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SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus
V937 is an oncolytic virus immunotherapy clinical drug candidate consisting of a proprietary formulation of Coxsackievirus A21 (CVA21). V937 specifically binds to and lyses cells with over-expressed ICAM-1 receptors in a range of tumor cell types and is currently in phase I and II clinical trials. I...
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/PMC8718657/ https://www.ncbi.nlm.nih.gov/pubmed/35024440 http://dx.doi.org/10.1016/j.omto.2021.12.009 |
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author | Deng, James Z. Rustandi, Richard R. Swartz, Andrew Shieh, Yvonne Baker, Jack B. Vlasak, Josef Wang, Shiyi Loughney, John W. |
author_facet | Deng, James Z. Rustandi, Richard R. Swartz, Andrew Shieh, Yvonne Baker, Jack B. Vlasak, Josef Wang, Shiyi Loughney, John W. |
author_sort | Deng, James Z. |
collection | PubMed |
description | V937 is an oncolytic virus immunotherapy clinical drug candidate consisting of a proprietary formulation of Coxsackievirus A21 (CVA21). V937 specifically binds to and lyses cells with over-expressed ICAM-1 receptors in a range of tumor cell types and is currently in phase I and II clinical trials. Infectious V937 particles consist of a ∼30 nm icosahedral capsid assembled from four structural viral proteins that encapsidate a viral RNA genome. Rapid and robust analytical methods to quantify and characterize CVA21 virus particles are important to support the process development, regulatory requirements, and validation of new manufacturing platforms. Herein, we describe a size-exclusion chromatography (SEC) method that was developed to characterize the V937 drug substance and process intermediates. Using a 4-in-1 combination of multi-detectors (UV, refractive index, dynamic and static light scattering), we demonstrate the use of SEC for the quantification of the virus particle count, the determination of virus size (molecular weight and hydrodynamic diameter), and the characterization of virus purity by assessing empty-to-full capsid ratios. Through a SEC analysis of stressed V937 samples, we propose CVA21 thermal degradation pathways that result in genome release and particle aggregation. |
format | Online Article Text |
id | pubmed-8718657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-87186572022-01-11 SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus Deng, James Z. Rustandi, Richard R. Swartz, Andrew Shieh, Yvonne Baker, Jack B. Vlasak, Josef Wang, Shiyi Loughney, John W. Mol Ther Oncolytics Original Article V937 is an oncolytic virus immunotherapy clinical drug candidate consisting of a proprietary formulation of Coxsackievirus A21 (CVA21). V937 specifically binds to and lyses cells with over-expressed ICAM-1 receptors in a range of tumor cell types and is currently in phase I and II clinical trials. Infectious V937 particles consist of a ∼30 nm icosahedral capsid assembled from four structural viral proteins that encapsidate a viral RNA genome. Rapid and robust analytical methods to quantify and characterize CVA21 virus particles are important to support the process development, regulatory requirements, and validation of new manufacturing platforms. Herein, we describe a size-exclusion chromatography (SEC) method that was developed to characterize the V937 drug substance and process intermediates. Using a 4-in-1 combination of multi-detectors (UV, refractive index, dynamic and static light scattering), we demonstrate the use of SEC for the quantification of the virus particle count, the determination of virus size (molecular weight and hydrodynamic diameter), and the characterization of virus purity by assessing empty-to-full capsid ratios. Through a SEC analysis of stressed V937 samples, we propose CVA21 thermal degradation pathways that result in genome release and particle aggregation. American Society of Gene & Cell Therapy 2021-12-11 /pmc/articles/PMC8718657/ /pubmed/35024440 http://dx.doi.org/10.1016/j.omto.2021.12.009 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 | Original Article Deng, James Z. Rustandi, Richard R. Swartz, Andrew Shieh, Yvonne Baker, Jack B. Vlasak, Josef Wang, Shiyi Loughney, John W. SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus |
title | SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus |
title_full | SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus |
title_fullStr | SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus |
title_full_unstemmed | SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus |
title_short | SEC coupled with in-line multiple detectors for the characterization of an oncolytic Coxsackievirus |
title_sort | sec coupled with in-line multiple detectors for the characterization of an oncolytic coxsackievirus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718657/ https://www.ncbi.nlm.nih.gov/pubmed/35024440 http://dx.doi.org/10.1016/j.omto.2021.12.009 |
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