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    Seroconversion following COVID-19 vaccination: can we optimize protective response in CD20-treated individuals? 
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    • Centre for Cancer Prevention
    • Seroconversion following COVID-19 vaccination: can we optimize protective response in CD20-treated individuals?
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    Seroconversion following COVID-19 vaccination: can we optimize protective response in CD20-treated individuals?

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    Accepted version (361.1Kb)
    Volume
    207
    Pagination
    263 - 271
    DOI
    10.1093/cei/uxab015
    Journal
    Clin Exp Immunol
    Issue
    3
    Metadata
    Show full item record
    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.
    Authors
    Baker, D; MacDougall, A; Kang, AS; Schmierer, K; Giovannoni, G; Dobson, R
    URI
    https://qmro.qmul.ac.uk/xmlui/handle/123456789/78814
    Collections
    • Centre for Cancer Prevention [858]
    Language
    eng
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