» Articles » PMID: 26176404

Process Development of Adenoviral Vector Production in Fixed Bed Bioreactor: From Bench to Commercial Scale

Overview
Journal Hum Gene Ther
Specialties Genetics
Pharmacology
Date 2015 Jul 16
PMID 26176404
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Large-scale vector manufacturing for phase III and beyond has proven to be challenging. Upscaling the process with suspension cells is increasingly feasible, but many viral production applications are still applicable only in adherent settings. Scaling up the adherent system has proven to be troublesome. The iCELLis(®) disposable fixed-bed bioreactors offer a possible option for viral vector manufacturing in large quantities in an adherent environment. In this study, we have optimized adenovirus serotype 5 manufacturing using iCELLis Nano with a cultivation area up to 4 m(2). HEK293 cell cultivation, infection, and harvest of the virus (by lysing the cells inside the bioreactor) proved possible, reaching total yield of up to 1.6×10(14) viral particles (vp)/batch. The iCELLis 500 is designed to satisfy demand for large-scale requirements. Inoculating a large quantity of cell mass into the iCELLis 500 was achieved by first expanding the cell mass in suspension. Upscaling the process into an iCELLis 500/100 m(2) cultivation area cassette was practical and produced up to 6.1×10(15) vp. Flask productivity per cm(2) in iCELLis Nano and iCELLis 500 was in the same range. As a conclusion, we showed for the first time that iCELLis 500 equipment has provided an effective way to manufacture large batches of adenoviral vectors.

Citing Articles

Quasi-perfusion studies for intensified lentiviral vector production using a continuous stable producer cell line.

Stibbs D, Couto P, Takeuchi Y, Rafiq Q, Jackson N, Rayat A Mol Ther Methods Clin Dev. 2024; 32(2):101264.

PMID: 38827249 PMC: 11141457. DOI: 10.1016/j.omtm.2024.101264.


Continuous manufacturing of lentiviral vectors using a stable producer cell line in a fixed-bed bioreactor.

Stibbs D, Couto P, Takeuchi Y, Rafiq Q, Jackson N, Rayat A Mol Ther Methods Clin Dev. 2024; 32(1):101209.

PMID: 38435128 PMC: 10907162. DOI: 10.1016/j.omtm.2024.101209.


Adenoviral Gene Therapy Vectors in Clinical Use-Basic Aspects with a Special Reference to Replication-Competent Adenovirus Formation and Its Impact on Clinical Safety.

Leikas A, Yla-Herttuala S, Hartikainen J Int J Mol Sci. 2023; 24(22).

PMID: 38003709 PMC: 10671366. DOI: 10.3390/ijms242216519.


Current avenues of gene therapy in Pompe disease.

Leon-Astudillo C, Trivedi P, Sun R, Gentry M, Fuller D, Byrne B Curr Opin Neurol. 2023; 36(5):464-473.

PMID: 37639402 PMC: 10911405. DOI: 10.1097/WCO.0000000000001187.


Optimizing and developing a scalable, chemically defined, animal component-free lentiviral vector production process in a fixed-bed bioreactor.

Fiol C, Collignon M, Welsh J, Rafiq Q Mol Ther Methods Clin Dev. 2023; 30:221-234.

PMID: 37528866 PMC: 10388200. DOI: 10.1016/j.omtm.2023.06.011.