| Reference : Immunoquantitative PCR for prion protein detection in sporadic Creutzfeldt-Jakob disease. |
| Scientific journals : Article | |||
| Human health sciences : Laboratory medicine & medical technology Life sciences : Biochemistry, biophysics & molecular biology Life sciences : Anatomy (cytology, histology, embryology...) & physiology | |||
| http://hdl.handle.net/2268/3465 | |||
| Immunoquantitative PCR for prion protein detection in sporadic Creutzfeldt-Jakob disease. | |
| English | |
Gofflot, Stéphanie [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Anatomie et cytologie pathologiques >] | |
Deprez, Manuel [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Anatomie et cytologie pathologiques >] | |
Elmoualij, Benaïssa [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Histologie humaine >] | |
| Osman, Awad [> > > >] | |
Thonnart, Jean-François [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Histologie humaine >] | |
Hougrand, Olivier [Centre Hospitalier Universitaire de Liège - CHU > > Anatomie pathologique >] | |
Heinen, Ernst [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Histologie humaine >] | |
Zorzi, Willy [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Histologie humaine - Département des sciences biomédicales et précliniques >] | |
| 2005 | |
| Clinical Chemistry | |
| American Association for Clinical Chemistry | |
| 51 | |
| 9 | |
| 1605-11 | |
| International | |
| 0009-9147 | |
| 1530-8561 | |
| Washington | |
| DC | |
| [en] Adolescent ; Aged ; Aged, 80 and over ; Blotting, Western ; Brain Chemistry ; Creutzfeldt-Jakob Syndrome/diagnosis ; Endopeptidase K/metabolism ; Enzyme-Linked Immunosorbent Assay ; Female ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Polymerase Chain Reaction ; Prions/analysis/metabolism ; Sensitivity and Specificity | |
| [en] BACKGROUND: The most common human prion disorder is Creutzfeldt-Jakob disease (CJD); it includes sporadic, familial, iatrogenic, and variant subtypes. Diagnostic tests aim at detection with the highest specificity of very small deposits of abnormal prion protein (PrP). METHODS: We used immunoquantitative PCR (iqPCR) to detect proteinase K-resistant PrP (PrPRes) in tissue from the middle frontal gyrus of 7 patients with sporadic CJD and 7 non-CJD cases. We compared iqPCR with routine optimized ELISA, Western blotting, and immunohistochemical analyses. RESULTS: The 4 methods showed similar 100% sensitivity and specificity for the diagnosis of CJD. Along with high specificity, however, iqPCR had a threshold for PrP(Res) detection at least 10-fold lower than that of the classic ELISA. CONCLUSIONS: iqPCR is a new method for PrPRes detection that combines 100% specificity with a detection threshold at least 10-fold lower than classic techniques. This method may improve the detection of minute PrPRes deposits in tissues and body fluids and thus be useful for diagnostic and sterilization applications. | |
| http://hdl.handle.net/2268/3465 | |
| also: http://hdl.handle.net/2268/26238 | |
| 10.1373/clinchem.2005.050120 |
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