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David A Hilton a Department of Histopathology, Derriford
Hospital, Plymouth PL6 8DH, b Department of Infectious Disease Epidemiology, Faculty of
Medicine, Imperial College of Science, Technology and Medicine, London
SW7 2AZ, c National CJD Surveillance Unit, University of Edinburgh,
Edinburgh EH4 2XU Correspondence to: D A Hilton
david.hilton@phnt.swest.nhs.uk
| The first 150 words of the full text of this article appear below. |
Variant Creutzfeldt-Jakob disease is almost certainly
caused by the bovine spongiform encephalopathy agent, and although the disease is rare (115 deaths to date) there is uncertainty about future
numbers of cases.1 The lack of a conventional immune response and the inability to detect abnormal prion protein in blood
has hampered the development of a blood test.1
Lymphoreticular accumulation of prion protein has been used as a
preclinical test for scrapie (the form of the disease in sheep and
goats) and is a consistent feature of variant Creutzfeldt-Jakob
disease, occurring before the onset of symptoms.2-4 We
screened large numbers of specimens from appendicectomies and
tonsillectomies for the presence of prion protein in lymphoreticular
tissue to determine the number of people with preclinical variant
Creutzfeldt-Jakob disease.
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Methods and results |
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We retrieved appendix and tonsil samples removed between
1995 and 1999 from patients aged 10-50 from histopathology departments across the United Kingdom. The samples were anonymised before testing.
We also
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