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Production and Purification of High-Titer Newcastle Disease Virus for Use in Preclinical Mouse Models of Cancer.
Santry, Lisa A; McAusland, Thomas M; Susta, Leonardo; Wood, Geoffrey A; Major, Pierre P; Petrik, Jim J; Bridle, Byram W; Wootton, Sarah K.
Afiliação
  • Santry LA; Department of Pathobiology, University of Guelph, Guelph, ON N1G 2W1, Canada.
  • McAusland TM; Department of Pathobiology, University of Guelph, Guelph, ON N1G 2W1, Canada.
  • Susta L; Department of Pathobiology, University of Guelph, Guelph, ON N1G 2W1, Canada.
  • Wood GA; Department of Pathobiology, University of Guelph, Guelph, ON N1G 2W1, Canada.
  • Major PP; Juravinski Cancer Centre, 699 Concession Street, Hamilton, ON L8V 5C2, Canada.
  • Petrik JJ; Department of Biomedical Sciences, University of Guelph, Guelph, ON N1G 2W1, Canada.
  • Bridle BW; Department of Pathobiology, University of Guelph, Guelph, ON N1G 2W1, Canada.
  • Wootton SK; Department of Pathobiology, University of Guelph, Guelph, ON N1G 2W1, Canada.
Mol Ther Methods Clin Dev ; 9: 181-191, 2018 Jun 15.
Article em En | MEDLINE | ID: mdl-29556508
ABSTRACT
Newcastle disease virus (NDV) is a single-stranded, negative-sense RNA virus in the Paramyxoviridae family. Although primarily an avian pathogen, NDV is a potent oncolytic virus that has been shown to be safe and effective in a variety of preclinical cancer models and human clinical trials. To produce virus for oncolytic trials, NDV is commonly amplified in embryonated chicken eggs and purified from the allantoic fluid. Conventional methods for purifying virus from allantoic fluid often result in relatively low-titer preparations containing high levels of impurities, including immunogenic chicken host cell proteins from allantoic fluid. However, large quantities of virus need to be delivered intravenously to administer oncolytic NDV systemically to mice. This route of administration requires virus preparations that are both highly concentrated (to enable delivery of small volumes) and highly pure (to limit toxic effects from contaminants). Given the accumulation of promising preclinical and clinical data demonstrating the efficacy of NDV as an oncolytic agent, strategies for increasing the titer and purity of NDV preparations are sorely needed to allow for effective intravenous administration in mice. Here, we describe an optimized protocol for the rescue, production, and purification of high-titer in vivo-grade NDV for preclinical studies in mouse models.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2018 Tipo de documento: Article