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Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab
Neuromyelitis optica (NMO) is a disabling autoimmune disease associated with an elevation of anti-aquaporin 4 (AQP4) autoantibodies. Here, we present a case with NMO who responded to monthly administration of the anti-IL-6 receptor antibody tocilizumab. The treatment rapidly reduced the elevated num...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3713263/ https://www.ncbi.nlm.nih.gov/pubmed/22782533 http://dx.doi.org/10.1007/s10165-012-0715-9 |
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author | Araki, Manabu Aranami, Toshimasa Matsuoka, Takako Nakamura, Masakazu Miyake, Sachiko Yamamura, Takashi |
author_facet | Araki, Manabu Aranami, Toshimasa Matsuoka, Takako Nakamura, Masakazu Miyake, Sachiko Yamamura, Takashi |
author_sort | Araki, Manabu |
collection | PubMed |
description | Neuromyelitis optica (NMO) is a disabling autoimmune disease associated with an elevation of anti-aquaporin 4 (AQP4) autoantibodies. Here, we present a case with NMO who responded to monthly administration of the anti-IL-6 receptor antibody tocilizumab. The treatment rapidly reduced the elevated numbers of plasmablasts and anti-AQP4 autoantibodies in the patient. Furthermore, neuropathic pain and disability scores gradually improved. Tocilizumab may be considered as a therapeutic option for NMO. |
format | Online Article Text |
id | pubmed-3713263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-37132632013-08-15 Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab Araki, Manabu Aranami, Toshimasa Matsuoka, Takako Nakamura, Masakazu Miyake, Sachiko Yamamura, Takashi Mod Rheumatol Case Report Neuromyelitis optica (NMO) is a disabling autoimmune disease associated with an elevation of anti-aquaporin 4 (AQP4) autoantibodies. Here, we present a case with NMO who responded to monthly administration of the anti-IL-6 receptor antibody tocilizumab. The treatment rapidly reduced the elevated numbers of plasmablasts and anti-AQP4 autoantibodies in the patient. Furthermore, neuropathic pain and disability scores gradually improved. Tocilizumab may be considered as a therapeutic option for NMO. Springer Japan 2012-07-11 2013-07 /pmc/articles/PMC3713263/ /pubmed/22782533 http://dx.doi.org/10.1007/s10165-012-0715-9 Text en © Japan College of Rheumatology 2012 |
spellingShingle | Case Report Araki, Manabu Aranami, Toshimasa Matsuoka, Takako Nakamura, Masakazu Miyake, Sachiko Yamamura, Takashi Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab |
title | Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab |
title_full | Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab |
title_fullStr | Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab |
title_full_unstemmed | Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab |
title_short | Clinical improvement in a patient with neuromyelitis optica following therapy with the anti-IL-6 receptor monoclonal antibody tocilizumab |
title_sort | clinical improvement in a patient with neuromyelitis optica following therapy with the anti-il-6 receptor monoclonal antibody tocilizumab |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3713263/ https://www.ncbi.nlm.nih.gov/pubmed/22782533 http://dx.doi.org/10.1007/s10165-012-0715-9 |
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