tetano
Editor, Senior Moderator
J Infect Chemother. 2019 Mar 29. pii: S1341-321X(19)30067-4. doi: 10.1016/j.jiac.2019.02.023. [Epub ahead of print]
[h=1]Efficacy of laninamivir octanoate in mice with advanced inflammation stage caused by infection of highly lethal influenza virus.[/h] Tomozawa T[SUP]1[/SUP], Hoshino K[SUP]1[/SUP], Yamashita M[SUP]2[/SUP], Kubo S[SUP]3[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Four neuraminidase (NA) inhibitors and an RNA synthesis inhibitor were recently approved and are currently in clinical use for influenza. Among NA inhibitors, oseltamivir phosphate (OSE, Tamiflu[SUP]?[/SUP]) and zanamivir are approved worldwide, whereas peramivir and laninamivir octanoate (LAN, Inavir[SUP]?[/SUP]) are regionally approved for human use. Therefore, OSE has been used to treat infections of highly pathogenic influenza viruses, such as H5N1 and H7N9, which caused epidemic in southeast Asia and Egypt, and China, respectively. Generally, OSE is administered twice daily for 5 days by oral administration, and LAN once by inhalation for completing influenza therapy. In this study, we compared the efficacy of OSE and LAN administered according to the regimens in mice infected with highly lethal influenza viruses. The drugs were administered at the early and late stages of infection, which correspond to mild and severe inflammation in the lungs, respectively. Based on the drugs' regimens for human, a single administration of LAN at both stages of inflammation showed superior efficacy to repeated administration of OSE. LAN, as in OSE, could also be efficacious in treating severe influenza in humans.
Copyright ? 2019 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
[h=4]KEYWORDS:[/h] Inflamed stage; Influenza virus; Laninamivir; Mouse; Oseltamivir; Treatment
PMID: 30935767 DOI: 10.1016/j.jiac.2019.02.023
[h=1]Efficacy of laninamivir octanoate in mice with advanced inflammation stage caused by infection of highly lethal influenza virus.[/h] Tomozawa T[SUP]1[/SUP], Hoshino K[SUP]1[/SUP], Yamashita M[SUP]2[/SUP], Kubo S[SUP]3[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Four neuraminidase (NA) inhibitors and an RNA synthesis inhibitor were recently approved and are currently in clinical use for influenza. Among NA inhibitors, oseltamivir phosphate (OSE, Tamiflu[SUP]?[/SUP]) and zanamivir are approved worldwide, whereas peramivir and laninamivir octanoate (LAN, Inavir[SUP]?[/SUP]) are regionally approved for human use. Therefore, OSE has been used to treat infections of highly pathogenic influenza viruses, such as H5N1 and H7N9, which caused epidemic in southeast Asia and Egypt, and China, respectively. Generally, OSE is administered twice daily for 5 days by oral administration, and LAN once by inhalation for completing influenza therapy. In this study, we compared the efficacy of OSE and LAN administered according to the regimens in mice infected with highly lethal influenza viruses. The drugs were administered at the early and late stages of infection, which correspond to mild and severe inflammation in the lungs, respectively. Based on the drugs' regimens for human, a single administration of LAN at both stages of inflammation showed superior efficacy to repeated administration of OSE. LAN, as in OSE, could also be efficacious in treating severe influenza in humans.
Copyright ? 2019 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
[h=4]KEYWORDS:[/h] Inflamed stage; Influenza virus; Laninamivir; Mouse; Oseltamivir; Treatment
PMID: 30935767 DOI: 10.1016/j.jiac.2019.02.023