Immunopathology of multiple sclerosis

Human gut microbiome viewed across age and geography

Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815

From inflammation to sickness and depression: when the immune system subjugates the brain

Dantzer, R., O'Connor, J. C., Freund, G. G., Johnson, R. W., & Kelley, K. W. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2297 · Cited by 7,395

Integrative analysis of 111 reference human epigenomes

Roadmap Epigenomics Consortium, Kundaje, A., Meuleman, W., Ernst, J., Bilenky, M., Yen, A., Heravi-Moussavi, A., Kheradpour, P., Zhang, Z., Wang, J., et al. (2015) · Nature · doi:10.1038/nature14248 · Cited by 6,368

Multiple sclerosis

Compston, A., & Coles, A. J. (2008) · The Lancet · doi:10.1016/s0140-6736(08)61620-7 · Cited by 4,699

Structural and functional features of central nervous system lymphatic vessels

Louveau, A., Smirnov, I., Keyes, T. J., Eccles, J. D., Rouhani, S. J., Peske, J. D., Derecki, N. C., Castle, D., Mandell, J. W., Lee, K. S., et al. (2015) · Nature · doi:10.1038/nature14432 · Cited by 4,413

Meta-Analysis of 74,046 Individuals Identifies 11 New Susceptibility Loci for Alzheimer’s Disease

(EADI), E. A. D. I., Lambert, J.-C., (GERAD), G. A. E. R. I. A. D., Alzheimer's Disease Genetic Consortium (ADGC), (CHARGE), C. F. H. A. A. R. I. G. E., Ibrahim-Verbaas, C. A., Harold, D., Naj, A. C., Sims, R., Bellenguez, C., et al. (2013) · Nature Genetics · doi:10.1038/ng.2802 · Cited by 4,336

T cell exhaustion

Wherry, E. J. (2011) · Nature Immunology · doi:10.1038/ni.2035 · Cited by 4,062

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

Bennett, C. L., Christie, J., Ramsdell, F., Brunkow, M., Ferguson, P., Whitesell, L., Kelly, T., Saulsbury, F., Chance, P., & Ochs, H. (2001) · Nature Genetics · doi:10.1038/83713 · Cited by 3,576

B-cell depletion with rituximab in relapsing-remitting multiple sclerosis

Hauser, S. L., Waubant, E., Arnold, D. L., Vollmer, T., Antel, J., Fox, R. J., Bar-Or, A., Panzara, M., Sarkar, N., Agarwal, S., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0706383 · Cited by 2,439

Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors

Gomez Perdiguero, E., Klapproth, K., Schulz, C., Busch, K., Azzoni, E., Crozet, L., Garner, H., Trouillet, C., de Bruijn, M. F., Geissmann, F., et al. (2015) · Nature · doi:10.1038/nature13989 · Cited by 2,339

Increased constitutive activation of NF-κB p65 (RelA) in peripheral blood cells of patients with progressive multiple sclerosis

Yan, J., Winterford, C. M., Catts, V. S., Pat, B., Pender, M. P., McCombe, P., & Greer, J. M. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.04.002 · Cited by 19

Cladribine tablets’ potential role as a key example of selective immune reconstitution therapy in multiple sclerosis

Boyко, A., & Boyko, O. V. (2018) · Degenerative Neurological and Neuromuscular Disease · doi:10.2147/dnnd.s161450 · Cited by 21

A Tolerogenic Artificial APC Durably Ameliorates Experimental Autoimmune Encephalomyelitis by Directly and Selectively Modulating Myelin Peptide–Autoreactive CD4+ and CD8+ T Cells

Wan, X., Pei, W., Shahzad, K. A., Zhang, L., Song, S., Jin, X., Wang, L., Zhao, C., & Shen, C. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800108 · Cited by 19

Genetic deletion of Autotaxin from CD11b+ cells decreases the severity of experimental autoimmune encephalomyelitis

Ninou, I., Sevastou, I. G., Magkrioti, C., Kaffe, E., Stamatakis, G. M., Thivaios, S., Panayotou, G., Aoki, J., Kollias, G. A., & Aidinis, V. (2020) · PLoS ONE · doi:10.1371/journal.pone.0226050 · Cited by 19

Overview of Brain-to-Gut Axis Exposed to Chronic CNS Bacterial Infection(s) and a Predictive Urinary Metabolic Profile of a Brain Infected by Mycobacterium tuberculosis

Isaiah, S., Loots, D. T., Solomons, R., van der Kuip, M., van Furth, A. M., & Mason, S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00296 · Cited by 20

Perivascular tissue resident memory T cells as therapeutic target in multiple sclerosis

Smolders, J., Fransen, N. L., Hsiao, C., Hamann, J., & Huitinga, I. (2020) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2020.1776609 · Cited by 22

B Cells in Multiple Sclerosis and Virus-Induced Neuroinflammation

Chunder, R., Schropp, V., & Küerten, S. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.591894 · Cited by 20

Reduction in Cognitive Processing Speed Surrounding Multiple Sclerosis Relapse

McKay, K. A., Bedri, S. K., Manouchehrinia, A., Stawiarz, L., Olsson, T. P., Hillert, J., & Fink, K. (2022) · Annals of Neurology · doi:10.1002/ana.26301 · Cited by 19

MS ‐Driven Metabolic Alterations Are Recapitulated in iPSC ‐Derived Astrocytes

Ghirotto, B., Oliveira, D., Cipelli, M., Basso, P. J., de Lima, J., Breda, C. N. D. S., Ribeiro, H. C., Silva, C. C. C., Sertie, A. L., Oliveira, A. E. R., et al. (2022) · Annals of Neurology · doi:10.1002/ana.26336 · Cited by 20

Time to first treatment and risk of disability pension in relapsing-remitting multiple sclerosis

Wandall‐Holm, M. F., Buron, M. D., Kopp, T. I., Thielen, K., Sellebjerg, F. T., & Magyari, M. (2022) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2022-329058 · Cited by 19

Exploiting Rational Assembly to Map Distinct Roles of Regulatory Cues during Autoimmune Therapy

Oakes, R. S., Tostanoski, L. H., Kapnick, S. M., Froimchuk, E., Black, S. K., Zeng, X., & Jewell, C. M. (2021) · ACS Nano · doi:10.1021/acsnano.0c07440 · Cited by 18

Sildenafil Alleviates Murine Experimental Autoimmune Encephalomyelitis by Triggering Autophagy in the Spinal Cord

Duarte-Silva, E. P., Araújo, S. M. D. R., de Oliveira, W. H., Lós, D. B., Bonfanti, A. P., Peron, G., Thomaz, L. D. L., Verinaud, L. M. C., & Peixoto, C. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.671511 · Cited by 18

The antimicrobial peptide cathelicidin drives development of experimental autoimmune encephalomyelitis in mice by affecting Th17 differentiation

Smith, K. J., Minns, D., McHugh, B. J., Holloway, R. K., O’Connor, R. A., Williams, A., Melrose, L. A., McPherson, R. C., Miron, V. E., Davidson, D. J., et al. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001554 · Cited by 20

Inhibition of Th1 activation and differentiation by dietary guar gum ameliorates experimental autoimmune encephalomyelitis

Fettig, N. M., Robinson, H. G., Allanach, J. R., Davis, K. M., Simister, R. L., Wang, E. J., Sharon, A. J., Ye, J., Popple, S., Seo, J. H., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111328 · Cited by 19

Humanized zebrafish as a tractable tool for in vivo evaluation of pro-myelinating drugs

Häberlein, F., Mingardo, E., Merten, N., Köhling, N.-K. S., Reinoß, P., Simon, K., Japp, A. S., Nagarajan, B., Schrage, R., Pégurier, C., et al. (2022) · Cell chemical biology · doi:10.1016/j.chembiol.2022.08.007 · Cited by 18

The influence of gut microbiota on circulating inflammatory cytokines and host: A Mendelian randomization study with meta-analysis

Fan, X., He, Z., Pang, M.-J., Wang, L.-L., Wang, X.-Y., Sun, D.-W., Wang, Z., Wu, D.-L., & Miao, Z. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122105 · Cited by 19

Single-cell profiling reveals preferential reduction of memory B cell subsets in cladribine patients that correlates with treatment response

Teschner, V. E., Fleck, A.-K., Walter, C., Schwarze, A.-S., Eschborn, M., Wirth, T., Steinberg, O. V., Schulte‐Mecklenbeck, A., Lu, I., Herrera-Rivero, M., et al. (2023) · Therapeutic Advances in Neurological Disorders · doi:10.1177/17562864231211077 · Cited by 18

Dysregulated lipid metabolism networks modulate T-cell function in people with relapsing-remitting multiple sclerosis

Martin‐Gutierrez, L., Waddington, K. E., Maggio, A., Coelewij, L., Oppong, A. E., Yang, N., Adriani, M., Nytrová, P., Farrell, R. A., Pineda‐Torra, I., et al. (2024) · Clinical & Experimental Immunology · doi:10.1093/cei/uxae032 · Cited by 18

Meningeal lymphatic vessel crosstalk with central nervous system immune cells in aging and neurodegenerative diseases

Gao, M., Wang, X., Su, S., Feng, W., Lai, Y., Huang, K., Cao, D., & Wang, Q. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01595 · Cited by 18

Progress and prospects for the use and the understanding of the mode of action of autologous hematopoietic stem cell transplantation in the treatment of multiple sclerosis

Collins, F., Kazmi, M. A., & Muraro, P. A. (2017) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2017.1297232 · Cited by 18

HIV and spinal cord disease

Levin, S. N., & Lyons, J. L. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63849-6.00017-7 · Cited by 18

Sulfatide isoform pattern in cerebrospinal fluid discriminates progressive MS from relapsing‐remitting MS

Novakova, L., Singh, A. K., Axelsson, M., Ståhlman, M., Adiels, M., Malmeström, C., Zetterberg, H., Borén, J., Lycke, J., Cardell, S., et al. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14452 · Cited by 18

CD28 between tolerance and autoimmunity: the side effects of animal models

Porciello, N., Kunkl, M., & Tuosto, L. (2018) · F1000Research · doi:10.12688/f1000research.14046.1 · Cited by 18

Alpinia oxyphylla Fruit Extract Ameliorates Experimental Autoimmune Encephalomyelitis through the Regulation of Th1/Th17 Cells

Huang, K., Lin, M.-N., Hsu, Y., Lu, I.-H., Pan, I.-H., & Yang, J. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/6797030 · Cited by 19

Peroxisome Proliferator–Activated Receptor-δ Acts within Peripheral Myeloid Cells to Limit Th Cell Priming during Experimental Autoimmune Encephalomyelitis

Drohomyrecky, P. C., Doroshenko, E. R., Akkermann, R., Moshkova, M., Yi, T. J., Zhao, F. L., Ahn, J. J., McGaha, T. L., Pahan, K., & Dunn, S. E. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1801200 · Cited by 18

Multiple Sclerosis and the Choroid Plexus: Emerging Concepts of Disease Immunopathophysiology

Dixon, G. A., & Pérez, C. A. (2019) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2019.08.007 · Cited by 19

Effects of interferon and glatiramer acetate on cytokine patterns in multiple sclerosis patients

Ganji, A., Monfared, M. E., Shapoori, S., Nourbakhsh, P., Ghazavi, A., Ghasami, K., & Mosayebi, G. (2019) · Cytokine · doi:10.1016/j.cyto.2019.154911 · Cited by 18

Novel phloroglucinol derivative Compound 21 protects experimental autoimmune encephalomyelitis rats via inhibiting Th1/Th17 cell infiltration

Zhao, Z., Bao, X.-Q., Zhang, Z., Li, F., Liu, H., & Zhang, D. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.03.009 · Cited by 18

Genetic Etiology Shared by Multiple Sclerosis and Ischemic Stroke

Tian, Z., Song, Y., Yao, Y., Guo, J., Gong, Z., & Wang, Z. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00646 · Cited by 18

Recent Advances in Nanomedicines for Multiple Sclerosis Therapy

Zeng, Y., Li, Z., Zhu, H., Gu, Z., Zhang, H., & Luo, K. (2020) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c00953 · Cited by 18

B-cells expressing NgR1 and NgR3 are localized to EAE-induced inflammatory infiltrates and are stimulated by BAFF

Bakhuraysah, M. M., Theotokis, P., Lee, J. Y., Alrehaili, A. A., Aui, P.-M., Figgett, W. A., Azari, M. F., Abou-Afech, J.-P., Mackay, F., Siatskas, C., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-82346-6 · Cited by 18

CSF-resident CD4+ T-cells display a distinct gene expression profile with relevance to immune surveillance and multiple sclerosis

Hrastelj, J., Andrews, R., Loveless, S., Morgan, J., Bishop, S. M., Bray, N. J., Williams, N. M., & Robertson, N. P. (2021) · Brain Communications · doi:10.1093/braincomms/fcab155 · Cited by 20

2-Chlorodeoxyadenosine (Cladribine) preferentially inhibits the biological activity of microglial cells

Aybar, F., Pérez, M. J., Marcora, M. S., Samman, M. E., Marrodán, M., Pasquini, J. M., & Correale, J. D. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108571 · Cited by 18

The role of B cells and their interactions with stromal cells in the context of inflammatory autoimmune diseases

Tout, I., & Miossec, P. (2022) · Autoimmunity Reviews · doi:10.1016/j.autrev.2022.103098 · Cited by 18

Transcription Factor c-Maf Promotes Immunoregulation of Programmed Cell Death 1–Expressed CD8 + T Cells in Multiple Sclerosis

Koto, S., Chihara, N., Akatani, R., Nakano, H., Hara, A., Sekiguchi, K., Matsumoto, R., & Toda, T. (2022) · Neurology Neuroimmunology & Neuroinflammation · doi:10.1212/nxi.0000000000001166 · Cited by 18

Serum neurofilament as a predictor of 10-year grey matter atrophy and clinical disability in multiple sclerosis: a longitudinal study

Lie, I. A., Kaçar, S., Wesnes, K., Brouwer, I., Kvistad, S. S., Wergeland, S., Holmøy, T., Midgard, R., Bru, A., Edland, A., et al. (2022) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2021-328568 · Cited by 18

What Have Failed, Interrupted, and Withdrawn Antibody Therapies in Multiple Sclerosis Taught Us?

Krämer, J., & Wiendl, H. (2022) · Neurotherapeutics · doi:10.1007/s13311-022-01246-3 · Cited by 18

Murine Cytomegalovirus Infection Induces Susceptibility to EAE in Resistant BALB/c Mice

Milovanović, J., Popović, B., Milovanović, M., Kveštak, D., Arsenijević, A., Stojanović, B., Tanasković, I., Krmpotić, A., Arsenijević, N., Jonjić, S., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00192 · Cited by 18

Pioglitazone is superior to quetiapine, clozapine and tamoxifen at alleviating experimental autoimmune encephalomyelitis in mice

Chedrawe, M. A. J., Holman, S. P., Lamport, A.-C., Akay, T., & Robertson, G. S. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.06.001 · Cited by 20

Regulation of lymphocyte trafficking in central nervous system autoimmunity

Oukka, M., & Bettelli, E. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.09.008 · Cited by 19

Association between Lipoprotein Levels and Humoral Reactivity to Mycobacterium avium subsp. paratuberculosis in Multiple Sclerosis, Type 1 Diabetes Mellitus and Rheumatoid Arthritis

Bo, M., Arru, G., Niegowska, M., Erre, G. L., Manchia, P., & Sechi, L. A. (2019) · Microorganisms · doi:10.3390/microorganisms7100423 · Cited by 18

Molecular Interventions towards Multiple Sclerosis Treatment

Metaxakis, A., Petratou, D., & Tavernarakis, N. (2020) · Brain Sciences · doi:10.3390/brainsci10050299 · Cited by 18

Mechanisms of astrocytic and microglial purinergic signaling in homeostatic regulation and implications for neurological disease

Naffaa, M. M. (2025) · Exploration of neuroscience · doi:10.37349/en.2025.100676 · Cited by 20

Notch3 destabilizes regulatory T cells to drive autoimmune neuroinflammation in multiple sclerosis

Benamar, M., Contini, P., Schmitz‐Abe, K., Lanzetta, O., Getachew, F., Bachelin, C., Leyva-Castillo, J. M., Wang, M., Öktelik, F. B., Perrot, O., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.09.007 · Cited by 17

The Link Among Neurological Diseases: Extracellular Vesicles as a Possible Brain Injury Footprint

Ciccocioppo, F., Lanuti, P., Centonze, D., Miscia, S., & Marchisio, M. (2019) · Neurosignals · doi:10.33594/000000116 · Cited by 17

Preventive exercise attenuates IL-2-driven mood disorders in multiple sclerosis

Gilio, L., Fresegna, D., Gentile, A., Guadalupi, L., Sanna, K., Vito, F. D., Balletta, S., Caioli, S., Rizzo, F. R., Musella, A., et al. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105817 · Cited by 17

Tissue‐Targeted Drug Delivery Strategies to Promote Antigen‐Specific Immune Tolerance

Rui, Y., Eppler, H. B., Yanes, A. A., & Jewell, C. M. (2022) · Advanced Healthcare Materials · doi:10.1002/adhm.202202238 · Cited by 17

GPX4 aggravates experimental autoimmune encephalomyelitis by inhibiting the functions of CD4+ T cells

Li, H., Zeng, Y., Luo, S., Li, Z., Huang, F., & Liu, Z. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.12.034 · Cited by 17

Harnessing two-dimensional nanomaterials for diagnosis and therapy in neurodegenerative diseases: Advances, challenges and prospects

Beura, S. K., Panigrahi, A. R., Yadav, P., Palacio, I., Casero, E., Quintana, C., Singh, J., Singh, S. K., Martín-Gago, J. Á., & Singh, S. K. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102205 · Cited by 17

Interleukin-9 protects from microglia- and TNF-mediated synaptotoxicity in experimental multiple sclerosis

Guadalupi, L., Vanni, V., Balletta, S., Caioli, S., Vito, F. D., Fresegna, D., Sanna, K., Nencini, M., Donninelli, G., Volpe, E., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03120-9 · Cited by 18

Glial cell crosstalk in Parkinson's disease: Mechanisms, implications, and therapeutic strategies

Wang, N., Xiao, X., Chen, Z., Xu, K., Cao, X., Kou, D., & Zeng, J. (2025) · Fundamental Research · doi:10.1016/j.fmre.2024.12.023 · Cited by 18

High-Resolution Expression Profiling of Peripheral Blood CD8+ Cells in Patients with Multiple Sclerosis Displays Fingolimod-Induced Immune Cell Redistribution

Roch, L., Hecker, M., Friess, J., Angerer, I. C., Koczan, D., Fitzner, B., Schröder, I., Flechtner, K., Thiesen, H., Meister, S., et al. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0075-0 · Cited by 17

Cathepsin C modulates myelin oligodendrocyte glycoprotein‐induced experimental autoimmune encephalomyelitis

Durose, W. W., Shimizu, T., Li, J., Abe, M., Sakimura, K., Chetsawang, B., Tanaka, K. F., Suzumura, A., Tohyama, K., & Ikenaka, K. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14581 · Cited by 17

Exploring the relationship between Endothelin-1 and peripheral inflammation in multiple sclerosis

Rocha, N. P., Colpo, G. D., Bravo-Alegria, J. B., Lincoln, J. A., Wolinsky, J. S., Lindsey, J. W., Teixeira, A. L., & Freeman, L. A. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.11.007 · Cited by 17

A robust pipeline with high replication rate for detection of somatic variants in the adaptive immune system as a source of common genetic variation in autoimmune disease

Horebeek, L. V., Hilven, K., Mallants, K., van Nieuwenhuijze, A. E. M., Kelkka, T., Savola, P., Mustjoki, S. M., Schlenner, S., Liston, A., Dubois, B., et al. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy425 · Cited by 17

Clinical trials in multiple sclerosis: potential future trial designs

Manouchehri, N., Zhang, Y., Salter, A. R., Hussain, R. Z., Hartung, H.-P., Hemmer, B., Linker, R. A., Segal, B. M., Cutter, G., & Stüve, O. (2019) · Therapeutic Advances in Neurological Disorders · doi:10.1177/1756286419847095 · Cited by 17

Autologous Hematopoietic Cell Transplantation in Multiple Sclerosis: Changing Paradigms in the Era of Novel Agents

Gavriilaki, M., Sakellari, I., Gavriilaki, E., Kimiskidis, V. Κ., & Anagnostopoulos, Α. (2019) · Stem Cells International · doi:10.1155/2019/5840286 · Cited by 19

Multiple Sclerosis: Epidemiology, Genetics, Symptoms, and Unmet Needs

Moreno‐Torres, I., Muñoz, J. S., & García‐Merino, A. (2019) · Royal Society of Chemistry eBooks · doi:10.1039/9781788016070-00001 · Cited by 18

Coupling the Paternò-Büchi (PB) Reaction With Mass Spectrometry to Study Unsaturated Fatty Acids in Mouse Model of Multiple Sclerosis

Chong, L., Tian, R., Shi, R., Ouyang, Z., & Xia, Y. (2019) · Frontiers in Chemistry · doi:10.3389/fchem.2019.00807 · Cited by 17

Amelioration of experimental autoimmune encephalomyelitis by Rhodiola rosea, a natural adaptogen

Lin, X., Liu, Y., Ma, L., Ma, X., Chen, Z., Chen, H. H., Si, L., Ma, X., Yu, Z., & Chen, X. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.109960 · Cited by 17

Dense module searching for gene networks associated with multiple sclerosis

Manuel, A. M., Dai, Y., Freeman, L. A., Jia, P., & Zhao, Z. (2020) · BMC Medical Genomics · doi:10.1186/s12920-020-0674-5 · Cited by 17

Perspective insights of repurposing the pleiotropic efficacy of statins in neurodegenerative disorders: An expository appraisal

Bhat, A., Dalvi, H., Jain, H., Rangaraj, N., Singh, S. B., & Srivastava, S. (2020) · Current Research in Pharmacology and Drug Discovery · doi:10.1016/j.crphar.2020.100012 · Cited by 17

In vivo detection of teriflunomide-derived fluorine signal during neuroinflammation using fluorine MR spectroscopy

Prinz, C., Starke, L., Millward, J. M., Fillmer, A., Delgado, P. R., Waiczies, H., Pohlmann, A., Rothe, M., Nazaré, M., Paul, F., et al. (2021) · Theranostics · doi:10.7150/thno.47130 · Cited by 18

Alternative Activation of Macrophages through Interleukin-13-Loaded Extra-Large-Pore Mesoporous Silica Nanoparticles Suppresses Experimental Autoimmune Encephalomyelitis

Park, J., Choi, S. W., Cha, B. G., Kim, J., & Kang, S. (2021) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.1c00946 · Cited by 17

Teriflunomide Preserves Neuronal Activity and Protects Mitochondria in Brain Slices Exposed to Oxidative Stress

Malla, B., Liotta, A., Bros, H., Ulshöfer, R., Paul, F., Hauser, A. E., Niesner, R. A., & Infante‐Duarte, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031538 · Cited by 18

Targeting IFN-λ Signaling Promotes Recovery from Central Nervous System Autoimmunity

Manivasagam, S., Williams, J. L., Vollmer, L. L., Bollman, B., Bartleson, J. M., Ai, S., Wu, G. F., & Klein, R. S. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2101041 · Cited by 16

CDX-modified chitosan nanoparticles remarkably reduce therapeutic dose of fingolimod in the EAE model of mice

Sepasi, T., Ghadiri, T., Kalan, A. E., Bani, F., Talebi, M., Rahbarghazi‬, R., Khodakarimi, S., Beyrampour-Basmenj, H., Seidi, K., Abbaspour‐Ravasjani, S., et al. (2023) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2023.122815 · Cited by 17

The sequence of regional structural disconnectivity due to multiple sclerosis lesions

Tozlu, C., Olafson, E. R., Jamison, K. W., Demmon, E., Kaunzner, U. W., Marcille, M., Zinger, N., Michaelson, N. M., Safi, N., Nguyen, T. D., et al. (2023) · Brain Communications · doi:10.1093/braincomms/fcad332 · Cited by 17

Cucurbitacin E Potently Modulates the Activity of Encephalitogenic Cells

Jevtić, B., Djedović, N., Stanisavljević, S., Despotović, J., Miljković, D. M., & Timotijević, G. S. (2016) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.6b00951 · Cited by 17

Amelioration of progressive autoimmune encephalomyelitis by epigenetic regulation involves selective repression of mature neutrophils during the preclinical phase

Jayaraman, A. K., Sharma, M., Prabhakar, B. S., Holterman, M., & Jayaraman, S. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.02.008 · Cited by 17

Cytomegalovirus and Epstein–Barr Virus Associations with Neurological Diseases and the Need for Vaccine Development

Maple, P. A. C. (2020) · Vaccines · doi:10.3390/vaccines8010035 · Cited by 17

Neutrophil to-lymphocyte ratio as a possible predictor of prognosis in recently diagnosed multiple sclerosis patients

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