Literature DB >> 15137902

Molecular diagnostic tools in Creutzfeldt-Jakob disease and other prion disorders.

Bart Van Everbroeck1, Jef Boons, Evelyn De Leenheir, Ursula Lübke, Patrick Cras.   

Abstract

Clinical criteria and cerebrospinal fluid biomarkers for the diagnosis of human prion diseases (sporadic, iatrogenic or variant Creutzfeldt-Jakob disease and genetic inherited transmissible spongiform encephalopathies) are now widely available and show a sensitivity and specificity of approximately 98%. Final diagnosis of prion diseases is obtained by post-mortem examination upon identification of the pathological conformer of the prion protein (PrPSc) in the brain. Several diagnostic kits are now available that facilitate the immunochemical measurement of PrPSc. Several new molecular diagnostic techniques, aimed at increasing the sensitivity and specificity of PrPSc detection and at identifying markers of disease other than PrPSc, are the subject of ongoing studies. The aim of these studies is to develop preclinical screening tests for the identification of infected but still healthy individuals. These tests are also essential to investigate the safety of blood or blood-derived products and to ensure meat safety in European countries.

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Year:  2004        PMID: 15137902     DOI: 10.1586/14737159.4.3.351

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  1 in total

1.  Generation of antisera to purified prions in lipid rafts.

Authors:  Robert Hnasko; Ana V Serban; George Carlson; Stanley B Prusiner; Larry H Stanker
Journal:  Prion       Date:  2010-04-09       Impact factor: 3.931

  1 in total

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