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Axo-glial antigens as targets in multiple sclerosis: implications for axonal and grey matter injury

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Derfuss,  T.
Department: Neuroimmunology / Wekerle, MPI of Neurobiology, Max Planck Society;

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Linington,  C.
Department: Neuroimmunology / Wekerle, MPI of Neurobiology, Max Planck Society;

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Hohlfeld,  R.
Department: Neuroimmunology / Wekerle, MPI of Neurobiology, Max Planck Society;

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Meinl,  E.
Department: Neuroimmunology / Wekerle, MPI of Neurobiology, Max Planck Society;

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Citation

Derfuss, T., Linington, C., Hohlfeld, R., & Meinl, E. (2010). Axo-glial antigens as targets in multiple sclerosis: implications for axonal and grey matter injury. Journal of Molecular Medicine, 88(8), 753-761.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0012-1F8C-5
Abstract
Multiple sclerosis is thought to be an autoimmune-mediated disease of the central nervous system. For many years, T-cells were regarded as the key players in the pathogenesis, and myelin of white matter was considered as the main victim. However, research during recent years showed a more complex picture. Besides T-cells, also B-cells, antibodies and the innate immunity contribute to the tissue damage. Modern imaging techniques and neuropathological examinations showed that not only myelin but also axons, cortical neurons and nodes of Ranvier are damaged. The autoimmune targets of this widespread injury are so far not known. The identification of the axo-glial proteins contactin-2 and neurofascin provides excellent examples how antibodies can induce axonal injury at the node of Ranvier and how T-cells can destruct cortical integrity. This review will discuss the pathogenic implications of an autoimmune response against these newly discovered antigens.