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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kluwer Academic Publishers
1999
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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. |
format | Online Article Text |
id | pubmed-3449936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Kluwer Academic Publishers |
record_format | MEDLINE/PubMed |
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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