Optimization of the quality by design approach for gene therapy products: A case study for adeno-associated viral vectors
Abstract
The development of gene therapy products has been expanding globally, and among them, the recombinant adeno-associated virus (rAAV) vector is one of the most promising vectors for gene transfer. For efficient and rapid development of the manufacturing process and quality control strategy, the quality by design (QbD) approach can be as effective for gene therapy products as it is for gene recombinant proteins, which have been developed for decades. However, prior available knowledge required for the QbD approach is limited in the field of gene therapy. Here, we comprehensively review rAAV study results that can form the basis of QbD-based development and propose a critical quality attribute identification method suitable for gene therapy development. As a case study for rAAV, we propose a series of practical development steps, including a quality target product profile (QTPP) setting, identification of critical quality attributes (CQAs), repetitive risk assessment associated with process optimization, design space (DS) establishment, and control strategy using the QbD method. Our case study, which was based on publicly available literature, is a basic model that can be augmented by unique data pertaining to specific products. An improvement in rAAV development is expected using this model as the first step.
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Although process-related attributes are not unique to rAAV manufacturing, critical quality attributes relating to the rAAV product or product-related impurities are just starting to be clearly identified.
“Although process-related attributes are not unique to rAAV manufacturing,11,14 CQAs relating to the rAAV product or product-related impurities are just starting to be clearly identified.15”
From Analytical methods for process and product characterization of recombinant adeno-associated virus-based gene therapies (2021) · cites this paper as [15]
Other critical quality attributes, such as capsids with host cell/plasmid DNA and replication-competent AAV, have been proposed.
“other CQAs (e.g., capsids with host cell/plasmid DNA, replication-competent AAV) have been proposed”
From Analytical methods for process and product characterization of recombinant adeno-associated virus-based gene therapies (2021) · cites this paper as [15]
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References 74 · Cited by 27
- Authors
- Tanaka, T., Hanaoka, H., & Sakurai, S.
- Affiliations
- Chiba University (JP)
- Corresponding author
- Tanaka, Toshimitsu
- Venue
- European Journal of Pharmaceutics and Biopharmaceutics
- Publisher
- Elsevier BV
- Published
- 2020-10
- Volume
- 155
- Pages
- 88-102
- ISSN
- 0939-6411 (ISSN-L)
- OpenAlex
- W3048151498
- Cited by
- 27
- References
- 74
- Citations by year
- 2026: 2 · 2025: 8 · 2024: 3 · 2023: 7 · 2022: 4 · 2021: 3
- FWCI
- 0.50
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Pharmaceutics and Biopharmaceutics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein purification and stability
- Keywords
- quality by design, gene therapy products, recombinant adeno-associated virus vectors, critical quality attributes, quality target product profile, design space, control strategy, risk assessment, process optimization, manufacturing process development, quality control strategies
- MeSH terms
- Dependovirus, Animals, Genetic Vectors, Humans, Genetic Therapy, Risk Assessment, Qualitative Research, HEK293 Cells
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