Evaluation of a downstream process for the recovery and concentration of a Cell-Culture-Derived rVSV-Spike COVID-19 vaccine candidate.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
26 11 2021
Historique:
received: 03 05 2021
revised: 17 10 2021
accepted: 17 10 2021
pubmed: 11 11 2021
medline: 27 11 2021
entrez: 10 11 2021
Statut: ppublish

Résumé

rVSV-Spike (rVSV-S) is a recombinant viral vaccine candidate under development to control the COVID-19 pandemic and is currently in phase II clinical trials. rVSV-S induces neutralizing antibodies and protects against SARS-CoV-2 infection in animal models. Bringing rVSV-S to clinical trials required the development of a scalable downstream process for the production of rVSV-S that can meet regulatory guidelines. The objective of this study was the development of the first downstream unit operations for cell-culture-derived rVSV-S, namely, the removal of nucleic acid contamination, the clarification and concentration of viral harvested supernatant, and buffer exchange. Retaining the infectivity of the rVSV-S during the downstream process was challenged by the shear sensitivity of the enveloped rVSV-S and its membrane protruding spike protein. Through a series of screening experiments, we evaluated and established the required endonuclease treatment conditions, filter train composition, and hollow fiber-tangential flow filtration parameters to remove large particles, reduce the load of impurities, and concentrate and exchange the buffer while retaining rVSV-S infectivity. The combined effect of the first unit operations on viral recovery and the removal of critical impurities was examined during scale-up experiments. Overall, approximately 40% of viral recovery was obtained and the regulatory requirements of less than 10 ng host cell DNA per dose were met. However, while 86-97% of the host cell proteins were removed, the regulatory acceptable HCP levels were not achieved, requiring subsequent purification and polishing steps. The results we obtained during the scale-up experiments were similar to those obtained during the screening experiments, indicating the scalability of the process. The findings of this study set the foundation for the development of a complete downstream manufacturing process, requiring subsequent purification and polishing unit operations for clinical preparations of rVSV-S.

Identifiants

pubmed: 34756612
pii: S0264-410X(21)01376-1
doi: 10.1016/j.vaccine.2021.10.045
pmc: PMC8531466
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
COVID-19 Vaccines 0
Spike Glycoprotein, Coronavirus 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7044-7051

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Arik Makovitzki (A)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Elad Lerer (E)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Yaron Kafri (Y)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Yaakov Adar (Y)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Lilach Cherry (L)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Edith Lupu (E)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Arik Monash (A)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Rona Levy (R)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Ofir Israeli (O)

Department of Biochemistry and Molecular Genetics, Israel Institute for Biological, Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Eyal Dor (E)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Eyal Epstein (E)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Lilach Levin (L)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Einat Toister (E)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Idan Hefetz (I)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Ophir Hazan (O)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Irit Simon (I)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Arnon Tal (A)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Meni Girshengorn (M)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Hanan Tzadok (H)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Osnat Rosen (O)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel.

Ziv Oren (Z)

Department of Biotechnology, Israel Institute for Biological Research, 24 Reuven Lerer St., Nes-Ziona, Israel. Electronic address: zivo@iibr.gov.il.

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