Extensive Multiple Sclerosis Reactivation after Switching from Fingolimod to Rituximab.
Trygve HolmøyØivind TorkildsenSvetozar ZarnovickyPublished in: Case reports in neurological medicine (2018)
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.
Keyphrases
- multiple sclerosis
- lymph node
- diffuse large b cell lymphoma
- disease activity
- white matter
- systemic lupus erythematosus
- rheumatoid arthritis
- hodgkin lymphoma
- chronic lymphocytic leukemia
- ankylosing spondylitis
- case report
- stem cells
- single cell
- cell therapy
- early onset
- early stage
- ms ms
- neoadjuvant chemotherapy
- juvenile idiopathic arthritis
- mass spectrometry
- locally advanced