It’s what’s on the inside that counts: Capsid content as a critical quality attribute for AAV characterization

Recombinant adeno-associated virus (rAAV) vectors exhibit complex heterogeneity in capsid content. Although a growing array of analytical platforms can interrogate different capsid attributes, no single method provides a comprehensive or unequivocal assessment. Critically, current approaches often fail to evaluate genome integrity, an emerging important quality attribute. Incomplete genomes can contribute to viral genome titers without conferring therapeutic benefit, while simultaneously increasing immunogenic burden and risk of adverse events. Discordant results from orthogonal assays further complicate interpretation and cross-laboratory comparisons. Here, we highlight the limitations of existing characterization strategies and advocate for robust analytical frameworks that directly assess genome completeness. We propose best-practice guidelines, including improved genome integrity assays and harmonized reporting, to better link capsid content analytics with potency and patient safety in gene therapy development.

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Publication Details

Journal
Molecular Therapy Advances
Published
2026-06-19
DOI
https://doi.org/10.1016/j.omta.2026.201765
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

It’s what’s on the inside that counts: Capsid content as a critical quality attribute for AAV characterization

David Dobnik, Ana Dolinar Češarek, Stuart Nelson, Lauriel F. Earley
Molecular Therapy Advances
Virus-based gene therapy research
article

It’s what’s on the inside that counts: Capsid content as a critical quality attribute for AAV characterization

David Dobnik, Ana Dolinar Češarek, Stuart Nelson, Lauriel F. Earley
article en

Abstract

Recombinant adeno-associated virus (rAAV) vectors exhibit complex heterogeneity in capsid content. Although a growing array of analytical platforms can interrogate different capsid attributes, no single method provides a comprehensive or unequivocal assessment. Critically, current approaches often fail to evaluate genome integrity, an emerging important quality attribute. Incomplete genomes can contribute to viral genome titers without conferring therapeutic benefit, while simultaneously increasing immunogenic burden and risk of adverse events. Discordant results from orthogonal assays further complicate interpretation and cross-laboratory comparisons. Here, we highlight the limitations of existing characterization strategies and advocate for robust analytical frameworks that directly assess genome completeness. We propose best-practice guidelines, including improved genome integrity assays and harmonized reporting, to better link capsid content analytics with potency and patient safety in gene therapy development.

Molecular Therapy AdvancesVol. 34(3)
Eli Lilly (United States) (US), National Institute of Biology (SI), University of Washington Tacoma (US), B2 (Slovenia) (SI)
Javna Agencija za Raziskovalno Dejavnost RS
Openalex Percentile: Top 7%
Virus-based gene therapy research
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