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10.1016/j.msard.2020.102306

http://scihub22266oqcxt.onion/10.1016/j.msard.2020.102306
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32585617!7295509!32585617
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suck abstract from ncbi

pmid32585617      Mult+Scler+Relat+Disord 2020 ; 44 (?): 102306
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  • COVID-19 in 7 multiple sclerosis patients in treatment with ANTI-CD20 therapies #MMPMID32585617
  • Meca-Lallana V; Aguirre C; Beatrizdel Rio; Cardenoso L; Alarcon T; Vivancos J
  • Mult Scler Relat Disord 2020[Sep]; 44 (?): 102306 PMID32585617show ga
  • BACKGROUND AND AIM: In December 2019, the first cases of SARS-CoV-2 infection were detected in Wuhan. Within two months, it had begun to spread around the world in what became an unprecedented pandemic. Patients with Multiple Sclerosis (MS) in a state of immunosuppression may be considered at risk for complications in the COVID-19 pandemic, although there is increasing evidence postulating a possible protective role of selective immunosuppression. One group of such immunosuppressants used in MS comprises the anti-CD20 monoclonal antibodies (mAbs) ocrelizumab and rituximab. Anti-CD20 mAbs bind to the surface of B cells, causing their depletion. We describe our experience in seven cases of patients with multiple sclerosis who have been affected by SARS-COV-2 (with a clinical/serological diagnosis or PCR diagnosis) and who were being treated with anti-CD20+ monoclonal antibodies. MATERIAL AND METHODS: We review the development of patients during infection as well as the resolution of their clinical picture. We also analyze the serology status against SARS-CoV-2 after resolution of the infection. RESULTS: Although the severity of the clinical pictures was variable, patients' development was good. Not all patients, however, developed antibodies against SARS-CoV-2. CONCLUSIONS: Patients treated with anti-CD20+ have adequate resolution of COVID-19 despite the fact that the presence of antibodies against SARS-CoV-2 was not detected in all cases. It is possible that the presence of humoral immunity is not always necessary fora good clinical course of SARS-CoV-2 infection.
  • |Adult[MESH]
  • |Antibodies, Monoclonal, Humanized/*therapeutic use[MESH]
  • |Antigens, CD20/*immunology[MESH]
  • |COVID-19/complications/*immunology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunologic Factors/*therapeutic use[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Multiple Sclerosis/complications/*drug therapy/*immunology[MESH]
  • |Rituximab/*therapeutic use[MESH]


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