Humoral immune response in multiple sclerosis patients following PfizerBNT162b2 COVID19 vaccination: Up to 6 months cross-sectional study
Appropriate immune response following COVID-19 vaccination is important in the context of disease-modifying treatments (DMTs). In a prospective cross-sectional study, we determined SARS-COV-2 IgG response up to 6 months following PfizerBNT162b2 vaccination in 414 multiple sclerosis (MS) patients and...
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Published in: | Journal of neuroimmunology Vol. 361; p. 577746 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Netherlands
Elsevier B.V
15-12-2021
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Subjects: | |
Online Access: | Get full text |
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Summary: | Appropriate immune response following COVID-19 vaccination is important in the context of disease-modifying treatments (DMTs). In a prospective cross-sectional study, we determined SARS-COV-2 IgG response up to 6 months following PfizerBNT162b2 vaccination in 414 multiple sclerosis (MS) patients and 89 healthy subjects. Protective response was demonstrated in untreated MS patients (N = 76, 100%), treated with Cladribine (N = 48, 100%), Dimethyl fumarate (N = 35, 100%), Natalizumab (N = 32, 100%), and Teriflunomide (N = 39, 100%), similarly to healthy subjects (N = 89, 97.8%). Response was decreased in Fingolimod (N = 42, 9.5%), Ocrelizumab (N = 114, 22.8%) and Alemtuzumab (N = 22, 86.4%) treated patients. IgG response can help tailor adequate vaccine guidelines for MS patients under various DMTs.
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•Immune responses after PfizerBioNTech COVID-19 vaccination differ in multiple sclerosis patients treated with various DMTs.•Durability of the anti-SARS-COV-2 IgG response to the vaccine was maintained up to 6 months post vaccination.•The relative impact of the time from the last dosing to vaccination is of significance to humoral IgG response.•Absence of SARS-COV-2 antibodies in patients treated with Fingolimod or Ocrelizumab suggests these patients will need a booster vaccine dose. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
ISSN: | 0165-5728 1872-8421 |
DOI: | 10.1016/j.jneuroim.2021.577746 |