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Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines

Impressive efforts have been made by researchers worldwide in the development of target vaccines against the novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and in improving the management of immunomodulating agents. Currently, different vaccine formulations, such as viral vector,...

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Autores principales: Picchianti Diamanti, Andrea, Rosado, Maria Manuela, Nicastri, Emanuele, Sesti, Giorgio, Pioli, Claudio, Laganà, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515900/
https://www.ncbi.nlm.nih.gov/pubmed/34659200
http://dx.doi.org/10.3389/fimmu.2021.708848
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author Picchianti Diamanti, Andrea
Rosado, Maria Manuela
Nicastri, Emanuele
Sesti, Giorgio
Pioli, Claudio
Laganà, Bruno
author_facet Picchianti Diamanti, Andrea
Rosado, Maria Manuela
Nicastri, Emanuele
Sesti, Giorgio
Pioli, Claudio
Laganà, Bruno
author_sort Picchianti Diamanti, Andrea
collection PubMed
description Impressive efforts have been made by researchers worldwide in the development of target vaccines against the novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and in improving the management of immunomodulating agents. Currently, different vaccine formulations, such as viral vector, mRNA, and protein-based, almost all directed toward the spike protein that includes the domain for receptor binding, have been approved. Although data are not conclusive, patients affected by autoimmune rheumatic diseases (ARDs) seem to have a slightly higher disease prevalence, risk of hospitalization, and death from coronavirus disease-2019 (COVID-19) than the general population. Therefore, ARD patients, under immunosuppressive agents, have been included among the priority target groups for vaccine administration. However, specific cautions are needed to optimize vaccine safety and effectiveness in these patients, such as modification in some of the ongoing immunosuppressive therapies and the preferential use of mRNA other than vector-based vaccines. Immunomodulating agents can be a therapeutic opportunity for the management of COVID-19 patients; however, their clinical impact depends on how they are handled. To place in therapy immunomodulating agents in the correct window of opportunity throughout the identification of surrogate markers of disease progression and host immune response is mandatory to optimize patient’s outcome.
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spelling pubmed-85159002021-10-15 Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines Picchianti Diamanti, Andrea Rosado, Maria Manuela Nicastri, Emanuele Sesti, Giorgio Pioli, Claudio Laganà, Bruno Front Immunol Immunology Impressive efforts have been made by researchers worldwide in the development of target vaccines against the novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and in improving the management of immunomodulating agents. Currently, different vaccine formulations, such as viral vector, mRNA, and protein-based, almost all directed toward the spike protein that includes the domain for receptor binding, have been approved. Although data are not conclusive, patients affected by autoimmune rheumatic diseases (ARDs) seem to have a slightly higher disease prevalence, risk of hospitalization, and death from coronavirus disease-2019 (COVID-19) than the general population. Therefore, ARD patients, under immunosuppressive agents, have been included among the priority target groups for vaccine administration. However, specific cautions are needed to optimize vaccine safety and effectiveness in these patients, such as modification in some of the ongoing immunosuppressive therapies and the preferential use of mRNA other than vector-based vaccines. Immunomodulating agents can be a therapeutic opportunity for the management of COVID-19 patients; however, their clinical impact depends on how they are handled. To place in therapy immunomodulating agents in the correct window of opportunity throughout the identification of surrogate markers of disease progression and host immune response is mandatory to optimize patient’s outcome. Frontiers Media S.A. 2021-09-30 /pmc/articles/PMC8515900/ /pubmed/34659200 http://dx.doi.org/10.3389/fimmu.2021.708848 Text en Copyright © 2021 Picchianti Diamanti, Rosado, Nicastri, Sesti, Pioli and Laganà https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Picchianti Diamanti, Andrea
Rosado, Maria Manuela
Nicastri, Emanuele
Sesti, Giorgio
Pioli, Claudio
Laganà, Bruno
Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines
title Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines
title_full Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines
title_fullStr Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines
title_full_unstemmed Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines
title_short Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Autoimmunity 1 Year Later: The Era of Vaccines
title_sort severe acute respiratory syndrome coronavirus-2 infection and autoimmunity 1 year later: the era of vaccines
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515900/
https://www.ncbi.nlm.nih.gov/pubmed/34659200
http://dx.doi.org/10.3389/fimmu.2021.708848
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