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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is an anti-CD25 monoclonal antibody developed for the treatment of relapsing remitting multiple sclerosis, which was withdrawn worldwide in March 2018, due to emerging serious immune-mediated systemic andcentral nervous system adverse events.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-...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2021
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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is an anti-CD25 monoclonal antibody developed for the treatment of relapsing remitting multiple sclerosis, which was withdrawn worldwide in March 2018, due to emerging serious immune-mediated systemic andcentral nervous system adverse events.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. |
format | Online Article Text |
id | pubmed-8137234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
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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