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Candidate cell substrates, vaccine production, and transmissible spongiform encephalopathies
Authors:Piccardo Pedro  Cervenakova Larisa  Vasilyeva Irina  Yakovleva Oksana  Bacik Igor  Cervenak Juraj  McKenzie Carroll  Kurillova Lubica  Gregori Luisa  Pomeroy Kitty  Asher David M
Affiliation:University of Edinburgh, Easter Bush, UK. pedro.piccardo@fda.hhs.gov
Abstract:
Transmissible spongiform encephalopathy (TSE) agents have contaminated human tissue-derived medical products, human blood components, and animal vaccines. The objective of this study was to determine the potential susceptibility to infection of 5 cell lines used or proposed for manufacture of biological products, as well as other lines. Cell lines were exposed to the infectious agents of sporadic and variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy (BSE). Exposed cultures were tested for TSE-associated prion protein (PrP(TSE)) and TSE infectivity by assay in rodents and nonhuman primates. No PrP(TSE) or infectivity has been detected in any exposed cell line under study so far. Animals inoculated with BSE brain homogenate developed typical spongiform encephalopathy. In contrast, animals inoculated with cells exposed to the BSE agent remained asymptomatic. All cell lines we studied resisted infection with 3 TSE agents, including the BSE agent.
Keywords:prion   prion protein   BSE   bovine spongiform encephalopathy   Creutzfeldt-Jakob disease   CJD   vaccines   TSE   transmissible spongiform encepthalopathy
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