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流感病毒对神经氨酸酶抑制剂的耐药性。

Influenza virus resistance to neuraminidase inhibitors.

机构信息

Research Center in Infectious Diseases of the CHUQ-CHUL and Laval University, Québec City, Québec, Canada.

出版信息

Antiviral Res. 2013 May;98(2):174-85. doi: 10.1016/j.antiviral.2013.03.014. Epub 2013 Mar 22.

Abstract

In addition to immunization programs, antiviral agents can play a major role for the control of seasonal influenza epidemics and may also provide prophylactic and therapeutic benefits during an eventual pandemic. The purpose of this article is to review the mechanism of action, pharmacokinetics and clinical indications of neuraminidase inhibitors (NAIs) with an emphasis on the emergence of antiviral drug resistance. There are two approved NAIs compounds in US: inhaled zanamivir and oral oseltamivir, which have been commercially available since 1999-2000. In addition, two other NAIs, peramivir (an intravenous cyclopentane derivative) and laninamivir (a long-acting NAI administered by a single nasal inhalation) have been approved in certain countries and are under clinical evaluations in others. As for other antivirals, the development and dissemination of drug resistance is a significant threat to the clinical utility of NAIs. The emergence and worldwide spread of oseltamivir-resistant seasonal A(H1N1) viruses during the 2007-2009 seasons emphasize the need for continuous monitoring of antiviral drug susceptibilities. Further research priorities should include a better understanding of the mechanisms of resistance to existing antivirals, the development of novel compounds which target viral or host proteins and the evaluation of combination therapies for improved treatment of severe influenza infections, particularly in immunocompromised individuals. This article forms part of a symposium in Antiviral Research on "Treatment of influenza: targeting the virus or the host."

摘要

除了免疫接种计划外,抗病毒药物在控制季节性流感流行方面可发挥重要作用,在最终发生大流行期间,也可能具有预防和治疗益处。本文的目的是综述神经氨酸酶抑制剂(NAI)的作用机制、药代动力学和临床适应证,重点关注抗病毒药物耐药性的出现。美国有两种批准的 NAI 化合物:吸入扎那米韦和口服奥司他韦,自 1999-2000 年以来已商业化。此外,还有两种其他 NAI,帕拉米韦(静脉内环戊烷衍生物)和拉尼米韦(通过单次鼻内吸入给予的长效 NAI)已在某些国家获得批准,并在其他国家进行临床评估。至于其他抗病毒药物,耐药性的发展和传播是对 NAI 临床应用的重大威胁。在 2007-2009 年季节期间,耐奥司他韦的季节性 A(H1N1)病毒的出现和在全球范围内的传播强调了需要持续监测抗病毒药物敏感性。进一步的研究重点应包括更好地了解对现有抗病毒药物的耐药机制,开发针对病毒或宿主蛋白的新型化合物,以及评估联合疗法以改善对严重流感感染的治疗,特别是在免疫功能低下的个体中。本文是抗病毒研究中“流感治疗:针对病毒还是宿主”专题研讨会的一部分。

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