Effect of zidovudine resistance mutations on virologic response to treatment with zidovudine-lamivudine-ritonavir: Genotypic analysis of human immunodeficiency virus type 1 isolates from AIDS Clinical Trials Group protocol 315

被引:37
作者
Kuritzkes, DR
Sevin, A
Young, B
Bakhtiari, M
Wu, HL
St Clair, M
Connick, E
Landay, A
Spritzler, J
Kessler, H
Lederman, MM
机构
[1] Univ Colorado, Hlth Sci Ctr, Div Infect Dis, Denver, CO 80262 USA
[2] Vet Affairs Med Ctr, Denver, CO USA
[3] Harvard Univ, Sch Publ Hlth, Ctr Biostat & AIDS Res, Boston, MA 02115 USA
[4] Glaxo Wellcome Inc, Res Triangle Pk, NC 27709 USA
[5] Rush Presbyterian St Lukes Med Ctr, Dept Med, Chicago, IL 60612 USA
[6] Rush Presbyterian St Lukes Med Ctr, Dept Immunol Microbiol, Chicago, IL 60612 USA
[7] Case Western Reserve Univ, Cleveland, OH 44106 USA
关键词
D O I
10.1086/315244
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The effect of baseline drug resistance mutations on response to zidovudine, lamivudine, and ritonavir was evaluated in zidovudine-experienced persons infected with human immunodeficiency virus type 1 (HIV-1), Presence of the K70R mutation was associated with significantly higher plasma HIV-1 RNA levels at baseline. However, presence of resistance mutations did not affect the increase in plasma HIV-1 RNA during a 5-week drug washout, nor was there any effect on first-phase virus decay rates after initiation of therapy or on the probability of having plasma HIV-1 RNA levels <100 copies/mL at week 48, Polymorphisms at protease codons 10, 36, and 71 were associated with significantly faster second-phase decay rates. Suppression of plasma HIV-1 RNA despite presence of zidovudine resistance mutations implies that the presence of these mutations does not preclude a durable response to treatment with a potent 3-drug regimen.
引用
收藏
页码:491 / 497
页数:7
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