In Vivo Tracking for Oncolytic Adenovirus Interactions with Liver Cells

• Published in: Biomedicines 2022-07, Vol.10 (7), p.1697
• Main Authors: Naumenko, Victor A., Vishnevskiy, Daniil A., Stepanenko, Aleksei A., Sosnovtseva, Anastasiia O., Chernysheva, Anastasiia A., Abakumova, Tatiana O., Valikhov, Marat P., Lipatova, Anastasiia V., Abakumov, Maxim A., Chekhonin, Vladimir P.
• Format: Article
• Language: English
• Subjects: adenovirus; Adenoviruses; Animals; Apoptosis; CD8 antigen; CD8+ T cells; Cell death; Cloning; Hepatocytes; Hepatotoxicity; Immunotherapy; Infections; Intravenous administration; Leukocytes (neutrophilic); Liver; Lymphocytes T; Macrophages; Membrane vesicles; Microscopy; neutrophils; Oncolysis; Propidium iodide; Toxicity; Transduction; Viruses; zeiosis
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10071697

Hepatotoxicity remains an as yet unsolved problem for adenovirus (Ad) cancer therapy. The toxic effects originate both from rapid Kupffer cell (KCs) death (early phase) and hepatocyte transduction (late phase). Several host factors and capsid components are known to contribute to hepatotoxicity, however, the complex interplay between Ad and liver cells is not fully understood. Here, by using intravital microscopy, we aimed to follow the infection and immune response in mouse liver from the first minutes up to 72 h post intravenous injection of three Ads carrying delta-24 modification (Ad5-RGD, Ad5/3, and Ad5/35). At 15–30 min following the infusion of Ad5-RGD and Ad5/3 (but not Ad5/35), the virus-bound macrophages demonstrated signs of zeiosis: the formation of long-extended protrusions and dynamic membrane blebbing with the virus release into the blood in the membrane-associated vesicles. Although real-time imaging revealed interactions between the neutrophils and virus-bound KCs within minutes after treatment, and long-term contacts of CD8+ T cells with transduced hepatocytes at 24–72 h, depletion of neutrophils and CD8+ T cells affected neither rate nor dynamics of liver infection. Ad5-RGD failed to complete replicative cycle in hepatocytes, and transduced cells remained impermeable for propidium iodide, with a small fraction undergoing spontaneous apoptosis. In Ad5-RGD-immune mice, the virus neither killed KCs nor transduced hepatocytes, while in the setting of hepatic regeneration, Ad5-RGD enhanced liver transduction. The clinical and biochemical signs of hepatotoxicity correlated well with KC death, but not hepatocyte transduction. Real-time in vivo tracking for dynamic interactions between virus and host cells provides a better understanding of mechanisms underlying Ad-related hepatotoxicity.