vCJD's Long Incubation Period Could Mean Many People May Be Infected
Main Category: CJD / vCJD / Mad Cow DiseaseArticle Date: 27 Mar 2006 - 3:00 PDT
| Patient / Public: | ![]() |
2.83 (12 votes) |
| Healthcare Prof: | ![]() |
3 (2 votes) |
| Article Opinions: | 1 posts |
According to an article published online today (Monday March 27, 2006) by The Lancet Neurology, all individuals could be susceptible to transmission of variant Creutzfeldt-Jakob disease (vCJD) through routes such as blood transfusion, and, because of long incubation times before onset of symptoms, a significant level of infection might already be present in the population.
Estimates of the extent of the UK epidemic of vCJD have varied greatly with the predicted number of future cases ranging from the low hundreds to hundreds of thousands. Variations and mutations in the prion protein (PrP) gene affect disease susceptibility, although the underlying mechanisms are unknown. Variations at a particular point on the PrP gene--codon 129--can affect the transformation of the PrP into the disease-associated form (PrPSc).
A team of researchers from Edinburgh, UK, led by Professor Jean Manson, have analysed the transmission of BSE and vCJD in four lines of genetically altered (transgenic) mice after they were injected with brain material from cases of vCJD and BSE. Transgenic mice were produced that express the variations found in human PrP gene at codon 129--methionine (MM), methionine/valine (MV), and valine (VV). The team found that vCJD was transmitted to mice with all three genetic variations with different pathological characteristics. Disease transmission occurred most readily with VV mice, followed by MV, and then MM. Furthermore, the long incubation periods during which PrPSc was deposited in the transgenic mice predict that infection could be present in human beings, with all genotypes, for a substantial time before clinical onset of symptoms. The authors conclude: "A lengthy preclinical disease is predicted by these models, which may represent a risk for further disease transmission and thus a significant public-health issue."
In an accompanying Reflection and Reaction article, Corinne Lasmézas comments that although a small number of VV individuals could become asymptomatic carriers, since only 10% of the population carries two V alles the impact of this partly reassuring finding is reduced.
The Reflection and Reaction article states that 40% of the Caucasian human population has the MM genetic variation, 10% VV, and 50% MV.
Joe Santangelo
Lancet
http://www.thelancet.com
Visit our cjd / vcjd / mad cow disease section for the latest news on this subject.
MLA
16 Feb. 2012. <http://www.medicalnewstoday.com/releases/40332.php>
APA
http://www.medicalnewstoday.com/releases/40332.php.
Please note: If no author information is provided, the source is cited instead.
|
Rate this article: (Hover over the stars then click to rate) |
Patient / Public: |
or |
Health Professional: |
Visitor Opinions In Chronological Order (1)
How Can We Know?
posted by Anon. on 15 Aug 2008 at 7:06 pmI'm seriously confused about all this I've recently decided to donate plasma and have been told that I cannot because of being in Germany on a military base for over 6 months in 1983. Though I now understand as to why it would affect things. I still don't know how we can find out if we truly area carrier and what can be done about it if we are.
Add Your Opinion
Please note that we publish your name, but we do not publish your email address. It is only used to let you know when your message is published. We do not use it for any other purpose. Please see our privacy policy for more information.
If you write about specific medications or operations, please do not name health care professionals by name.
All opinions are moderated before being included (to stop spam)
Contact Our News Editors
For any corrections of factual information, or to contact the editors please use our feedback form.
![]()
Please send any medical news or health news press releases to:
Note: Any medical information published on this website is not intended as a substitute for informed medical advice and you should not take any action before consulting with a health care professional. For more information, please read our terms and conditions.



