1)プリオン病及び遅発性ウイルス感染症に関する調査研究班,プリオン病のサーベイランスと感染予防に関する調査研究班編:プリオン病診療ガイドライン2014
2)Will RG, et al:A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 347:921-925, 1996
3)Shinde A, et al:The first Japanese patient with variant Creutzfeldt-Jakob disease(vCJD). Neuropathology 29(6):713-719, 2009
4)EFSA:Quantitative assessment of the human and animal BSE risk posed by gelatine with respect to residual BSE risk. The EFSA Journal 312:1-29, 2006
5)Llewelyn CA, et al:Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. Lancet 363:417-421, 2004
6)Gill ON, et al:Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic:large scale survey. BMJ 347:f5675, 2013
7)Comoy EE, et al:Atypical BSE(BASE)transmitted from asymptomatic aging cattle to a primate. PLoS One 3(8):e3017, 2008
8)Ono F, et al:Atypical L-type bovine spongiform encephalopathy(L-BSE)transmission to cynomolgus macaques, a non-human primate. Jpn J Infect Dis 64(1):81-84, 2011
9)Capobianco R, et al:Conversion of the BASE prion strain into the BSE strain:the origin of BSE? PLoS Pathog 3(3):e31, 2007
10)Baron T, et al:Emergence of classical BSE strain properties during serial passages of H-BSE in wild-type mice. PLoS One 6(1):e15839, 2011
11)Kong Q, et al:Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. J Virol 82(7):3697-3701, 2008
12)Marsh RF, et al:Epidemiologic and experimental studies on transmissible mink encephalopathy. Dev Biol Stand 80:111-118, 1993
13)Nicholson EM, et al:Identification of a heritable polymorphism in bovine PRNP associated with genetic transmissible spongiform encephalopathy:evidence of heritable BSE. PLoS One 3(8):e2912, 2008