| Literature DB >> 28931216 |
Maki Kiso1, Kiyoko Iwatsuki-Horimoto1, Seiya Yamayoshi1, Ryuta Uraki1, Mutsumi Ito1, Noriko Nakajima2, Shinya Yamada1, Masaki Imai1, Eiryo Kawakami3, Yuriko Tomita1, Satoshi Fukuyama1,4, Yasushi Itoh5, Kazumasa Ogasawara5, Tiago J S Lopes1,6, Tokiko Watanabe1,4, Louise H Moncla6,7, Hideki Hasegawa2, Thomas C Friedrich6,7, Gabriele Neumann6, Yoshihiro Kawaoka1,4,6.
Abstract
Antiviral compounds (eg, the neuraminidase inhibitor oseltamivir) are invaluable for the treatment of individuals infected with influenza A viruses of the H7N9 subtype (A[H7N9]), which have infected and killed hundreds of persons. However, oseltamivir treatment often leads to the emergence of resistant viruses in immunocompromised individuals. To better understand the emergence and properties of oseltamivir-resistant A(H7N9) viruses in immunosuppressed individuals, we infected immunosuppressed cynomolgus macaques with an A(H7N9) virus and treated them with oseltamivir. Disease severity and mortality were higher in immunosuppressed than in immunocompetent animals. Oseltamivir treatment at 2 different doses reduced A(H7N9) viral titers in infected animals, but even high-dose oseltamivir did not block viral replication sufficiently to suppress the emergence of resistant variants. Some resistant variants were not appreciably attenuated in cultured cells, but an oseltamivir-resistant A(H7N9) virus did not transmit among ferrets. These findings are useful for the control of A(H7N9) virus infections in clinical settings.Entities:
Keywords: Influenza virus; immunosuppression; nonhuman primates; oseltamivir resistance
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Year: 2017 PMID: 28931216 DOI: 10.1093/infdis/jix296
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226