Cargando…
SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome
Aicardi Goutières Syndrome (AGS) is an autoinflammatory disorder resulting in sustained interferon activation through defects in nucleic acid modification and sensing pathways. Thus, mRNA-based vaccination used against SARS-CoV-2, raise disease-specific safety concerns. To assess interferon signalin...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550281/ https://www.ncbi.nlm.nih.gov/pubmed/36334423 http://dx.doi.org/10.1016/j.ymgme.2022.10.001 |
_version_ | 1784805846502342656 |
---|---|
author | Takanohashi, Asako Alameh, Mohamad-Gabriel Woidill, Sarah Hacker, Julia Davis, Benjamin Helman, Guy Gavazzi, Francesco Adang, Laura D'Aiello, Russell Winters, Patrick Cordova, Devon Khandaker, Taibeen Ni, Houping Tam, Ying Lin, Paulo Weissman, Drew Shults, Justine Vanderver, Adeline |
author_facet | Takanohashi, Asako Alameh, Mohamad-Gabriel Woidill, Sarah Hacker, Julia Davis, Benjamin Helman, Guy Gavazzi, Francesco Adang, Laura D'Aiello, Russell Winters, Patrick Cordova, Devon Khandaker, Taibeen Ni, Houping Tam, Ying Lin, Paulo Weissman, Drew Shults, Justine Vanderver, Adeline |
author_sort | Takanohashi, Asako |
collection | PubMed |
description | Aicardi Goutières Syndrome (AGS) is an autoinflammatory disorder resulting in sustained interferon activation through defects in nucleic acid modification and sensing pathways. Thus, mRNA-based vaccination used against SARS-CoV-2, raise disease-specific safety concerns. To assess interferon signaling, we tested mRNA SARS-CoV-2 vaccines in AGS whole blood samples. Interferon activation is measured through quantitation of interferon signaling gene (ISG) expression and is increased in AGS patients. There was no increase in ISG scores from baseline following treatment with the nucleoside modified mRNA formulation compared to an increase with unmodified. A patient-family survey reported that the vaccines were well tolerated. These findings suggest that COVID vaccination using nucleoside-modified forms of mRNA vaccines are unlikely to directly stimulate ISG expression in response to mRNA internalization in AGS tissues. With continued community spread, we recommend vaccination using nucleoside-modified mRNA vaccines in this rare disease group in individuals for whom vaccines were previously well tolerated. |
format | Online Article Text |
id | pubmed-9550281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95502812022-10-11 SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome Takanohashi, Asako Alameh, Mohamad-Gabriel Woidill, Sarah Hacker, Julia Davis, Benjamin Helman, Guy Gavazzi, Francesco Adang, Laura D'Aiello, Russell Winters, Patrick Cordova, Devon Khandaker, Taibeen Ni, Houping Tam, Ying Lin, Paulo Weissman, Drew Shults, Justine Vanderver, Adeline Mol Genet Metab Article Aicardi Goutières Syndrome (AGS) is an autoinflammatory disorder resulting in sustained interferon activation through defects in nucleic acid modification and sensing pathways. Thus, mRNA-based vaccination used against SARS-CoV-2, raise disease-specific safety concerns. To assess interferon signaling, we tested mRNA SARS-CoV-2 vaccines in AGS whole blood samples. Interferon activation is measured through quantitation of interferon signaling gene (ISG) expression and is increased in AGS patients. There was no increase in ISG scores from baseline following treatment with the nucleoside modified mRNA formulation compared to an increase with unmodified. A patient-family survey reported that the vaccines were well tolerated. These findings suggest that COVID vaccination using nucleoside-modified forms of mRNA vaccines are unlikely to directly stimulate ISG expression in response to mRNA internalization in AGS tissues. With continued community spread, we recommend vaccination using nucleoside-modified mRNA vaccines in this rare disease group in individuals for whom vaccines were previously well tolerated. Elsevier Inc. 2022-12 2022-10-10 /pmc/articles/PMC9550281/ /pubmed/36334423 http://dx.doi.org/10.1016/j.ymgme.2022.10.001 Text en © 2022 Elsevier Inc. 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 Takanohashi, Asako Alameh, Mohamad-Gabriel Woidill, Sarah Hacker, Julia Davis, Benjamin Helman, Guy Gavazzi, Francesco Adang, Laura D'Aiello, Russell Winters, Patrick Cordova, Devon Khandaker, Taibeen Ni, Houping Tam, Ying Lin, Paulo Weissman, Drew Shults, Justine Vanderver, Adeline SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome |
title | SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome |
title_full | SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome |
title_fullStr | SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome |
title_full_unstemmed | SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome |
title_short | SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome |
title_sort | sars-cov-2 mrna-based vaccines in the aicardi goutières syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550281/ https://www.ncbi.nlm.nih.gov/pubmed/36334423 http://dx.doi.org/10.1016/j.ymgme.2022.10.001 |
work_keys_str_mv | AT takanohashiasako sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT alamehmohamadgabriel sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT woidillsarah sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT hackerjulia sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT davisbenjamin sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT helmanguy sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT gavazzifrancesco sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT adanglaura sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT daiellorussell sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT winterspatrick sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT cordovadevon sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT khandakertaibeen sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT nihouping sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT tamying sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT linpaulo sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT weissmandrew sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT shultsjustine sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome AT vanderveradeline sarscov2mrnabasedvaccinesintheaicardigoutieressyndrome |