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Variant CJD: 18 years of research and surveillance

It is now 18 years since the first identification of a case of vCJD in the UK. Since that time, there has been much speculation over how vCJD might impact human health. To date there have been 177 case reports in the UK and a further 51 cases worldwide in 11 different countries. Since establishing t...

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Autores principales: Diack, Abigail B, Head, Mark W, McCutcheon, Sandra, Boyle, Aileen, Knight, Richard, Ironside, James W, Manson, Jean C, Will, Robert G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601215/
https://www.ncbi.nlm.nih.gov/pubmed/25495404
http://dx.doi.org/10.4161/pri.29237
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author Diack, Abigail B
Head, Mark W
McCutcheon, Sandra
Boyle, Aileen
Knight, Richard
Ironside, James W
Manson, Jean C
Will, Robert G
author_facet Diack, Abigail B
Head, Mark W
McCutcheon, Sandra
Boyle, Aileen
Knight, Richard
Ironside, James W
Manson, Jean C
Will, Robert G
author_sort Diack, Abigail B
collection PubMed
description It is now 18 years since the first identification of a case of vCJD in the UK. Since that time, there has been much speculation over how vCJD might impact human health. To date there have been 177 case reports in the UK and a further 51 cases worldwide in 11 different countries. Since establishing that BSE and vCJD are of the same strain of agent, we have also shown that there is broad similarity between UK and non-UK vCJD cases on first passage to mice. Transgenic mouse studies have indicated that all codon 129 genotypes are susceptible to vCJD and that genotype may influence whether disease appears in a clinical or asymptomatic form, supported by the appearance of the first case of potential asymptomatic vCJD infection in a PRNP 129MV patient. Following evidence of blood transfusion as a route of transmission, we have ascertained that all blood components and leucoreduced blood in a sheep model of vCJD have the ability to transmit disease. Importantly, we recently established that a PRNP 129MV patient blood recipient with an asymptomatic infection and limited PrP(Sc) deposition in the spleen could readily transmit disease into mice, demonstrating the potential for peripheral infection in the absence of clinical disease. This, along with the recent appendix survey which identified 16 positive appendices in a study of 32 441 cases, underlines the importance of continued CJD surveillance and maintaining control measures already in place to protect human health.
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spelling pubmed-46012152015-11-01 Variant CJD: 18 years of research and surveillance Diack, Abigail B Head, Mark W McCutcheon, Sandra Boyle, Aileen Knight, Richard Ironside, James W Manson, Jean C Will, Robert G Prion Review It is now 18 years since the first identification of a case of vCJD in the UK. Since that time, there has been much speculation over how vCJD might impact human health. To date there have been 177 case reports in the UK and a further 51 cases worldwide in 11 different countries. Since establishing that BSE and vCJD are of the same strain of agent, we have also shown that there is broad similarity between UK and non-UK vCJD cases on first passage to mice. Transgenic mouse studies have indicated that all codon 129 genotypes are susceptible to vCJD and that genotype may influence whether disease appears in a clinical or asymptomatic form, supported by the appearance of the first case of potential asymptomatic vCJD infection in a PRNP 129MV patient. Following evidence of blood transfusion as a route of transmission, we have ascertained that all blood components and leucoreduced blood in a sheep model of vCJD have the ability to transmit disease. Importantly, we recently established that a PRNP 129MV patient blood recipient with an asymptomatic infection and limited PrP(Sc) deposition in the spleen could readily transmit disease into mice, demonstrating the potential for peripheral infection in the absence of clinical disease. This, along with the recent appendix survey which identified 16 positive appendices in a study of 32 441 cases, underlines the importance of continued CJD surveillance and maintaining control measures already in place to protect human health. Taylor & Francis 2014-11-01 /pmc/articles/PMC4601215/ /pubmed/25495404 http://dx.doi.org/10.4161/pri.29237 Text en © 2014 The Author(s). Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Review
Diack, Abigail B
Head, Mark W
McCutcheon, Sandra
Boyle, Aileen
Knight, Richard
Ironside, James W
Manson, Jean C
Will, Robert G
Variant CJD: 18 years of research and surveillance
title Variant CJD: 18 years of research and surveillance
title_full Variant CJD: 18 years of research and surveillance
title_fullStr Variant CJD: 18 years of research and surveillance
title_full_unstemmed Variant CJD: 18 years of research and surveillance
title_short Variant CJD: 18 years of research and surveillance
title_sort variant cjd: 18 years of research and surveillance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601215/
https://www.ncbi.nlm.nih.gov/pubmed/25495404
http://dx.doi.org/10.4161/pri.29237
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