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CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity

Heat shock proteins (HSPs) have been known for decades for their ability to protect cells under stressful conditions. In the 1980s a new role was ascribed for several HSPs given their ability to elicit specific immune responses in the setting of cancer and infectious disease. These immune responses...

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Detalles Bibliográficos
Autores principales: Binder, Robert J., Zhou, Yu Jerry, Messmer, Michelle N., Pawaria, Sudesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507052/
https://www.ncbi.nlm.nih.gov/pubmed/23209886
http://dx.doi.org/10.1155/2012/863041
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author Binder, Robert J.
Zhou, Yu Jerry
Messmer, Michelle N.
Pawaria, Sudesh
author_facet Binder, Robert J.
Zhou, Yu Jerry
Messmer, Michelle N.
Pawaria, Sudesh
author_sort Binder, Robert J.
collection PubMed
description Heat shock proteins (HSPs) have been known for decades for their ability to protect cells under stressful conditions. In the 1980s a new role was ascribed for several HSPs given their ability to elicit specific immune responses in the setting of cancer and infectious disease. These immune responses have primarily been harnessed for the immunotherapy of cancer in the clinical setting. However, because of the ability of HSPs to prime diverse immune responses, they have also been used for modulation of immune responses during autoimmunity. The apparent dichotomy of immune responses elicited by HSPs is discussed here on a molecular and cellular level. The potential clinical application of HSP-mediated immune responses for therapy of autoimmune diseases is reviewed.
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spelling pubmed-35070522012-12-03 CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity Binder, Robert J. Zhou, Yu Jerry Messmer, Michelle N. Pawaria, Sudesh Autoimmune Dis Review Article Heat shock proteins (HSPs) have been known for decades for their ability to protect cells under stressful conditions. In the 1980s a new role was ascribed for several HSPs given their ability to elicit specific immune responses in the setting of cancer and infectious disease. These immune responses have primarily been harnessed for the immunotherapy of cancer in the clinical setting. However, because of the ability of HSPs to prime diverse immune responses, they have also been used for modulation of immune responses during autoimmunity. The apparent dichotomy of immune responses elicited by HSPs is discussed here on a molecular and cellular level. The potential clinical application of HSP-mediated immune responses for therapy of autoimmune diseases is reviewed. Hindawi Publishing Corporation 2012 2012-11-19 /pmc/articles/PMC3507052/ /pubmed/23209886 http://dx.doi.org/10.1155/2012/863041 Text en Copyright © 2012 Robert J. Binder et al. 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
Binder, Robert J.
Zhou, Yu Jerry
Messmer, Michelle N.
Pawaria, Sudesh
CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity
title CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity
title_full CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity
title_fullStr CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity
title_full_unstemmed CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity
title_short CD91-Dependent Modulation of Immune Responses by Heat Shock Proteins: A Role in Autoimmunity
title_sort cd91-dependent modulation of immune responses by heat shock proteins: a role in autoimmunity
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507052/
https://www.ncbi.nlm.nih.gov/pubmed/23209886
http://dx.doi.org/10.1155/2012/863041
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