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Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects

BACKGROUND: Several concerns exist on the immunogenicity of SARS-CoV-2 vaccines in multiple sclerosis (MS) subjects due to their immunomodulating disease modifying therapies (DMTs). Here we report a comparison of the humoral response to BNT162b2-mRNA coronavirus (COVID)-19 vaccine and the immunologi...

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Autores principales: Maniscalco, Giorgia Teresa, Manzo, Valentino, Ferrara, Anne Lise, Perrella, Alessandro, Di Battista, Mariaelena, Salvatore, Simona, Graziano, Daniela, Viola, Assunta, Amato, Gerardino, Moreggia, Ornella, Di Giulio Cesare, Daniele, Barbato, Stefano, Servillo, Giovanna, Longo, Katia, Di Giovanni, Mario, Scarpati, Barbara, Muggianu, Simona Maria, Longo, Giuseppe, Russo, Giuseppe, Andreone, Vincenzo, De Rosa, Veronica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683261/
https://www.ncbi.nlm.nih.gov/pubmed/34929455
http://dx.doi.org/10.1016/j.msard.2021.103455
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author Maniscalco, Giorgia Teresa
Manzo, Valentino
Ferrara, Anne Lise
Perrella, Alessandro
Di Battista, Mariaelena
Salvatore, Simona
Graziano, Daniela
Viola, Assunta
Amato, Gerardino
Moreggia, Ornella
Di Giulio Cesare, Daniele
Barbato, Stefano
Servillo, Giovanna
Longo, Katia
Di Giovanni, Mario
Scarpati, Barbara
Muggianu, Simona Maria
Longo, Giuseppe
Russo, Giuseppe
Andreone, Vincenzo
De Rosa, Veronica
author_facet Maniscalco, Giorgia Teresa
Manzo, Valentino
Ferrara, Anne Lise
Perrella, Alessandro
Di Battista, Mariaelena
Salvatore, Simona
Graziano, Daniela
Viola, Assunta
Amato, Gerardino
Moreggia, Ornella
Di Giulio Cesare, Daniele
Barbato, Stefano
Servillo, Giovanna
Longo, Katia
Di Giovanni, Mario
Scarpati, Barbara
Muggianu, Simona Maria
Longo, Giuseppe
Russo, Giuseppe
Andreone, Vincenzo
De Rosa, Veronica
author_sort Maniscalco, Giorgia Teresa
collection PubMed
description BACKGROUND: Several concerns exist on the immunogenicity of SARS-CoV-2 vaccines in multiple sclerosis (MS) subjects due to their immunomodulating disease modifying therapies (DMTs). Here we report a comparison of the humoral response to BNT162b2-mRNA coronavirus (COVID)-19 vaccine and the immunological phenotype in a cohort of 125 MS subjects undergoing different DMTs, with no history of SARS-CoV-2 infection. METHODS: We collected serum and blood samples at the first day of vaccine (T0) and 21 days after the second vaccine dose (T1) from 125 MS subjects, undergoing eight different DMTs. Sera were tested using the Elecsys anti-SARS-CoV-2-IgG assay for the detection of IgG antibodies to SARS-CoV-2 spike protein. The anti-spike IgG titres from MS subjects were compared with 24 age- and sex-matched healthy controls (HC). Percentage and absolute number of B and T lymphocytes were evaluated by cytofluorimetric analysis in the same study cohort. RESULTS: When compared with SARS-CoV-2 IgG levels in HC (n = 24, median 1089 (IQR 652.5–1625) U/mL), we observed an increased secretion of SARS-CoV-2 IgG in interferon-beta 1a (IFN)-treated MS subjects (n = 22, median 1916 (IQR 1024–2879) U/mL) and an impaired humoral response in MS subjects undergoing cladribine (CLAD) (n = 10, median 396.9 (IQR 37.52–790.9) U/mL), fingolimod (FTY) (n = 19, median 7.9 (IQR 4.8–147.6) U/mL) and ocrelizumab (OCRE) (n = 15, median 0.67 (IQR 0.4–5.9) U/mL) treatment. Moreover, analysis of geometric mean titre ratio (GMTR) between different DMT's groups of MS subjects revealed that, when compared with IFN-treated MS subjects, intrinsic antibody production was impaired in teriflunomide (TERI)-, natalizumab (NAT)-, CLAD-, FTY- and OCRE-, while preserved in DMF- and GA-treated MS subjects. CONCLUSION: Humoral response to BNT162b2-mRNA-vaccine was increased in IFN-treated MS subjects while clearly blunted in those under CLAD, FTY and OCRE treatment. This suggests that the DMTs could have a key role in the protection from SARS-CoV-2 related disease and complication in MS subjects, underlying a novel aspect that should be considered in the selection of the most appropriate therapy under COVID-19 pandemic.
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spelling pubmed-86832612021-12-20 Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects Maniscalco, Giorgia Teresa Manzo, Valentino Ferrara, Anne Lise Perrella, Alessandro Di Battista, Mariaelena Salvatore, Simona Graziano, Daniela Viola, Assunta Amato, Gerardino Moreggia, Ornella Di Giulio Cesare, Daniele Barbato, Stefano Servillo, Giovanna Longo, Katia Di Giovanni, Mario Scarpati, Barbara Muggianu, Simona Maria Longo, Giuseppe Russo, Giuseppe Andreone, Vincenzo De Rosa, Veronica Mult Scler Relat Disord Article BACKGROUND: Several concerns exist on the immunogenicity of SARS-CoV-2 vaccines in multiple sclerosis (MS) subjects due to their immunomodulating disease modifying therapies (DMTs). Here we report a comparison of the humoral response to BNT162b2-mRNA coronavirus (COVID)-19 vaccine and the immunological phenotype in a cohort of 125 MS subjects undergoing different DMTs, with no history of SARS-CoV-2 infection. METHODS: We collected serum and blood samples at the first day of vaccine (T0) and 21 days after the second vaccine dose (T1) from 125 MS subjects, undergoing eight different DMTs. Sera were tested using the Elecsys anti-SARS-CoV-2-IgG assay for the detection of IgG antibodies to SARS-CoV-2 spike protein. The anti-spike IgG titres from MS subjects were compared with 24 age- and sex-matched healthy controls (HC). Percentage and absolute number of B and T lymphocytes were evaluated by cytofluorimetric analysis in the same study cohort. RESULTS: When compared with SARS-CoV-2 IgG levels in HC (n = 24, median 1089 (IQR 652.5–1625) U/mL), we observed an increased secretion of SARS-CoV-2 IgG in interferon-beta 1a (IFN)-treated MS subjects (n = 22, median 1916 (IQR 1024–2879) U/mL) and an impaired humoral response in MS subjects undergoing cladribine (CLAD) (n = 10, median 396.9 (IQR 37.52–790.9) U/mL), fingolimod (FTY) (n = 19, median 7.9 (IQR 4.8–147.6) U/mL) and ocrelizumab (OCRE) (n = 15, median 0.67 (IQR 0.4–5.9) U/mL) treatment. Moreover, analysis of geometric mean titre ratio (GMTR) between different DMT's groups of MS subjects revealed that, when compared with IFN-treated MS subjects, intrinsic antibody production was impaired in teriflunomide (TERI)-, natalizumab (NAT)-, CLAD-, FTY- and OCRE-, while preserved in DMF- and GA-treated MS subjects. CONCLUSION: Humoral response to BNT162b2-mRNA-vaccine was increased in IFN-treated MS subjects while clearly blunted in those under CLAD, FTY and OCRE treatment. This suggests that the DMTs could have a key role in the protection from SARS-CoV-2 related disease and complication in MS subjects, underlying a novel aspect that should be considered in the selection of the most appropriate therapy under COVID-19 pandemic. Elsevier B.V. 2022-02 2021-12-18 /pmc/articles/PMC8683261/ /pubmed/34929455 http://dx.doi.org/10.1016/j.msard.2021.103455 Text en © 2021 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Maniscalco, Giorgia Teresa
Manzo, Valentino
Ferrara, Anne Lise
Perrella, Alessandro
Di Battista, Mariaelena
Salvatore, Simona
Graziano, Daniela
Viola, Assunta
Amato, Gerardino
Moreggia, Ornella
Di Giulio Cesare, Daniele
Barbato, Stefano
Servillo, Giovanna
Longo, Katia
Di Giovanni, Mario
Scarpati, Barbara
Muggianu, Simona Maria
Longo, Giuseppe
Russo, Giuseppe
Andreone, Vincenzo
De Rosa, Veronica
Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects
title Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects
title_full Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects
title_fullStr Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects
title_full_unstemmed Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects
title_short Interferon Beta-1a treatment promotes SARS-CoV-2 mRNA vaccine response in multiple sclerosis subjects
title_sort interferon beta-1a treatment promotes sars-cov-2 mrna vaccine response in multiple sclerosis subjects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683261/
https://www.ncbi.nlm.nih.gov/pubmed/34929455
http://dx.doi.org/10.1016/j.msard.2021.103455
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