Biodistribution of an oncolytic adenovirus after intracranial injection in permissive animals: a comparative study of Syrian hamsters and cotton rats

AM Sonabend, IV Ulasov, Y Han, CE Rolle… - Cancer gene …, 2009 - nature.com
AM Sonabend, IV Ulasov, Y Han, CE Rolle, S Nandi, D Cao, MA Tyler, MS Lesniak
Cancer gene therapy, 2009nature.com
Conditionally replicative adenoviruses (CRAds) are often evaluated in mice; however,
normal and cancerous mouse tissues are poorly permissive for human CRAds. As the cotton
rat (CR) is a semipermissive animal and the Syrian hamster (SH) is a fully permissive model
for adenoviral replication, we compared them in a single study following intracranial (ic)
injection of a novel glioma-targeting CRAd. Viral genomic copies were quantified by real-
time PCR in brain, blood, liver and lung. The studies were corroborated by …
Abstract
Conditionally replicative adenoviruses (CRAds) are often evaluated in mice; however, normal and cancerous mouse tissues are poorly permissive for human CRAds. As the cotton rat (CR) is a semipermissive animal and the Syrian hamster (SH) is a fully permissive model for adenoviral replication, we compared them in a single study following intracranial (ic) injection of a novel glioma-targeting CRAd. Viral genomic copies were quantified by real-time PCR in brain, blood, liver and lung. The studies were corroborated by immunohistochemical, serological and immunological assays. CR had a multiple log higher susceptibility for adenoviral infection than SH. A similar amount of genomic copies of CRAd-Survivin-pk7 and human adenovirus serotype 5 (AdWT) was found in the brain of CR and in all organs from SH. In blood and lung of CR, AdWT had more genomic copies than CRAd-Survivin-pk7 in some of the time points studied. Viral antigens were confirmed in brain slices, an elevation of serum transaminases was observed in both models, and an increase in anti-adenoviral antibodies was detected in SH sera. In conclusion, CR represents a sensitive model for studying biodistribution of CRAds after ic delivery, allowing for the detection of differences in the replication of CRAd-Survivin-pk7 and AdWT that were not evident in SH.
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