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Neutralizing antibody responses against SARS-CoV-2 in vaccinated people with multiple sclerosis
BACKGROUND: Patients with multiple sclerosis (pwMS) are often treated with disease modifying therapies (DMT) with immunomodulatory effects. This is of particular concern following the development of several vaccines to combat coronavirus disease 19 (COVD-19), a potentially fatal illness caused by SA...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941285/ https://www.ncbi.nlm.nih.gov/pubmed/35342640 http://dx.doi.org/10.1177/20552173221087357 |
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author | Gyang, Tirisham V. Evans, John P. Miller, Joseph S. Alcorn, Kariss Peng, Juan Bell, Erica H. Zeng, Cong Gumina, Richard Liu, Shan-Lu Segal, Benjamin M. |
author_facet | Gyang, Tirisham V. Evans, John P. Miller, Joseph S. Alcorn, Kariss Peng, Juan Bell, Erica H. Zeng, Cong Gumina, Richard Liu, Shan-Lu Segal, Benjamin M. |
author_sort | Gyang, Tirisham V. |
collection | PubMed |
description | BACKGROUND: Patients with multiple sclerosis (pwMS) are often treated with disease modifying therapies (DMT) with immunomodulatory effects. This is of particular concern following the development of several vaccines to combat coronavirus disease 19 (COVD-19), a potentially fatal illness caused by SARS-CoV-2. OBJECTIVES: To determine the efficacy of SARS-CoV-2 vaccination in pwMS and the impact of disease modifying therapies (DMT) on vaccine response. METHODS: This is a prospective longitudinal study in pwMS. Longitudinal serum samples were obtained prior to, and after SARS-CoV-2 mRNA vaccination. A novel neutralizing antibody (nAb) assay was used to determine nAbs titres against SARS-CoV-2 spike. RESULTS: We observed that (1) pwMS on B-cell depleting therapies exhibited reduced response to vaccination compared to other pwMS, correlating with time from last anti-CD20 infusion, (2) prior COVID-19 illness, DMT category, and pyramidal function were significant predictors of vaccine responsiveness, and (3) circulating absolute lymphocyte count (ALC) and IgG levels correlated with nAb levels. CONCLUSIONS: We demonstrate that pwMS exhibit reduced nAb response to mRNA vaccination dependent on DMT status and identify predictive biomarkers for vaccine efficacy. We conclude that additional vaccination strategies may be necessary to achieve protective immunity in pwMS. |
format | Online Article Text |
id | pubmed-8941285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-89412852022-03-24 Neutralizing antibody responses against SARS-CoV-2 in vaccinated people with multiple sclerosis Gyang, Tirisham V. Evans, John P. Miller, Joseph S. Alcorn, Kariss Peng, Juan Bell, Erica H. Zeng, Cong Gumina, Richard Liu, Shan-Lu Segal, Benjamin M. Mult Scler J Exp Transl Clin Original Research Article BACKGROUND: Patients with multiple sclerosis (pwMS) are often treated with disease modifying therapies (DMT) with immunomodulatory effects. This is of particular concern following the development of several vaccines to combat coronavirus disease 19 (COVD-19), a potentially fatal illness caused by SARS-CoV-2. OBJECTIVES: To determine the efficacy of SARS-CoV-2 vaccination in pwMS and the impact of disease modifying therapies (DMT) on vaccine response. METHODS: This is a prospective longitudinal study in pwMS. Longitudinal serum samples were obtained prior to, and after SARS-CoV-2 mRNA vaccination. A novel neutralizing antibody (nAb) assay was used to determine nAbs titres against SARS-CoV-2 spike. RESULTS: We observed that (1) pwMS on B-cell depleting therapies exhibited reduced response to vaccination compared to other pwMS, correlating with time from last anti-CD20 infusion, (2) prior COVID-19 illness, DMT category, and pyramidal function were significant predictors of vaccine responsiveness, and (3) circulating absolute lymphocyte count (ALC) and IgG levels correlated with nAb levels. CONCLUSIONS: We demonstrate that pwMS exhibit reduced nAb response to mRNA vaccination dependent on DMT status and identify predictive biomarkers for vaccine efficacy. We conclude that additional vaccination strategies may be necessary to achieve protective immunity in pwMS. SAGE Publications 2022-03-22 /pmc/articles/PMC8941285/ /pubmed/35342640 http://dx.doi.org/10.1177/20552173221087357 Text en © The Author(s), 2022 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 | Original Research Article Gyang, Tirisham V. Evans, John P. Miller, Joseph S. Alcorn, Kariss Peng, Juan Bell, Erica H. Zeng, Cong Gumina, Richard Liu, Shan-Lu Segal, Benjamin M. Neutralizing antibody responses against SARS-CoV-2 in vaccinated people with multiple sclerosis |
title | Neutralizing antibody responses against SARS-CoV-2 in vaccinated
people with multiple sclerosis |
title_full | Neutralizing antibody responses against SARS-CoV-2 in vaccinated
people with multiple sclerosis |
title_fullStr | Neutralizing antibody responses against SARS-CoV-2 in vaccinated
people with multiple sclerosis |
title_full_unstemmed | Neutralizing antibody responses against SARS-CoV-2 in vaccinated
people with multiple sclerosis |
title_short | Neutralizing antibody responses against SARS-CoV-2 in vaccinated
people with multiple sclerosis |
title_sort | neutralizing antibody responses against sars-cov-2 in vaccinated
people with multiple sclerosis |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941285/ https://www.ncbi.nlm.nih.gov/pubmed/35342640 http://dx.doi.org/10.1177/20552173221087357 |
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