Issues associated with residual cell-substrate DNA in viral vaccines
Abstract
The presence of some residual cellular DNA derived from the production-cell substrate in viral vaccines is inevitable. Whether this DNA represents a safety concern, particularly if the cell substrate is derived from a tumor or is tumorigenic, is unknown. DNA has two biological activities that need to be considered. First, DNA can be oncogenic; second, DNA can be infectious. As part of our studies to assess the risk of residual cell-substrate DNA in viral vaccines, we have established assays that can quantify the biological activities of DNA. From data obtained using these assays, we have estimated the risk of an oncogenic or an infectious event from DNA. Because these estimates were derived from the most sensitive assays identified so far, they likely represent worst-case estimates. In addition, methods that inactivate the biological activities of DNA can be assessed and estimations of risk reduction by these treatments can be made. In this paper, we discuss our approaches to address potential safety issues associated with residual cellular DNA from neoplastic cell substrates in viral vaccines, summarize the development of assays to quantify the oncogenic and infectivity activities of DNA, and discuss methods to reduce the biological activities of DNA.
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The main risks associated with rcDNA in viral vaccines are infectivity and oncogenicity.
“The main risks associated with rcDNA in viral vaccines are infectivity and oncogenicity; rcDNA might be capable of transmitting viral infections if retroviral proviruses, integrated copies of DNA viruses, or extra chromosomal genomes are present (FDA, 2010;Sheng-Fowler et al., 2009), or may pose a potential risk for oncogenesis if viral or cell substrate (derived from tumors or which are tumorigen”
From Comparative analysis of the performance of residual host cell DNA assays for viral vaccines produced in Vero cells (2019) · cites this paper as Sheng-Fowler et al., 2009
Residual host cell DNA (rcDNA) from continuous cell lines used for manufacturing biological medicinal products has been considered a safety risk.
“Residual host cell DNA (rcDNA) from continuous cell lines used for manufacturing of biological medicinal products has been considered as safety risk.”
From Comparative analysis of the performance of residual host cell DNA assays for viral vaccines produced in Vero cells (2019) · cites this paper as Sheng-Fowler et al., 2009
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Cloning of infectious adeno-associated virus genomes in bacterial plasmids
Laughlin, C. A., Tratschin, J.-D., Coon, H., & Carter, B. J. (1983) · Gene · doi:10.1016/0378-1119(83)90217-2 · Cited by 266 · see citing works
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Vernay, O., Sarcey, E., Detrez, V., Abachin, E., Riou, P., Mouterde, B., Bonnevay, T., & Mallet, L. (2019) · Journal of Virological Methods · doi:10.1016/j.jviromet.2019.01.001 · Cited by 14 · see citing works
- Authors
- Sheng-Fowler, L., Lewis, A. M., & Peden, K.
- Affiliations
- Center for Biologics Evaluation and Research (US)
- Corresponding author
- Peden, Keith
- Venue
- Biologicals
- Publisher
- Elsevier BV
- Published
- 2009-06
- Volume
- 37
- Issue
- 3
- Pages
- 190-195
- ISSN
- 1045-1056 (ISSN-L)
- OpenAlex
- W2060372252
- Cited by
- 53
- References
- 1
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 4 · 2023: 4 · 2021: 5 · 2020: 2 · 2019: 3 · 2018: 1 · 2017: 4 · 2016: 3 · 2015: 2 · 2014: 7 · 2013: 4
- FWCI
- 0.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biologicals (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
- Keywords
- viral vaccines, vaccine safety, tumorigenic cell lines, DNA inactivation, risk assessment
- MeSH terms
- Algorithms, DNA, Viral Vaccines
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