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Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis

BACKGROUND: Several studies have demonstrated reduced serological response to vaccines in patients treated with anti-CD20 agents. However, limited data exist surrounding the clinical effect of disease modifying therapy (DMT) use on vaccine efficacy. OBJECTIVES: To investigate breakthrough coronaviru...

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Autores principales: Rose, Deja R, Mahadeen, Ahmad Z, Carlson, Alise K, Planchon, Sarah M, Sedlak, Jennifer, Husak, Scott, Bermel, Robert A, Cohen, Jeffrey A, Moss, Brandon P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673876/
https://www.ncbi.nlm.nih.gov/pubmed/34925875
http://dx.doi.org/10.1177/20552173211057110
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author Rose, Deja R
Mahadeen, Ahmad Z
Carlson, Alise K
Planchon, Sarah M
Sedlak, Jennifer
Husak, Scott
Bermel, Robert A
Cohen, Jeffrey A
Moss, Brandon P
author_facet Rose, Deja R
Mahadeen, Ahmad Z
Carlson, Alise K
Planchon, Sarah M
Sedlak, Jennifer
Husak, Scott
Bermel, Robert A
Cohen, Jeffrey A
Moss, Brandon P
author_sort Rose, Deja R
collection PubMed
description BACKGROUND: Several studies have demonstrated reduced serological response to vaccines in patients treated with anti-CD20 agents. However, limited data exist surrounding the clinical effect of disease modifying therapy (DMT) use on vaccine efficacy. OBJECTIVES: To investigate breakthrough coronavirus disease 2019 (COVID-19) in vaccinated people with multiple sclerosis (PwMS) on DMT. METHODS: PwMS on DMT diagnosed with COVID-19 after full vaccination were identified from an existing Cleveland Clinic COVID-19 registry, supplemented by provider-identified cases. Demographics, disease history, DMTs, comorbidities, exposures, vaccination status, and COVID-19 outcomes were confirmed by review of the electronic medical record. RESULTS: Thirteen (3.8%) of 344 fully vaccinated people with multiple sclerosis on disease modifying therapy were diagnosed with COVID-19 after vaccination. Ten patients (76.9%) were on an anti-CD20 therapy, the remaining 3 (23.1%) on fingolimod. Only 2 patients (15.4%), both on anti-CD20 therapy, required hospitalization and steroid treatment. Neither required Intensive Care Unit admission. CONCLUSION: Patients treated with anti-CD20 agents and sphingosine 1-phosphate receptor modulators may still be at risk for COVID-19 despite vaccination. While still at risk for hospitalization, intubation and death from COVID-19 appear rare. Larger studies analyzing how this may differ in the setting of emerging variants are needed.
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spelling pubmed-86738762021-12-16 Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis Rose, Deja R Mahadeen, Ahmad Z Carlson, Alise K Planchon, Sarah M Sedlak, Jennifer Husak, Scott Bermel, Robert A Cohen, Jeffrey A Moss, Brandon P Mult Scler J Exp Transl Clin Brief Report BACKGROUND: Several studies have demonstrated reduced serological response to vaccines in patients treated with anti-CD20 agents. However, limited data exist surrounding the clinical effect of disease modifying therapy (DMT) use on vaccine efficacy. OBJECTIVES: To investigate breakthrough coronavirus disease 2019 (COVID-19) in vaccinated people with multiple sclerosis (PwMS) on DMT. METHODS: PwMS on DMT diagnosed with COVID-19 after full vaccination were identified from an existing Cleveland Clinic COVID-19 registry, supplemented by provider-identified cases. Demographics, disease history, DMTs, comorbidities, exposures, vaccination status, and COVID-19 outcomes were confirmed by review of the electronic medical record. RESULTS: Thirteen (3.8%) of 344 fully vaccinated people with multiple sclerosis on disease modifying therapy were diagnosed with COVID-19 after vaccination. Ten patients (76.9%) were on an anti-CD20 therapy, the remaining 3 (23.1%) on fingolimod. Only 2 patients (15.4%), both on anti-CD20 therapy, required hospitalization and steroid treatment. Neither required Intensive Care Unit admission. CONCLUSION: Patients treated with anti-CD20 agents and sphingosine 1-phosphate receptor modulators may still be at risk for COVID-19 despite vaccination. While still at risk for hospitalization, intubation and death from COVID-19 appear rare. Larger studies analyzing how this may differ in the setting of emerging variants are needed. SAGE Publications 2021-11-26 /pmc/articles/PMC8673876/ /pubmed/34925875 http://dx.doi.org/10.1177/20552173211057110 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Brief Report
Rose, Deja R
Mahadeen, Ahmad Z
Carlson, Alise K
Planchon, Sarah M
Sedlak, Jennifer
Husak, Scott
Bermel, Robert A
Cohen, Jeffrey A
Moss, Brandon P
Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis
title Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis
title_full Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis
title_fullStr Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis
title_full_unstemmed Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis
title_short Clinical features and outcomes of COVID-19 despite SARS-CoV-2 vaccination in people with multiple sclerosis
title_sort clinical features and outcomes of covid-19 despite sars-cov-2 vaccination in people with multiple sclerosis
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673876/
https://www.ncbi.nlm.nih.gov/pubmed/34925875
http://dx.doi.org/10.1177/20552173211057110
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