Safety and Tolerability of the Adeno-Associated Virus Vector, AAV6.2FF, Expressing a Monoclonal Antibody in Murine and Ovine Animal Models.
Amira D RgheiLaura P van LieshoutBenjamin M McLeodYanlong PeiJordyn A LopesNicole ZielinskaEnzo M BaracuhyBrenna A Y StevensSylvia P ThomasJacob G E YatesBryce M WarnerDarwyn KobasaHugues Fausther-BovendoGary P KobingerKhalil KarimiBrad ThompsonByram W BridleLeonardo SustaSarah K WoottonPublished in: Biomedicines (2021)
Adeno-associated virus (AAV) vector mediated expression of therapeutic monoclonal antibodies is an alternative strategy to traditional vaccination to generate immunity in immunosuppressed or immunosenescent individuals. In this study, we vectorized a human monoclonal antibody (31C2) directed against the spike protein of SARS-CoV-2 and determined the safety profile of this AAV vector in mice and sheep as a large animal model. In both studies, plasma biochemical parameters and hematology were comparable to untreated controls. Except for mild myositis at the site of injection, none of the major organs revealed any signs of toxicity. AAV-mediated human IgG expression increased steadily throughout the 28-day study in sheep, resulting in peak concentrations of 21.4-46.7 µg/ mL, demonstrating practical scale up from rodent to large animal models. This alternative approach to immunity is worth further exploration after this demonstration of safety, tolerability, and scalability in a large animal model.
Keyphrases
- monoclonal antibody
- gene therapy
- sars cov
- endothelial cells
- poor prognosis
- binding protein
- induced pluripotent stem cells
- oxidative stress
- clinical trial
- randomized controlled trial
- type diabetes
- small molecule
- case control
- coronavirus disease
- amino acid
- high fat diet induced
- study protocol
- interstitial lung disease