Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab

During treatment with fingolimod, B cells are redistributed from blood to secondary lymphoid organs, where they are protected from the effect of anti-CD20 and other cell-depleting therapies. We describe a multiple sclerosis patient who had almost complete depletion of B cells in blood during and sho...

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Main Authors: Trygve Holmøy, Øivind Torkildsen, Svetozar Zarnovicky
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Case Reports in Neurological Medicine
Online Access:http://dx.doi.org/10.1155/2018/5190794
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spelling doaj-d9250688ec944657b0cc9443a4e50f1c2020-11-24T20:42:53ZengHindawi LimitedCase Reports in Neurological Medicine2090-66682090-66762018-01-01201810.1155/2018/51907945190794Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to RituximabTrygve Holmøy0Øivind Torkildsen1Svetozar Zarnovicky2Department of Neurology, Akershus University Hospital, Lørenskog, NorwayDepartment of Neurology, Haukeland University Hospital, Bergen, NorwayDepartment of Radiology, Akershus University Hospital, Lørenskog, NorwayDuring treatment with fingolimod, B cells are redistributed from blood to secondary lymphoid organs, where they are protected from the effect of anti-CD20 and other cell-depleting therapies. We describe a multiple sclerosis patient who had almost complete depletion of B cells in blood during and shortly after treatment with fingolimod. He developed severe disease activity resembling immune reconstitution syndrome after switching from fingolimod to rituximab, with first dose being six weeks after fingolimod cessation. Following recommendations from the Swedish MS Association, rituximab treatment was started as one single dose of 1000 mg. In patients treated with fingolimod, pathogenic B cells may still be sequestered in secondary lymph nodes if this dose is given early. To deplete such B cells as they egress from the lymph nodes, we propose that a second dose of rituximab a few weeks after the first dose should be considered.http://dx.doi.org/10.1155/2018/5190794
collection DOAJ
language English
format Article
sources DOAJ
author Trygve Holmøy
Øivind Torkildsen
Svetozar Zarnovicky
spellingShingle Trygve Holmøy
Øivind Torkildsen
Svetozar Zarnovicky
Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab
Case Reports in Neurological Medicine
author_facet Trygve Holmøy
Øivind Torkildsen
Svetozar Zarnovicky
author_sort Trygve Holmøy
title Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab
title_short Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab
title_full Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab
title_fullStr Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab
title_full_unstemmed Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab
title_sort extensive multiple sclerosis reactivation after switching from fingolimod to rituximab
publisher Hindawi Limited
series Case Reports in Neurological Medicine
issn 2090-6668
2090-6676
publishDate 2018-01-01
description During treatment with fingolimod, B cells are redistributed from blood to secondary lymphoid organs, where they are protected from the effect of anti-CD20 and other cell-depleting therapies. We describe a multiple sclerosis patient who had almost complete depletion of B cells in blood during and shortly after treatment with fingolimod. He developed severe disease activity resembling immune reconstitution syndrome after switching from fingolimod to rituximab, with first dose being six weeks after fingolimod cessation. Following recommendations from the Swedish MS Association, rituximab treatment was started as one single dose of 1000 mg. In patients treated with fingolimod, pathogenic B cells may still be sequestered in secondary lymph nodes if this dose is given early. To deplete such B cells as they egress from the lymph nodes, we propose that a second dose of rituximab a few weeks after the first dose should be considered.
url http://dx.doi.org/10.1155/2018/5190794
work_keys_str_mv AT trygveholmøy extensivemultiplesclerosisreactivationafterswitchingfromfingolimodtorituximab
AT øivindtorkildsen extensivemultiplesclerosisreactivationafterswitchingfromfingolimodtorituximab
AT svetozarzarnovicky extensivemultiplesclerosisreactivationafterswitchingfromfingolimodtorituximab
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