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CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder

Here we report 3 cases of neuromyelitis optica spectrum disorder (NMOSD), who were all treated with eculizumab and could be observed with monitoring serum C3, C4 and 50% hemolytic complement (CH50) before and after the treatment. Serum C3 and C4 were not dramatically changed during the treatment, in...

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Autores principales: Namatame, Chihiro, Misu, Tatsuro, Takai, Yoshiki, Nishiyama, Shuhei, Nakashima, Ichiro, Fujihara, Kazuo, Aoki, Masashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809378/
https://www.ncbi.nlm.nih.gov/pubmed/33490671
http://dx.doi.org/10.1016/j.heliyon.2021.e05899
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author Namatame, Chihiro
Misu, Tatsuro
Takai, Yoshiki
Nishiyama, Shuhei
Nakashima, Ichiro
Fujihara, Kazuo
Aoki, Masashi
author_facet Namatame, Chihiro
Misu, Tatsuro
Takai, Yoshiki
Nishiyama, Shuhei
Nakashima, Ichiro
Fujihara, Kazuo
Aoki, Masashi
author_sort Namatame, Chihiro
collection PubMed
description Here we report 3 cases of neuromyelitis optica spectrum disorder (NMOSD), who were all treated with eculizumab and could be observed with monitoring serum C3, C4 and 50% hemolytic complement (CH50) before and after the treatment. Serum C3 and C4 were not dramatically changed during the treatment, in contrast serum CH50 level of each patient had diminished and kept under the detection limit after the treatment without clinical worsening, even in the situation of extending dosing. Serum CH50 level is useful to monitor the drug efficacy during eculizumab treatment.
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spelling pubmed-78093782021-01-22 CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder Namatame, Chihiro Misu, Tatsuro Takai, Yoshiki Nishiyama, Shuhei Nakashima, Ichiro Fujihara, Kazuo Aoki, Masashi Heliyon Research Article Here we report 3 cases of neuromyelitis optica spectrum disorder (NMOSD), who were all treated with eculizumab and could be observed with monitoring serum C3, C4 and 50% hemolytic complement (CH50) before and after the treatment. Serum C3 and C4 were not dramatically changed during the treatment, in contrast serum CH50 level of each patient had diminished and kept under the detection limit after the treatment without clinical worsening, even in the situation of extending dosing. Serum CH50 level is useful to monitor the drug efficacy during eculizumab treatment. Elsevier 2021-01-08 /pmc/articles/PMC7809378/ /pubmed/33490671 http://dx.doi.org/10.1016/j.heliyon.2021.e05899 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Namatame, Chihiro
Misu, Tatsuro
Takai, Yoshiki
Nishiyama, Shuhei
Nakashima, Ichiro
Fujihara, Kazuo
Aoki, Masashi
CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
title CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
title_full CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
title_fullStr CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
title_full_unstemmed CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
title_short CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
title_sort ch50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809378/
https://www.ncbi.nlm.nih.gov/pubmed/33490671
http://dx.doi.org/10.1016/j.heliyon.2021.e05899
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