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 |
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15.12.2021
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Abstract | 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.
[Display omitted]
•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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AbstractList | 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.
Unlabelled Image 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.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. 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. [Display omitted] •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. 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. |
ArticleNumber | 577746 |
Author | Achiron, Anat Flechter, Shlomo Zilkha-Falb, Rina Gurevich, Michael Sonis, Polina Guber, Diana Harari, Gil Menascu, Shay Dolev, Mark Magalashvili, David Givon, Uri Mandel, Mathilda Dreyer-Alster, Sapir |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34655991$$D View this record in MEDLINE/PubMed |
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Keywords | COVID-19 Multiple sclerosis IgG antibody Disease modifying treatments Vaccination Humoral immunity |
Language | English |
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SubjectTerms | Adult Antibodies, Viral - blood Antirheumatic Agents - therapeutic use BNT162 Vaccine - immunology COVID-19 COVID-19 - prevention & control Cross-Sectional Studies Disease modifying treatments Female Humans Humoral immunity IgG antibody Immunity, Humoral - immunology Immunoglobulin G - blood Immunosuppressive Agents - therapeutic use Male Middle Aged Multiple sclerosis Multiple Sclerosis - drug therapy Multiple Sclerosis - immunology Prospective Studies SARS-CoV-2 Vaccination |
Title | Humoral immune response in multiple sclerosis patients following PfizerBNT162b2 COVID19 vaccination: Up to 6 months cross-sectional study |
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