Targeting B cells to modify MS, NMOSD, and MOGAD Part 2

被引:25
作者
Graf, Jonas [1 ]
Mares, Jan [2 ]
Barnett, Michael [3 ]
Aktas, Orhan [1 ]
Albrecht, Philipp [1 ]
Zamvil, Scott S. [4 ]
Hartung, Hans-Peter [1 ,3 ]
机构
[1] Heinrich Heine Univ, Med Fac, Univ Hosp, Dept Neurol, Dusseldorf, Germany
[2] Palacky Univ, Dept Neurol, Olomouc, Czech Republic
[3] Univ Sydney, Dept Neurol, Brain & Mind Ctr, Sydney, NSW, Australia
[4] Univ Calif San Francisco, UCSF Weill Inst Neurosci, Dept Neurol, San Francisco, CA 94143 USA
来源
NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION | 2021年 / 8卷 / 01期
关键词
OPTICA SPECTRUM DISORDERS; MYELIN OLIGODENDROCYTE GLYCOPROTEIN; ANTIBODY-ASSOCIATED DISEASE; LONG-TERM SAFETY; NEUROMYELITIS-OPTICA; ANTI-CD19; ANTIBODY; CLINICAL PRESENTATION; TREATMENT RESPONSES; MULTIPLE-SCLEROSIS; DOUBLE-BLIND;
D O I
10.1212/NXI.0000000000000919
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Ocrelizumab, rituximab, ofatumumab, ublituximab, inebilizumab, and evobrutinib are immunotherapies that target various B cell-related proteins. Most of these treatments have proven efficacy in relapsing and progressive forms of MS and neuromyelitis optica spectrum disease (NMOSD) or are in advanced stages of clinical development. Currently, ocrelizumab and inebilizumab are licensed for treatment of MS and NMOSD, respectively. This part of the review focuses on monoclonal antibody B cell-depleting strategies in NMOSD and the emerging related myelin oligodendrocyte glycoprotein (MOG) immunoglobulin G-associated disease (MOGAD). Case series and phase 2/3 studies in these inflammatory disorders are assessed. The safety profile of long-term B-cell depletion in MS, NMOSD, and MOGAD will be highlighted. Finally implications of the current coronavirus disease 2019 pandemic on the management of patients with these disorders and the use of B cell-depleting agents will be discussed.
引用
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页数:7
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