
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:language>eng</dc:language>
  <dc:creator>Drulović, Jelena</dc:creator>
  <dc:creator>Pekmezović, Tatjana</dc:creator>
  <dc:creator>Mesaroš, Šarlota</dc:creator>
  <dc:creator id="https://orcid.org/0000-0001-8233-1636">Gnjatović, Marija</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-6145-3850">Ćujić, Danica</dc:creator>
  <dc:creator>Veselinović, Nikola</dc:creator>
  <dc:creator>Tamas, Olivera</dc:creator>
  <dc:creator>Martinović, Vanja</dc:creator>
  <dc:creator>Ivanović, Jovana</dc:creator>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:identifier>https://phaidrabg.bg.ac.rs/o:26024</dc:identifier>
  <dc:identifier>doi:10.1016/j.msard.2021.103150</dc:identifier>
  <dc:description xml:lang="eng">ABSTRACT
Background: It has been generally accepted that people with MS (PwMS) should be vaccinated against COVID-19. The aim of our investigation was to evaluate the humoral response to natural SARS-CoV-2 infection and to two COVID-19 vaccines (BNT162b2 Pfizer-BioNTech and Beijing/Sinopharm BBIBP-CorV) in our cohort of PwMS under high efficacy disease modifying therapies (DMTs), cladribine and alemtuzumab.
Methods: Twenty two PwMS treated at the Clinic of Neurology, in Belgrade, who developed COVID-19 and/or were vaccinated against SARS-CoV-2, during treatment with cladribine and alemtuzumab, were included. Out of 18 patients treated with cladribine, 11 developed COVID-19, and 11 were vaccinated against SARS-CoV-2 (four with mRNA vaccine, 7 with Sinopharm). Four MS patients under alemtuzumab were vaccinated against SARS-CoV-2; three with mRNA, and one with Sinopharm vaccine. SARS-Cov-2 IgG response was measured using ELISA anti- spike protein-based serology (INEP, Belgrade, Serbia).
Results: All 7 patients under cladribine treatment who suffered from COVID-19, developed IgG antibodies, 2.0-5.5 months after last symptoms. All four (100%) patients under cladribine who were vaccinated with Pfizer-BioNTech vaccine, and three out of seven (42.9%) vaccinated with Sinopharm, developed antibodies. All 4 patients under alemtuzumab developed antibodies after vaccination. In all cases, seroprotection occurred, irrespective of timing of vaccination and absolute lymphocyte count.
Conclusion: Our findings in a small number of highly active PwMS in whom, lymphodepleting, immune reconstitution therapies, were applied in order to successfully manage MS, indicate that in a number of these patients it was possible to develop at the same time seroprotection in these patients after COVID-19 vaccination in these complex circumstances.</dc:description>
  <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/legalcode</dc:rights>
  <dc:title xml:lang="eng">Humoral response to SARS-CoV-2 COVID-19 vaccines in patients with multiple sclerosis treated with immune reconstitution therapies</dc:title>
  <dc:format>application/pdf</dc:format>
  <dc:format>656697 bytes</dc:format>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:date>2021</dc:date>
  <dc:source>Multiple Sclerosis and Related Disorders 54</dc:source>
  <dc:subject xml:lang="eng">COVID-19, Pfizer-BioNTech, Sinopharm, alemtuzumab, cladribine, humoral response, multiple sclerosis, vaccination</dc:subject>
</oai_dc:dc>
