Bovine spongiform encephalopathy (BSE) incidence.
The number of new cases continues to fall as forecast (from the peak of 37 487 in 1992 to 13 825 in 1995, to 7406 in 1996 to 3980 in 1997) and is on track to bring the epidemic to an end.
Findings since 1996 indicate that the agents of BSE and new-variant Creutzfeldt-Jakob disease (nvCJD) possess the same'fingerprint'This is consistent with the transmission of BSE infection to humans.
Although it remains possible that both BSE and nvCJD may have been triggered by some currently unknown cause, it is difficult to conceive what that might be. nvCJD incidence.
The UK Department of Health reported 24 cases of nvCJD up to the 6 April 1998.
Assuming that nvCJD is the result of consumption of BSE infective materials before 1989, it is too soon to draw any conclusions about likely future incidence.
Infectivity of bovine materials.
In its report dated 9 December 1997, the EU Scientific Steering Committee has set out the most up-to-date information and assessment of the infectivities of various bovine materials.
Beef, milk and bones.
Assays in mice have not detected BSE infectivity in muscle meat (beef) or milk from confirmed cases.
The more sensitive assay in calves is yet to be concluded, but to date results are negative.
Thus, although low levels of infectivity cannot be excluded, the risk from beef or milk is currently considered to be extremely small. (...)
Mots-clés Pascal : Encéphalopathie spongiforme, Bétail, Encéphalopathie spongiforme Creutzfeldt Jakob, Infection, Homme, Transmission animal homme, Viande boeuf, Gélatine, Sang, Lait vache, Contamination, Epidémiologie, Réglementation, Lutte sanitaire, Article synthèse, Prion, Système nerveux pathologie, Système nerveux central pathologie, Encéphale pathologie, Maladie dégénérative, Royaume Uni, Europe
Mots-clés Pascal anglais : Spongiform encephalopathy, Livestock, Creutzfeldt Jakob disease, Infection, Human, Transmission from animal to man, Beef, Gelatin, Blood, Cow milk, Contamination, Epidemiology, Regulation, Sanitary control, Review, Prion, Nervous system diseases, Central nervous system disease, Cerebral disorder, Degenerative disease, United Kingdom, Europe
Notice produite par :
Inist-CNRS - Institut de l'Information Scientifique et Technique
Cote : 99-0157340
Code Inist : 002B17G. Création : 16/11/1999.