Production of resistant HIV mutants during antiretroviral therapy

被引:152
作者
Ribeiro, RM
Bonhoeffer, S [1 ]
机构
[1] Friedrich Miescher Inst, POB 2543, CH-4002 Basel, Switzerland
[2] Univ Oxford, Dept Zool, Wellcome Trust Ctr Epidemiol Infect Dis, Oxford OX1 3PS, England
关键词
D O I
10.1073/pnas.97.14.7681
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
HIV drug therapy often fails because of the appearance of multidrug-resistant virus. There are two possible scenarios for the outgrowth of multidrug-resistant virus in response to therapy, Resistant virus may preexist at low frequencies in drug-naive patients and is rapidly selected in the presence of drugs. Alternatively, resistant virus is absent at the start of therapy but is generated by residual viral replication during therapy. Currently available experimental methods are generally too insensitive to distinguish between these two scenarios, Here we use deterministic and stochastic models to investigate the origin of multidrug resistance. We quantify the probabilities that resistant mutants preexist, and that resistant mutants are generated during therapy. The models suggest that under a wide range of conditions, treatment failure is most likely caused by the preexistence of resistant mutants.
引用
收藏
页码:7681 / 7686
页数:6
相关论文
共 37 条
[1]  
ANDERSON R M, 1991
[2]  
[Anonymous], 1980, TABLES INTEGRALS SER
[3]   Variations in HIV-1 pol gene associated with reduced sensitivity to antiretroviral drugs in treatment-naive patients [J].
Birk, M ;
Sönnerborg, A .
AIDS, 1998, 12 (18) :2369-2375
[4]   Virus dynamics and drug therapy [J].
Bonhoeffer, S ;
May, RM ;
Shaw, GM ;
Nowak, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) :6971-6976
[5]  
Bonhoeffer S, 1997, P ROY SOC B-BIOL SCI, V264, P631
[6]   Models of viral kinetics and drug resistance in HIV-1 infection [J].
Bonhoeffer, S .
AIDS PATIENT CARE AND STDS, 1998, 12 (10) :769-774
[7]   Report of the NIH Panel to Define Principles of Therapy of HIV Infection [J].
Carpenter, C ;
Feinberg, M ;
Aubry, W ;
Averitt, D ;
Coffin, J ;
Cooper, D ;
Follansbee, S ;
Hamburg, P ;
Harrington, M ;
Hidalgo, J ;
Jaffe, H ;
Landers, D ;
Masur, H ;
Pizzo, P ;
Richman, D ;
Saag, M ;
Schooley, R ;
Stone, V ;
Thompson, M ;
Trono, D ;
Vella, S ;
Walker, B ;
Yeni, P .
ANNALS OF INTERNAL MEDICINE, 1998, 128 (12) :1057-1078
[8]   Antiretroviral therapy for HIV infection in 1997 - Updated recommendations of the International AIDS Society USA panel [J].
Carpenter, CCJ ;
Fischl, MA ;
Hammer, SM ;
Hirsch, MS ;
Jacobsen, DM ;
Katzenstein, DA ;
Montaner, JSG ;
Richman, DD ;
Saag, MS ;
Schooley, RT ;
Thompson, MA ;
Vella, S ;
Yeni, PG ;
Volberding, PA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (24) :1962-1969
[9]   Target cell limited and immune control models of HIV infection: A comparison [J].
De Boer, RJ ;
Perelson, AS .
JOURNAL OF THEORETICAL BIOLOGY, 1998, 190 (03) :201-214
[10]   Anti-CD4 therapy for AIDS suggested by mathematical models [J].
DeBoer, RJ ;
Boucher, CAB .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1996, 263 (1372) :899-905