Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: McLean, Catriona A.
Formato: Texto
Lenguaje:English
Publicado: The Royal Society 2008
Materias:
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
_version_ 1782171254658170880
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
work_keys_str_mv AT mcleancatrionaa theneuropathologyofkuruandvariantcreutzfeldtjakobdisease
AT mcleancatrionaa neuropathologyofkuruandvariantcreutzfeldtjakobdisease