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COVID-19 vaccine response in people with multiple sclerosis
Emma C Tallantyre; Nicola Vickaryous; Valerie Anderson; Aliye Nazli Asardag; David Baker; Jonathan P Bestwick; Kathryn Bramhall; Randy Chance; Nikos Evangelou; Katila George; Gavin Giovannoni; Leanne Grant; Katharine E Harding; Aimee Hibbert; Gillian Ingram; Meleri Jones; Angray S Kang; Samantha Loveless; Stuart Moat; Neil P Robertson; Klaus Schmierer; Sitash Navin Shah; Jessica Simmons; Matthew Upcott; Mark D Willis; Stephen Jolles; Ruth Dobson.
Afiliação
  • Emma C Tallantyre; Cardiff University
  • Nicola Vickaryous; Preventive Neurology Unit, Queen Mary University London
  • Valerie Anderson; Department of Neurology, Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, UK
  • Aliye Nazli Asardag; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • David Baker; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • Jonathan P Bestwick; Preventive Neurology Unit, Queen Mary University London
  • Kathryn Bramhall; Immunodeficiency Centre for Wales, University Hospital of Wales, Cardiff, UK
  • Randy Chance; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • Nikos Evangelou; Department of Clinical Neurology, University of Nottingham
  • Katila George; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • Gavin Giovannoni; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • Leanne Grant; Immunodeficiency Centre for Wales, University Hospital of Wales, Cardiff, UK
  • Katharine E Harding; Department of Neurology, Royal Gwent Hopsital, Newport, UK
  • Aimee Hibbert; Nottingham University Hospitals
  • Gillian Ingram; Department of Neurology, Morriston Hospital, Swansea
  • Meleri Jones; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • Angray S Kang; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • Samantha Loveless; Department of Neurology, Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, UK
  • Stuart Moat; Wales Newborn Screening Laboratory, Department of Medical Biochemistry, Immunology and Toxicology, University Hospital of Wales, Cardiff, Wales, UK
  • Neil P Robertson; Department of Neurology, Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, UK
  • Klaus Schmierer; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
  • Sitash Navin Shah; Preventive Neurology Unit, Queen Mary University London
  • Jessica Simmons; Preventive Neurology Unit, Queen Mary University London
  • Matthew Upcott; School of Medicine, Cardiff University, UK
  • Mark D Willis; Department of Neurology, Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, UK
  • Stephen Jolles; Immunodeficiency Centre for Wales, University Hospital of Wales, Cardiff, UK
  • Ruth Dobson; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21261326
ABSTRACT
ObjectiveTo investigate the effect of disease modifying therapies on serological response to SARS-CoV2 vaccines in people with multiple sclerosis Methods473 people with multiple sclerosis from 5 centres provided one or more dried blood spot samples and questionnaires about COVID-19. Information about disease and drug history was extracted from their medical records. Dried blood spots were eluted and tested for antibodies to SARS-CoV2 receptor binding domain. Seropositivity was expressed according to validated cut-off indices. Antibody titers were partitioned into tertiles using data from 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 SARS-CoV2 vaccine according to disease modifying therapy. We used regression modelling to explore the effect of factors including vaccine timing, treatment duration, age, vaccine type and lymphocyte count on vaccine response. ResultsCompared to no disease modifying therapy, the use of anti-CD20 monoclonal antibodies (odds ratio 0.03; 95% confidence interval 0.01-0.06, p<0.001) and fingolimod (odds ratio 0.41; 95% confidence interval 0.01-0.12) were associated with lower seroconversion following SARS-CoV2 vaccine. All other drug groups did not differ significantly from the untreated cohort. Time since last anti-CD20 treatment and total time on treatment were significantly related with response to vaccination. Vaccine type significantly predicted seroconversion, but not in those on anti-CD20 medications. InterpretationSome disease modifying therapies carry a risk of attenuated response to SARS-CoV2 vaccination in people with MS. We provide recommendations for the practical management of this patient group.
Licença
cc_by_nd
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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