Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Perspective
  • Published:

Pathogenic autoantibodies in multiple sclerosis — from a simple idea to a complex concept

Abstract

The role of autoantibodies in multiple sclerosis (MS) has been enigmatic since the first description, many decades ago, of intrathecal immunoglobulin production in people with this condition. Some studies have indicated that MS pathology is heterogeneous, with an antibody-associated subtype — characterized by B cells (in varying quantities), antibodies and complement — existing alongside other subtypes with different pathologies. However, subsequent evidence suggested that some cases originally diagnosed as MS with autoantibody-mediated demyelination were more likely to be neuromyelitis optica spectrum disorder or myelin oligodendrocyte glycoprotein antibody-associated disease. These findings raise the important question of whether an autoantibody-mediated MS subtype exists and whether pathogenic MS-associated autoantibodies remain to be identified. Potential roles of autoantibodies in MS could range from specific antibodies defining the disease to a non-disease-specific amplification of cellular immune responses and other pathophysiological processes. In this Perspective, we review studies that have attempted to identify MS-associated autoantibodies and provide our opinions on their possible roles in the pathophysiology of MS.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Potential mechanisms of antibody pathogenicity in multiple sclerosis.
Fig. 2: Neuropathology of tumefactive MS and MOGAD.

Similar content being viewed by others

References

  1. Frohman, E. M., Racke, M. K. & Raine, C. S. Multiple sclerosis–the plaque and its pathogenesis. N. Engl. J. Med. 354, 942–955 (2006).

    Article  CAS  PubMed  Google Scholar 

  2. Lassmann, H., Bruck, W. & Lucchinetti, C. F. The immunopathology of multiple sclerosis: an overview. Brain Pathol. 17, 210–218 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  3. Sospedra, M. & Martin, R. Immunology of multiple sclerosis. Annu. Rev. Immunol. 23, 683–747 (2005).

    Article  CAS  PubMed  Google Scholar 

  4. Reindl, M., Khalil, M. & Berger, T. Antibodies as biological markers for pathophysiological processes in MS. J. Neuroimmunol. 180, 50–62 (2006).

    Article  CAS  PubMed  Google Scholar 

  5. Kuenz, B. et al. Cerebrospinal fluid B cells correlate with early brain inflammation in multiple sclerosis. PLoS ONE 3, e2559 (2008).

    Article  PubMed  PubMed Central  Google Scholar 

  6. Cepok, S. et al. Patterns of cerebrospinal fluid pathology correlate with disease progression in multiple sclerosis. Brain 124, 2169–2176 (2001).

    Article  CAS  PubMed  Google Scholar 

  7. Freedman, M. S. et al. Recommended standard of cerebrospinal fluid analysis in the diagnosis of multiple sclerosis: a consensus statement. Arch. Neurol. 62, 865–870 (2005).

    Article  PubMed  Google Scholar 

  8. Berger, T. & Reindl, M. Antibody biomarkers in CNS demyelinating diseases–a long and winding road. Eur. J. Neurol. 22, 1162–1168 (2015).

    Article  CAS  PubMed  Google Scholar 

  9. Hohlfeld, R., Dornmair, K., Meinl, E. & Wekerle, H. The search for the target antigens of multiple sclerosis, part 2: CD8+ T cells, B cells, and antibodies in the focus of reverse-translational research. Lancet Neurol. 15, 317–331 (2016).

    Article  CAS  PubMed  Google Scholar 

  10. Schirmer, L., Srivastava, R. & Hemmer, B. To look for a needle in a haystack: the search for autoantibodies in multiple sclerosis. Mult. Scler. 20, 271–279 (2014).

    Article  PubMed  Google Scholar 

  11. Hardy, T. A. et al. Atypical inflammatory demyelinating syndromes of the CNS. Lancet Neurol. 15, 967–981 (2016).

    Article  CAS  PubMed  Google Scholar 

  12. Dalmau, J. & Graus, F. Antibody-mediated encephalitis. N. Engl. J. Med. 378, 840–851 (2018).

    Article  PubMed  Google Scholar 

  13. Marignier, R. et al. Myelin-oligodendrocyte glycoprotein antibody-associated disease. Lancet Neurol. 20, 762–772 (2021).

    Article  CAS  PubMed  Google Scholar 

  14. Jarius, S. et al. Neuromyelitis optica. Nat. Rev. Dis. Prim. 6, 85 (2020).

    Article  PubMed  Google Scholar 

  15. Pruss, H. Autoantibodies in neurological disease. Nat. Rev. Immunol. 21, 798–813 (2021).

    Article  PubMed  PubMed Central  Google Scholar 

  16. Lucchinetti, C. et al. Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination. Ann. Neurol. 47, 707–717 (2000).

    Article  CAS  PubMed  Google Scholar 

  17. Tobin, W. O. et al. Clinical correlation of multiple sclerosis immunopathologic subtypes. Neurology 97, e1906–e1913 (2021).

    Article  CAS  PubMed  Google Scholar 

  18. Prineas, J. W. & Graham, J. S. Multiple sclerosis: capping of surface immunoglobulin G on macrophages engaged in myelin breakdown. Ann. Neurol. 10, 149–158 (1981).

    Article  CAS  PubMed  Google Scholar 

  19. Barnett, M. H., Parratt, J. D., Cho, E. S. & Prineas, J. W. Immunoglobulins and complement in postmortem multiple sclerosis tissue. Ann. Neurol. 65, 32–46 (2009).

    Article  PubMed  Google Scholar 

  20. Henderson, A. P., Barnett, M. H., Parratt, J. D. & Prineas, J. W. Multiple sclerosis: distribution of inflammatory cells in newly forming lesions. Ann. Neurol. 66, 739–753 (2009).

    Article  PubMed  Google Scholar 

  21. Michailidou, I. et al. Complement C3 on microglial clusters in multiple sclerosis occur in chronic but not acute disease: implication for disease pathogenesis. Glia 65, 264–277 (2017).

    Article  PubMed  Google Scholar 

  22. Werneburg, S. et al. Targeted complement inhibition at synapses prevents microglial synaptic engulfment and synapse loss in demyelinating disease. Immunity 52, 167–182.e7 (2020).

    Article  CAS  PubMed  Google Scholar 

  23. Bornstein, M. B. & Appel, S. H. Tissue culture studies of demyelination. Ann. N. Y. Acad. Sci. 122, 280–286 (1965).

    Article  CAS  PubMed  Google Scholar 

  24. Appel, S. H. & Bornstein, M. B. The application of tissue culture to the study of experimental allergic encephalomyelitis. II. Serum factors responsible for demyelination. J. Exp. Med. 119, 303–312 (1964).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Grundke-Iqbal, I. & Bornstein, M. B. Multiple sclerosis: serum gamma globulin and demyelination in organ culture. Neurology 30, 749–754 (1980).

    Article  CAS  PubMed  Google Scholar 

  26. Seil, F. J. Myelin antigens and antimyelin antibodies. Antibodies 7, 2 (2018).

    Article  PubMed Central  Google Scholar 

  27. Lisak, R. P. et al. Secretory products of multiple sclerosis B cells are cytotoxic to oligodendroglia in vitro. J. Neuroimmunol. 246, 85–95 (2012).

    Article  CAS  PubMed  Google Scholar 

  28. Linington, C., Webb, M. & Woodhams, P. L. A novel myelin-associated glycoprotein defined by a mouse monoclonal antibody. J. Neuroimmunol. 6, 387–396 (1984).

    Article  Google Scholar 

  29. Brunner, C., Lassmann, H., Waehneldt, T. V., Matthieu, J. M. & Linington, C. Differential ultrastructural localization of myelin basic protein, myelin/oligodendroglial glycoprotein, and 2′,3′-cyclic nucleotide 3′-phosphodiesterase in the CNS of adult rats. J. Neurochem. 52, 296–304 (1989).

    Article  CAS  PubMed  Google Scholar 

  30. Lassmann, H. & Bradl, M. Multiple sclerosis: experimental models and reality. Acta Neuropathol. 133, 223–244 (2017).

    Article  CAS  PubMed  Google Scholar 

  31. Lucchinetti, C. F. et al. A role for humoral mechanisms in the pathogenesis of Devic’s neuromyelitis optica. Brain 125, 1450–1461 (2002).

    Article  PubMed  Google Scholar 

  32. Lennon, V. A. et al. A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet 364, 2106–2112 (2004).

    Article  CAS  PubMed  Google Scholar 

  33. Lennon, V. A., Kryzer, T. J., Pittock, S. J., Verkman, A. S. & Hinson, S. R. IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel. J. Exp. Med. 202, 473–477 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Bennett, J. L. et al. Intrathecal pathogenic anti-aquaporin-4 antibodies in early neuromyelitis optica. Ann. Neurol. 66, 617–629 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Bradl, M. et al. Neuromyelitis optica: pathogenicity of patient immunoglobulin in vivo. Ann. Neurol. 66, 630–643 (2009).

    Article  CAS  PubMed  Google Scholar 

  36. Saadoun, S. et al. Intra-cerebral injection of neuromyelitis optica immunoglobulin G and human complement produces neuromyelitis optica lesions in mice. Brain 133, 349–361 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  37. Wingerchuk, D. M. et al. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders. Neurology 85, 177–189 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  38. Lucchinetti, C. F. et al. The pathology of an autoimmune astrocytopathy: lessons learned from neuromyelitis optica. Brain Pathol. 24, 83–97 (2014).

    Article  CAS  PubMed  Google Scholar 

  39. Jarius, S. et al. MOG encephalomyelitis: international recommendations on diagnosis and antibody testing. J. Neuroinflamm. 15, 134 (2018).

    Article  CAS  Google Scholar 

  40. Lopez-Chiriboga, A. S. et al. Association of MOG-IgG serostatus with relapse after acute disseminated encephalomyelitis and proposed diagnostic criteria for MOG-IgG-associated disorders. JAMA Neurol. 75, 1355–1363 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  41. Reindl, M. & Waters, P. Myelin oligodendrocyte glycoprotein antibodies in neurological disease. Nat. Rev. Neurol. 15, 89–102 (2019).

    Article  CAS  PubMed  Google Scholar 

  42. Jarius, S. et al. Screening for MOG-IgG and 27 other anti-glial and anti-neuronal autoantibodies in ‘pattern II multiple sclerosis’ and brain biopsy findings in a MOG-IgG-positive case. Mult. Scler. 22, 1541–1549 (2016).

    Article  CAS  PubMed  Google Scholar 

  43. Ricken, G. et al. Detection methods for autoantibodies in suspected autoimmune encephalitis. Front. Neurol. 9, 841 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  44. Waters, P., Pettingill, P. & Lang, B. Detection methods for neural autoantibodies. Handb. Clin. Neurol. 133, 147–163 (2016).

    Article  PubMed  Google Scholar 

  45. O’Connor, K. C. et al. Myelin basic protein-reactive autoantibodies in the serum and cerebrospinal fluid of multiple sclerosis patients are characterized by low-affinity interactions. J. Neuroimmunol. 136, 140–148 (2003).

    Article  PubMed  Google Scholar 

  46. Srivastava, R. et al. Potassium channel KIR4.1 as an immune target in multiple sclerosis. N. Engl. J. Med. 367, 115–123 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Brickshawana, A. et al. Investigation of the KIR4.1 potassium channel as a putative antigen in patients with multiple sclerosis: a comparative study. Lancet Neurol. 13, 795–806 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Nerrant, E. et al. Lack of confirmation of anti-inward rectifying potassium channel 4.1 antibodies as reliable markers of multiple sclerosis. Mult. Scler. 20, 1699–1703 (2014).

    Article  CAS  PubMed  Google Scholar 

  49. Probstel, A. K. et al. Multiple sclerosis and antibodies against KIR4.1. N. Engl. J. Med. 374, 1496–1498 (2016).

    Article  PubMed  Google Scholar 

  50. Chastre, A., Hafler, D. A. & O’Connor, K. C. Evaluation of KIR4.1 as an immune target in multiple sclerosis. N. Engl. J. Med. 374, 1495–1496 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  51. Higuchi, O. et al. Lack of KIR4.1 autoantibodies in Japanese patients with MS and NMO. Neurol. Neuroimmunol. Neuroinflamm. 3, e263 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  52. Navas-Madronal, M. et al. Absence of antibodies against KIR4.1 in multiple sclerosis: a three-technique approach and systematic review. PLoS ONE 12, e0175538 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  53. Mathey, E. K. et al. Neurofascin as a novel target for autoantibody-mediated axonal injury. J. Exp. Med. 204, 2363–2372 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Devaux, J. J. et al. Neurofascin-155 IgG4 in chronic inflammatory demyelinating polyneuropathy. Neurology 86, 800–807 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Sokmen, O., Demirci, M. & Tan, E. A case with neurofascin-155 IgG antibody-associated combined central and peripheral demyelination: successfully treated with anti-CD20 monoclonal antibody. Clin. Neurol. Neurosurg. 210, 106961 (2021).

    Article  PubMed  Google Scholar 

  56. Verghese, A., Krishnan, D., Chia, Y. K., Querol, L. & Hiew, F. L. Optic nerve demyelination in IgG4 anti-neurofascin 155 antibody-positive combined central and peripheral demyelination syndrome. J. Cent. Nerv. Syst. Dis. 13, 11795735211039913 (2021).

    Article  PubMed  PubMed Central  Google Scholar 

  57. Elliott, C. et al. Functional identification of pathogenic autoantibody responses in patients with multiple sclerosis. Brain 135, 1819–1833 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  58. Owens, G. P. et al. Antibodies produced by clonally expanded plasma cells in multiple sclerosis cerebrospinal fluid. Ann. Neurol. 65, 639–649 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Blauth, K. et al. Antibodies produced by clonally expanded plasma cells in multiple sclerosis cerebrospinal fluid cause demyelination of spinal cord explants. Acta Neuropathol. 130, 765–781 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Liu, Y. et al. Myelin-specific multiple sclerosis antibodies cause complement-dependent oligodendrocyte loss and demyelination. Acta Neuropathol. Commun. 5, 25 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  61. Brennan, K. M. et al. Lipid arrays identify myelin-derived lipids and lipid complexes as prominent targets for oligoclonal band antibodies in multiple sclerosis. J. Neuroimmunol. 238, 87–95 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Menon, K. K., Piddlesden, S. J. & Bernard, C. C. Demyelinating antibodies to myelin oligodendrocyte glycoprotein and galactocerebroside induce degradation of myelin basic protein in isolated human myelin. J. Neurochem. 69, 214–222 (1997).

    Article  CAS  PubMed  Google Scholar 

  63. Fierz, W. et al. Synergism in the pathogenesis of EAE induced by an MBP-specific T-cell line and monoclonal antibodies to galactocerebroside or a myelin oligodendroglial glycoprotein. Ann. N. Y. Acad. Sci. 540, 360–363 (1988).

    Article  CAS  PubMed  Google Scholar 

  64. Menge, T. et al. Antibody responses against galactocerebroside are potential stage-specific biomarkers in multiple sclerosis. J. Allergy Clin. Immunol. 116, 453–459 (2005).

    Article  CAS  PubMed  Google Scholar 

  65. Breij, E. C. et al. Myelin flow cytometry assay detects enhanced levels of antibodies to human whole myelin in a subpopulation of multiple sclerosis patients. J. Neuroimmunol. 176, 106–114 (2006).

    Article  CAS  PubMed  Google Scholar 

  66. Lily, O., Palace, J. & Vincent, A. Serum autoantibodies to cell surface determinants in multiple sclerosis: a flow cytometric study. Brain 127, 269–279 (2004).

    Article  PubMed  Google Scholar 

  67. Rivas, J. R. et al. Peripheral VH4+ plasmablasts demonstrate autoreactive B cell expansion toward brain antigens in early multiple sclerosis patients. Acta Neuropathol. 133, 43–60 (2017).

    Article  CAS  PubMed  Google Scholar 

  68. Miyachi, Y. et al. Serum anti-oligodendrocyte autoantibodies in patients with multiple sclerosis detected by a tissue-based immunofluorescence assay. Front. Neurol. 12, 681980 (2021).

    Article  PubMed  PubMed Central  Google Scholar 

  69. Sun, X. et al. Quantified CSF antibody reactivity against myelin in multiple sclerosis. Ann. Clin. Transl. Neurol. 2, 1116–1123 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  70. Brändle, S. M. et al. Distinct oligoclonal band antibodies in multiple sclerosis recognize ubiquitous self-proteins. Proc. Natl Acad. Sci. USA 113, 7864–7869 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  71. Lanz, T. V. et al. Clonally expanded B cells in multiple sclerosis bind EBV EBNA1 and GlialCAM. Nature 603, 321–327 (2022).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  72. Shimizu, F. et al. Glucose-regulated protein 78 autoantibody associates with blood-brain barrier disruption in neuromyelitis optica. Sci. Transl. Med. 9, eaai9111 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  73. Shimizu, F. et al. GRP78 antibodies are associated with blood-brain barrier breakdown in anti-myelin oligodendrocyte glycoprotein antibody-associated disorder. Neurol. Neuroimmunol. Neuroinflamm. 9, e1038 (2022).

    Article  PubMed  Google Scholar 

  74. Linington, C., Bradl, M., Lassmann, H., Brunner, C. & Vass, K. Augmentation of demyelination in rat acute allergic encephalomyelitis by circulating mouse monoclonal antibodies directed against a myelin/oligodendrocyte glycoprotein. Am. J. Pathol. 130, 443–454 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  75. Vass, K., Heininger, K., Schafer, B., Linington, C. & Lassmann, H. Interferon-γ potentiates antibody-mediated demyelination in vivo. Ann. Neurol. 32, 198–206 (1992).

    Article  CAS  PubMed  Google Scholar 

  76. Spadaro, M. et al. Pathogenicity of human antibodies against myelin oligodendrocyte glycoprotein. Ann. Neurol. 84, 315–328 (2018).

    Article  CAS  PubMed  Google Scholar 

  77. Beltran, E. et al. Archeological neuroimmunology: resurrection of a pathogenic immune response from a historical case sheds light on human autoimmune encephalomyelitis and multiple sclerosis. Acta Neuropathol. 141, 67–83 (2021).

    Article  CAS  PubMed  Google Scholar 

  78. Hillebrand, S. et al. Circulating AQP4-specific auto-antibodies alone can induce neuromyelitis optica spectrum disorder in the rat. Acta Neuropathol. 137, 467–485 (2019).

    Article  CAS  PubMed  Google Scholar 

  79. Pellerin, K. et al. MOG autoantibodies trigger a tightly-controlled FcR and BTK-driven microglia proliferative response. Brain 144, 2361–2374 (2021).

    Article  PubMed  Google Scholar 

  80. Carta, S. et al. Antibodies to MOG in CSF only: pathological findings support the diagnostic value. Acta Neuropathol. 141, 801–804 (2021).

    Article  CAS  PubMed  Google Scholar 

  81. Dubois-Dalcq, M., Niedieck, B. & Buyse, M. Action of anti-cerebroside sera on myelinated nervous tissue cultures. Pathol. Eur. 5, 331–347 (1970).

    CAS  PubMed  Google Scholar 

  82. Seil, F. J. & Agrawal, H. C. Myelin-proteolipid protein does not induce demyelinating or myelination-inhibiting antibodies. Brain Res. 194, 273–277 (1980).

    Article  CAS  PubMed  Google Scholar 

  83. Piddlesden, S., Lassmann, H., Laffafian, I., Morgan, B. P. & Linington, C. Antibody-mediated demyelination in experimental allergic encephalomyelitis is independent of complement membrane attack complex formation. Clin. Exp. Immunol. 83, 245–250 (1991).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. Piddlesden, S. J., Lassmann, H., Zimprich, F., Morgan, B. P. & Linington, C. The demyelinating potential of antibodies to myelin oligodendrocyte glycoprotein is related to their ability to fix complement. Am. J. Pathol. 143, 555–564 (1993).

    CAS  PubMed  PubMed Central  Google Scholar 

  85. Iorio, R. et al. Astrocytic autoantibody of neuromyelitis optica (NMO-IgG) binds to aquaporin-4 extracellular loops, monomers, tetramers and high order arrays. J. Autoimmun. 40, 21–27 (2013).

    Article  CAS  PubMed  Google Scholar 

  86. Owens, G. P. et al. Mutagenesis of the aquaporin 4 extracellular domains defines restricted binding patterns of pathogenic neuromyelitis optica IgG. J. Biol. Chem. 290, 12123–12134 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  87. Peschl, P. et al. Human antibodies against the myelin oligodendrocyte glycoprotein can cause complement-dependent demyelination. J. Neuroinflamm. 14, 208 (2017).

    Article  Google Scholar 

  88. Hoftberger, R. et al. The pathology of central nervous system inflammatory demyelinating disease accompanying myelin oligodendrocyte glycoprotein autoantibody. Acta Neuropathol. 139, 875–892 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  89. Takai, Y. et al. Myelin oligodendrocyte glycoprotein antibody-associated disease: an immunopathological study. Brain 143, 1431–1446 (2020).

    Article  PubMed  Google Scholar 

  90. Macrini, C. et al. Features of MOG required for recognition by patients with MOG antibody-associated disorders. Brain 144, 2375–2389 (2021).

    Article  PubMed  Google Scholar 

  91. Titulaer, M. J. et al. Overlapping demyelinating syndromes and anti-N-methyl-D-aspartate receptor encephalitis. Ann. Neurol. 75, 411–428 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  92. Zrzavy, T. et al. Neuropathological variability within a spectrum of NMDAR-encephalitis. Ann. Neurol. 90, 725–737 (2021).

    Article  CAS  PubMed  Google Scholar 

  93. Hughes, E. G. et al. Cellular and synaptic mechanisms of anti-NMDA receptor encephalitis. J. Neurosci. 30, 5866–5875 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  94. Matute, C. et al. N-methyl-D-aspartate receptor antibodies in autoimmune encephalopathy alter oligodendrocyte function. Ann. Neurol. 87, 670–676 (2020).

    Article  CAS  PubMed  Google Scholar 

  95. Phillips, O. R. et al. Superficial white matter damage in anti-NMDA receptor encephalitis. J. Neurol. Neurosurg. Psychiatry 89, 518–525 (2018).

    Article  PubMed  Google Scholar 

  96. Koneczny, I. et al. IgG4 autoantibodies in organ-specific autoimmunopathies: reviewing class switching, antibody-producing cells, and specific immunotherapies. Front. Immunol. 13, 834342 (2022).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  97. Bhat, M. A. et al. Axon-glia interactions and the domain organization of myelinated axons requires neurexin IV/Caspr/Paranodin. Neuron 30, 369–383 (2001).

    Article  CAS  PubMed  Google Scholar 

  98. Boyle, M. E. et al. Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve. Neuron 30, 385–397 (2001).

    Article  CAS  PubMed  Google Scholar 

  99. Sherman, D. L. et al. Neurofascins are required to establish axonal domains for saltatory conduction. Neuron 48, 737–742 (2005).

    Article  CAS  PubMed  Google Scholar 

  100. Pomicter, A. D. et al. Novel forms of neurofascin 155 in the central nervous system: alterations in paranodal disruption models and multiple sclerosis. Brain 133, 389–405 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  101. Manso, C. et al. Anti-neurofascin-155 IgG4 antibodies prevent paranodal complex formation in vivo. J. Clin. Invest. 129, 2222–2236 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  102. Kinzel, S. et al. Myelin-reactive antibodies initiate T cell-mediated CNS autoimmune disease by opsonization of endogenous antigen. Acta Neuropathol. 132, 43–58 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  103. Flach, A. C. et al. Autoantibody-boosted T-cell reactivation in the target organ triggers manifestation of autoimmune CNS disease. Proc. Natl Acad. Sci. USA 113, 3323–3328 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  104. Breij, E. C. et al. Homogeneity of active demyelinating lesions in established multiple sclerosis. Ann. Neurol. 63, 16–25 (2008).

    Article  CAS  PubMed  Google Scholar 

  105. Levin, M. C. et al. Autoantibodies to non-myelin antigens as contributors to the pathogenesis of multiple sclerosis. J. Clin. Cell. Immunol. https://doi.org/10.4172/2155-9899.1000148 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  106. Puentes, F. et al. Neurofilament light as an immune target for pathogenic antibodies. Immunology 152, 580–588 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  107. Liddelow, S. A. et al. Neurotoxic reactive astrocytes are induced by activated microglia. Nature 541, 481–487 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  108. Cubas-Nunez, L. et al. Potential role of CHI3L1+ astrocytes in progression in MS. Neurol. Neuroimmunol. Neuroinflamm. 8, e972 (2021).

    Article  PubMed  PubMed Central  Google Scholar 

  109. van der Poel, M., Hoepel, W., Hamann, J., Huitinga, I. & Dunnen, J. D. IgG immune complexes break immune tolerance of human microglia. J. Immunol. 205, 2511–2518 (2020).

    Article  PubMed  Google Scholar 

  110. Robinson, W. H. et al. Autoantigen microarrays for multiplex characterization of autoantibody responses. Nat. Med. 8, 295–301 (2002).

    Article  CAS  PubMed  Google Scholar 

  111. Robinson, W. H. et al. Protein microarrays guide tolerizing DNA vaccine treatment of autoimmune encephalomyelitis. Nat. Biotechnol. 21, 1033–1039 (2003).

    Article  CAS  PubMed  Google Scholar 

  112. Kanter, J. L. et al. Lipid microarrays identify key mediators of autoimmune brain inflammation. Nat. Med. 12, 138–143 (2006).

    Article  CAS  PubMed  Google Scholar 

  113. Van Haren, K. et al. Serum autoantibodies to myelin peptides distinguish acute disseminated encephalomyelitis from relapsing-remitting multiple sclerosis. Mult. Scler. 19, 1726–1733 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  114. Quintana, F. J. et al. Antigen microarrays identify unique serum autoantibody signatures in clinical and pathologic subtypes of multiple sclerosis. Proc. Natl Acad. Sci. USA 105, 18889–18894 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  115. Quintana, F. J. et al. Antigen microarrays identify CNS-produced autoantibodies in RRMS. Neurology 78, 532–539 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  116. Metz, I. et al. Serum peptide reactivities may distinguish neuromyelitis optica subgroups and multiple sclerosis. Neurol. Neuroimmunol. Neuroinflamm. 3, e204 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  117. Stork, L. et al. Antibody signatures in patients with histopathologically defined multiple sclerosis patterns. Acta Neuropathol. 139, 547–564 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  118. Kuerten, S. et al. Autoantibodies against central nervous system antigens in a subset of B cell-dominant multiple sclerosis patients. Proc. Natl Acad. Sci. USA 117, 21512–21518 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  119. Bakshi, R. et al. Serum lipid antibodies are associated with cerebral tissue damage in multiple sclerosis. Neurol. Neuroimmunol. Neuroinflamm. 3, e200 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  120. Lucchinetti, C. F., Bruck, W., Rodriguez, M. & Lassmann, H. Distinct patterns of multiple sclerosis pathology indicates heterogeneity on pathogenesis. Brain Pathol. 6, 259–274 (1996).

    Article  CAS  PubMed  Google Scholar 

  121. Storch, M. K. et al. Multiple sclerosis: in situ evidence for antibody- and complement-mediated demyelination. Ann. Neurol. 43, 465–471 (1998).

    Article  CAS  PubMed  Google Scholar 

  122. Metz, I. et al. Magnetic resonance imaging correlates of multiple sclerosis immunopathological patterns. Ann. Neurol. 90, 440–454 (2021).

    Article  CAS  PubMed  Google Scholar 

  123. Lucchinetti, C. F. et al. Clinical and radiographic spectrum of pathologically confirmed tumefactive multiple sclerosis. Brain 131, 1759–1775 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  124. Di Gregorio, M. et al. Defining the course of tumefactive multiple sclerosis: a large retrospective multicentre study. Eur. J. Neurol. 28, 1299–1307 (2021).

    Article  PubMed  Google Scholar 

  125. Keegan, M. et al. Relation between humoral pathological changes in multiple sclerosis and response to therapeutic plasma exchange. Lancet 366, 579–582 (2005).

    Article  PubMed  Google Scholar 

  126. Jarius, S. et al. Pattern II and pattern III MS are entities distinct from pattern I MS: evidence from cerebrospinal fluid analysis. J. Neuroinflamm. 14, 171 (2017).

    Article  CAS  Google Scholar 

  127. Torkildsen, O. et al. Upregulation of immunoglobulin-related genes in cortical sections from multiple sclerosis patients. Brain Pathol. 20, 720–729 (2010).

    Article  CAS  PubMed  Google Scholar 

  128. Brink, B. P. et al. The pathology of multiple sclerosis is location-dependent: no significant complement activation is detected in purely cortical lesions. J. Neuropathol. Exp. Neurol. 64, 147–155 (2005).

    Article  CAS  PubMed  Google Scholar 

  129. Lucchinetti, C. F. et al. Inflammatory cortical demyelination in early multiple sclerosis. N. Engl. J. Med. 365, 2188–2197 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  130. Graus, F. et al. A clinical approach to diagnosis of autoimmune encephalitis. Lancet Neurol. 15, 391–404 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  131. Joung, J. et al. Genome-scale CRISPR-Cas9 knockout and transcriptional activation screening. Nat. Protoc. 12, 828–863 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  132. Paul, F. et al. Antibody to aquaporin 4 in the diagnosis of neuromyelitis optica. PLoS Med. 4, e133 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  133. Tanaka, M., Tanaka, K., Komori, M. & Saida, T. Anti-aquaporin 4 antibody in Japanese multiple sclerosis: the presence of optic spinal multiple sclerosis without long spinal cord lesions and anti-aquaporin 4 antibody. J. Neurol. Neurosurg. Psychiatry 78, 990–992 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  134. Mader, S. et al. Patterns of antibody binding to aquaporin-4 isoforms in neuromyelitis optica. PLoS ONE 5, e10455 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  135. Waters, P. et al. Multicentre comparison of a diagnostic assay: aquaporin-4 antibodies in neuromyelitis optica. J. Neurol. Neurosurg. Psychiatry 87, 1005–1015 (2016).

    Article  PubMed  Google Scholar 

  136. Long, Y. et al. Development of a cell-based assay for the detection of anti-aquaporin 1 antibodies in neuromyelitis optica spectrum disorders. J. Neuroimmunol. 273, 103–110 (2014).

    Article  CAS  PubMed  Google Scholar 

  137. Tzartos, J. S. et al. Anti-aquaporin-1 autoantibodies in patients with neuromyelitis optica spectrum disorders. PLoS ONE 8, e74773 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  138. Schanda, K. et al. Antibodies to aquaporin-1 are not present in neuromyelitis optica. Neurol. Neuroimmunol. Neuroinflamm. 2, e160 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  139. Flanagan, E. P. et al. Glial fibrillary acidic protein immunoglobulin G as biomarker of autoimmune astrocytopathy: analysis of 102 patients. Ann. Neurol. 81, 298–309 (2017).

    Article  CAS  PubMed  Google Scholar 

  140. Quintana, F. J. et al. Epitope spreading as an early pathogenic event in pediatric multiple sclerosis. Neurology 83, 2219–2226 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  141. Sadaba, M. C. et al. Serum antibodies to phosphatidylcholine in MS. Neurol. Neuroimmunol. Neuroinflamm. 7, e765 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  142. Amor, S. et al. Neurofilament light antibodies in serum reflect response to natalizumab treatment in multiple sclerosis. Mult. Scler. 20, 1355–1362 (2014).

    Article  PubMed  Google Scholar 

  143. Ramberger, M. et al. NMDA receptor antibodies: a rare association in inflammatory demyelinating diseases. Neurol. Neuroimmunol. Neuroinflamm. 2, e141 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  144. Bar-Or, A. et al. Induction of antigen-specific tolerance in multiple sclerosis after immunization with DNA encoding myelin basic protein in a randomized, placebo-controlled phase 1/2 trial. Arch. Neurol. 64, 1407–1415 (2007).

    Article  PubMed  Google Scholar 

  145. O’Connor, K. C. et al. Self-antigen tetramers discriminate between myelin autoantibodies to native or denatured protein. Nat. Med. 13, 211–217 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  146. Ousman, S. S. et al. Protective and therapeutic role for αB-crystallin in autoimmune demyelination. Nature 448, 474–479 (2007).

    Article  CAS  PubMed  Google Scholar 

  147. Tengvall, K. et al. Molecular mimicry between anoctamin 2 and Epstein-Barr virus nuclear antigen 1 associates with multiple sclerosis risk. Proc. Natl Acad. Sci. USA 116, 16955–16960 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

The research of R.H. is supported by research grants from the Austrian Science Funds (FWF; project I4685-B SYNABS; DOC 33-B27 and I3334-B27 SILENCE). The research of M.R. is supported by research grants from FWF (project P32699) and the Austrian Research Promotion Agency (FFG, COMET Centre VASCage).

Author information

Authors and Affiliations

Authors

Contributions

The authors contributed equally to all aspects of the article.

Corresponding author

Correspondence to Markus Reindl.

Ethics declarations

Competing interests

The University Hospital and Medical University of Innsbruck, Austria (M.R.) and Vienna, Austria (R.H. and T.B.) receive payments for antibody assays (MOG, AQP4 and other autoantibodies) and for MOG and AQP4 antibody validation experiments organized by Euroimmun (Lübeck, Germany). H.L. declares no competing interests.

Peer review

Peer review information

Nature Reviews Neurology thanks I. Nakashima and I. Metz for their contribution to the peer review of this work.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Höftberger, R., Lassmann, H., Berger, T. et al. Pathogenic autoantibodies in multiple sclerosis — from a simple idea to a complex concept. Nat Rev Neurol 18, 681–688 (2022). https://doi.org/10.1038/s41582-022-00700-2

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41582-022-00700-2

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing