4.7 Article

Antibody response elicited by the SARS-CoV-2 vaccine booster in patients with multiple sclerosis: Who gains from it?

Journal

EUROPEAN JOURNAL OF NEUROLOGY
Volume 30, Issue 8, Pages 2357-2364

Publisher

WILEY
DOI: 10.1111/ene.15830

Keywords

anti-CD20; booster dose; COVID-19; fingolimod; multiple sclerosis; SARS-CoV-2 vaccine

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This study evaluates the differences in immune response after a third vaccine dose in patients with multiple sclerosis (pwMS). The results show that patients on anti-CD20 drugs rituximab and ocrelizumab had a lower increase in antibody levels compared to patients treated with other drugs, while patients on fingolimod showed a higher increase. All pwMS increased their serum antibody levels after the third vaccine dose.
Background and purpose: Although two doses of COVID-19 vaccine elicited a protective humoral response in most persons with multiple sclerosis (pwMS), a significant group of them treated with immunosuppressive disease-modifying therapies (DMTs) showed less efficient responses. Methods: This prospective multicenter observational study evaluates differences in immune response after a third vaccine dose in pwMS. Results: Four hundred seventy-three pwMS were analyzed. Compared to untreated patients, there was a 50-fold decrease (95% confidence interval [CI]=14.3-100.0, p < 0.001) in serum SARS-CoV-2 antibody levels in those on rituximab, a 20-fold decrease (95% CI=8.3-50.0, p < 0.001) in those on ocrelizumab, and a 2.3-fold decrease (95% CI = 1.2-4.6, p = 0.015) in those on fingolimod. As compared to the antibody levels after the second vaccine dose, patients on the anti-CD20 drugs rituximab and ocrelizumab showed a 2.3-fold lower gain (95% CI = 1.4-3.8, p=0.001), whereas those on fingolimod showed a 1.7-fold higher gain (95% CI = 1.1-2.7, p = 0.012), compared to patients treated with other DMTs. Conclusions: All pwMS increased their serum SARS-CoV-2 antibody levels after the third vaccine dose. The mean antibody values of patients treated with ocrelizumab/rituximab remained well below the empirical protective threshold for risk of infection identified in the CovaXiMS study (>659 binding antibody units/mL), whereas for patients treated with fingolimod this value was significantly closer to the cutoff.

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