Why the study?
Adenovirus infections can cause serious illness, particularly in immunocompromised individuals, but there is currently no approved treatment.
Does LAVR-289 inhibit viral replication and improve survival in models of adenovirus infection?
Does LAVR-289 inhibit viral replication and improve survival in models of adenovirus infection?
LAVR-289 demonstrates potent in vitro and in vivo antiviral activity against adenovirus, suggesting potential as a future therapy for immunocompromised patients.
Supports antiviral development for adenovirus in immunocompromised hosts; leaves open human translation pending further studies.
Adenoviruses are responsible for a range of pathologies, including respiratory infections in children. Although most adenovirus infections are self-resolving, they can cause serious illness, particularly in immunocompromised individuals. There is currently no approved treatment for adenovirus infections. Here, we report on the antiviral activity of LAVR-289, a broad-spectrum acyclonucleoside phosphonate exhibiting potent in vitro efficacy against several adenovirus serotypes, comparable to that of brincidofovir. LAVR-289 specifically inhibits viral replication, blocking the formation of viral replication centers and preventing late protein expression without affecting viral entry or delivery of viral genomes to the nucleus. In vivo, using immunocompromised Syrian hamsters infected with HAdV-C6, oral administration of LAVR-289 resulted in 100% animal survival. These results suggest that LAVR-289 holds promise as a potential therapy for adenovirus infections paving the way for a future treatment of immunocompromised patients.
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Quentin-Froignant et al. (2025) studied this question.
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