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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...

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Autores principales: Deng, James Z., Rustandi, Richard R., Swartz, Andrew, Shieh, Yvonne, Baker, Jack B., Vlasak, Josef, Wang, Shiyi, Loughney, John W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
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.
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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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