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Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy
Poxviruses have been used extensively as vaccine vectors for human and veterinary medicine and have recently entered the clinical realm as immunotherapies for cancer. We present a comprehensive method for producing high-quality lots of the poxvirus Parapoxvirus ovis (OrfV) for use in preclinical mod...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579082/ https://www.ncbi.nlm.nih.gov/pubmed/34786436 http://dx.doi.org/10.1016/j.omtm.2021.08.004 |
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author | van Vloten, Jacob P. Minott, Jessica A. McAusland, Thomas M. Ingrao, Joelle C. Santry, Lisa A. McFadden, Grant Petrik, James J. Bridle, Byram W. Wootton, Sarah K. |
author_facet | van Vloten, Jacob P. Minott, Jessica A. McAusland, Thomas M. Ingrao, Joelle C. Santry, Lisa A. McFadden, Grant Petrik, James J. Bridle, Byram W. Wootton, Sarah K. |
author_sort | van Vloten, Jacob P. |
collection | PubMed |
description | Poxviruses have been used extensively as vaccine vectors for human and veterinary medicine and have recently entered the clinical realm as immunotherapies for cancer. We present a comprehensive method for producing high-quality lots of the poxvirus Parapoxvirus ovis (OrfV) for use in preclinical models of vaccinology and cancer therapy. OrfV is produced using a permissive sheep skin-derived cell line and is released from infected cells by repeated freeze-thaw combined with sonication. We present two methods for isolation and purification of bulk virus. Isolated virus is concentrated to high titer using polyethylene glycol to produce the final in vivo-grade product. We also describe methods for quantifying OrfV infectious virions and determining genomic copy number to evaluate virus stocks. The methods herein will provide researchers with the ability to produce high-quality, high-titer OrfV for use in preclinical studies, and support the translation of OrfV-derived technologies into the clinic. |
format | Online Article Text |
id | pubmed-8579082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-85790822021-11-15 Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy van Vloten, Jacob P. Minott, Jessica A. McAusland, Thomas M. Ingrao, Joelle C. Santry, Lisa A. McFadden, Grant Petrik, James J. Bridle, Byram W. Wootton, Sarah K. Mol Ther Methods Clin Dev Protocol Poxviruses have been used extensively as vaccine vectors for human and veterinary medicine and have recently entered the clinical realm as immunotherapies for cancer. We present a comprehensive method for producing high-quality lots of the poxvirus Parapoxvirus ovis (OrfV) for use in preclinical models of vaccinology and cancer therapy. OrfV is produced using a permissive sheep skin-derived cell line and is released from infected cells by repeated freeze-thaw combined with sonication. We present two methods for isolation and purification of bulk virus. Isolated virus is concentrated to high titer using polyethylene glycol to produce the final in vivo-grade product. We also describe methods for quantifying OrfV infectious virions and determining genomic copy number to evaluate virus stocks. The methods herein will provide researchers with the ability to produce high-quality, high-titer OrfV for use in preclinical studies, and support the translation of OrfV-derived technologies into the clinic. American Society of Gene & Cell Therapy 2021-08-26 /pmc/articles/PMC8579082/ /pubmed/34786436 http://dx.doi.org/10.1016/j.omtm.2021.08.004 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol van Vloten, Jacob P. Minott, Jessica A. McAusland, Thomas M. Ingrao, Joelle C. Santry, Lisa A. McFadden, Grant Petrik, James J. Bridle, Byram W. Wootton, Sarah K. Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy |
title | Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy |
title_full | Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy |
title_fullStr | Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy |
title_full_unstemmed | Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy |
title_short | Production and purification of high-titer OrfV for preclinical studies in vaccinology and cancer therapy |
title_sort | production and purification of high-titer orfv for preclinical studies in vaccinology and cancer therapy |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579082/ https://www.ncbi.nlm.nih.gov/pubmed/34786436 http://dx.doi.org/10.1016/j.omtm.2021.08.004 |
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