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COVID-19 Vaccine Response in People with Multiple Sclerosis

Tallantyre, Emma C.; Vickaryous, Nicola; Anderson, Valerie; Asardag, Aliye Nazli; Baker, David; Bestwick, Jonathan; Bramhall, Kath; Chance, Randy; Evangelou, Nikos; George, Katila; Giovannoni, Gavin; Godkin, Andrew; Grant, Leanne; Harding, Katharine E.; Hibbert, Aimee; Ingram, Gillian; Jones, Meleri; Kang, Angray S.; Loveless, Samantha; Moat, Stuart J.; Robertson, Neil P.; Schmierer, Klaus; Scurr, Martin J.; Shah, Sita Navin; Simmons, Jessica; Upcott, Matthew; Willis, Mark; Jolles, Stephen; Dobson, Ruth

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Authors

Emma C. Tallantyre

Nicola Vickaryous

Valerie Anderson

Aliye Nazli Asardag

David Baker

Jonathan Bestwick

Kath Bramhall

Randy Chance

Katila George

Gavin Giovannoni

Andrew Godkin

Leanne Grant

Katharine E. Harding

Aimee Hibbert

Gillian Ingram

Meleri Jones

Angray S. Kang

Samantha Loveless

Stuart J. Moat

Neil P. Robertson

Klaus Schmierer

Martin J. Scurr

Sita Navin Shah

Jessica Simmons

Matthew Upcott

Mark Willis

Stephen Jolles

Ruth Dobson



Abstract

Objective: The purpose of this study was to investigate the effect of disease modifying therapies on immune response to severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) vaccines in people with multiple sclerosis (MS). Methods: Four hundred seventy-three people with MS provided one or more dried blood spot samples. Information about coronavirus disease 2019 (COVID-19) and vaccine history, medical, and drug history were extracted from questionnaires and medical records. Dried blood spots were eluted and tested for antibodies to SARS-CoV-2. Antibody titers were partitioned into tertiles with people on no disease modifying therapy as a reference. We calculated the odds ratio of seroconversion (univariate logistic regression) and compared quantitative vaccine response (Kruskal Wallis) following the SARS-CoV-2 vaccine according to disease modifying therapy. We used regression modeling to explore the effect of vaccine timing, treatment duration, age, vaccine type, and lymphocyte count on vaccine response. Results: Compared to no disease modifying therapy, the use of anti-CD20 monoclonal antibodies (odds ratio=0.03, 95% confidence interval [CI] = 0.01–0.06, p < 0.001) and fingolimod (odds ratio=0.04; 95% CI=0.01–0.12) were associated with lower seroconversion following the SARS-CoV-2 vaccine. All other drugs did not differ significantly from the untreated cohort. Both time since last anti-CD20 treatment and total time on treatment were significantly associated with the response to the vaccination. The vaccine type significantly predicted seroconversion, but not in those on anti-CD20 medications. Preliminary data on cellular T-cell immunity showed 40% of seronegative subjects had measurable anti-SARS-CoV-2 T cell responses. Interpretation: Some disease modifying therapies convey risk of attenuated serological response to SARS-CoV-2 vaccination in people with MS. We provide recommendations for the practical management of this patient group. ANN NEUROL 20219999:n/a–n/a.

Citation

Tallantyre, E. C., Vickaryous, N., Anderson, V., Asardag, A. N., Baker, D., Bestwick, J., …Dobson, R. (2022). COVID-19 Vaccine Response in People with Multiple Sclerosis. Annals of Neurology, 91(1), 89-100. https://doi.org/10.1002/ana.26251

Journal Article Type Article
Acceptance Date Oct 18, 2021
Online Publication Date Oct 22, 2021
Publication Date Jan 1, 2022
Deposit Date Nov 18, 2021
Publicly Available Date Nov 18, 2021
Journal Annals of Neurology
Print ISSN 0364-5134
Electronic ISSN 1531-8249
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 91
Issue 1
Pages 89-100
DOI https://doi.org/10.1002/ana.26251
Keywords Clinical Neurology; Neurology
Public URL https://nottingham-repository.worktribe.com/output/6729552
Publisher URL https://onlinelibrary.wiley.com/doi/full/10.1002/ana.26251

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