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Seroconversion following COVID-19 vaccination: can we optimize protective response in CD20-treated individuals?
Baker, David; MacDougall, Amy; Kang, Angray S; Schmierer, Klaus; Giovannoni, Gavin; Dobson, Ruth.
  • Baker D; The Blizard Institute, Barts and The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
  • MacDougall A; Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.
  • Kang AS; The Blizard Institute, Barts and The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
  • Schmierer K; Centre for Oral Immunobiology and Regenerative Medicine, Dental Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Giovannoni G; The Blizard Institute, Barts and The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
  • Dobson R; Clinical Board Medicine (Neuroscience), The Royal London Hospital, Barts Health NHS Trust, London, UK.
Clin Exp Immunol ; 207(3): 263-271, 2022 05 12.
Article in English | MEDLINE | ID: covidwho-2291810
ABSTRACT
Although there is an ever-increasing number of disease-modifying treatments for relapsing multiple sclerosis (MS), few appear to influence coronavirus disease 2019 (COVID-19) severity. There is concern about the use of anti-CD20-depleting monoclonal antibodies, due to the apparent increased risk of severe disease following severe acute respiratory syndrome corona virus two (SARS-CoV-2) infection and inhibition of protective anti-COVID-19 vaccine responses. These antibodies are given as maintenance infusions/injections and cause persistent depletion of CD20+ B cells, notably memory B-cell populations that may be instrumental in the control of relapsing MS. However, they also continuously deplete immature and mature/naïve B cells that form the precursors for infection-protective antibody responses, thus blunting vaccine responses. Seroconversion and maintained SARS-CoV-2 neutralizing antibody levels provide protection from COVID-19. However, it is evident that poor seroconversion occurs in the majority of individuals following initial and booster COVID-19 vaccinations, based on standard 6 monthly dosing intervals. Seroconversion may be optimized in the anti-CD20-treated population by vaccinating prior to treatment onset or using extended/delayed interval dosing (3-6 month extension to dosing interval) in those established on therapy, with B-cell monitoring until (1-3%) B-cell repopulation occurs prior to vaccination. Some people will take more than a year to replete and therefore protection may depend on either the vaccine-induced T-cell responses that typically occur or may require prophylactic, or rapid post-infection therapeutic, antibody or small-molecule antiviral treatment to optimize protection against COVID-19. Further studies are warranted to demonstrate the safety and efficacy of such approaches and whether or not immunity wanes prematurely as has been observed in the other populations.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Multiple Sclerosis Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Clin Exp Immunol Year: 2022 Document Type: Article Affiliation country: Cei

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Multiple Sclerosis Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Clin Exp Immunol Year: 2022 Document Type: Article Affiliation country: Cei