Abstract:
:Neuromyelitis optica (NMO) is an uncommon, life-threatening demyelinating disease that produces transverse myelitis and optic neuritis. An important pathogenetic mechanism belongs to NMO-IgG autoantibodies directed against the ultrastructure of the water channel aquaporin-4 (AQP4), the so-called orthogonal arrays of particles (OAPs). With respect to the yet known data about OAP formation it is suggested to modulate the AQP4-M23 isoform to prevent the aggregation of AQP4 tetramers into higher organized structures. Without specific target for the NMO-IgGs the inflammation and thus the resulting demyelination may be stopped without the need for immunosuppressive agents with severe side-effects.
journal_name
Med Hypothesesjournal_title
Medical hypothesesauthors
Warth Adoi
10.1016/j.mehy.2009.02.036subject
Has Abstractpub_date
2009-09-01 00:00:00pages
361-2issue
3eissn
0306-9877issn
1532-2777pii
S0306-9877(09)00230-8journal_volume
73pub_type
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