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- Juan I Rojas, Ricardo Alonso, Mariela Cabrera, Edgar Carnero Contentti, Edgardo Cristiano, Norma Deri, Javier Hryb, Pablo Lopez, Geraldine Luetic, Liliana Patrucco, Veronica Tkachuk, María C Ysrraelit, Gisela Zanga, Leonel Cruces, Gabriela Turk, Yesica Longueira, Natalia Laufer, and Sebastian Nuñez.
- Centro de Esclerosis Múltiple de Buenos Aires, Buenos Aires, Argentina. E-mail: rojasjuanignacio@gmail.com.
- Medicina (B Aires). 2023 Jan 1; 83 (3): 358365358-365.
IntroductionThe objective was to assess the immunogenicity and effectiveness of vaccines against SARSCoV-2 in multiple sclerosis (MS) patients included in the Argentinean MS registry.MethodsA prospective cohort study between May and December 2021. The primary outcome was immunogenicity and effectiveness of vaccines during a three-month follow-up. Immunogenicity was evaluated based on detection of total antibodies (Ab) against spike protein and neutralizing Ab in serum 4 weeks after the second vaccine dose. A positive COVID-19 case was defined according to Argentinean Ministry of Health.Results94 patients were included, mean age: 41.7 ± 12.1 years. Eighty (85.1%) had relapsing remitting multiple sclerosis (RRMS); 30 (31.9%) were under fingolimod treatment. The Sputnik V vaccine was the first dose in 33 (35.1%), and AstraZeneca in 61 (64.9%). In 60 (63.8%), the vaccine elicited a specific humoral response. Immunological response according to the vaccination schemes showed no qualitative differences (p = 0.45). Stratified analysis according to the MS treatment showed that a significantly smaller number of subjects developed antibodies against spike antigen among those that were on ocrelizumab compared to other groups (p = 0.001), while a reduced number of patients under ocrelizumab where evaluated (n = 7). This was also observed for neutralizing antibodies in the ocrelizumab group (p < 0.001). During the three-month follow-up, two individuals were diagnosed with COVID-19.ConclusionWe found that MS patients that received Sputnik V or AstraZeneca vaccines for SARS-CoV-2 developed a serological response with no differences between the vaccines used.
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