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Immunotherapy against Prion Disease

The term “prion disease” encompasses a group of neurodegenerative diseases affecting both humans and animals. Currently, there is no effective therapy and all forms of prion disease are invariably fatal. Because of (a) the outbreak of bovine spongiform encephalopathy in cattle and variant Creutzfeld...

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Detalles Bibliográficos
Autores principales: Ma, Yue, Ma, Jiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157205/
https://www.ncbi.nlm.nih.gov/pubmed/32183309
http://dx.doi.org/10.3390/pathogens9030216
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author Ma, Yue
Ma, Jiyan
author_facet Ma, Yue
Ma, Jiyan
author_sort Ma, Yue
collection PubMed
description The term “prion disease” encompasses a group of neurodegenerative diseases affecting both humans and animals. Currently, there is no effective therapy and all forms of prion disease are invariably fatal. Because of (a) the outbreak of bovine spongiform encephalopathy in cattle and variant Creutzfeldt–Jakob disease in humans; (b) the heated debate about the prion hypothesis; and (c) the availability of a natural prion disease in rodents, the understanding of the pathogenic process in prion disease is much more advanced compared to that of other neurodegenerative disorders, which inspired many attempts to develop therapeutic strategies against these fatal diseases. In this review, we focus on immunotherapy against prion disease. We explain our rationale for immunotherapy as a plausible therapeutic choice, review previous trials using either active or passive immunization, and discuss potential strategies for overcoming the hurdles in developing a successful immunotherapy. We propose that immunotherapy is a plausible and practical therapeutic strategy and advocate more studies in this area to develop effective measures to control and treat these devastating disorders.
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spelling pubmed-71572052020-05-01 Immunotherapy against Prion Disease Ma, Yue Ma, Jiyan Pathogens Review The term “prion disease” encompasses a group of neurodegenerative diseases affecting both humans and animals. Currently, there is no effective therapy and all forms of prion disease are invariably fatal. Because of (a) the outbreak of bovine spongiform encephalopathy in cattle and variant Creutzfeldt–Jakob disease in humans; (b) the heated debate about the prion hypothesis; and (c) the availability of a natural prion disease in rodents, the understanding of the pathogenic process in prion disease is much more advanced compared to that of other neurodegenerative disorders, which inspired many attempts to develop therapeutic strategies against these fatal diseases. In this review, we focus on immunotherapy against prion disease. We explain our rationale for immunotherapy as a plausible therapeutic choice, review previous trials using either active or passive immunization, and discuss potential strategies for overcoming the hurdles in developing a successful immunotherapy. We propose that immunotherapy is a plausible and practical therapeutic strategy and advocate more studies in this area to develop effective measures to control and treat these devastating disorders. MDPI 2020-03-14 /pmc/articles/PMC7157205/ /pubmed/32183309 http://dx.doi.org/10.3390/pathogens9030216 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ma, Yue
Ma, Jiyan
Immunotherapy against Prion Disease
title Immunotherapy against Prion Disease
title_full Immunotherapy against Prion Disease
title_fullStr Immunotherapy against Prion Disease
title_full_unstemmed Immunotherapy against Prion Disease
title_short Immunotherapy against Prion Disease
title_sort immunotherapy against prion disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157205/
https://www.ncbi.nlm.nih.gov/pubmed/32183309
http://dx.doi.org/10.3390/pathogens9030216
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