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Vaccine ; 25(39-40): 6872-81, 2007 Sep 28.
Artigo em Inglês | MEDLINE | ID: mdl-17707954

RESUMO

Ensuring complete viral inactivation is critical for the safety of vaccines based on an inactivated virus. Detection of residual infectious virus is dependent on sensitivity of the assay, sample volume analyzed and the absence of interference with viral infection. Here we describe the development and qualification of a sensitive cell-based assay for the detection of residual infectious West Nile Virus (WNV). The results of the assay are in good agreement with the assumption that at low concentrations the number of infectious units in relatively small samples follows a Poisson distribution. The assay can detect 1 infectious unit with a confidence of 99%, provides statistical controls for interference and can easily be scaled up to test large amounts of vaccine material. Furthermore, we show equivalence in sensitivity between the cell-based assay and an in vivo assay for detection of infectious WNV. Finally, the assay has been used for successful release testing of clinical lots of inactivated WNV vaccine. Given the principle and generic setup of the method we envision broad applicability to the detection of very low concentrations of infectious virus.


Assuntos
Propiolactona/farmacologia , Vacinas de Produtos Inativados , Inativação de Vírus , Vacinas contra o Vírus do Nilo Ocidental , Vírus do Nilo Ocidental/patogenicidade , Animais , Animais Lactentes , Linhagem Celular , Chlorocebus aethiops , Modelos Animais de Doenças , Camundongos , Camundongos Endogâmicos C3H , Células Vero , Febre do Nilo Ocidental/mortalidade , Febre do Nilo Ocidental/virologia , Vírus do Nilo Ocidental/efeitos dos fármacos , Vírus do Nilo Ocidental/isolamento & purificação , Vírus do Nilo Ocidental/fisiologia
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