The DOI matches its Crossref record; 362 of the 362 references it cites were found in a registry or an index.
IMMUNOLOGY OF MULTIPLE SCLEROSIS
Abstract
Multiple sclerosis (MS) develops in young adults with a complex predisposing genetic trait and probably requires an inciting environmental insult such as a viral infection to trigger the disease. The activation of CD4+ autoreactive T cells and their differentiation into a Th1 phenotype are a crucial events in the initial steps, and these cells are probably also important players in the long-term evolution of the disease. Damage of the target tissue, the central nervous system, is, however, most likely mediated by other components of the immune system, such as antibodies, complement, CD8+ T cells, and factors produced by innate immune cells. Perturbations in immunomodulatory networks that include Th2 cells, regulatory CD4+ T cells, NK cells, and others may in part be responsible for the relapsing-remitting or chronic progressive nature of the disease. However, an important paradigmatic shift in the study of MS has occurred in the past decade. It is now clear that MS is not just a disease of the immune system, but that factors contributed by the central nervous system are equally important and must be considered in the future.
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
“Neurological deficits in MS patients result from two pathogenic events: acute inflammatory demyelination and axonal injury [150,151].”
From Beneficial Effects of Spirulina Consumption on Brain Health (2022) · cites this paper as [150]
Citations
Cites
Control of Regulatory T Cell Development by the Transcription Factor Foxp3
Hori, S., Nomura, T., & Sakaguchi, S. (2003) · Science · doi:10.1126/science.1079490 · Cited by 8,187
Axonal transection in the lesions of multiple sclerosis
Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029
Cua, D. J., Sherlock, J., Chen, Y., Murphy, C. A., Joyce, B., Seymour, B., Lucian, L., To, W., Kwan, S., Churakova, T., et al. (2003) · Nature · doi:10.1038/nature01355 · Cited by 2,906
Toll Pathway-Dependent Blockade of CD4 + CD25 + T Cell-Mediated Suppression by Dendritic Cells
Pasare, C., & Medzhitov, R. M. (2003) · Science · doi:10.1126/science.1078231 · Cited by 2,000
Use of a cDNA microarray to analyse gene expression patterns in human cancer
DeRisi, J. L., Penland, L., Brown, P. O., Bittner, M. L., Meltzer, P. S., Ray, M., Chen, Y.-W., Su, Y. A., & Trent, J. M. (1996) · Nature Genetics · doi:10.1038/ng1296-457 · Cited by 1,952
Counting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection
Murali‐Krishna, K., Altman, J. D., Suresh, M., Sourdive, D. J. D., Zajac, A. J., Miller, J. D., Slansky, J. E., & Ahmed, R. (1998) · Immunity · doi:10.1016/s1074-7613(00)80470-7 · Cited by 1,918
Loss of Functional Suppression by CD4+CD25+ Regulatory T Cells in Patients with Multiple Sclerosis
Viglietta, V., Baecher‐Allan, C., Weiner, H. L., & Hafler, D. A. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20031579 · Cited by 1,858
Dendritic Cells Induce Peripheral T Cell Unresponsiveness under Steady State Conditions in Vivo
Hawiger, D., Inaba, K., Dorsett, Y., Guo, M., Mahnke, K., Rivera, M. N., Ravetch, J. V., Steinman, R. M., & Nussenzweig, M. C. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.194.6.769 · Cited by 1,848
Monney, L., Sabatos, C. A., Gaglia, J. L., Ryu, A., Waldner, H., Chernova, T., Manning, S., Greenfield, E. A., Coyle, A. J., Sobel, R. A., et al. (2002) · Nature · doi:10.1038/415536a · Cited by 1,683
Copolymer 1 reduces relapse rate and improves disability in relapsing‐remitting multiple sclerosis
Johnson, K., Brooks, B., Cohen, J. A., Ford, C., Goldstein, J., Lisak, R., Myers, L., Panitch, H., Rose, J., Schiffer, R., et al. (1995) · Neurology · doi:10.1212/wnl.45.7.1268 · Cited by 1,667
Research works printed but not linked: 12
- McFarland HF, 1999, Am. J. Neuroradiol., 20, 1777
- 10.1172/JCI200421357 · DOI
- Charcot J, 1868, Gaz. Hopitaux, 41, 554
- Remlinger J, 1905, Ann. Inst. Pasteur, 19, 625
- Berger T, 1997, Lab. Invest., 76, 355
- 10.1097/00019052-200306000-00004 · DOI
- Sharief MK, 1991, Brain, 114, 181
- Bornstein MB, 1959, Trans. Am. Neurol. Assoc., 84, 165
- 10.1002/1531-8249(200006)47:6<694::AID-ANA2>3.0.CO;2-W · DOI
- Linington C, 1988, Am. J. Pathol., 130, 443
- Benczur M, 1980, Clin. Exp. Immunol., 39, 657
- 10.1002/1531-8249(199909)46:3<296::AID-ANA4>3.0.CO;2-# · DOI
Cited by
Sorted by citations
Items 101–200 of 1,006
IL-17 receptor signaling and T helper 17-mediated autoimmune demyelinating disease
Zepp, J. A., Wu, L., & Li, X. (2011) · Trends in Immunology · doi:10.1016/j.it.2011.02.007 · Cited by 227
Enhanced number and activity of mitochondria in multiple sclerosis lesions
Witte, M. E., Bø, L., Rodenburg, R. J., Beliën, J. A. M., Musters, R. J. P., Hazes, T., Wintjes, L. T., Smeitink, J. A. M., Geurts, J. J. G., de Vries, H. E., et al. (2009) · The Journal of Pathology · doi:10.1002/path.2582 · Cited by 223
Circulating exosomes suppress the induction of regulatory T cells via let-7i in multiple sclerosis
Kimura, K., Hohjoh, H., Fukuoka, M., Sato, W., Oki, S., Tomi, C., Yamaguchi, H., Kondo, T., Takahashi, R., & Yamamura, T. (2017) · Nature Communications · doi:10.1038/s41467-017-02406-2 · Cited by 223
Passive induction of experimental allergic encephalomyelitis
Stromnes, I. M., & Goverman, J. M. (2006) · Nature Protocols · doi:10.1038/nprot.2006.284 · Cited by 238
Current Views on the Roles of Th1 and Th17 Cells in Experimental Autoimmune Encephalomyelitis
Behi, M. E., Rostami, A. M., & Ćirić, B. (2010) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-009-9188-9 · Cited by 222
Carbajal, K. S., Schaumburg, C. S., Strieter, R. M., Kane, J. A. C., & Lane, T. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006375107 · Cited by 226
Act1 mediates IL-17-induced EAE pathogenesis selectively in NG2+ glial cells
Kang, Z., Wang, C., Zepp, J., Wu, L., Sun, K., Zhao, J., Chandrasekharan, U., DiCorleto, P. E., Trapp, B. D., Ransohoff, R. M., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3505 · Cited by 218
Th17 Cells and Autoimmune Encephalomyelitis (EAE/MS)
Aranami, T., & Yamamura, T. (2008) · Allergology International · doi:10.2332/allergolint.r-07-159 · Cited by 218
Zeis, T., Graumann, U., Reynolds, R., & Schaeren‐Wiemers, N. (2007) · Brain · doi:10.1093/brain/awm291 · Cited by 214
Kwon, H.-K., Kim, G.-C., Kim, Y., Hwang, W., Jash, A., Sahoo, A., Kim, J.-E., Nam, J. H., & Im, S.-H. (2013) · Clinical Immunology · doi:10.1016/j.clim.2013.01.001 · Cited by 212
Hedegaard, C. J., Krakauer, M., Bendtzen, K., Lund, H., Sellebjerg, F. T., & Nielsen, C. H. (2008) · Immunology · doi:10.1111/j.1365-2567.2008.02837.x · Cited by 215
The Master Switch: The Role of Mast Cells in Autoimmunity and Tolerance
Sayed, B. A., Christy, A. L., Quirion, M. R., & Brown, M. A. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090320 · Cited by 214
Benkhoucha, M., Santiago‐Raber, M., Schneiter, G., Chofflon, M., Funakoshi, H., Nakamura, T., & Lalive, P. H. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912437107 · Cited by 210
A basic overview of multiple sclerosis immunopathology
Grigoriadis, N., & Pesch, V. V. (2015) · European Journal of Neurology · doi:10.1111/ene.12798 · Cited by 220
Functional epistasis on a common MHC haplotype associated with multiple sclerosis
Gregersen, J. W., Kranc, K. R., Ke, X., Svendsen, P., Madsen, L. S., Thomsen, A. R., Cardon, L. R., Bell, J. I., & Fugger, L. H. (2006) · Nature · doi:10.1038/nature05133 · Cited by 207
Environmental risk factors for multiple sclerosis
Salzer, J. (2013) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 202
Sex: A Significant Risk Factor for Neurodevelopmental and Neurodegenerative Disorders
Pinares-Garcia, P., Stratikopoulos, M., Zagato, A., Loke, H., & Lee, J. (2018) · Brain Sciences · doi:10.3390/brainsci8080154 · Cited by 200
Oxidative Stress-Induced Signaling Pathways Implicated in the Pathogenesis of Parkinson’s Disease
Gaki, G. S., & Papavassiliou, A. G. (2014) · NeuroMolecular Medicine · doi:10.1007/s12017-014-8294-x · Cited by 206
Leist, T. P., & Weissert, R. (2011) · Clinical Neuropharmacology · doi:10.1097/wnf.0b013e318204cd90 · Cited by 200
Temporal dynamics of anti-MOG antibodies in CNS demyelinating diseases
Pauli, F. D., Mader, S., Rostasy, K. M., Schanda, K., Bajer-Kornek, B., Ehling, R., Deisenhammer, F., Reindl, M., & Berger, T. (2010) · Clinical Immunology · doi:10.1016/j.clim.2010.11.013 · Cited by 200
Zhang, X., Jin, J., Peng, X., Ramgolam, V. S., & Markovic‐Plese, S. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.10.6988 · Cited by 203
Thewissen, M. M., Somers, V. A., Hellings, N., Fraussen, J., Damoiseaux, J. G. M. C., & Stinissen, P. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.10.6514 · Cited by 199
Ifergan, I., Kébir, H., Bernard, M., Wosik, K., Dodelet-Devillers, A., Cayrol, R., Arbour, N., & Prat, A. (2007) · Brain · doi:10.1093/brain/awm295 · Cited by 199
Hohlfeld, R., Dornmair, K., Meinl, E., & Wekerle, H. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(15)00334-8 · Cited by 205
The epigenetics of autoimmunity
Meda, F., Folci, M., Baccarelli, A., & Selmi, C. F. (2011) · Cellular and Molecular Immunology · doi:10.1038/cmi.2010.78 · Cited by 198
Estrogen and testosterone therapies in multiple sclerosis
Gold, S. M., & Voskuhl, R. R. (2009) · Progress in brain research · doi:10.1016/s0079-6123(09)17516-7 · Cited by 200
Zajonc, D. M., Maricic, I., Wu, D., Halder, R. C., Roy, K. C., Wong, C., Kumar, V., & Wilson, I. A. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20051625 · Cited by 192
Unraveling the complexities of cannabinoid receptor 2 (CB2) immune regulation in health and disease
Basu, S., & Dittel, B. N. (2011) · Immunologic Research · doi:10.1007/s12026-011-8210-5 · Cited by 197
Akt1 is critical for acute inflammation and histamine-mediated vascular leakage
Lorenzo, A. D., Fernandez-Hernando, C. F., Cirino, G., & Sessa, W. C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904073106 · Cited by 191
Mucosal-associated invariant T cells regulate Th1 response in multiple sclerosis
Miyazaki, Y., Miyake, S., Chiba, A., Lantz, O. J., & Yamamura, T. (2011) · International Immunology · doi:10.1093/intimm/dxr047 · Cited by 201
microRNA-301a regulation of a T-helper 17 immune response controls autoimmune demyelination
Mycko, M. P., Cichalewska, M., Machlańska, A., Ćwiklińska, H., Mariasiewicz, M., & Selmaj, K. W. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114325109 · Cited by 190
T Cell-Mediated Autoimmune Disease Due to Low-Affinity Crossreactivity to Common Microbial Peptides
Harkiolaki, M., Holmes, S. L., Svendsen, P., Gregersen, J. W., Jensen, L. T., McMahon, R. M., Friese, M. A., van Boxel, G., Etzensperger, R., Tzartos, J. S., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.01.009 · Cited by 198
Gaforio, J. J., Visioli, F., Alarcón-de-la-Lastra, C., Castañer, O., Delgado-Rodríguez, M., Fitó, M., Hernández, A. F., Huertas, J. R., Martínez-González, M. A., Menendez, J. A., et al. (2019) · Nutrients · doi:10.3390/nu11092039 · Cited by 187
Downregulation of macrophage inhibitory molecules in multiple sclerosis lesions
Koning, N., Bö, L., Hoek, R. M., & Huitinga, I. (2007) · Annals of Neurology · doi:10.1002/ana.21220 · Cited by 186
Murugaiyan, G., Mittal, A., & Weiner, H. L. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.11.7480 · Cited by 186
Li, Y., Huang, Y., Lue, J., Quandt, J. A., Martinꝉ, R., & Mariuzza, R. A. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600771 · Cited by 185
Self-citationNFKB and NFKBI polymorphisms in relation to susceptibility of tumour and other diseases.
Sun, X.-F., & Zhang, H. (2007) · PubMed · doi:10.14670/hh-22.1387 · Cited by 185
Opposing effects of HLA class I molecules in tuning autoreactive CD8+ T cells in multiple sclerosis
Friese, M. A., Jakobsen, K. B., Friis, L. S., Etzensperger, R., Craner, M. J., McMahon, R. M., Jensen, L. T., Huygelen, V., Jones, E. Y., Bell, J. I., et al. (2008) · Nature Medicine · doi:10.1038/nm.1881 · Cited by 184
Dousset, V., Brochet, B., Deloire, M. S. A., Lagoarde, L., Barroso, B., Caillé, J. M., & Petry, K. G. (2006) · PubMed Central · Cited by 182
Fas–Fas Ligand: Checkpoint of T Cell Functions in Multiple Sclerosis
Volpe, E., Sambucci, M., Battistini, L., & Borsellino, G. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00382 · Cited by 197
Rus, H., Pardo, C. A., Hu, L., Darrah, E., Cudrici, C. D., Niculescu, T., Niculescu, F. I., Mullen, K. M., Allie, R., Guo, L., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501770102 · Cited by 181
Wüst, S., van den Brandt, J., Tischner, D., Kleiman, A., Tuckermann, J. P., Gold, R., Lühder, F., & Reichardt, H. M. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.12.8434 · Cited by 181
Phase 2 trial of a DNA vaccine encoding myelin basic protein for multiple sclerosis
Garren, H., Robinson, W. H., Krasulová, E., Havrdová, E., Nadj, Č., Selmaj, K. W., Losy, J., Nadj, I., Radue, E. W., Kidd, B. A., et al. (2008) · Annals of Neurology · doi:10.1002/ana.21370 · Cited by 180
Autoantibodies to myelin basic protein catalyze site-specific degradation of their antigen
Ponomarenko, N. A., Durova, O. M., Vorobiev, I. I., Belogurov, A. A., Kurkova, I. N., Petrenko, A. G., Telegin, G. B., Suchkov, S. V., Киселев, С. Л., Lagarkova, M. A., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509849103 · Cited by 179
Current and Future Biomarkers in Multiple Sclerosis
Yang, J., Hamade, M., Wu, Q., Wang, Q., Axtell, R. C., Giri, S., & Mao‐Draayer, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23115877 · Cited by 190
Glial toll-like receptor signaling in central nervous system infection and autoimmunity
Carpentier, P. A., Duncan, D. S., & Miller, S. D. (2007) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2007.08.011 · Cited by 182
Karni, A., Abraham, M., Monsonego, A., Cai, G., Freeman, G. J., Hafler, D. A., Khoury, S. J., & Weiner, H. L. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.6.4196 · Cited by 177
The complement cascade: Yin-Yang in neuroinflammation—neuro-protection and -degeneration
Alexander, J. J., Anderson, A. J., Barnum, S. R., Stevens, B., & Tenner, A. J. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05668.x · Cited by 177
Zhang, J., Cheng, Y., Cui, W., Li, M., Li, B., & Guo, L. (2013) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2013.09.019 · Cited by 178
The Immunopathophysiology of Multiple Sclerosis
Wu, G. F., & Álvarez, E. (2011) · Neurologic Clinics · doi:10.1016/j.ncl.2010.12.009 · Cited by 186
Modeling the heterogeneity of multiple sclerosis in animals
Simmons, S. B., Pierson, E. R., Lee, S. Y., & Goverman, J. M. (2013) · Trends in Immunology · doi:10.1016/j.it.2013.04.006 · Cited by 184
Singh, N. P., Hegde, V. L., Hofseth, L. J., Nagarkatti, M., & Nagarkatti, P. S. (2007) · Molecular Pharmacology · doi:10.1124/mol.107.038984 · Cited by 174
Perriot, S., Mathias, A., Perriard, G., Canales, M., Jonkmans, N., Merienne, N., Meunier, C., El Kassar, L., Perrier, A. L., Laplaud, D.-A., et al. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.09.015 · Cited by 171
Pathogenic CD8+ T cells in multiple sclerosis
Friese, M. A., & Fugger, L. H. (2009) · Annals of Neurology · doi:10.1002/ana.21744 · Cited by 170
Lower motor neuron loss in multiple sclerosis and experimental autoimmune encephalomyelitis
Vogt, J., Paul, F., Aktas, O., Müller‐Wielsch, K., Dörr, J., Dörr, S., Bharathi, B. S., Glumm, R., Schmitz, C., Steinbusch, H., et al. (2009) · Annals of Neurology · doi:10.1002/ana.21719 · Cited by 157
Calderon, T. M., Eugenín, E. A., Lopez, L., Kumar, S. S., Hesselgesser, J., Raine, C. S., & Berman, J. W. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.05.003 · Cited by 166
Increased IL-23p19 expression in multiple sclerosis lesions and its induction in microglia
Li, Y., Chu, N., Hu, A., Gran, B., Rostami, A. M., & ZHANG, G. (2006) · Brain · doi:10.1093/brain/awl273 · Cited by 170
Cao, W., Yang, Y., Wang, Z., Liu, A., Fang, L., Wu, F., Hong, J., Shi, Y., Leung, S., Dong, C., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.06.011 · Cited by 168
Bar‐Or, A., Vollmer, T. R., Antel, J. P., Arnold, D. L., Bodner, C., Campagnolo, D. I., Gianettoni, J., Jalili, F., Kachuck, N. J., Lapierre, Y., et al. (2007) · Archives of Neurology · doi:10.1001/archneur.64.10.nct70002 · Cited by 166
Ponomarev, E. D., Shriver, L. P., & Dittel, B. N. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.3.1402 · Cited by 165
Christy, A. L., Walker, M. E., Hessner, M. J., & Brown, M. A. (2012) · Journal of Autoimmunity · doi:10.1016/j.jaut.2012.11.003 · Cited by 172
Type I interferon pathway in CNS homeostasis and neurological disorders
Blank, T., & Prinz, M. (2017) · Glia · doi:10.1002/glia.23154 · Cited by 172
Activation of p38 MAPK in CD4 T cells controls IL-17 production and autoimmune encephalomyelitis
Noubade, R., Krementsov, D. N., del Río, R., Thornton, T. M., Nagaleekar, V. K., Saligrama, N., Spitzack, A., Spach, K. M., Sabio, G., Davis, R. J., et al. (2011) · Blood · doi:10.1182/blood-2011-02-336552 · Cited by 167
Sayed, B. A., Christy, A. L., Walker, M. E., & Brown, M. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000126 · Cited by 163
Central nervous system-directed effects of FTY720 (fingolimod)
Miron, V. E., Schubart, A., & Antel, J. P. (2008) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2008.06.031 · Cited by 166
Inhibition of the immunoproteasome ameliorates experimental autoimmune encephalomyelitis
Basler, M., Mundt, S., Muchamuel, T., Moll, C., Jiang, J., Groettrup, M., & Kirk, C. J. (2014) · EMBO Molecular Medicine · doi:10.1002/emmm.201303543 · Cited by 163
Role of gender in multiple sclerosis: Clinical effects and potential molecular mechanisms
Greer, J. M., & McCombe, P. (2011) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2011.03.003 · Cited by 165
Glucocorticoids and endothelial cell barrier function
Salvador, E., Shityakov, S., & Förster, C. Y. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1762-z · Cited by 164
Potential targeting of B7‐H4 for the treatment of cancer
Podojil, J. R., & Miller, S. D. (2017) · Immunological Reviews · doi:10.1111/imr.12530 · Cited by 160
The value of animal models for drug development in multiple sclerosis
Friese, M. A. (2006) · Brain · doi:10.1093/brain/awl083 · Cited by 159
Hucke, S., Eschborn, M., Liebmann, M., Herold, M. V. B., Freise, N., Engbers, A., Ehling, P., Meuth, S. G., Roth, J., Kuhlmann, T., et al. (2015) · Journal of Autoimmunity · doi:10.1016/j.jaut.2015.11.001 · Cited by 161
The Essential Role of Epstein-Barr Virus in the Pathogenesis of Multiple Sclerosis
Pender, M. P. (2010) · The Neuroscientist · doi:10.1177/1073858410381531 · Cited by 157
Ben‐Nun, A., Kaushansky, N., Kawakami, N., Krishnamoorthy, G., Berer, K., Liblau, R., Hohlfeld, R., & Wekerle, H. (2014) · Journal of Autoimmunity · doi:10.1016/j.jaut.2014.06.004 · Cited by 165
Farez, M., Correale, J. D., Armstrong, M. J., Rae-Grant, A. D., Gloss, D. S., Donley, D. K., Holler‐Managan, Y., Kachuck, N. J., Jeffery, D., Beilman, M., et al. (2019) · Neurology · doi:10.1212/wnl.0000000000008157 · Cited by 156
Noorbakhsh, F., Tsutsui, S., Vergnolle, N., Boven, L. A., Shariat, N., Vodjgani, M., Warren, K. G., Andrade‐Gordon, P., Hollenberg, M. D., & Power, C. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20052148 · Cited by 153
Autoreactive lymphocytes in multiple sclerosis: Pathogenesis and treatment target
Liu, R., Du, S., Zhao, L., Jain, S., Sahay, K., Rizvanov, A. A., Lezhnyova, V., Хайбуллин, Т. И., Martynova, E. V., Khaiboullina, S. F., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.996469 · Cited by 170
van Zwam, M., Huizinga, R., Heijmans, N., van Meurs, M., Wierenga‐Wolf, A. F., Melief, M., Hintzen, R. Q., Hart, B. A. ‘., Amor, S., Boven, L. A., et al. (2008) · The Journal of Pathology · doi:10.1002/path.2476 · Cited by 151
Microbial view of central nervous system autoimmunity
Berer, K., & Krishnamoorthy, G. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.04.007 · Cited by 153
Microglial autophagy–associated phagocytosis is essential for recovery from neuroinflammation
Berglund, R., Guerreiro-Cacais, A. O., Adzemovic, M. Z., Zeitelhofer, M., Lund, H., Ewing, E., Ruhrmann, S., Nutma, E., Parsa, R., Thessen-Hedreul, M., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.abb5077 · Cited by 149
Disturbed regulatory T cell homeostasis in multiple sclerosis
Venken, K., Hellings, N., Liblau, R., & Stinissen, P. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2009.12.003 · Cited by 150
Stüve, O., Cepok, S., Elias, B., Saleh, A., Hartung, H.-P., Hemmer, B., & Kieseier, B. C. (2005) · Archives of Neurology · doi:10.1001/archneur.62.10.1620 · Cited by 149
A Population-based Ecologic Study of Inflammatory Bowel Disease: Searching for Etiologic Clues
Green, C. A., Elliott, L. J., Beaudoin, C. M., & Bernstein, C. N. (2006) · American Journal of Epidemiology · doi:10.1093/aje/kwj260 · Cited by 148
Sécher, T., Kassem, S., Benamar, M., Bernard, I., Boury, M., Barreau, F., Oswald, É., & Saoudi, A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01096 · Cited by 148
Innate, innate-like and adaptive lymphocytes in the pathogenesis of MS and EAE
Van Kaer, L., Postoak, J. L., Wang, C., Yang, G., & Wu, L. (2019) · Cellular & Molecular Immunology · doi:10.1038/s41423-019-0221-5 · Cited by 148
HIV Infection of the Central Nervous System: Clinical Features and Neuropathogenesis
Lomax, L. B., Gill, M. J., & Power, C. (2008) · Neurologic Clinics · doi:10.1016/j.ncl.2008.04.002 · Cited by 147
Modulating the immune system through nanotechnology
Dacoba, T. G., Ana, O., Torres, D., Crecente‐Campo, J., & Alonso, M. J. (2017) · Seminars in Immunology · doi:10.1016/j.smim.2017.09.007 · Cited by 150
CURCUMIN AND AUTOIMMUNE DISEASE
Bright, J. J. (2007) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-46401-5_19 · Cited by 147
Harauz, G., & Musse, A. A. (2006) · Neurochemical Research · doi:10.1007/s11064-006-9108-9 · Cited by 146
Larochelle, C., Cayrol, R., Kebir, H., Alvarez, J. I., Lécuyer, M.-A., Ifergan, I., Viel, É., Bourbonnière, L., Beauseigle, D., Terouz, S., et al. (2012) · Brain · doi:10.1093/brain/aws212 · Cited by 145
Regulation of the severity of neuroinflammation and demyelination by TLR‐ASK1‐p38 pathway
Guo, X., Harada, C., Namekata, K., Matsuzawa, A., Camps, M., Ji, H., Swinnen, D., Jorand‐Lebrun, C., Muzerelle, M., Vitte, P., et al. (2010) · EMBO Molecular Medicine · doi:10.1002/emmm.201000103 · Cited by 146
Shaw, P. J., Barr, M., Lukens, J. R., McGargill, M. A., Chi, H., Mak, T. W., & Kanneganti, T. (2011) · Immunity · doi:10.1016/j.immuni.2010.12.015 · Cited by 144
van Zwam, M., Huizinga, R., Melief, M., Wierenga‐Wolf, A. F., van Meurs, M., Voerman, J. S. A., Biber, K. P. H., Boddeke, H. W. G. M., Höpken, U. E., Meisel, C., et al. (2008) · Journal of Molecular Medicine · doi:10.1007/s00109-008-0421-4 · Cited by 148
Lithium Prevents and Ameliorates Experimental Autoimmune Encephalomyelitis
Sarno, P. D., Axtell, R. C., Raman, C., Roth, K. A., Alessi, D. R., & Jope, R. S. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.1.338 · Cited by 146
The role of immune cells, glia and neurons in white and gray matter pathology in multiple sclerosis
Mallucci, G., Peruzzotti‐Jametti, L., Bernstock, J. D., & Pluchino, S. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.02.003 · Cited by 153
Natalizumab treatment is associated with peripheral sequestration of proinflammatory T cells
Kivisäkk, P., Healy, B. C., Viglietta, V., Quintana, F. J., Hootstein, M. A., Weiner, H. L., & Khoury, S. J. (2009) · Neurology · doi:10.1212/wnl.0b013e3181a8266f · Cited by 145
Oreja‐Guevara, C., Ramos‐Cejudo, J., Aroeira, L. S., Chamorro, B., & Díez‐Tejedor, E. (2012) · BMC Neurology · doi:10.1186/1471-2377-12-95 · Cited by 141
Novakova, L., Axelsson, M., Khademi, M., Zetterberg, H., Blennow, K., Malmeström, C., Piehl, F., Olsson, T. P., & Lycke, J. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13881 · Cited by 147
Podojil, J. R., & Miller, S. D. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2009.00773.x · Cited by 144
Critical regulation of CD4+ T cell survival and autoimmunity by β-arrestin 1
Shi, Y., Feng, Y., Kang, J., Liu, C., Li, Z., Li, D., Cao, W., Qiu, J., Guo, Z., Bi, E., et al. (2007) · Nature Immunology · doi:10.1038/ni1489 · Cited by 141
IL‐10 suppressor activity and ex vivo Tr1 cell function are impaired in multiple sclerosis
Martínez‐Forero, I., García‐Muñoz, R., Martinez‐Pasamar, S., Inogés, S., de Cerio, A. L.-D., Palacios, R., Sepulcre, J., Moreno, B., Gonzalez, Z., Fernández-Díez, B., et al. (2008) · European Journal of Immunology · doi:10.1002/eji.200737271 · Cited by 141
Metadata
- Authors
- Sospedra, M., & Martin, R.
- Affiliations
- National Institutes of Health (US)
- Cellular Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892-1400;
- ORCID
- Sospedra, Mireia
- Venue
- Annual Review of Immunology
- Publisher
- Annual Reviews
- Published
- 2005-04-01
- Volume
- 23
- Issue
- 1
- Pages
- 683-747
- ISSN
- 0732-0582 (ISSN-L)
- 1545-3278
- OpenAlex
- W2113291839
- Cited by
- 2,149
- References
- 362
- Citations by year
- 2026: 27 · 2025: 43 · 2024: 62 · 2023: 64 · 2022: 69 · 2021: 72 · 2020: 78 · 2019: 84 · 2018: 71 · 2017: 110 · 2016: 107 · 2015: 149 · 2014: 133 · 2013: 144 · 2012: 120
- FWCI
- 19.06
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- multiple sclerosis, autoimmunity, CD4+ T cells, Th1 cells, Th2 cells, regulatory T cells, natural killer cells, CD8+ T cells, complement system, autoantibodies, innate immunity, viral triggers, genetic susceptibility, relapsing-remitting disease, chronic progressive disease, central nervous system, neuroimmune interactions
- MeSH terms
- Autoantibodies, Autoantigens, Central Nervous System, HLA Antigens, Humans, Immunity, Innate, Immunogenetics, Infections, Multiple Sclerosis, Myelin Proteins, T-Lymphocyte Subsets, Cytokines, Models, Immunological, Molecular Mimicry, Chemokines, Genomics
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