| Literature DB >> 25387545 |
Kelley Weinfurtner1, Jennifer Graves2, Jayne Ness3, Lauren Krupp4, Maria Milazzo5, Emmanuelle Waubant6.
Abstract
Neuromyelitis optica is an autoimmune disease characterized by acute episodes of transverse myelitis and optic neuritis. Several small, open-label studies suggest rituximab, a monoclonal antibody against CD20, prevents relapses in neuromyelitis optica; however, there is little consensus on timing or duration of treatment. Here we report four patients with severe relapsing neuromyelitis optica who were stabilized on rituximab and, after discontinuing treatment, continued to experience prolonged remission of their disease. Remission ranged from 4.5 to 10.5 years total, including 3 to 9 years off all therapies. The patients had sustained clinical responses despite normal B-lymphocyte levels and, in at least 2 patients, continued seropositivity for aquaporin-4 antibodies. These cases suggest that rituximab may induce prolonged remission in certain neuromyelitis optica patients, and they highlight the need for further elucidation of rituximab's mechanism in neuromyelitis optica.Entities:
Keywords: CNS demyelinating disease; neuromyelitis optica; rituximab
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Year: 2014 PMID: 25387545 DOI: 10.1177/0883073814553974
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987