Influenza virus resistance to neuraminidase inhibitors

被引:360
作者
Samson, Melanie
Pizzorno, Andres
Abed, Yacine
Boivin, Guy
机构
[1] CHUQ CHUL, Res Ctr Infect Dis, Quebec City, PQ, Canada
[2] Univ Laval, Quebec City, PQ, Canada
关键词
Influenza; Antivirals; Resistance; Neuraminidase inhibitors; Oseltamivir; Zanamivir; PANDEMIC H1N1 2009; OSELTAMIVIR-RESISTANT; A VIRUS; B VIRUS; ZANAMIVIR RESISTANCE; ACTIVE-SITE; IN-VITRO; IMMUNOCOMPROMISED PATIENTS; CLINICAL PHARMACOKINETICS; REDUCED SUSCEPTIBILITY;
D O I
10.1016/j.antiviral.2013.03.014
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
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." (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:174 / 185
页数:12
相关论文
共 149 条
[1]
Abed Y, 2004, ANTIVIR THER, V9, P577
[2]
Characterization of 2 influenza A(H3N2) clinical isolates with reduced susceptibility to neuraminidase inhibitors due to mutations in the hemagglutinin gene [J].
Abed, Y ;
Bourgault, AM ;
Fenton, RJ ;
Morley, PJ ;
Gower, D ;
Owens, IJ ;
Tisdale, M ;
Boivin, G .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (08) :1074-1080
[3]
Activity of the neuraminidase inhibitor A-315675 against oseltamivir-resistant influenza neuraminidases of N1 and N2 subtypes [J].
Abed, Yacine ;
Nehme, Benjamin ;
Baz, Mariana ;
Boivin, Guy .
ANTIVIRAL RESEARCH, 2008, 77 (02) :163-166
[4]
Abed Y, 2006, ANTIVIR THER, V11, P971
[5]
Role of Permissive Neuraminidase Mutations in Influenza A/Brisbane/59/2007-like (H1N1) Viruses [J].
Abed, Yacine ;
Pizzorno, Andres ;
Bouhy, Xavier ;
Boivin, Guy .
PLOS PATHOGENS, 2011, 7 (12)
[6]
Parenteral Peramivir Treatment for Oseltamivir-Resistant 2009 Pandemic Influenza A H1N1 Viruses [J].
Abed, Yacine ;
Boivin, Guy ;
Yoshida, Ryu ;
Kodama, Makoto ;
Hernandez, Jaime E. .
JOURNAL OF INFECTIOUS DISEASES, 2011, 204 (10) :1641-1642
[7]
A Novel Neuraminidase Deletion Mutation Conferring Resistance to Oseltamivir in Clinical Influenza A/H3N2 Virus [J].
Abed, Yacine ;
Baz, Mariana ;
Boivin, Guy .
JOURNAL OF INFECTIOUS DISEASES, 2009, 199 (02) :180-183
[8]
[Anonymous], 49 INT C ANT AG CHEM
[9]
Aoki FY, 2007, ANTIVIR THER, V12, P603
[10]
BCX-1812 (RWJ-270201): Discovery of a novel, highly potent, orally active, and selective influenza neuraminidase inhibitor through structure-based drug design [J].
Babu, YS ;
Chand, P ;
Bantia, S ;
Kotian, P ;
Dehghani, A ;
El-Kattan, Y ;
Lin, TH ;
Hutchison, TL ;
Elliott, AJ ;
Parker, CD ;
Ananth, SL ;
Horn, LL ;
Laver, GW ;
Montgomery, JA .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (19) :3482-3486