Unknown

Dataset Information

0

Combinations of Oseltamivir and T-705 Extend the Treatment Window for Highly Pathogenic Influenza A(H5N1) Virus Infection in Mice.


ABSTRACT: Current anti-influenza therapy depends on administering drugs soon after infection, which is often impractical. We assessed whether combinations of oseltamivir (a neuraminidase inhibitor) and T-705 (a nonspecific inhibitor of viral polymerases) could extend the window for treating lethal infection with highly pathogenic A(H5N1) influenza virus in mice. Combination therapy protected 100% of mice, even when delayed until 96?h postinoculation. Compared to animals receiving monotherapy, mice receiving combination therapy had reduced viral loads and restricted viral spread in lung tissues, limited lung damage, and decreased inflammatory cytokine production. Next-generation sequencing showed that virus populations in T-705-treated mice had greater genetic variability, with more frequent transversion events, than did populations in control and oseltamivir-treated mice, but no substitutions associated with resistance to oseltamivir or T-705 were detected. Thus, combination therapy extended the treatment window for A(H5N1) influenza infection in mice and should be considered for evaluation in a clinical setting.

SUBMITTER: Marathe BM 

PROVIDER: S-EPMC4879667 | biostudies-literature | 2016 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Combinations of Oseltamivir and T-705 Extend the Treatment Window for Highly Pathogenic Influenza A(H5N1) Virus Infection in Mice.

Marathe Bindumadhav M BM   Wong Sook-San SS   Vogel Peter P   Garcia-Alcalde Fernando F   Webster Robert G RG   Webby Richard J RJ   Najera Isabel I   Govorkova Elena A EA  

Scientific reports 20160525


Current anti-influenza therapy depends on administering drugs soon after infection, which is often impractical. We assessed whether combinations of oseltamivir (a neuraminidase inhibitor) and T-705 (a nonspecific inhibitor of viral polymerases) could extend the window for treating lethal infection with highly pathogenic A(H5N1) influenza virus in mice. Combination therapy protected 100% of mice, even when delayed until 96 h postinoculation. Compared to animals receiving monotherapy, mice receivi  ...[more]

Similar Datasets

| S-EPMC6977371 | biostudies-literature
| S-EPMC2916532 | biostudies-literature
| S-EPMC3679007 | biostudies-literature
| S-EPMC2888842 | biostudies-other
| S-EPMC2818889 | biostudies-other
| S-EPMC2798555 | biostudies-literature
| S-EPMC3320388 | biostudies-literature
| S-EPMC10579283 | biostudies-literature
| S-EPMC2657001 | biostudies-literature
| S-EPMC1803015 | biostudies-other