Improved conformation-dependent immunoassay:: suitability for human prion detection with enhanced sensitivity

被引:75
作者
Bellon, A
Seyfert-Brandt, W
Lang, W
Baron, H
Gröner, A
Vey, M
机构
[1] Aventis Behring GmbH, Virol, D-35002 Marburg, Germany
[2] Aventis Behring SA, Ind & Hlth Policy, F-75601 Paris 12, France
关键词
D O I
10.1099/vir.0.18996-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The presence of pathogenic prion protein (PrPSc) in lymphoid tissues of variant Creutzfeldt-Jakob disease (vCJD) patients raises questions as to whether prions may be present in bodily fluids as well. Currently, transgenic mice are highly sensitive in vivo tools for the study of prions in tissues or fluids containing high levels of normal prion protein (PrPC). We report here an in vitro assay with virtually equivalent sensitivity incorporating a capture antibody into a sandwich conformation-dependent immunoassay (CDl), resulting in 30- to 100-fold increased sensitivity compared with the original, direct CDl. Furthermore, spiking plasma with vCJD prions in different preparations demonstrated that sandwich CDl detects prions with different biophysical properties at high sensitivity, even without proteinase K pretreatment of samples. Thus, sandwich CDl represents a powerful tool to study prions in bodily fluids of CJD/vCJD patients, with a turnaround time of less than 24 h.
引用
收藏
页码:1921 / 1925
页数:5
相关论文
共 18 条
[1]  
BARON H, 2000, BIOL SAFETY PRINCIPL, P187
[2]   ISOLATION AND STRUCTURAL STUDIES OF THE INTACT SCRAPIE AGENT PROTEIN [J].
BOLTON, DC ;
BENDHEIM, PE ;
MARMORSTEIN, AD ;
POTEMPSKA, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 258 (02) :579-590
[3]   HUMAN SPONGIFORM ENCEPHALOPATHY - THE NATIONAL-INSTITUTES-OF-HEALTH SERIES OF 300 CASES OF EXPERIMENTALLY TRANSMITTED DISEASE [J].
BROWN, P ;
GIBBS, CJ ;
RODGERSJOHNSON, P ;
ASHER, DM ;
SULIMA, MP ;
BACOTE, A ;
GOLDFARB, LG ;
GAJDUSEK, DC .
ANNALS OF NEUROLOGY, 1994, 35 (05) :513-529
[4]   The distribution of infectivity in blood components and plasma derivatives in experimental models of transmissible spongiform encephalopathy [J].
Brown, P ;
Rohwer, RG ;
Dunstan, BC ;
MacAuley, C ;
Gajdusek, DC ;
Drohan, WN .
TRANSFUSION, 1998, 38 (09) :810-816
[5]   Detection of variant Creutzfeld-Jakob disease infectivity in extraneural tissues [J].
Bruce, ME ;
McConnell, I ;
Will, RG ;
Ironside, JW .
LANCET, 2001, 358 (9277) :208-209
[6]   The safety of human blood: experimental TSE/prion infectivity studies [J].
Cervenakova, L .
TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2001, 8 (03) :260-260
[7]   Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy [J].
Hill, AF ;
Zeidler, M ;
Ironside, J ;
Collinge, J .
LANCET, 1997, 349 (9045) :99-100
[8]   Transmission of BSE by blood transfusion in sheep [J].
Houston, F ;
Foster, JD ;
Chong, A ;
Hunter, N ;
Bostock, CJ .
LANCET, 2000, 356 (9234) :999-1000
[9]   Transmission of prion diseases by blood transfusion [J].
Hunter, N ;
Foster, J ;
Chong, A ;
McCutcheon, S ;
Parnham, D ;
Eaton, S ;
MacKenzie, C ;
Houston, F .
JOURNAL OF GENERAL VIROLOGY, 2002, 83 :2897-2905
[10]   Identification of an epitope in the C terminus of normal prion protein whose expression is modulated by binding events in the N terminus [J].
Li, RL ;
Liu, T ;
Wong, BS ;
Pan, T ;
Morillas, M ;
Swietnicki, W ;
O'Rourke, K ;
Gambetti, P ;
Surewicz, WK ;
Sy, MS .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 301 (03) :567-573