Abstract
Transmissible spongiform encephalopathies (TSE) are a group of rare neurodegenerative diseases that affect humans and animals. There is compelling evidence that variant Creutzfeldt-Jakob disease (vCJD) in humans results from the consumption of cattle affected by bovine spongiform encephalopathy (BSE) [2]. Although there is no reported case of transmittance of vCJD by blood or blood products, this theoretical risk has not yet been ruled out.A pre-symptomatic test, which would assess the potential threat to public health, is still lacking. In this study we used a new ELISA which detects IgG against prionins, a possible new serum marker for TSEs. Prionins are species-specific proteins, encoded from genes within the prion genes (Fig. 1).
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Budka H. Prions and transfusion medicine. Vox Sang, 2000; 78: 231–238
Collinge J. Variant Creutzfeldt-Jakob disease. Lancet, 1999; 354: 317–324
Kaneko K. et al. Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation. Proc Natl Acad Sci, 1997; 94: 10069
Korth C. et al. Prion (PrPsc)-specific epitope defined by a monoclonal antibody. Nature, 1997; 74–78
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© 2004 Springer-Verlag Berlin Heidelberg
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Schön, A., Bergmann, J., Kühnl, P., Gutensohn, K. (2004). Anti-Prionin IgG, Possible new Serum Markers for Contact and Infection with Transmissible Spongiform Encephalopathies: Preliminary Results from Screening 100 Blood Donors. In: Scharrer, I., Schramm, W. (eds) 33rd Hemophilia Symposium. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-18260-0_20
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DOI: https://doi.org/10.1007/978-3-642-18260-0_20
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-00902-3
Online ISBN: 978-3-642-18260-0
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