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Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture

Disabled Infectious Single Cycle (DISC) HSV-2 has been cultured in the complimentary cell line CR2 to provide high titre bulk material suitable for the purification of the virus as a live viral vaccine. CR2 cells are cultured on the microcarrier Cytodex-1 at 5 g l-1 in small scale (1 l) and larger s...

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Detalles Bibliográficos
Autores principales: Zecchini, T.A., Smith, R.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kluwer Academic Publishers 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449936/
https://www.ncbi.nlm.nih.gov/pubmed/19003370
http://dx.doi.org/10.1023/A:1008005200711
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author Zecchini, T.A.
Smith, R.J.
author_facet Zecchini, T.A.
Smith, R.J.
author_sort Zecchini, T.A.
collection PubMed
description Disabled Infectious Single Cycle (DISC) HSV-2 has been cultured in the complimentary cell line CR2 to provide high titre bulk material suitable for the purification of the virus as a live viral vaccine. CR2 cells are cultured on the microcarrier Cytodex-1 at 5 g l-1 in small scale (1 l) and larger scale (15 l) reactors. The cells are infected at an MOI of 0.01 pfu cell-1 and the culture harvested 60–72 h later. The infected cells are removed from the microcarriers by the addition of a hypotonic saline and the virus released by low-pressure disruption techniques. Virus titres achieved are compared to the standard roller bottle process. The resulting material is the starting point for the purification of the DISC-HSV virus.
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spelling pubmed-34499362012-10-31 Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture Zecchini, T.A. Smith, R.J. Cytotechnology Article Disabled Infectious Single Cycle (DISC) HSV-2 has been cultured in the complimentary cell line CR2 to provide high titre bulk material suitable for the purification of the virus as a live viral vaccine. CR2 cells are cultured on the microcarrier Cytodex-1 at 5 g l-1 in small scale (1 l) and larger scale (15 l) reactors. The cells are infected at an MOI of 0.01 pfu cell-1 and the culture harvested 60–72 h later. The infected cells are removed from the microcarriers by the addition of a hypotonic saline and the virus released by low-pressure disruption techniques. Virus titres achieved are compared to the standard roller bottle process. The resulting material is the starting point for the purification of the DISC-HSV virus. Kluwer Academic Publishers 1999-07 /pmc/articles/PMC3449936/ /pubmed/19003370 http://dx.doi.org/10.1023/A:1008005200711 Text en © Kluwer Academic Publishers 1999
spellingShingle Article
Zecchini, T.A.
Smith, R.J.
Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture
title Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture
title_full Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture
title_fullStr Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture
title_full_unstemmed Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture
title_short Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture
title_sort production of high titre disabled infectious single cycle (disc) hsv from a microcarrier culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449936/
https://www.ncbi.nlm.nih.gov/pubmed/19003370
http://dx.doi.org/10.1023/A:1008005200711
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