Abstract | BACKGROUND & OBJECTIVES: The persistence of the severe acute respiratory syndrome coronavirus (SARS-CoV)-2 pandemic, partly due to the appearance of highly infectious variants, has made booster vaccinations necessary for vulnerable groups. Here, we present data regarding the decline of the SARS-CoV-2 BNT162b2 mRNA vaccine-induced humoral immune response in a monocentric cohort of MS patients. METHODS: 96 MS patients undergoing eight different DMTs, all without previous SARS-CoV-2 infection, were evaluated for anti-Spike IgG levels, 21 days (T1) and 5-6 months (T2) after the second SARS-CoV-2 BNT162b2 mRNA vaccine dose. The anti-Spike IgG titre from MS subjects was compared with 21 age- and sex-matched healthy controls (HC). RESULTS: CONCLUSION:
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Authors | Giorgia Teresa Maniscalco, Anne Lise Ferrara, Antonietta Liotti, Valentino Manzo, Maria Elena Di Battista, Simona Salvatore, Daniela Graziano, Assunta Viola, Gerardino Amato, Ornella Moreggia, Daniele Di Giulio Cesare, Gennaro Alfieri, Walter Di Iorio, Gennaro Della Rocca, Vincenzo Andreone, Veronica De Rosa |
Journal | Multiple sclerosis and related disorders
(Mult Scler Relat Disord)
Vol. 62
Pg. 103800
(Jun 2022)
ISSN: 2211-0356 [Electronic] Netherlands |
PMID | 35462168
(Publication Type: Journal Article)
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Copyright | Copyright © 2022 Elsevier B.V. All rights reserved. |
Chemical References |
- Antibodies, Viral
- COVID-19 Vaccines
- Immunoglobulin G
- Natalizumab
- Vaccines, Synthetic
- mRNA Vaccines
- Glatiramer Acetate
- Dimethyl Fumarate
- BNT162 Vaccine
- Interferon beta-1a
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Topics |
- Antibodies, Viral
- BNT162 Vaccine
- COVID-19
- COVID-19 Vaccines
- Dimethyl Fumarate
(therapeutic use)
- Glatiramer Acetate
(therapeutic use)
- Humans
- Immunoglobulin G
(therapeutic use)
- Interferon beta-1a
(therapeutic use)
- Multiple Sclerosis
(drug therapy)
- Natalizumab
(therapeutic use)
- SARS-CoV-2
- Vaccines, Synthetic
- mRNA Vaccines
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