Multi‐omics kinetic analysis of recombinant adeno‐associated virus production by plasmid transfection of HEK293 cells

Abstract

Recombinant adeno‐associated virus (rAAV) is among the most commonly used vectors for gene therapy. It is commonly produced by transfection of HEK293 cells with three plasmids each containing the vector genome including gene of interest (GOI), helper functions, and rep and cap genes for genome replication and capsid formation. To meet the potential clinical needs, the productivity of the production system needs to be enhanced. A better process characterization of the production system will further advance our insights into ways to enhance productivity. Here, we employed transcriptomic analysis to quantify the dynamics of different isoforms of viral transcripts and to assess the shift of cellular physiology, and deployed targeted proteomic analysis for absolute quantification of viral proteins and tandem mass tags (TMTs) for assessing cellular responses at the protein level. Functional analysis at transcriptome and proteome levels identified defense and immune response, unfolded protein response, p53 signaling as enriched. The small molecule additive intervention study based on functional analysis showed the potential of such omics‐guided productivity enhancement. Together, multi‐omics analysis advanced understanding of rAAV production and provided insight into enhancing rAAV production by plasmid transfection.

Comparative transcriptomic and proteomic kinetic analysis of adeno-associated virus production systems

“…Nevertheless, in all three cases, regardless of whether the genome was wtAAV or rAAV, whether the viral components were encoded by virus, plasmid vector, or integrated genetic modules, the host cell responded in a broadly similar manner, invoking pathways in immune response, inflammation, and MAPK signaling pathways. The earlier study on omic dynamics of rAAV-DJ transfection system also found that functional classes in inflammatory and immune response as well as MAPK signaling were enriched (Lu et al 2024b ).…”

“…A recent study reported the transcriptome and proteome dynamics of rAAV-DJ production by triple plasmid transient transfection of HEK293 cells (Lu et al 2024b ). Although that study used a different AAV serotype, we nonetheless plotted the data from that case along with the three cases from this study as shown in Supplemental Fig.…”