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Transfusion Medicine Reviews
Volume 22, Issue 3
, Pages 234-242
, July 2008
The In Vitro Bioassay Systems for the Amplification and Detection of Abnormal Prion PrPSc in Blood and Tissues
References
- . Variant Creutzfeldt-Jakob disease transmission by plasma products: Assessing and communicating risk in an era of scientific uncertainty. Vox Sang. 2005;89:186–192
- . Approaches to therapy of prion diseases. Annu Rev Med. 2005;56:321–344
- Creutzfeldt-Jakob disease and blood transfusion: Results of the UK Transfusion Medicine Epidemiological Review study. Vox Sang. 2006;91:221–230
- . Verses, viruses, and the vulnerability of the blood supply in industrialized countries. J Med Virol. 2007;79:1229–1237
- . Detection of prions in blood. Nat Med. 2005;11:982–985
- . On the horizon: A blood test for prions. Trends Microbiol. 2006;14:149–151
- . Presymptomatic detection of prions in blood. Science. 2006;313:92–94
- In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrP(Sc). J Pathol. 2007;213:21–26
- Test for detection of disease-associated prion aggregate in the blood of infected but asymptomatic animals. Clin Vaccine Immunol. 2007;14:36–43
- Interaction of scrapie agent and cells of the lymphoreticular system. Arch Virol. 1994;136:255–268
- . Cultured cell sublines highly susceptible to prion infection. J Virol. 2000;74:4377–4386
- Immune system and peripheral nerves in propagation of prions to CNS. Br Med Bull. 2003;66:141–159
- Cultured peripheral neuroglial cells are highly permissive to sheep prion infection. J Virol. 2004;78:482–490
- The cellular prion protein modulates phagocytosis and inflammatory response. J Leukoc Biol. 2005;77:238–246
- Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease. N Engl J Med. 2004;349:1812–1820
- . Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification. J Biol Chem. 2006;281:35245–35252
- . Cyclic amplification of protein misfolding: Application to prion-related disorders and beyond. Trends Neurosci. 2002;25:390–394
- Standards for the assay of Creutzfeldt-Jakob disease specimens. J Gen Virol. 2004;85:1777–1784(Pt 6)
- Health Protection Agency. 4th case of variant CJD infection associated with blood transfusion. http://www.hpa.org.uk/hpa/news/articles/press_releases/2007/070118_vCJD.htm.
- Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. Lancet. 2004;63:417–421
- Recent developments in prion disease research: Diagnostic tools and in vitro cell culture models. J Vet Med Sci. 2007;69:329–337
- . Current and future molecular diagnostics for prion diseases. Expert Rev Mol Diagn. 2006;6:597–611
- Protein misfolding cyclic amplification for diagnosis and prion propagation studies. Methods Enzymol. 2006;412:3–21
- Cationic phosphorus-containing dendrimers reduce prion replication both in cell culture and in mice infected with scrapie. J Gen Virol. 2004;85:1791–1799(Pt 6)
- Proteinase-resistant protein in human neuroblastoma cells infected with brain material from Creutzfeld-Jakob patient. Lancet. 1995;345:594–595
- Two Creutzfeldt-Jakob disease agents reproduce prion protein-independent identities in cell cultures. Proc Natl Acad Sci U S A. 2004;101:8768–8773
- A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions. Proc Natl Acad Sci U S A. 2003;100:11666–11671
- Mouse-adapted scrapie infection of SN56 cells: Greater efficiency with microsome-associated versus purified PrP-res. J Virol. 2006;80:2106–2117
- Inhibition of protease-resistant prion protein formation in a transformed deer cell line infected with chronic wasting disease. J Virol. 2006;80:596–604
- . Prion propagation in cultured cells. Br Med Bull. 2003;66:87–97
- Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents. J Infect Dis. 2004;189:431–439
- Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins. J Virol. 1988;62:1558–1564
- Prion protein expression in Chinese hamster ovary cells using a glutamine synthetase selection and amplification system. Protein Eng. 1997;10:1465–1473
- Cell culture models of transmissible spongiform encephalopathies. Biochem Biophys Res Commun. 2001;289:311–316
- . Reciprocal interference between specific CJD and scrapie agents in neural cell cultures. Science. 2005;310:493–496
- . A wild-type prion protein does not acquire properties of the scrapie isoform when coexpressed with a mutant prion protein in cultured cells. Brain Res Mol Brain Res. 1997;52:139–145
- . Birth of a prion: Spontaneous generation revisited. Cell. 2005;122:165–168
- Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system. Proc Natl Acad Sci U S A. 1996;93:13148–13151
- Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein. J Virol. 2001;74:320–325
- . Gene expression profile following stable expression of the cellular prion protein. Cell Mol Neurobiol. 2004;24:793–814
- Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein. Proc Natl Acad Sci U S A. 2001;98:4055–4059
- New in vivo and ex vivo models for the experimental study of sheep scrapie: Development and perspectives. C R Biol. 2002;325:49–57
- . Prion diseases: From molecular biology to intervention strategies. Chembiochem. 2003;4:1268–1284
- PrPSc binding antibodies are potent inhibitors of prion replication in cell lines. J Biol Chem. 2004;279:39671–39676
- Anti-PrP antibodies block PrPSc replication in prion-infected cell cultures by accelerating PrPC degradation. J Neurochem. 2004;89:454–463
- . Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature. 2001;411:810–813
- Cell-free formation of misfolded prion protein with authentic prion infectivity. Proc Natl Acad Sci U S A. 2006;103:15818–15823
- Generation of genuine prion infectivity by serial PMCA. Vet Microbiol. 2007;123:346–357
- . Prion protein conversion in vitro. J Mol Med. 2004;82:348–356
- Efficient in vitro amplification of chronic wasting disease PrPres. J Virol. 2007;81:9605–9608
- Efficient in vitro amplification of a mouse-adapted scrapie prion protein. Neurosci Lett. 2007;413:270–273
- Protein misfolding cyclic amplification as a rapid test for assessment of prion inactivation. Biochem Biophys Res Commun. 2006;348:758–762
- Autocatalytic self-propagation of misfolded prion protein. Proc Natl Acad Sci U S A. 2004;101:12207–12211
- The stoichiometry of host PrPC glycoforms modulates the efficiency of PrPSc formation in vitro. Biochemistry. 2006;45:14129–14139
- From the cover: Formation of native prions from minimal components in vitro. Proc Natl Acad Sci U S A. 2007;104:9741–9746
- Eight prion strains have PrP(Sc) molecules with different conformations. Nat Med. 1998;4:1157–1165
- Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice. Nat Biotechnol. 2002;20:1147–1150
- Diagnosis of human prion disease. Proc Natl Acad Sci U S A. 2005;102:3501–3506
- Improved conformation-dependent immunoassay: Suitability for human prion detection with enhanced sensitivity. J Gen Virol. 2003;84:1921–1925(Pt 7)
- Prusiner SB, Safar JG: Method of concentrating prion proteins in blood samples. US Patent #6166187 (2000).
- A prion protein epitope selective for the pathologically misfolded conformation. Nat Med. 2003;9:893–899
- . Probing for prions: Recognizing misfolded PrP. Nat Med. 2003;9:819–820
PII: S0887-7963(08)00016-3
doi: 10.1016/j.tmrv.2008.02.004
© 2008 Elsevier Inc. All rights reserved.
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Transfusion Medicine Reviews
Volume 22, Issue 3
, Pages 234-242
, July 2008
