Antiviral resistance and the control of pandemic influenza

被引:155
作者
Lipsitch, Marc [1 ]
Cohen, Ted
Murray, Megan
Levin, Bruce R.
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Div Social Med & Hlth Inequal, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Div Infect Dis & Gen Med, Boston, MA 02114 USA
[5] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
关键词
D O I
10.1371/journal.pmed.0040015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The response to the next influenza pandemic will likely include extensive use of antiviral drugs (mainly oseltamivir), combined with other transmission-reducing measures. Animal and in vitro studies suggest that some strains of influenza may become resistant to oseltamivir while maintaining infectiousness (fitness). Use of antiviral agents on the scale anticipated for the control of pandemic influenza will create an unprecedented selective pressure for the emergence and spread of these strains. Nonetheless, antiviral resistance has received little attention when evaluating these plans. Methods and Findings: We designed and analyzed a deterministic compartmental model of the transmission of oseltamivir-sensitive and -resistant influenza infections during a pandemic. The model predicts that even if antiviral treatment or prophylaxis leads to the emergence of a transmissible resistant strain in as few as 1 in 50,000 treated persons and 1 in 500,000 prophylaxed persons, widespread use of antivirals may strongly promote the spread of resistant strains at the population level, leading to a prevalence of tens of percent by the end of a pandemic. On the other hand, even in circumstances in which a resistant strain spreads widely, the use of antivirals may significantly delay and/or reduce the total size of the pandemic. If resistant strains carry some fitness cost, then, despite widespread emergence of resistance, antivirals could slow pandemic spread by months or more, and buy time for vaccine development; this delay would be prolonged by nondrug control measures (e.g., social distancing) that reduce transmission, or use of a stockpiled suboptimal vaccine. Surprisingly, the model suggests that such nondrug control measures would increase the proportion of the epidemic caused by resistant strains. Conclusions: The benefits of antiviral drug use to control an influenza pandemic may be reduced, although not completely offset, by drug resistance in the virus. Therefore, the risk of resistance should be considered in pandemic planning and monitored closely during a pandemic.
引用
收藏
页码:111 / 121
页数:11
相关论文
共 42 条
[1]  
ANDERSON R M, 1991
[2]   The biological cost of antibiotic resistance [J].
Andersson, DI ;
Levin, BR .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (05) :489-493
[3]  
Balcells ME, 2006, EMERG INFECT DIS, V12, P744
[4]   BIOLOGIC POTENTIAL OF AMANTADINE-RESISTANT INFLUENZA-A VIRUS IN AN AVIAN MODEL [J].
BEAN, WJ ;
THRELKELD, SC ;
WEBSTER, RG .
JOURNAL OF INFECTIOUS DISEASES, 1989, 159 (06) :1050-1056
[5]   Evaluating treatment protocols to prevent antibiotic resistance [J].
Bonhoeffer, S ;
Lipsitch, M ;
Levin, BR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (22) :12106-12111
[6]   Resistance of human immunodeficiency virus type 1 to protease inhibitors: Selection of resistance mutations in the presence and absence of the drug [J].
Borman, AM ;
Paulous, S ;
Clavel, F .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :419-426
[7]   Adamantane resistance among influenza A viruses isolated early during the 2005-2006 influenza season in the United States [J].
Bright, RA ;
Shay, DK ;
Shu, B ;
Cox, NJ ;
Klimov, AI .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (08) :891-894
[8]   Distribution of amantadine-resistant H5N1 avian influenza variants in Asia [J].
Cheung, Chung-Lam ;
Rayner, Jane M. ;
Smith, Gavin J. D. ;
Wang, Pui ;
Naipospos, T. S. P. ;
Zhang, Jinxia ;
Yuen, Kwok-Yung ;
Webster, Robert G. ;
Peiris, J. S. Malik ;
Guan, Yi ;
Chen, Honglin .
JOURNAL OF INFECTIOUS DISEASES, 2006, 193 (12) :1626-1629
[9]   Seasonal intermittent preventive treatment with artesunate and sulfadoxine-pyrimethamine for prevention of malaria in Senegalese children:: a randomised, placebo-controlled, double-blind trial [J].
Cissé, B ;
Sokhna, C ;
Boulanger, D ;
Milet, J ;
Bâ, EH ;
Richardson, K ;
Hallett, R ;
Sutherland, C ;
Simondon, K ;
Simondon, F ;
Alexander, N ;
Gaye, O ;
Targett, G ;
Lines, J ;
Greenwood, B ;
Trape, JF .
LANCET, 2006, 367 (9511) :659-667
[10]   Beneficial and perverse effects of isoniazid preventive therapy for latent tuberculosis infection in HIV-tuberculosis coinfected populations [J].
Cohen, T ;
Lipsitch, M ;
Walensky, RP ;
Murray, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (18) :7042-7047