ECTRIMS 2021 – Late Breaking News ePoster

نویسندگان

چکیده

Objective: To compare humoral and T-cell responses to COVID- 19 vaccines in 400 MS patients who were on Ocrelizumab ('OCR') v. other disease-modifying therapies ('non-OCR') at the time of vaccination. Introduction: Peripheral B-cell depletion with anti-CD20 attenuates vaccines. Whether immune COVID-19 differ between depleted non-B cell is not known. Methods: Consecutive from NYU Care Center invited participate if they completed vaccination ?6 weeks previously. Immune testing included anti-spike RBD antibody (Elecsys Anti-SARS-CoV-2) (Roche Diagnostics);multiplex bead-based immunoassays antibody-responses SARS-COV-2 spike proteins;T-cell SARS-CoV-2 Spike protein using IFN? enzyme-linked immune-absorbent spot (Invitrogen) TruCulture (Myriad RBM) assays;high dimensional immunophenotyping;and live virus immunofluorescencebased microneutralization assay. Results: As 7/15/2021, 105 subjects enrolled (mean age: 40.5 years;76% female;41% non-white;38% OCR;12% prior infection). 95% fully vaccinated mRNA (Pfizer/Moderna);5% - adenovirus-based vaccine (JohnsonJp<0.0001). Positive response by multiplex assay (threshold 'positive' defined as 2 SD below mean for non-OCR) detected 10/27 (37%) OCR 29/31 (94%) non-OCR (p<0.00001). activation based induced secretion (TruCulture) was 20/25 (80%) 16/19 (84%) (p=0.71). Conclusions: Preliminary results suggest robust SARS-CoV2 approximately 80% both patients. Antibody markedly attenuated compared group. Updated will be presented.

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ژورنال

عنوان ژورنال: Multiple Sclerosis Journal

سال: 2021

ISSN: ['1352-4585', '1477-0970']

DOI: https://doi.org/10.1177/13524585211047080