神経治療学
Online ISSN : 2189-7824
Print ISSN : 0916-8443
ISSN-L : 2189-7824
シンポジウム1:多発性硬化症と視神経脊髄炎の病態と治療Update
視神経脊髄炎の病態と治療のUP–TO–DATE;アクアポリン4抗体の発見で何が変わったのか?
河内 泉
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ジャーナル フリー

2019 年 36 巻 3 号 p. 217-219

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Neuromyelitis optica spectrum disorders (NMOSD) and multiple sclerosis (MS) are the two main autoimmune disorders of the central nervous system (CNS). The discovery of diagnostic biomarkers for NMOSD, aquaporin–4 (AQP4) autoantibodies, provides significant research progresses of NMOSD as follows ; 1) accurate diagnosis and prompt therapeutic option for patients with NMOSD and MS, 2) newly pathomechanistic insights of AQP4 autoantibodies and complements as significant pathogenic immune molecules for NMOSD, resulting in primary damages of astrocytes and ependymal cells, and secondary but severe neuroaxonal damages and demyelination, and 3) future possible developments of new disease–modifying therapies that target aberrant immune systems (e.g. complements, interleukin–6 and B cells) for NMOSD. The NMOSD landscape has been comprehensively transformed by these progresses since the discovery of AQP4 autoantibodies in 2004.

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