Rath Barbara, Chen Xi, Spies Vera, Muehlhans Susann, Obermeier Patrick, Tief Franziska, Seeber Lea, Karsch Katharina, Milde Jeanette, Skopnik Heino, Schweiger Brunhilde, Duwe Susanne C
Charité University Medical Center, Department of Pediatrics, Berlin, Germany.
Vienna Vaccine Safety Initiative, Berlin, Germany.
Antivir Ther. 2017;22(6):515-522. doi: 10.3851/IMP3141. Epub 2017 Feb 16.
Infants exhibit elevated influenza virus loads and prolonged viral shedding, which may increase the risk for resistance development, especially in cases of suboptimal exposure to antiviral therapy.
We performed a prospective surveillance of hospitalized infants undergoing oseltamivir therapy during the 2008-2009 and 2011-2012 influenza seasons at two paediatric hospitals in Germany. A total of 37 infants less than 1 year of age with laboratory confirmed influenza A(H3N2) infection received oseltamivir as per physician's order for 5 days (2008-2009 season: 2 mg/kg twice daily; 2011-2012 season: 2.0 mg/kg; 2.5 mg/kg and 3.0 mg/kg twice daily for infants <1 month; 2-3 months and 4-12 months, respectively). Virus load, the susceptibility to neuraminidase inhibitors (NAIs), and the presence of molecular markers of resistance to NAIs was assessed for influenza viruses recovered from respiratory samples collected at baseline and during follow-up visits.
Overall, 73% of the infants continued to shed viral RNA detectable by reverse transcription (RT)-PCR after dose number 10 of oseltamivir; 12 infants shed viruses, 2 of them (both 9 months of age) shed resistant viruses. Resistance was characterized by ≥1,000-fold increase of 50% inhibitory concentration (IC) for oseltamivir, up to 50-fold for zanamivir and elevated Km values when compared to susceptible A(H3N2) strains. Sanger sequencing revealed the selection of the NA-R292K substitution in both instances (after dose number 10 on day 6).
Our data suggest that it may be relevant to monitor antiviral resistance systematically in all infants, considering that the European Medicines Agency has recently extended the licensure for oseltamivir to include full-term infants.
婴儿表现出较高的流感病毒载量和较长的病毒排泄期,这可能会增加产生耐药性的风险,尤其是在抗病毒治疗暴露不足的情况下。
我们对2008 - 2009年和2011 - 2012年流感季节期间在德国两家儿童医院接受奥司他韦治疗的住院婴儿进行了前瞻性监测。共有37名1岁以下实验室确诊为甲型(H3N2)流感感染的婴儿按照医生的医嘱接受了5天的奥司他韦治疗(2008 - 2009年季节:每日两次,每次2毫克/千克;2011 - 2012年季节:1个月以下婴儿每日两次,每次2.0毫克/千克;2 - 3个月婴儿每日两次,每次2.5毫克/千克;4 - 12个月婴儿每日两次,每次3.0毫克/千克)。对从基线和随访期间采集的呼吸道样本中分离出的流感病毒,评估其病毒载量、对神经氨酸酶抑制剂(NAIs)的敏感性以及对NAIs耐药的分子标志物的存在情况。
总体而言,73%的婴儿在接受第10剂奥司他韦治疗后,通过逆转录(RT)-PCR仍可检测到病毒RNA;12名婴儿排出病毒,其中2名(均为9个月大)排出耐药病毒。与敏感的甲型(H3N2)毒株相比,耐药性表现为奥司他韦的50%抑制浓度(IC)增加≥1000倍,扎那米韦增加至50倍,且米氏常数(Km)值升高。桑格测序显示在这两例中(第6天第10剂后)均出现了NA-R292K替代的选择。
我们的数据表明,鉴于欧洲药品管理局最近已将奥司他韦的许可范围扩大至包括足月儿,在所有婴儿中系统监测抗病毒耐药性可能具有重要意义。