Jul 2026· International Journal of Drug Delivery Technology· Vol 16· 1 citation· 42 references
TL;DR
It is suggested that TAF exerts time-dependent inhibitory effects on Influenza A virus while preserving cellular viability, supporting further investigation of nucleotide-analogue–based strategies for RNA virus replication control.
Abstract
Influenza A virus (IAV) remains a significant global health threat due to its rapid mutation rate, seasonal epidemics,
and pandemic potential. Continuous viral evolution and emerging resistance to existing antivirals necessitate the
evaluation of alternative or repurposed antiviral strategies. Tenofovir alafenamide (TAF), a phosphonamidite prodrug of tenofovir primarily used in antiretroviral therapy, has demonstrated intracellular stability and a favorable
safety profile. In this study, we investigated the time- and concentration-dependent antiviral activity and cytotoxicity
of TAF in Influenza A–infected cell culture over a 120-h period. Antiviral efficacy was quantified as percentage
inhibition of viral replication, while cytotoxicity was assessed using the MTT assay to determine cell viability. TAF
exhibited progressive, exposure-dependent suppression of Influenza A replication, with inhibition exceeding 80% at
higher concentrations after prolonged incubation. Importantly, host cell viability remained ≥70% under
corresponding conditions, and the CC₅₀ was not reached within the tested concentration range. The estimated EC₅₀
values indicated significant antiviral activity with a favourable selectivity window. These findings suggest that TAF
exerts time-dependent inhibitory effects on Influenza A virus while preserving cellular viability, supporting further
investigation of nucleotide-analogue–based strategies for RNA virus replication control.
This integrated approach highlights the viability of Optimized HVEM-derived peptides as promising candidates with demonstrated antiviral efficacy, offering a strong foundation for future anti-HSV drug development.
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