An emerald ribbon hangs from her lips. A coy smile circles the corners of her mouth. She stares out of the fogged-up window and into the cosy gloom the Autumn rain gives her. She hugs her knees close to her chest and sighs. She believes she is happiest alone. Finally the trees close around her.
09 March 2014
Variant Creutzfeldt-Jakob disease (vCJD) is a rare and invariably fatal brain-wasting condition. It’s the human form of bovine spongiform encephalopathy (BSE), commonly known as ‘mad-cow disease’. At the root of both diseases are prion proteins – misfolded proteins that coax other proteins to misfold as well. This self-amplifying process results in an accumulation of toxic protein clumps (the large, fibrous blobs seen here) that destroy neurons. A BSE outbreak in the 1980s led to a surge of vCJD cases in the UK, and a recent study found that 1 in every 2,000 people there carries the disease-causing prion protein. But that doesn’t necessarily mean they will develop vCJD, because prion proteins were only found in the lymphoid system – including the spleen and tonsils – which is more easily infected than the brain. Nevertheless, scientists will be watching closely as it’s still not clear if the infection can spread from the lymphoid system.
Written by Daniel Cossins
Image courtesy of Theresa Hammett
Public Health Image Library
This image is in the public domain and can be freely reused
Research published in Biomedical Journal, October 2013