Department of Infection, The Royal London Hospital, Barts Health NHS Trust, London, UK.
Eur J Clin Microbiol Infect Dis. 2020 Jul;39(7):1201-1208. doi: 10.1007/s10096-020-03840-9. Epub 2020 Feb 13.
Influenza affects approximately 1 billion individuals each year resulting in between 290,000 and 650,000 deaths. Young children and immunocompromised individuals are at a particularly high risk of severe illness attributable to influenza and these are also the groups of individuals in which reduced susceptibility to neuraminidase inhibitors is most frequently seen. High levels of resistance emerged with previous adamantane therapy for influenza A and despite no longer being used to treat influenza and therefore lack of selection pressure, high levels of adamantane resistance continue to persist in currently circulating influenza A strains. Resistance to neuraminidase inhibitors has remained at low levels to date and the majority of resistance is seen in influenza A H1N1 pdm09 infected immunocompromised individuals receiving oseltamivir but is also seen less frequently with influenza A H3N2 and B. Rarely, resistance is also seen in the immunocompetent. There is evidence to suggest that these resistant strains (particularly H1N1 pdm09) are able to maintain their replicative fitness and transmissibility, although there is no clear evidence that being infected with a resistant strain is associated with a worse clinical outcome. Should neuraminidase inhibitor resistance become more problematic in the future, there are a small number of alternative novel agents within the anti-influenza armoury with different mechanisms of action to neuraminidase inhibitors and therefore potentially effective against neuraminidase inhibitor resistant strains. Limited data from use of novel agents such as baloxavir marboxil and favipiravir, does however show that resistance variants can also emerge in the presence of these drugs.
流感每年影响约 10 亿人,导致 29 万至 65 万人死亡。儿童和免疫功能低下者患流感后发生严重疾病的风险特别高,而这些人群也是对神经氨酸酶抑制剂的敏感性降低最常见的人群。甲型流感之前使用金刚烷胺治疗后出现了高水平的耐药性,尽管不再用于治疗流感,因此缺乏选择压力,但目前仍在流行的甲型流感病毒株中继续存在高水平的金刚烷胺耐药性。到目前为止,神经氨酸酶抑制剂的耐药性仍处于低水平,大多数耐药性见于接受奥司他韦治疗的甲型 H1N1 pdm09 感染免疫功能低下者,但在甲型 H3N2 和乙型流感中也较少见。在免疫功能正常者中也很少见耐药性。有证据表明,这些耐药株(特别是 H1N1 pdm09)能够保持其复制适应性和传染性,尽管没有明确证据表明感染耐药株与临床结局较差有关。如果神经氨酸酶抑制剂的耐药性在未来变得更加成问题,那么在抗流感武器库中还有少数其他新型药物,这些药物具有与神经氨酸酶抑制剂不同的作用机制,因此可能对神经氨酸酶抑制剂耐药株有效。然而,新型药物(如巴洛沙韦马罗匹韦和法维拉韦)的使用数据有限,表明在这些药物存在的情况下也会出现耐药变异体。