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The neuropathology of kuru and variant Creutzfeldt–Jakob disease
A comparison of the pathological profiles of two spongiform encephalopathies with a similar presumptive route of infection was performed. Archival kuru and recent variant Creutzfeldt–Jakob disease (vCJD) cases reveal distinct lesional differences, particularly with respect to prion protein, suggesti...
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Formato: | Texto |
Lenguaje: | English |
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The Royal Society
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735511/ https://www.ncbi.nlm.nih.gov/pubmed/18849282 http://dx.doi.org/10.1098/rstb.2008.0086 |
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author | McLean, Catriona A. |
author_facet | McLean, Catriona A. |
author_sort | McLean, Catriona A. |
collection | PubMed |
description | A comparison of the pathological profiles of two spongiform encephalopathies with a similar presumptive route of infection was performed. Archival kuru and recent variant Creutzfeldt–Jakob disease (vCJD) cases reveal distinct lesional differences, particularly with respect to prion protein, suggesting that the strain of agent is important in determining the phenotype. Genotype analysis of the polymorphism on codon 129 reveals (in conjunction with updated information from more kuru cases) that all three genotypes (VV, MV and MM (where M is methionine and V is valine)) are detected in kuru with some preference for MM homozygosity. The presence of valine does not therefore appear to determine peripheral selection of PrP(CJD). vCJD remains restricted to date to MM homozygosity on codon 129. It remains to be determined whether this genotype is dictating a shorter incubation period. |
format | Text |
id | pubmed-2735511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-27355112009-09-21 The neuropathology of kuru and variant Creutzfeldt–Jakob disease McLean, Catriona A. Philos Trans R Soc Lond B Biol Sci Review A comparison of the pathological profiles of two spongiform encephalopathies with a similar presumptive route of infection was performed. Archival kuru and recent variant Creutzfeldt–Jakob disease (vCJD) cases reveal distinct lesional differences, particularly with respect to prion protein, suggesting that the strain of agent is important in determining the phenotype. Genotype analysis of the polymorphism on codon 129 reveals (in conjunction with updated information from more kuru cases) that all three genotypes (VV, MV and MM (where M is methionine and V is valine)) are detected in kuru with some preference for MM homozygosity. The presence of valine does not therefore appear to determine peripheral selection of PrP(CJD). vCJD remains restricted to date to MM homozygosity on codon 129. It remains to be determined whether this genotype is dictating a shorter incubation period. The Royal Society 2008-11-27 /pmc/articles/PMC2735511/ /pubmed/18849282 http://dx.doi.org/10.1098/rstb.2008.0086 Text en Copyright © 2008 The Royal Society http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review McLean, Catriona A. The neuropathology of kuru and variant Creutzfeldt–Jakob disease |
title | The neuropathology of kuru and variant Creutzfeldt–Jakob disease |
title_full | The neuropathology of kuru and variant Creutzfeldt–Jakob disease |
title_fullStr | The neuropathology of kuru and variant Creutzfeldt–Jakob disease |
title_full_unstemmed | The neuropathology of kuru and variant Creutzfeldt–Jakob disease |
title_short | The neuropathology of kuru and variant Creutzfeldt–Jakob disease |
title_sort | neuropathology of kuru and variant creutzfeldt–jakob disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735511/ https://www.ncbi.nlm.nih.gov/pubmed/18849282 http://dx.doi.org/10.1098/rstb.2008.0086 |
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