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Humoral immune response following SARS-CoV-2 mRNA vaccination concomitant to anti-CD20 therapy in multiple sclerosis.
Novak, Frederik; Nilsson, Anna Christine; Nielsen, Christian; Holm, Dorte K; Østergaard, Kamilla; Bystrup, Anna; Byg, Keld-Erik; Johansen, Isik S; Mittl, Kristen; Rowles, William; Mcpolin, Kira; Spencer, Collin; Sagan, Sharon; Gerungan, Chloe; Wilson, Michael R; Zamvil, Scott S; Bove, Riley; Sabatino, Joseph J; Sejbaek, Tobias.
  • Novak F; Department of Neurology, Hospital Southwest Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.
  • Nilsson AC; Department of Clinical Immunology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
  • Nielsen C; Department of Clinical Immunology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
  • Holm DK; Department of Clinical Immunology, Odense University Hospital, Odense, Denmark.
  • Østergaard K; Department of Neurology, Nordsjællands Hospital, Hillerød, Denmark.
  • Bystrup A; Department of Neurology, Hospitalsenhed Midt, Viborg, Denmark.
  • Byg KE; Department of Clinical Research, University of Southern Denmark, Odense, Denmark; Department of Rheumatology, Odense University Hospital, Odense, Denmark.
  • Johansen IS; Department of Clinical Research, University of Southern Denmark, Odense, Denmark; Department of Infectious Diseases, Odense University Hospital, Odense, Denmark.
  • Mittl K; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Rowles W; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Mcpolin K; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Spencer C; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Sagan S; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Gerungan C; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Wilson MR; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Zamvil SS; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Bove R; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Sabatino JJ; Weill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
  • Sejbaek T; Department of Neurology, Hospital Southwest Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark. Electronic address: tobias.sejbaek@rsyd.dk.
Mult Scler Relat Disord ; 56: 103251, 2021 Nov.
Article in English | MEDLINE | ID: covidwho-1401726
ABSTRACT

BACKGROUND:

The immunogenicity of COVID-19 vaccine among patients receiving anti-CD20 monoclonal antibody (Ab) treatment has not been fully investigated. Detectable levels of SARS-CoV-2 immunoglobulin G (IgG) are believed to have a predictive value for immune protection against COVID-19 and is currently a surrogate indicator for vaccine efficacy.

OBJECTIVE:

To determine IgG Abs in anti-CD20 treated patients with multiple sclerosis (MS).

METHOD:

IgG Abs against SARS-CoV-2 spike receptor-binding domain were measured with the SARS-CoV-2 IgG II Quant assay (Abbott Laboratories) before and after vaccination (n = 60).

RESULTS:

36.7% of patients mounted a positive SARS-CoV-2 spike Ab response after the second dose of vaccine. Five patients (8.3%) developed Abs >264 BAU/mL, another 12 patients (20%) developed intermediate Abs between 54 BAU/mL and 264 BAU/mL and five patients (8.3%) had low levels <54 BAU/mL. Of all seropositive patients, 63.6% converted from seronegative to seropositive after the 2nd vaccine.

CONCLUSION:

Our study demonstrates decreased humoral response after BNT162b2 mRNA SARS-CoV-2 vaccine in MS patients receiving B-cell depleting therapy. Clinicians should advise patients treated with anti-CD20 to avoid exposure to SARS-CoV-2. Future studies should investigate the implications of a third booster vaccine in patients with low or absent Abs after vaccination.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Multiple Sclerosis Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Mult Scler Relat Disord Year: 2021 Document Type: Article Affiliation country: J.msard.2021.103251

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Multiple Sclerosis Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Mult Scler Relat Disord Year: 2021 Document Type: Article Affiliation country: J.msard.2021.103251