| Literature DB >> 27153814 |
Udaya S Rangaswamy1, Christopher R Cotter1, Xing Cheng1, Hong Jin1, Zhongying Chen1.
Abstract
Newcastle disease virus (NDV) is being developed as an oncolytic virus for virotherapy. In this study we analysed the regulation of complement-mediated inactivation of a recombinant NDV in different host cells. NDV grown in human cells was less sensitive to complement-mediated virus inactivation than NDV grown in embryonated chicken eggs. Additionally, NDV produced from HeLa-S3 cells is more resistant to complement than NDV from 293F cells, which correlated with higher expression and incorporation of complement regulatory proteins (CD46, CD55 and CD59) into virions from HeLa-S3 cells. Further analysis of the recombinant NDVs individually expressing the three CD molecules showed that CD55 is the most potent in counteracting complement-mediated virus inactivation. The results provide important information on selecting NDV manufacture substrate to mitigate complement-mediated virus inactivation.Entities:
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Year: 2016 PMID: 27153814 DOI: 10.1099/jgv.0.000498
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891