z. (2023) · Biology · doi:10.3390/biology12121463 · Cited by 5
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Lynch, C. M. K., O’Riordan, K. J., Clarke, G. A., & Cryan, J. F. (2023) · Springer eBooks · doi:10.1007/978-3-031-46712-7_4 · Cited by 5
Role of diet, gut microbiota, and metabolism in multiple sclerosis and neuromyelitis optica
Okuno, T., Kinoshita, M., Ishikura, T., & Mochizuki, H. (2019) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12499 · Cited by 5
Lin, C. D., Poretto, A., Scodro, M., Marra, M. P., Iliceto, S., & Tona, F. (2015) · Journal of Integrative Cardiology · doi:10.15761/jic.1000137 · Cited by 5
Mentrup, H. L., Hartman, A., Thames, E. L., Basheer, W. A., & Matesic, L. E. (2017) · Differentiation · doi:10.1016/j.diff.2017.12.003 · Cited by 5
The gut-brain axis: microglia in the spotlight
Mezö, C., Mossad, O., Erny, D., & Blank, T. (2019) · e-Neuroforum · doi:10.1515/nf-2019-0014 · Cited by 5
Microbiota and enteric viruses infection
Huang, P.-N. (2020) · Medicine in Microecology · doi:10.1016/j.medmic.2020.100006 · Cited by 5
Szablewski, L. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00065-6 · Cited by 5
Schröder, T., & Ibrahim, S. M. (2017) · Der Internist · doi:10.1007/s00108-017-0221-4 · Cited by 5
Tsigalou, C., Tsolou, A., Konstantinidis, T. G., Zafiriou, E., Efthimios, D., Tsirogianni, A., & Bogdanos, D. P. (2020) · Preprints.org · doi:10.20944/preprints202001.0228.v1 · Cited by 5
Álvarez‐López, A. I., Ponce‐España, E., Cruz‐Chamorro, I., Santos‐Sánchez, G., Bejarano, I., Álvarez‐Sánchez, N., Lardone, P. J., & Carrillo‐Vico, A. (2025) · MedComm · doi:10.1002/mco2.70228 · Cited by 4
van Pamelen, J., Rodriguez-Mogeda, C., van Olst, L., van der Pol, S. M. A., Boon, M. L., de Beukelaar, J., Gerlach, O. H. H., Budding, A. E., Killestein, J., de Vries, H. E., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1514762 · Cited by 4
Gut microbiota modulates CNS barrier function in murine model for multiple sclerosis
Xie, J., Burgelman, M., Dujardin, P., Castelein, J., Imschoot, G. V., Wonterghem, E. V., Lernout, H., Schetters, S. T. T., Vandendriessche, C., Hoecke, L. V., et al. (2025) · Fluids and Barriers of the CNS · doi:10.1186/s12987-025-00724-y · Cited by 4
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Abdurasulova, I. N., Тарасова, Е. А., Matsulevich, A. V., Eliseev, A. V., Ермоленко, Е. И., Suvorov, A. N., & Клименко, В. М. (2017) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-017-0401-7 · Cited by 4
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Quintana, F. J., & Prinz, M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714260114 · Cited by 4
Gastrointestinal influences in multiple sclerosis: Focus on the role of the microbiome
Francis, A. G., & Constantinescu, C. S. (2018) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12432 · Cited by 4
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Gerdes, L. A., Yoon, H., & Peters, A. (2020) · Der Nervenarzt · doi:10.1007/s00115-020-01012-w · Cited by 4
Abdurasulova, I. N. (2022) · Medical academic journal · doi:10.17816/maj108241 · Cited by 5
Microbiomes and Pediatric onset multiple sclerosis (MS): A systematic review
Mehrabani, S., Rastkar, M., Ebrahimi, N., & Ghajarzadeh, M. (2023) · AIMS neuroscience · doi:10.3934/neuroscience.2023031 · Cited by 4
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Muñoz-Jurado, A., Escribano, B. M., & Túnez, I. (2024) · Methods in cell biology · doi:10.1016/bs.mcb.2024.03.013 · Cited by 5
Dale, R. C., Banwell, B., Bar‐Or, A., & Brilot, F. (2012) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2012.03.003 · Cited by 4
Consuming cholera toxin counteracts age-associated obesity
Varian, B. J., Poutahidis, T., Haner, G., Hardas, A., Lau, V., & Erdman, S. E. (2019) · Oncotarget · doi:10.18632/oncotarget.27137 · Cited by 4
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Qiao, Y., Hayashi, H., & Teo, S. C. (2020) · Chemistry - An Asian Journal · doi:10.1002/asia.202000541 · Cited by 4
Kaczor‐Urbanowicz, K. E., & Wong, D. T. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813762-8.00004-9 · Cited by 5
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Ouerdane, Y., El-Nahas, Z. S., Ouerdane, F., Hamam, K. M., & Ebada, M. A. (2022) · Springer eBooks · doi:10.1007/978-981-16-7606-2_12 · Cited by 4
Th17 Cells in Autoimmune Inflammation and Demyelination in the Central Nervous System
Kuchroo, V. K., & Korn, T. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7953-6_1 · Cited by 4
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Selmin, O. I., Romagnolo, A. P. G., & Romagnolo, D. F. (2016) · Springer eBooks · doi:10.1007/978-3-319-27969-5_12 · Cited by 4
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Hickman, R. A., Hussein, M. A., & Pei, Z. (2016) · InTech eBooks · doi:10.5772/64690 · Cited by 5
Coppedè, F., Bosco, P., Fuso, A., & Troen, A. M. (2012) · Current Gerontology and Geriatrics Research · doi:10.1155/2012/926082 · Cited by 5
Development of an In Vitro Fermentation Model to Culture the Human Distal Gut Microbiota
McDonald, J. A. K. (2013) · The Atrium (University of Guelph) · Cited by 4
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Gold, R., Montalbán, X., & Haghikia, A. (2020) · Therapeutic Advances in Neurological Disorders · doi:10.1177/1756286420936165 · Cited by 4
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Takahashi, D., & Hase, K. (2015) · Inflammation and Regeneration · doi:10.2492/inflammregen.35.129 · Cited by 3
Influence of the Microbiota Through the Gut-Brain Axis in Neurological Diseases
Guarnotta, V., Mandarino, F. V., Fasulo, E., Maida, M. F., Laterza, L., Sferrazza, S., Raimondo, D., & Sinagra, E. (2024) · Integrated science · doi:10.1007/978-3-031-73061-0_20 · Cited by 3
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Siewert, L. K., Berve, K., Pössnecker, E., Dyckow, J., Zulji, A., Baumann, R., Muñoz-Blázquez, A., Krishnamoorthy, G., Schreiner, D., Sagan, S. A., et al. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2601430 · Cited by 3
Self-citationCellular Immunity and Multiple Sclerosis: Current Understanding
Sato, W., & Yamamura, T. (2016) · Springer eBooks · doi:10.1007/978-4-431-55594-0_1 · Cited by 2
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Jose, J. V., & Aliya, S. (2022) · Nutritional neurosciences · doi:10.1007/978-981-19-4530-4_10 · Cited by 3
Mungan, S., Güzel, I., & Demirdöğen, B. C. (2023) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x2023e12776 · Cited by 3
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Yeh, Y., Chen, K.-D., Huang, C., Tsai, J.-R., & Kuo, H. (2025) · Virulence · doi:10.1080/21505594.2025.2512401 · Cited by 3
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Gagliani, N., & Huber, S. (2012) · InTech eBooks · doi:10.5772/48183 · Cited by 6
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Loebermann, M., Reisinger, E. C., Zettl, U. K., & Winkelmann, A. (2014) · Nervenheilkunde · doi:10.1055/s-0038-1627755 · Cited by 3
Imaging the execution phase of neuroinflammatory disease models
Schumacher, A.-M., Misgeld, T., Kerschensteiner, M., & Snaidero, N. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.112968 · Cited by 3
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Phelps, C. M., & Meisel, M. (2022) · Cell · doi:10.1016/j.cell.2022.08.013 · Cited by 3
Ju, B., Xiu, N.-N., Xu, J. M. S., Yang, X., Sun, X.-Y., & Zhao, X.-C. (2023) · World Journal of Clinical Cases · doi:10.12998/wjcc.v11.i17.4105 · Cited by 3
Tréfond, L., Billard, E., Pereira, B., Richard, D., Vazeille, E., Bonnet, R., Barnich, N., & André, M. F. J. (2023) · BMJ Open · doi:10.1136/bmjopen-2023-073776 · Cited by 3
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Shahid, A., Fatima, M., Khan, M. S. I., Ali, U., Fareed, S. Z., & Qureshi, M. A. (2023) · Journal of Health and Rehabilitation Research · doi:10.61919/jhrr.v3i2.238 · Cited by 3
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Sprenger‐Svačina, A., Klein, I., Svačina, M. K. R., Bobylev, I., Kohle, F., Schneider, C. A., Schweitzer, F., Piekarek, N., Barham, M., Vehreschild, M. J. G. T., et al. (2024) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-024-10119-9 · Cited by 3
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Sand, I. K., & Baranzini, S. E. (2018) · Multiple Sclerosis Journal · doi:10.1177/1352458518761167 · Cited by 3
The Promise of Personalized Medicine
Stoll, M. L. (2018) · Springer eBooks · doi:10.1007/978-3-319-79026-8_35 · Cited by 3
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Frahm, C., & Witte, O. W. (2019) · Die Gastroenterologie · doi:10.1007/s11377-019-0345-2 · Cited by 3
Joscelyn, J., Ochoa‐Repáraz, J., & Kasper, L. H. (2019) · Current clinical neurology · doi:10.1007/978-3-030-24436-1_2 · Cited by 3
Zhao, X.-C., Ju, B., Xiu, N.-N., Sun, X.-Y., & Meng, F. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1339971 · Cited by 4
Bărcuţean, L., Farczádi, L., Mănescu, I. B., Imre, S., Maier, S., & Bălașa, R. (2024) · Biologics · doi:10.2147/btt.s489523 · Cited by 3
Seo, J., Hasan, M., Han, J., Kim, N., Lee, J. E., Lee, K. M., Park, J.-H., Kim, H. J., Son, J. J., Lee, J., et al. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1732-9 · Cited by 3
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Veldhoen, M. (2017) · Immunity · doi:10.1016/j.immuni.2016.12.016 · Cited by 3
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Webb, D. R. (2018) · Springer eBooks · doi:10.1007/978-3-319-79026-8_6 · Cited by 3
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Castillo-Álvarez, F., & Marzo-Sola, M. E. (2019) · Medicina Clínica (English Edition) · doi:10.1016/j.medcle.2018.08.012 · Cited by 3
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Ba, S., Sinitsa, A. V., Zakharchenko, M. M., & Lang, C. (2020) · Springer eBooks · doi:10.1007/978-3-030-34167-1_9 · Cited by 3
Romeo, A. R., & Segal, B. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-7020-8165-1.00066-6 · Cited by 5
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Gil, C., Dorca‐Arévalo, J., & Blasi, J. (2018) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2018.08.003 · Cited by 3
Wilson, M. (2016) · Wiley eBooks · doi:10.1002/9781118982907.ch1 · Cited by 3
«Gut-brain» axis and multiple sclerosis
Omarova, М. А., & Boyko, A. N. (2023) · Neurology neuropsychiatry Psychosomatics · doi:10.14412/2074-2711-2023-6-122-127 · Cited by 2
He, J., Meng, Q., Miao, C., Hao, J., & Dai, M. (2024) · Postgraduate Medical Journal · doi:10.1093/postmj/qgae125 · Cited by 2
RetractedRahamathulla, M., Kumar, R., Alrashdan, Y., Bose, M. M., Muthukumar, A., Salahuddin, M., Ahmed, M. M., Shivanandappa, T. B., & Pasha, I. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-04934-1 · Cited by 2
Wang, W., Xu, Y., Chu, Y., Zhang, H., Zhou, L., Zhu, H., Li, J., Zhang, Z., Cheng, J., Zhou, F., et al. (2025) · International Journal of Clinical and Experimental Pathology · doi:10.62347/usll6631 · Cited by 3
Ferreira, C., Carvalho, F. S., Vieira, P., Alves, A. D. C., Palavra, F., Almeida, J., Alves, V., Coscueta, E. R., Dias‐Pereira, P., Pintado, M., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1682183 · Cited by 2
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Yun, Y., Xu, G., Jiang, X., Ren, X., Lu, M., Chen, J., & Zhang, S. (2025) · Comprehensive physiology · doi:10.1002/cph4.70078 · Cited by 2
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Metadata
- Authors
- Berer, K., Mues, M., Koutrolos, M., Rasbi, Z. A., Boziki, M., Johner, C., Wekerle, H., & Krishnamoorthy, G.
- Affiliations
- Max Planck Institute of Neurobiology (DE)
- Max Planck Society (DE)
- Corresponding author
- Wekerle, Hartmut
- Krishnamoorthy, Gurumoorthy
- Venue
- Nature
- Published
- 2011-10-26
- Volume
- 479
- Issue
- 7374
- Pages
- 538-541
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2037907937
- Cited by
- 1,251
- References
- 29
- Citations by year
- 2026: 34 · 2025: 45 · 2024: 74 · 2023: 78 · 2022: 107 · 2021: 101 · 2020: 100 · 2019: 93 · 2018: 110 · 2017: 105 · 2016: 113 · 2015: 87 · 2014: 74 · 2013: 72 · 2012: 47
- FWCI
- 44.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Max Planck Digital Library (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Division of Materials Research
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Keywords
- commensal gut microbiota, myelin autoantigens, myelin oligodendrocyte glycoprotein, multiple sclerosis, experimental autoimmune encephalomyelitis, autoimmune demyelination, autoantibody-producing B cells, CD4+ T cells, diet and microbiome, relapsing-remitting multiple sclerosis
- MeSH terms
- Animals, Autoantigens, B-Lymphocytes, Brain, Cell Movement, Diet, Encephalomyelitis, Autoimmune, Experimental, Germ-Free Life, Lymph Nodes, Lymphocyte Activation, Myelin Proteins, Myelin Sheath, Stomach, T-Lymphocytes, Autoimmunity, Cytokines, Germinal Center, Adoptive Transfer, Multiple Sclerosis, Relapsing-Remitting, Mice, Metagenome, Myelin-Oligodendrocyte Glycoprotein
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