z-logo
Premium
Evaluation of a test for its suitability in the diagnosis of variant C reutzfeldt– J akob disease
Author(s) -
Cooper J. K.,
Andrews N.,
Ladhani K.,
Bujaki E.,
Minor P. D.
Publication year - 2013
Publication title -
vox sanguinis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.68
H-Index - 83
eISSN - 1423-0410
pISSN - 0042-9007
DOI - 10.1111/vox.12037
Subject(s) - bovine spongiform encephalopathy , medicine , disease , virology , whole blood , transmission (telecommunications) , blood transfusion , diagnostic test , scrapie , prion protein , emergency medicine , electrical engineering , engineering
Background and Objectives Evaluation of variant C reutzfeldt– J akob disease ( vCJD ) diagnostic/donor screening tests is made complicated by the very limited supply of blood samples from clinically confirmed cases of vCJD . To determine appropriate access for test developers to rare C reutzfeldt– J akob disease ( CJD ) blood samples, the oversight committee of the NIBSC CJD Resource Centre has developed a process and protocols detailing minimum requirements for both test sensitivity and specificity. This protocol is broadly similar to that outlined in the common technical specification (European Directive 98/79/EC). Materials and Methods Tests are subjected to a stepwise evaluation (step 1). vCJD tissue homogenates spiked into pooled human plasma (step 2). Blood samples from animals known to be incubating (Transmissible spongiform encephalopathy) TSE disease (scrapie/Bovine Spongiform encephalopathy (BSE)‐infected sheep, BSE‐infected primates) and appropriate controls (step 3). Fresh or frozen plasma from normal UK blood donors and (step 4). Plasma samples from individuals with confirmed clinical stage variant CJD (transfusion transmission) or sporadic CJD (no evidence of blood transmission). Results The assay evaluated performed with good sensitivity with vCJD ‐spiked tissue homogenates, poor sensitivity for ovine TSE ‐infected blood samples and failed with plasma from BSE ‐infected non‐human primates and with true vCJD clinical samples. Conclusions The test evaluated here is currently unsuitable for use in blood donor screening or diagnosis using blood.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here