Evidence map›Paper›PMID 34571415›Full record

ArticleMultiple sclerosis and related disorders2021

Humoral immune response following SARS-CoV-2 mRNA vaccination concomitant to anti-CD20 therapy in multiple sclerosis.

Frederik Novak, Anna Christine Nilsson, Christian Nielsen, Dorte K Holm, Kamilla Østergaard, Anna Bystrup, Keld-Erik Byg, Isik S Johansen, Kristen Mittl, William Rowles and 9 more

Abstract read
In one paragraph

Article in Multiple sclerosis and related disorders, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Frederik NovakDepartment of Neurology, Hospital Southwest Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Anna Christine NilssonDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Christian NielsenDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Dorte K HolmDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark.
Kamilla ØstergaardDepartment of Neurology, Nordsjællands Hospital, Hillerød, Denmark.
Anna BystrupDepartment of Neurology, Hospitalsenhed Midt, Viborg, Denmark.
Keld-Erik BygDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark; Department of Rheumatology, Odense University Hospital, Odense, Denmark.
Isik S JohansenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark; Department of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Kristen MittlWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
William RowlesWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Kira McpolinWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Collin SpencerWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Sharon SaganWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Chloe GerunganWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Michael R WilsonWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Scott S ZamvilWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Riley BoveWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Joseph J SabatinoWeill Institute for Neurosciences, Department of Neurology, University California San Francisco, San Francisco, United States.
Tobias SejbaekDepartment 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.

Funding

Repertoire selection of AQP4-specific T cells that cause CNS autoimmunediseaseR01AI131624 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZAMVIL, SCOTT S · 2019 to 2023
$2.2M
Next-Generation Diagnostics for Acute EncephalitisK08NS096117 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WILSON, MICHAEL R · 2017 to 2021
$999k
NIAID NIH HHS R01 AI131624NINDS NIH HHS K08 NS096117
6 · The paper itself

Abstract

backgroundThe 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.

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

methodIgG 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).

results36.7% 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.

conclusionOur 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.

Indexed as

COVID-19Multiple SclerosisAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesHumansImmunity, HumoralRNA, MessengerSARS-CoV-2VaccinationVaccine EfficacyAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesRNA, MessengerAnti-cd20Clinical trialsCovid-19OcrelizumabSars-cov-2Vaccination

Identifiers

PMID34571415
PMCPMC8426319

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.