Serological response to SARS-CoV-2 vaccination in multiple sclerosis patients treated with fingolimod or ocrelizumab: an initial real-life experience.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 31 05 2021
accepted: 11 06 2021
revised: 10 06 2021
pubmed: 1 7 2021
medline: 11 1 2022
entrez: 30 6 2021
Statut: ppublish

Résumé

Recent observations suggest a lack of humoral response after SARS-CoV-2 vaccination in multiple sclerosis (MS) patients treated with fingolimod or ocrelizumab OBJECTIVES: To assess serological response to SARS-CoV-2 vaccination in MS patients receiving these disease-modifying treatments (DMTs) in a real-life setting. Retrospective clinical data collection from MS patients followed at San Raffaele Hospital MS Centre (Milan, Italy). All patients treated with fingolimod or ocrelizumab who had received a complete anti-COVID-19 vaccination course, with no clinical history suggestive of previous SARS-CoV-2 infection and with an available post-vaccination serological assay obtained at least 14 days after vaccination completion were considered for the study. We collected data from 32 MS patients, 16 treated with fingolimod and 16 receiving ocrelizumab. Among the fingolimod group 10 patients (62.5%) had a positive serological response after vaccination and among ocrelizumab-treated patients a positive serological test was found in six cases (37.5%). No relation between serological response and clinical features (i.e., treatment duration, time between vaccination and last treatment dose, and white blood cells count) was identified. Our initial real-life experience suggests a variable antibody production in MS patients receiving these DMTs. At present, there are no sufficient data to do not recommend anti-SARS-CoV-2 vaccine in these patients.

Sections du résumé

BACKGROUND BACKGROUND
Recent observations suggest a lack of humoral response after SARS-CoV-2 vaccination in multiple sclerosis (MS) patients treated with fingolimod or ocrelizumab OBJECTIVES: To assess serological response to SARS-CoV-2 vaccination in MS patients receiving these disease-modifying treatments (DMTs) in a real-life setting.
METHODS METHODS
Retrospective clinical data collection from MS patients followed at San Raffaele Hospital MS Centre (Milan, Italy). All patients treated with fingolimod or ocrelizumab who had received a complete anti-COVID-19 vaccination course, with no clinical history suggestive of previous SARS-CoV-2 infection and with an available post-vaccination serological assay obtained at least 14 days after vaccination completion were considered for the study.
RESULTS RESULTS
We collected data from 32 MS patients, 16 treated with fingolimod and 16 receiving ocrelizumab. Among the fingolimod group 10 patients (62.5%) had a positive serological response after vaccination and among ocrelizumab-treated patients a positive serological test was found in six cases (37.5%). No relation between serological response and clinical features (i.e., treatment duration, time between vaccination and last treatment dose, and white blood cells count) was identified.
CONCLUSIONS CONCLUSIONS
Our initial real-life experience suggests a variable antibody production in MS patients receiving these DMTs. At present, there are no sufficient data to do not recommend anti-SARS-CoV-2 vaccine in these patients.

Identifiants

pubmed: 34189719
doi: 10.1007/s00415-021-10663-x
pii: 10.1007/s00415-021-10663-x
pmc: PMC8241206
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antibodies, Viral 0
COVID-19 Vaccines 0
ocrelizumab A10SJL62JY
Fingolimod Hydrochloride G926EC510T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-43

Informations de copyright

© 2021. The Author(s).

Références

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doi: 10.1016/S1474-4422(20)30221-0 pubmed: 32622375 pmcid: 7332267
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doi: 10.1001/jamaneurol.2020.2581 pubmed: 32589189
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Auteurs

Guerrieri S (G)

Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Lazzarin S (L)

Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Zanetta C (Z)

Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Neurorehabilitation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Nozzolillo A (N)

Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Filippi M (F)

Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Neurorehabilitation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Neurophysiology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Vita-Salute San Raffaele University, Milan, Italy.

Moiola L (M)

Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy. Moiola.lucia@hsr.it.

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Classifications MeSH