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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.
  • Tallantyre EC; Division of Psychological Medicine and Clinical Neuroscience, School of Medicine, Cardiff University, Cardiff, UK.
  • Vickaryous N; Department of Neurology, University Hospital of Wales, Cardiff, UK.
  • Anderson V; Preventive Neurology Unit, Wolfson Institute of Population Health, Queen Mary University London, London, UK.
  • Asardag AN; Division of Psychological Medicine and Clinical Neuroscience, School of Medicine, Cardiff University, Cardiff, UK.
  • Baker D; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Bestwick J; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Bramhall K; Preventive Neurology Unit, Wolfson Institute of Population Health, Queen Mary University London, London, UK.
  • Chance R; Immunodeficiency Centre for Wales, University Hospital of Wales, Cardiff, UK.
  • Evangelou N; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • George K; Centre for Oral Immunobiology and Regenerative Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Giovannoni G; Department of Clinical Neurology, University of Nottingham, Nottingham, UK.
  • Godkin A; Preventive Neurology Unit, Wolfson Institute of Population Health, Queen Mary University London, London, UK.
  • Grant L; Preventive Neurology Unit, Wolfson Institute of Population Health, Queen Mary University London, London, UK.
  • Harding KE; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Hibbert A; Department of Neurology, Barts Health NHS Trust, London, UK.
  • Ingram G; Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
  • Jones M; Department of Gastroenterology and Hepatology, University Hospital of Wales, Cardiff, UK.
  • Kang AS; Immunodeficiency Centre for Wales, University Hospital of Wales, Cardiff, UK.
  • Loveless S; Department of Neurology, Royal Gwent Hospital, Newport, UK.
  • Moat SJ; Department of Clinical Neurology, University of Nottingham, Nottingham, UK.
  • Robertson NP; Department of Neurology, Morriston Hospital, Swansea, UK.
  • Schmierer K; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Scurr MJ; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Shah SN; Centre for Oral Immunobiology and Regenerative Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Simmons J; Division of Psychological Medicine and Clinical Neuroscience, School of Medicine, Cardiff University, Cardiff, UK.
  • Upcott M; Wales Newborn Screening Laboratory, Department of Medical Biochemistry, Immunology and Toxicology, University Hospital of Wales, Cardiff, UK.
  • Willis M; School of Medicine, Cardiff University, Cardiff, UK.
  • Jolles S; Division of Psychological Medicine and Clinical Neuroscience, School of Medicine, Cardiff University, Cardiff, UK.
  • Dobson R; Department of Neurology, University Hospital of Wales, Cardiff, UK.
Ann Neurol ; 91(1): 89-100, 2022 01.
Article in English | MEDLINE | ID: covidwho-1479378
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 20219999n/a-n/a.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunocompromised Host / Antirheumatic Agents / Seroconversion / COVID-19 Vaccines / COVID-19 / Multiple Sclerosis Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Ann Neurol Year: 2022 Document Type: Article Affiliation country: Ana.26251

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunocompromised Host / Antirheumatic Agents / Seroconversion / COVID-19 Vaccines / COVID-19 / Multiple Sclerosis Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Ann Neurol Year: 2022 Document Type: Article Affiliation country: Ana.26251