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Vaccines, adjuvants and autoimmunity

Vaccines and autoimmunity are linked fields. Vaccine efficacy is based on whether host immune response against an antigen can elicit a memory T-cell response over time. Although the described side effects thus far have been mostly transient and acute, vaccines are able to elicit the immune system to...

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Autores principales: Guimarães, Luísa Eça, Baker, Britain, Perricone, Carlo, Shoenfeld, Yehuda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129276/
https://www.ncbi.nlm.nih.gov/pubmed/26275795
http://dx.doi.org/10.1016/j.phrs.2015.08.003
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author Guimarães, Luísa Eça
Baker, Britain
Perricone, Carlo
Shoenfeld, Yehuda
author_facet Guimarães, Luísa Eça
Baker, Britain
Perricone, Carlo
Shoenfeld, Yehuda
author_sort Guimarães, Luísa Eça
collection PubMed
description Vaccines and autoimmunity are linked fields. Vaccine efficacy is based on whether host immune response against an antigen can elicit a memory T-cell response over time. Although the described side effects thus far have been mostly transient and acute, vaccines are able to elicit the immune system towards an autoimmune reaction. The diagnosis of a definite autoimmune disease and the occurrence of fatal outcome post-vaccination have been less frequently reported. Since vaccines are given to previously healthy hosts, who may have never developed the disease had they not been immunized, adverse events should be carefully accessed and evaluated even if they represent a limited number of occurrences. In this review of the literature, there is evidence of vaccine-induced autoimmunity and adjuvant-induced autoimmunity in both experimental models as well as human patients. Adjuvants and infectious agents may exert their immune-enhancing effects through various functional activities, encompassed by the adjuvant effect. These mechanisms are shared by different conditions triggered by adjuvants leading to the autoimmune/inflammatory syndrome induced by adjuvants (ASIA syndrome). In conclusion, there are several case reports of autoimmune diseases following vaccines, however, due to the limited number of cases, the different classifications of symptoms and the long latency period of the diseases, every attempt for an epidemiological study has so far failed to deliver a connection. Despite this, efforts to unveil the connection between the triggering of the immune system by adjuvants and the development of autoimmune conditions should be undertaken. Vaccinomics is a field that may bring to light novel customized, personalized treatment approaches in the future.
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spelling pubmed-71292762020-04-08 Vaccines, adjuvants and autoimmunity Guimarães, Luísa Eça Baker, Britain Perricone, Carlo Shoenfeld, Yehuda Pharmacol Res Article Vaccines and autoimmunity are linked fields. Vaccine efficacy is based on whether host immune response against an antigen can elicit a memory T-cell response over time. Although the described side effects thus far have been mostly transient and acute, vaccines are able to elicit the immune system towards an autoimmune reaction. The diagnosis of a definite autoimmune disease and the occurrence of fatal outcome post-vaccination have been less frequently reported. Since vaccines are given to previously healthy hosts, who may have never developed the disease had they not been immunized, adverse events should be carefully accessed and evaluated even if they represent a limited number of occurrences. In this review of the literature, there is evidence of vaccine-induced autoimmunity and adjuvant-induced autoimmunity in both experimental models as well as human patients. Adjuvants and infectious agents may exert their immune-enhancing effects through various functional activities, encompassed by the adjuvant effect. These mechanisms are shared by different conditions triggered by adjuvants leading to the autoimmune/inflammatory syndrome induced by adjuvants (ASIA syndrome). In conclusion, there are several case reports of autoimmune diseases following vaccines, however, due to the limited number of cases, the different classifications of symptoms and the long latency period of the diseases, every attempt for an epidemiological study has so far failed to deliver a connection. Despite this, efforts to unveil the connection between the triggering of the immune system by adjuvants and the development of autoimmune conditions should be undertaken. Vaccinomics is a field that may bring to light novel customized, personalized treatment approaches in the future. Elsevier Ltd. 2015-10 2015-08-12 /pmc/articles/PMC7129276/ /pubmed/26275795 http://dx.doi.org/10.1016/j.phrs.2015.08.003 Text en Copyright © 2015 Elsevier Ltd. 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
Guimarães, Luísa Eça
Baker, Britain
Perricone, Carlo
Shoenfeld, Yehuda
Vaccines, adjuvants and autoimmunity
title Vaccines, adjuvants and autoimmunity
title_full Vaccines, adjuvants and autoimmunity
title_fullStr Vaccines, adjuvants and autoimmunity
title_full_unstemmed Vaccines, adjuvants and autoimmunity
title_short Vaccines, adjuvants and autoimmunity
title_sort vaccines, adjuvants and autoimmunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129276/
https://www.ncbi.nlm.nih.gov/pubmed/26275795
http://dx.doi.org/10.1016/j.phrs.2015.08.003
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