Fulminant MS Reactivation Following Combined Fingolimod Cessation and Yellow Fever Vaccination.
Adult
Drug Administration Schedule
Female
Fingolimod Hydrochloride
/ administration & dosage
Humans
Immunosuppressive Agents
/ administration & dosage
Lymphocytes
/ immunology
Multiple Sclerosis, Relapsing-Remitting
/ diagnosis
Natalizumab
/ therapeutic use
Yellow Fever Vaccine
/ administration & dosage
autoimmune disease
fingolimod
multiple sclerosis
vaccination
yellow fever
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
28 Nov 2019
28 Nov 2019
Historique:
received:
12
11
2019
revised:
24
11
2019
accepted:
26
11
2019
entrez:
5
12
2019
pubmed:
5
12
2019
medline:
15
4
2020
Statut:
epublish
Résumé
A major concern caused by the discontinuation of disease modifying treatment for multiple sclerosis (MS) is a rebound of disease activity. Hypotheses about the underlying mechanism of fingolimod (FTY) induced exaggerated inflammatory responses are diverse. So far, vaccinations as a trigger for rebound activity following FTY suspension have not been described. However, several reports have highlighted the occurrence of neurological and autoimmune side effects after single or combined multi-vaccination procedures. Here, we describe the case of a highly active female MS patient demonstrating recurrent, severe MS relapses accompanied by extensive MRI activity, subsequent to yellow fever vaccination two months following FTY withdrawal. Blood and cerebrospinal fluid immunophenotyping indicated a B cell/plasma cell autoreactivity. Following a therapy with natalizumab the clinical, laboratory, MRI, and disease course improved significantly. This case hints towards a combined immunological mechanism characterized by molecular mimicry, bystander activation, and lymphocyte re-egress, resulting in extensive neurological impairment and shows that natalizumab represents a therapeutic option to counteract B cell mediated autoreactivity. Especially, the diagnostic and therapeutic management of this complex scenario might be instructive for clinical practice.
Identifiants
pubmed: 31795084
pii: ijms20235985
doi: 10.3390/ijms20235985
pmc: PMC6929059
pii:
doi:
Substances chimiques
Immunosuppressive Agents
0
Natalizumab
0
Yellow Fever Vaccine
0
Fingolimod Hydrochloride
G926EC510T
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Références
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