Population
Latently infected murine ganglia
Comparison
Acyclovir or WAY-150138 vs Untreated ganglia
Design
Preclinical
Follow-up
48 hours postexplant
Authors
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High late expression reflects secondary spread, not initial reactivation; leaves open relevance to in vivo HSV dynamics.
High levels of viral gene expression at 48 h postexplant are largely due to the production of infectious virus and subsequent spread through the tissue, rather than initial reactivation events.
Pesola et al. (2005) studied this question.
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