| Literature DB >> 18423946 |
Douglas G Widman1, Tomohiro Ishikawa, Rafik Fayzulin, Nigel Bourne, Peter W Mason.
Abstract
Safer vaccines are needed to prevent flavivirus diseases. To help develop these products we have produced a pseudoinfectious West Nile virus (WNV) lacking a functional C gene which we have named RepliVAX WN. Here we demonstrate that RepliVAX WN can be safely propagated at high titer in BHK cells and vaccine-certified Vero cells engineered to stably express the C protein needed to trans-complement RepliVAX WN growth. Using these BHK cells we selected a better growing mutant RepliVAX WN population and used this to generate a second-generation RepliVAX WN (RepliVAX WN.2). RepliVAX WN.2 grown in these C-expressing cell lines safely elicit strong protective immunity against WNV disease in mice and hamsters. Taken together, these results indicate the clinical utility of RepliVAX WN.2 as a vaccine candidate against West Nile encephalitis.Entities:
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Year: 2008 PMID: 18423946 DOI: 10.1016/j.vaccine.2008.03.009
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641