Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives

Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disease of the central nervous system characterized by relapses and autoimmunity caused by antibodies against the astrocyte water channel protein aquaporin-4. Over the past decade, there have been significant advances in the biologic...

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Main Authors: Tzu-Lun Huang, Jia-Kang Wang, Pei-Yao Chang, Yung-Ray Hsu, Cheng-Hung Lin, Kung-Hung Lin, Rong-Kung Tsai
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/14/7908
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author Tzu-Lun Huang
Jia-Kang Wang
Pei-Yao Chang
Yung-Ray Hsu
Cheng-Hung Lin
Kung-Hung Lin
Rong-Kung Tsai
author_facet Tzu-Lun Huang
Jia-Kang Wang
Pei-Yao Chang
Yung-Ray Hsu
Cheng-Hung Lin
Kung-Hung Lin
Rong-Kung Tsai
author_sort Tzu-Lun Huang
collection DOAJ
description Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disease of the central nervous system characterized by relapses and autoimmunity caused by antibodies against the astrocyte water channel protein aquaporin-4. Over the past decade, there have been significant advances in the biologic knowledge of NMOSD, which resulted in the IDENTIFICATION of variable disease phenotypes, biomarkers, and complex inflammatory cascades involved in disease pathogenesis. Ongoing clinical trials are looking at new treatments targeting NMOSD relapses. This review aims to provide an update on recent studies regarding issues related to NMOSD, including the pathophysiology of the disease, the potential use of serum and cerebrospinal fluid cytokines as disease biomarkers, the clinical utilization of ocular coherence tomography, and the comparison of different animal models of NMOSD.
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spelling doaj.art-e0bd50b4369949789eb9a496845fc0772023-12-03T15:10:17ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-07-012314790810.3390/ijms23147908Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical PerspectivesTzu-Lun Huang0Jia-Kang Wang1Pei-Yao Chang2Yung-Ray Hsu3Cheng-Hung Lin4Kung-Hung Lin5Rong-Kung Tsai6Department of Ophthalmology, Far Eastern Memorial Hospital, Banqiao Dist., New Taipei City 220, TaiwanDepartment of Ophthalmology, Far Eastern Memorial Hospital, Banqiao Dist., New Taipei City 220, TaiwanDepartment of Ophthalmology, Far Eastern Memorial Hospital, Banqiao Dist., New Taipei City 220, TaiwanDepartment of Ophthalmology, Far Eastern Memorial Hospital, Banqiao Dist., New Taipei City 220, TaiwanDepartment of Electrical Engineering, Yuan Ze University, Chung-Li, Taoyuan 320, TaiwanDepartment of Neurology, Taiwan Adventist Hospital, Taipei City 105, TaiwanInstitute of Eye Research, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Tzu Chi University, 707 Sec. 3 Chung-Yung Road, Hualien 970, TaiwanNeuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disease of the central nervous system characterized by relapses and autoimmunity caused by antibodies against the astrocyte water channel protein aquaporin-4. Over the past decade, there have been significant advances in the biologic knowledge of NMOSD, which resulted in the IDENTIFICATION of variable disease phenotypes, biomarkers, and complex inflammatory cascades involved in disease pathogenesis. Ongoing clinical trials are looking at new treatments targeting NMOSD relapses. This review aims to provide an update on recent studies regarding issues related to NMOSD, including the pathophysiology of the disease, the potential use of serum and cerebrospinal fluid cytokines as disease biomarkers, the clinical utilization of ocular coherence tomography, and the comparison of different animal models of NMOSD.https://www.mdpi.com/1422-0067/23/14/7908neuromyelitis optica spectrum diseaseaquaporin-4myelin oligodendrocyte glycoproteinocular coherence tomographycomplementmicrocystic macular degeneration
spellingShingle Tzu-Lun Huang
Jia-Kang Wang
Pei-Yao Chang
Yung-Ray Hsu
Cheng-Hung Lin
Kung-Hung Lin
Rong-Kung Tsai
Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives
International Journal of Molecular Sciences
neuromyelitis optica spectrum disease
aquaporin-4
myelin oligodendrocyte glycoprotein
ocular coherence tomography
complement
microcystic macular degeneration
title Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives
title_full Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives
title_fullStr Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives
title_full_unstemmed Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives
title_short Neuromyelitis Optica Spectrum Disorder: From Basic Research to Clinical Perspectives
title_sort neuromyelitis optica spectrum disorder from basic research to clinical perspectives
topic neuromyelitis optica spectrum disease
aquaporin-4
myelin oligodendrocyte glycoprotein
ocular coherence tomography
complement
microcystic macular degeneration
url https://www.mdpi.com/1422-0067/23/14/7908
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