TSE Diagnostics: Recent Advances in Immunoassaying Prions

被引:7
作者
Lukan, Anja [1 ]
Vranac, Tanja [1 ]
Serbec, Vladka Curin [1 ]
机构
[1] Blood Transfus Ctr Slovenia, Dept Prod Diagnost Reagents & Res, Ljubljana 1000, Slovenia
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2013年
关键词
CREUTZFELDT-JAKOB-DISEASE; BOVINE SPONGIFORM ENCEPHALOPATHY; LINKED-IMMUNOSORBENT-ASSAY; PROTEINASE K; PRP ACCUMULATION; TRUNCATED FORMS; STEEL-SURFACE; BRAIN-TISSUE; WESTERN-BLOT; SCRAPIE;
D O I
10.1155/2013/360604
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Transmissible spongiform encephalopathies (TSEs) or prion diseases are a group of rare fatal neurodegenerative diseases, affecting humans and animals. They are believed to be the consequence of the conversion of the cellular prion protein to its aggregation-prone, beta-sheet -rich isoform, named prion. Definite diagnosis of TSEs is determined post mortem. For this purpose, immunoassays for analyzing brain tissue have been developed. However, the ultimate goal of TSE diagnostics is an ante mortem test, which would be sensitive enough to detect prions in body fluids, that is, in blood, cerebrospinal fluid, or urine. Such a test would be of paramount importance also for screening of asymptomatic carriers of the disease with the aim of increasing food, drugs, and blood-derived products safety. In the present paper, we have reviewed recent advances in the development of immunoassays for the detection of prions.
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页数:8
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