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Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases

Systemic autoimmune and rheumatic diseases (SAIRDs) are thought to develop due to the failure of autoimmune regulation and tolerance. Current therapies, such as biologics, have improved the clinical results of SAIRDs; however, they are not curative treatments. Recently, new discoveries have been mad...

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Detalles Bibliográficos
Autores principales: Takakubo, Yuya, Konttinen, Yrjö T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207139/
https://www.ncbi.nlm.nih.gov/pubmed/22110541
http://dx.doi.org/10.1155/2012/941346
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author Takakubo, Yuya
Konttinen, Yrjö T.
author_facet Takakubo, Yuya
Konttinen, Yrjö T.
author_sort Takakubo, Yuya
collection PubMed
description Systemic autoimmune and rheumatic diseases (SAIRDs) are thought to develop due to the failure of autoimmune regulation and tolerance. Current therapies, such as biologics, have improved the clinical results of SAIRDs; however, they are not curative treatments. Recently, new discoveries have been made in immune tolerance and inflammation, such as tolerogenic dendritic cells, regulatory T and B cells, Th 17 cells, inflammatory and tolerogenic cytokines, and intracellular signaling pathways. They lay the foundation for the next generation of the therapies beyond the currently used biologic therapies. New drugs should target the core processes involved in disease mechanisms with the aim to attain complete cure combined with safety and low costs compared to the biologic agents. Re-establishment of autoimmune regulation and tolerance in SAIRDs by the end of the current decade should be the final and realistic target.
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spelling pubmed-32071392011-11-22 Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases Takakubo, Yuya Konttinen, Yrjö T. Clin Dev Immunol Review Article Systemic autoimmune and rheumatic diseases (SAIRDs) are thought to develop due to the failure of autoimmune regulation and tolerance. Current therapies, such as biologics, have improved the clinical results of SAIRDs; however, they are not curative treatments. Recently, new discoveries have been made in immune tolerance and inflammation, such as tolerogenic dendritic cells, regulatory T and B cells, Th 17 cells, inflammatory and tolerogenic cytokines, and intracellular signaling pathways. They lay the foundation for the next generation of the therapies beyond the currently used biologic therapies. New drugs should target the core processes involved in disease mechanisms with the aim to attain complete cure combined with safety and low costs compared to the biologic agents. Re-establishment of autoimmune regulation and tolerance in SAIRDs by the end of the current decade should be the final and realistic target. Hindawi Publishing Corporation 2012 2011-10-27 /pmc/articles/PMC3207139/ /pubmed/22110541 http://dx.doi.org/10.1155/2012/941346 Text en Copyright © 2012 Y. Takakubo and Y. T. Konttinen. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Takakubo, Yuya
Konttinen, Yrjö T.
Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases
title Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases
title_full Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases
title_fullStr Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases
title_full_unstemmed Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases
title_short Immune-Regulatory Mechanisms in Systemic Autoimmune and Rheumatic Diseases
title_sort immune-regulatory mechanisms in systemic autoimmune and rheumatic diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207139/
https://www.ncbi.nlm.nih.gov/pubmed/22110541
http://dx.doi.org/10.1155/2012/941346
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