首页> 外文期刊>Antimicrobial agents and chemotherapy. >Therapeutic activity of intramuscular peramivir in mice infected with a recombinant influenza A/WSN/33 (H1N1) virus containing the H275Y neuraminidase mutation
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Therapeutic activity of intramuscular peramivir in mice infected with a recombinant influenza A/WSN/33 (H1N1) virus containing the H275Y neuraminidase mutation

机译:肌内帕拉米韦对含有H275Y神经氨酸酶突变的重组A / WSN / 33(H1N1)流感病毒感染的小鼠的治疗活性

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The therapeutic activity of intramuscular (IM) peramivir was evaluated in mice infected with a recombinant influenza A/WSN/33 virus containing the H275Y neuraminidase (NA) mutation known to confer oseltamivir resistance. Regimens consisted of single (90 mg/kg of body weight) or multiple (45 mg/kg daily for 5 days) IM peramivir doses that were initiated 24 h or 48 h postinfection (p.i.). An oral oseltamivir regimen (1 or 10 mg/kg daily for 5 days) was used for comparison. Untreated animals had a mortality rate of 75% and showed a mean weight loss of 16.9% on day 5 p.i. When started at 24 h p.i., both peramivir regimens prevented mortality and significantly reduced weight loss (P<0.001) and lung viral titers (LVT) (P<0.001). A high dose (10 mg/kg) of oseltamivir initiated at 24 h p.i. also prevented mortality and significantly decreased weight loss (P<0.05) and LVT (P<0.001) compared to the untreated group results. In contrast, a low dose (1 mg/kg) of oseltamivir did not show any benefits. When started at 48 h p.i., both peramivir regimens prevented mortality and significantly reduced weight loss (P<0.01) and LVT (P<0.001) whereas low-dose or high-dose oseltamivir regimens had no effect on mortality rates, body weight loss, and LVT. Our results show that single-dose and multiple-dose IM peramivir regimens retain clinical and virological activities against the A/H1N1 H275Y variant despite some reduction in susceptibility when assessed in vitro using enzymatic assays. IM peramivir could constitute an alternative for treatment of oseltamivir-resistant A/H1N1 infections, although additional studies are warranted to support such a recommendation.
机译:在感染重组流感A / WSN / 33病毒的小鼠中评估了肌内(IM)帕拉米韦的治疗活性,该重组流感病毒包含已知赋予奥司他韦耐药性的H275Y神经氨酸酶(NA)突变。方案包括单一(90毫克/千克体重)或多次(每天45毫克/千克体重,连续5天)IM帕拉米韦剂量,这些剂量在感染后24小时或48小时开始服用(p.i.)。口服奥司他韦方案(每天1或10 mg / kg,共5天)用于比较。未经治疗的动物的死亡率为75%,在p.i的第5天平均体重减轻了16.9%。在每天24小时开始时,两种帕拉米韦治疗方案均能防止死亡,并显着降低体重减轻(P <0.001)和肺病毒滴度(LVT)(P <0.001)。大剂量(10 mg / kg)的奥司他韦在p.i 24 h开始服用。与未治疗组相比,该药还可以预防死亡率并显着降低体重减轻(P <0.05)和LVT(P <0.001)。相反,低剂量的奥司他韦(1 mg / kg)没有显示任何益处。在pi 48小时开始时,两种peramivir方案均能预防死亡率并显着降低体重减轻(P <0.01)和LVT(P <0.001),而小剂量或大剂量的oseltamivir方案对死亡率,体重减轻,和LVT。我们的结果表明,单剂量和多剂量IM帕拉米韦方案在使用酶法体外评估时,尽管敏感性有所降低,但仍保留了针对A / H1N1 H275Y变体的临床和病毒学活性。 IM Peramivir可能是治疗耐奥司他韦A / H1N1感染的替代药物,尽管有必要进行更多研究以支持这一建议。

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