
<ns0:uwmetadata xmlns:ns0="http://phaidra.univie.ac.at/XML/metadata/V1.0" xmlns:ns1="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0" xmlns:ns10="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0" xmlns:ns11="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0/entity" xmlns:ns12="http://phaidra.univie.ac.at/XML/metadata/digitalbook/V1.0" xmlns:ns13="http://phaidra.univie.ac.at/XML/metadata/etheses/V1.0" xmlns:ns2="http://phaidra.univie.ac.at/XML/metadata/extended/V1.0" xmlns:ns3="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/entity" xmlns:ns4="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/requirement" xmlns:ns5="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/educational" xmlns:ns6="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/annotation" xmlns:ns7="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/classification" xmlns:ns8="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/organization" xmlns:ns9="http://phaidra.univie.ac.at/XML/metadata/histkult/V1.0">
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    <ns1:identifier>o:26024</ns1:identifier>
    <ns1:title language="en">Humoral response to SARS-CoV-2 COVID-19 vaccines in patients with multiple sclerosis treated with immune reconstitution therapies</ns1:title>
    <ns1:language>en</ns1:language>
    <ns1:description language="en">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.</ns1:description>
    <ns1:keyword language="en">COVID-19, Pfizer-BioNTech, Sinopharm, alemtuzumab, cladribine, humoral response, multiple sclerosis, vaccination</ns1:keyword>
    <ns2:identifiers>
      <ns2:resource>1552099</ns2:resource>
      <ns2:identifier>10.1016/j.msard.2021.103150</ns2:identifier>
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    <ns1:upload_date>2022-06-12T18:10:56.776Z</ns1:upload_date>
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        <ns3:firstname>Jelena</ns3:firstname>
        <ns3:lastname>Drulović</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Medicine, Clinic of Neurology, University Clinical Center of Serbia, Serbia</ns3:institution>
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        <ns3:firstname>Tatjana</ns3:firstname>
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        <ns3:institution>University of Belgrade, Faculty of Medicine, Institute of Epidemiology, Serbia</ns3:institution>
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        <ns3:firstname>Šarlota</ns3:firstname>
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        <ns3:institution>University of Belgrade, Faculty of Medicine, Clinic of Neurology, University Clinical Center of Serbia, Serbia</ns3:institution>
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        <ns3:firstname>Marija</ns3:firstname>
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        <ns3:institution>University of Belgrade, Institute for the Application of Nuclear Energy INEP, Serbia</ns3:institution>
        <ns3:title1>doktor biotehničkih nauka</ns3:title1>
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        <ns3:firstname>Danica</ns3:firstname>
        <ns3:lastname>Ćujić</ns3:lastname>
        <ns3:institution>University of Belgrade, Institute for the Application of Nuclear Energy INEP, Serbia</ns3:institution>
        <ns3:title1>doktor medicinskih nauka-farmacija</ns3:title1>
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        <ns3:firstname>Nikola</ns3:firstname>
        <ns3:lastname>Veselinović</ns3:lastname>
        <ns3:institution>University of Belgrade, Faculty of Medicine, Clinic of Neurology, University Clinical Center of Serbia, Serbia</ns3:institution>
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        <ns3:institution>University of Belgrade, Faculty of Medicine, Clinic of Neurology, University Clinical Center of Serbia, Serbia</ns3:institution>
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        <ns3:firstname>Vanja</ns3:firstname>
        <ns3:lastname>Martinović</ns3:lastname>
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        <ns3:firstname>Jovana</ns3:firstname>
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  <ns12:digitalbook>
    <ns12:name_magazine language="en">Multiple Sclerosis and Related Disorders</ns12:name_magazine>
    <ns12:volume>54</ns12:volume>
    <ns12:publisher>Elsevier</ns12:publisher>
    <ns12:releaseyear>2021</ns12:releaseyear>
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