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Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis

BACKGROUND: Daclizumab is an anti-CD25 monoclonal antibody developed for the treatment of relapsing remitting multiple sclerosis, which was withdrawn worldwide in March 2018, due to emerging serious immune-mediated systemic andcentral nervous system adverse events. We report a case of anti-N-methyl-...

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Autores principales: Karunaratne, Kushan, Ahrabian, Dariush, Monaghan, Bernadette, Campion, Tom, Yousry, Tarek, Lunn, Michael P, Zandi, Michael S, Howard, Robin S, Kullmann, Dimitri M, Spillane, Jennifer, Walker, Matthew, Chataway, Jeremy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8137234/
https://www.ncbi.nlm.nih.gov/pubmed/34079936
http://dx.doi.org/10.1136/bmjno-2020-000096
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author Karunaratne, Kushan
Ahrabian, Dariush
Monaghan, Bernadette
Campion, Tom
Yousry, Tarek
Lunn, Michael P
Zandi, Michael S
Howard, Robin S
Kullmann, Dimitri M
Spillane, Jennifer
Walker, Matthew
Chataway, Jeremy
author_facet Karunaratne, Kushan
Ahrabian, Dariush
Monaghan, Bernadette
Campion, Tom
Yousry, Tarek
Lunn, Michael P
Zandi, Michael S
Howard, Robin S
Kullmann, Dimitri M
Spillane, Jennifer
Walker, Matthew
Chataway, Jeremy
author_sort Karunaratne, Kushan
collection PubMed
description BACKGROUND: Daclizumab is an anti-CD25 monoclonal antibody developed for the treatment of relapsing remitting multiple sclerosis, which was withdrawn worldwide in March 2018, due to emerging serious immune-mediated systemic andcentral nervous system adverse events. We report a case of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis occurring 14 weeks after stopping daclizumab, which responded to the proteasome inhibitor bortezomib. METHODS: Following lack of effective clinical response to first line (corticosteroid, plasma exchange, intravenous immunoglobulin) and second line (rituximab) treatments, bortezomib therapy was commenced. The patient received six cycles of bortezomib treatment. RESULTS: Clinical improvement was noted 4 weeks after the first of six cycles of bortezomib and the patient experienced sustained clinical improvement. CONCLUSION: Our case provides further class IV evidence of the use of bortezomib therapy for treatment refractory anti-NMDAR encephalitis.
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spelling pubmed-81372342021-06-01 Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis Karunaratne, Kushan Ahrabian, Dariush Monaghan, Bernadette Campion, Tom Yousry, Tarek Lunn, Michael P Zandi, Michael S Howard, Robin S Kullmann, Dimitri M Spillane, Jennifer Walker, Matthew Chataway, Jeremy BMJ Neurol Open Short Report BACKGROUND: Daclizumab is an anti-CD25 monoclonal antibody developed for the treatment of relapsing remitting multiple sclerosis, which was withdrawn worldwide in March 2018, due to emerging serious immune-mediated systemic andcentral nervous system adverse events. We report a case of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis occurring 14 weeks after stopping daclizumab, which responded to the proteasome inhibitor bortezomib. METHODS: Following lack of effective clinical response to first line (corticosteroid, plasma exchange, intravenous immunoglobulin) and second line (rituximab) treatments, bortezomib therapy was commenced. The patient received six cycles of bortezomib treatment. RESULTS: Clinical improvement was noted 4 weeks after the first of six cycles of bortezomib and the patient experienced sustained clinical improvement. CONCLUSION: Our case provides further class IV evidence of the use of bortezomib therapy for treatment refractory anti-NMDAR encephalitis. BMJ Publishing Group 2021-05-18 /pmc/articles/PMC8137234/ /pubmed/34079936 http://dx.doi.org/10.1136/bmjno-2020-000096 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Short Report
Karunaratne, Kushan
Ahrabian, Dariush
Monaghan, Bernadette
Campion, Tom
Yousry, Tarek
Lunn, Michael P
Zandi, Michael S
Howard, Robin S
Kullmann, Dimitri M
Spillane, Jennifer
Walker, Matthew
Chataway, Jeremy
Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis
title Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis
title_full Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis
title_fullStr Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis
title_full_unstemmed Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis
title_short Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis
title_sort bortezomib for anti-nmdar encephalitis following daclizumab treatment in a patient with multiple sclerosis
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8137234/
https://www.ncbi.nlm.nih.gov/pubmed/34079936
http://dx.doi.org/10.1136/bmjno-2020-000096
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