A French study of prion transmission between species has shown that the misfolded protein structures that are the cause for Mad Cow Disease make interspecies and human-to-human communications more readily than previously known. Autopsies on brains to determine if the disease was communicated does not necessarily indicate if the disease had been broadcast to organs it might lurk in. Perhaps the blood-brain barrier had protected brains better than in the remainder of the body. In the French investigation the prions were transmitted successfully 26 of 41 times to organs rather than being a minority occurrence in the brains of the targets.
http://www.physorg.com/news/2012-01-prions-species-easily-thought.html
In Britain as many as 1 in 4000 people may be media for PrPSc prion transmission according to samples of appendixes of the populous. Evidently the prions find lymphoid tissue a friendlier ecosystem than brain tissue.
In Humans the disease is called Creutzfeldt-Jakob Disease. The disease causes a rotting of the brain resembling ordinary dementia or an over-abundance of concussions.
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