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Implementation of Novel Affinity Ligand for Lentiviral Vector Purification

The use of viral vectors as therapeutic products for multiple applications such as vaccines, cancer treatment, or gene therapies, has been growing exponentially. Therefore, improved manufacturing processes are needed to cope with the high number of functional particles required for clinical trials a...

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Autores principales: Moreira, Ana Sofia, Bezemer, Sandra, Faria, Tiago Q., Detmers, Frank, Hermans, Pim, Sierkstra, Laurens, Coroadinha, Ana Sofia, Peixoto, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966744/
https://www.ncbi.nlm.nih.gov/pubmed/36834764
http://dx.doi.org/10.3390/ijms24043354
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author Moreira, Ana Sofia
Bezemer, Sandra
Faria, Tiago Q.
Detmers, Frank
Hermans, Pim
Sierkstra, Laurens
Coroadinha, Ana Sofia
Peixoto, Cristina
author_facet Moreira, Ana Sofia
Bezemer, Sandra
Faria, Tiago Q.
Detmers, Frank
Hermans, Pim
Sierkstra, Laurens
Coroadinha, Ana Sofia
Peixoto, Cristina
author_sort Moreira, Ana Sofia
collection PubMed
description The use of viral vectors as therapeutic products for multiple applications such as vaccines, cancer treatment, or gene therapies, has been growing exponentially. Therefore, improved manufacturing processes are needed to cope with the high number of functional particles required for clinical trials and, eventually, commercialization. Affinity chromatography (AC) can be used to simplify purification processes and generate clinical-grade products with high titer and purity. However, one of the major challenges in the purification of Lentiviral vectors (LVs) using AC is to combine a highly specific ligand with a gentle elution condition assuring the preservation of vector biological activity. In this work, we report for the first time the implementation of an AC resin to specifically purify VSV-G pseudotyped LVs. After ligand screening, different critical process parameters were assessed and optimized. A dynamic capacity of 1 × 10(11) total particles per mL of resin was determined and an average recovery yield of 45% was found for the small-scale purification process. The established AC robustness was confirmed by the performance of an intermediate scale providing an infectious particles yield of 54%, which demonstrates the scalability and reproducibility of the AC matrix. Overall, this work contributes to increasing downstream process efficiency by delivering a purification technology that enables high purity, scalability, and process intensification in a single step, contributing to time-to-market reduction.
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spelling pubmed-99667442023-02-26 Implementation of Novel Affinity Ligand for Lentiviral Vector Purification Moreira, Ana Sofia Bezemer, Sandra Faria, Tiago Q. Detmers, Frank Hermans, Pim Sierkstra, Laurens Coroadinha, Ana Sofia Peixoto, Cristina Int J Mol Sci Article The use of viral vectors as therapeutic products for multiple applications such as vaccines, cancer treatment, or gene therapies, has been growing exponentially. Therefore, improved manufacturing processes are needed to cope with the high number of functional particles required for clinical trials and, eventually, commercialization. Affinity chromatography (AC) can be used to simplify purification processes and generate clinical-grade products with high titer and purity. However, one of the major challenges in the purification of Lentiviral vectors (LVs) using AC is to combine a highly specific ligand with a gentle elution condition assuring the preservation of vector biological activity. In this work, we report for the first time the implementation of an AC resin to specifically purify VSV-G pseudotyped LVs. After ligand screening, different critical process parameters were assessed and optimized. A dynamic capacity of 1 × 10(11) total particles per mL of resin was determined and an average recovery yield of 45% was found for the small-scale purification process. The established AC robustness was confirmed by the performance of an intermediate scale providing an infectious particles yield of 54%, which demonstrates the scalability and reproducibility of the AC matrix. Overall, this work contributes to increasing downstream process efficiency by delivering a purification technology that enables high purity, scalability, and process intensification in a single step, contributing to time-to-market reduction. MDPI 2023-02-08 /pmc/articles/PMC9966744/ /pubmed/36834764 http://dx.doi.org/10.3390/ijms24043354 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Moreira, Ana Sofia
Bezemer, Sandra
Faria, Tiago Q.
Detmers, Frank
Hermans, Pim
Sierkstra, Laurens
Coroadinha, Ana Sofia
Peixoto, Cristina
Implementation of Novel Affinity Ligand for Lentiviral Vector Purification
title Implementation of Novel Affinity Ligand for Lentiviral Vector Purification
title_full Implementation of Novel Affinity Ligand for Lentiviral Vector Purification
title_fullStr Implementation of Novel Affinity Ligand for Lentiviral Vector Purification
title_full_unstemmed Implementation of Novel Affinity Ligand for Lentiviral Vector Purification
title_short Implementation of Novel Affinity Ligand for Lentiviral Vector Purification
title_sort implementation of novel affinity ligand for lentiviral vector purification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966744/
https://www.ncbi.nlm.nih.gov/pubmed/36834764
http://dx.doi.org/10.3390/ijms24043354
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