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Vaccination against autoimmune diseases moves closer to the clinic

Biologicals, e.g. TNF inhibitors, have improved dramatically the efficacy of medical interventions in autoimmune diseases, such as in rheumatoid arthritis (RA). However, although progressive inflammation can be halted in this way, no drug-free remissions or lasting cures are reached. For this to bec...

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Autor principal: van Eden, Willem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062450/
https://www.ncbi.nlm.nih.gov/pubmed/30900933
http://dx.doi.org/10.1080/21645515.2019.1593085
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author van Eden, Willem
author_facet van Eden, Willem
author_sort van Eden, Willem
collection PubMed
description Biologicals, e.g. TNF inhibitors, have improved dramatically the efficacy of medical interventions in autoimmune diseases, such as in rheumatoid arthritis (RA). However, although progressive inflammation can be halted in this way, no drug-free remissions or lasting cures are reached. For this to become real, therapies based on induction antigen-specific immune tolerance are sought. This review describes mechanisms of tolerance and the current possibilities for induction of therapeutic tolerance through antigen-specific vaccination approaches. And despite the fact that for various diseases the search for appropriate autoantigens is ongoing, pioneering studies are now already developed that use more broadly inflammation associated antigens. Through their capacity to preferentially induce regulatory T cells, heat shock proteins are an attractive source of such broadly inflammation associated antigens.
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spelling pubmed-70624502020-03-16 Vaccination against autoimmune diseases moves closer to the clinic van Eden, Willem Hum Vaccin Immunother Review Biologicals, e.g. TNF inhibitors, have improved dramatically the efficacy of medical interventions in autoimmune diseases, such as in rheumatoid arthritis (RA). However, although progressive inflammation can be halted in this way, no drug-free remissions or lasting cures are reached. For this to become real, therapies based on induction antigen-specific immune tolerance are sought. This review describes mechanisms of tolerance and the current possibilities for induction of therapeutic tolerance through antigen-specific vaccination approaches. And despite the fact that for various diseases the search for appropriate autoantigens is ongoing, pioneering studies are now already developed that use more broadly inflammation associated antigens. Through their capacity to preferentially induce regulatory T cells, heat shock proteins are an attractive source of such broadly inflammation associated antigens. Taylor & Francis 2019-04-22 /pmc/articles/PMC7062450/ /pubmed/30900933 http://dx.doi.org/10.1080/21645515.2019.1593085 Text en © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Review
van Eden, Willem
Vaccination against autoimmune diseases moves closer to the clinic
title Vaccination against autoimmune diseases moves closer to the clinic
title_full Vaccination against autoimmune diseases moves closer to the clinic
title_fullStr Vaccination against autoimmune diseases moves closer to the clinic
title_full_unstemmed Vaccination against autoimmune diseases moves closer to the clinic
title_short Vaccination against autoimmune diseases moves closer to the clinic
title_sort vaccination against autoimmune diseases moves closer to the clinic
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062450/
https://www.ncbi.nlm.nih.gov/pubmed/30900933
http://dx.doi.org/10.1080/21645515.2019.1593085
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